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Research > Chapter 11029
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Mutants defective in secretory/vacuolar pathways in the EUROPEAN collection of yeast disruptants
Mutants for biochemical and molecular insights into embryogenesis in plants
Mutants in flaI and flaJ of the archaeon Methanococcus voltae are deficient in flagellum assembly
Mutants in the ptlA-H genes of Bordetella pertussis are deficient for pertussis toxin secretion
Mutants obtained by chronic gamma irradiation from a Carpathian-Ukrainian local soybean (Glycine max (L.) Merrill) variety: I. M3 and M4 generations
Mutants obtained by chronical gamma irradiation from a Karpatalja local soybean variety: II. M4 and M5 generations
Mutants of Arabidopsis thaliana defective in the acquisition of tolerance to high temperature stress
Mutants of Chlamydomonas reinhardtii resistant to very high light
Mutants of Chlamydomonas: Tools to study thylakoid membrane structure, function and biogenesis
Mutants of Discosoma red fluorescent protein with a GFP-like chromophore
Mutants of Escherichia coli heat-labile toxin act as effective mucosal adjuvants for nasal delivery of an acellular pertussis vaccine: Differential effects of the nontoxic AB complex and enzyme activity on Th1 and Th2 cells
Mutants of Kluyveromyces lactis with altered protein glycosylation are affected in cell wall morphogenesis
Mutants of Listeria monocytogenes defective in in vitro invasion and cell-to-cell spreading still invade and proliferate in hepatocytes of neutropenic mice
Mutants of Tobacco mosaic virus with temperature-sensitive coat proteins induce heat shock response in tobacco leaves
Mutants of Xanthomonas oryzae pv. oryzae deficient in general secretory pathway are virulence deficient and unable to secrete xylanase
Mutants of cholera toxin as an effective and safe adjuvant for nasal influenza vaccine
Mutants of cyanobacterium Synechocystis sp. PCC6803 with insertional inactivation of the sodB gene encoding Fe-superoxide dismutase
Mutants of immunotoxin anti-Tac(dsFv)-PE38 with variable number of lysine residues as candidates for site-specific chemical modification. 1. Properties of mutant molecules
Mutants of p53 gene presence in laryngeal carcinoma and adjacent histopathologically normal tissue
Mutants of phosphorylase a altered in recognition by protein phosphatase-1
Mutants of phycomyces with decreased gallic acid content
Mutants of protein kinase A that mimic the ATP-binding site of protein kinase B (AKT)
Mutants of the CuA site in cytochrome c oxidase of Rhodobacter sphaeroides: I. Spectral and functional properties
Mutants of the CuA site in cytochrome c oxidase of Rhodobacter sphaeroides: II. Rapid kinetic analysis of electron transfer
Mutants of the major ryegrass pollen allergen, Lol p 5, with reduced IgE-binding capacity: Candidates for grass pollen-specific immunotherapy
Mutatect: A mouse tumour model for detecting radiation-induced mutations in vivo
Mutated APC and Asef are involved in the migration of colorectal tumour cells
Mutated N-ras upregulates Bcl-2 in human melanoma in vitro and in SCID mice
Mutated alleles of the rod and cone Na-Ca+K-exchanger genes in patients with retinal diseases
Mutated alpha-synuclein gene in two Greek kindreds with familial PD: Incomplete penetrance?
Mutated cytochrome b as a determinant of a new monoclonal antibody (H8.98) on renal carcinoma cell lines recognized by a Vgamma3Vdelta1+ T-cell clone
Mutated focal adhesion kinase induces apoptosis in a human glioma cell line, T98G
Mutated gene-specific phenotypes of dinucleotide repeat instability in human colorectal carcinoma cell lines deficient in DNA mismatch repair
Mutated human beta3-adrenergic receptor (Trp64Arg) lowers the response to beta3-adrenergic agonists in transfected 3T3-L1 preadipocytes
Mutated nicotinic receptors responsible for autosomal dominant nocturnal frontal lobe epilepsy are more sensitive to carbamazepine
Mutated p53 as a molecular marker for the diagnosis of head and neck cancer
Mutated ras p21 as a target for cancer therapy in mouse transitional cell carcinoma
Mutated tau binds less avidly to microtubules than wildtype tau in living cells
Mutated-gamma-actin restores growth to a yeast amino acid transport defective mutant
Mutating a critical lysine in ShK toxin alters its binding configuration in the pore-vestibule region of the voltage-gated potassium channel, Kv1.3
Mutating aspartate in the calcium-binding site of alpha-lactalbumin: Effects on the protein stability and cation binding
Mutating the four extracellular cysteines in the chemokine receptor CCR6 reveals their differing roles in receptor trafficking, ligand binding, and signaling
Mutation MELAS (A3243G) de l'ADN mitochondrial: Etude chez 19 patients des relations entre le phenotype clinique, les donnees morphologiques et moleculaires
Mutation hot spot in HLA class I-restricted T cell epitope on hepatitis B surface antigen in chronic carriers and hepatocellular carcinoma
Mutation (Ser284Leu) of neuronal nicotinic acetylcholine receptor alpha4 subunit associated with frontal lobe epilepsy causes faster desensitization of the rat receptor expressed in oocytes
Mutation A1298C of methylenetetrahydrofolate reductase: Risk for early coronary disease not associated with hyperhomocysteinemia
Mutation Arg336 to Lys in Saccharomyces cerevisiae phosphoenolpyruvate carboxykinase originates an enzyme with increased oxaloacetate decarboxylase activity
Mutation BRCA1 gene in 186 breast cancer patients
Mutation C677T of methylenetetrahydrofolate reductase gene is not associated with coronary artery disease, but possibly with albuminuria, in type 2 diabetic patients
Mutation Detection 2001: Sixth International Symposium on Mutations in the Human Genome, May 3-7, 2001, Bled, Slovenia
Mutation L210W of HIV-1 reverse transcriptase in patients receiving combination therapy: Incidence, association with other mutations, and effects on the structure of mutated reverse transcriptase
Mutation S543N in the thumb subdomain of the Taq DNA polymerase large fragment suppresses pausing associated with the template structure
Mutation W284L of the human delta opioid receptor reveals agonist specific receptor conformations for G protein activation
Mutation analyses of 268 candidate genes in human tumor cell lines
Mutation analyses of North American APS-1 patients
Mutation analyses of a series of TNT-related compounds using the CHO-hprt assay
Mutation analyses of the NFAT1 gene in chondrosarcomas and enchondromas
Mutation analysis and association studies of the UCHL1 gene in German Parkinson's disease patients
Mutation analysis and association studies of the ubiquitin carboxy-terminal hydrolase L1 gene in Huntington's disease
Mutation analysis and bacterial expression of the chimerical oncoprotein Bcr/Abl Dbl-homology domain
Mutation analysis and clinical implications of von Willebrand factor-cleaving protease deficiency
Mutation analysis and description of sixteen RSH/Smith-Lemli-Opitz syndrome patients: Polymerase chain reaction-based assays to simplify genotyping
Mutation analysis and mRNA expression of trail-receptors in human breast cancer
Mutation analysis and molecular genetics of epidermolysis bullosa
Mutation analysis and the correlation between genotype and phenotype of Arg778Leu mutation in Chinese patients with Wilson disease
Mutation analysis impact on the genetic counseling of sporadic hemophilia B families
Mutation analysis in PKD1 of Japanese autosomal dominant polycystic kidney disease patients
Mutation analysis in Rett syndrome
Mutation analysis in a patient with succinic semialdehyde dehydrogenase deficiency: A compound heterozygote with 103-121 del and 1460T > A of the ALDH5A1 gene
Mutation analysis in a small cohort of New Zealand patients originating from the United Kingdom demonstrates genetic heterogeneity in familial hypercholesterolemia
Mutation analysis in adenylosuccinate lyase deficiency: Eight novel mutations in the re-evaluated full ADSL coding sequence
Mutation analysis in congenital Long QT Syndrome: A case with missense mutations in KCNQ1 and SCN5A
Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationship
Mutation analysis in patients with N-acetylglutamate synthase deficiency
Mutation analysis in patients with congenital adrenal hyperplasia in the Spanish population: Identification of putative novel steroid 21-hydroxylase deficiency alleles associated with the classic form of the disease
Mutation analysis in the HFE gene in patients with hereditary haemochromatosis in Saguenay-Lac-Saint-Jean (Quebec, Canada)
Mutation analysis in the coding sequence of thymidine kinase 1 in breast and colorectal cancer
Mutation analysis in the family of a Taiwanese boy with epidermolysis bullosa simplex Dowling-Meara
Mutation analysis of 20 SARS virus genome sequences: Evidence for negative selection in replicase ORF1b and spike gene
Mutation analysis of 3 genes in patients with Leber congenital amaurosis
Mutation analysis of ATP2C1 gene in Taiwanese patients with Hailey-Hailey disease
Mutation analysis of BRCA1 and BRCA2 cancer predisposition genes in radiation hypersensitive cancer patients
Mutation analysis of BRCA1 and BRCA2 in Turkish cancer families: A novel mutation BRCA2 3414del4 found in male breast cancer
Mutation analysis of BRCA1 gene in African-American patients with breast cancer
Mutation analysis of BRCA1, TP53, and KRAS2 in ovarian and related pelvic tumors
Mutation analysis of BrCA1, BrCA2, and p53 versus soluble HLA class I and class II in a case of familial endometriosis
Mutation analysis of C-KIT in patients with myelodysplastic syndromes without mastocytosis and cases of systemic mastocytosis
Mutation analysis of CBP and PCAF reveals rare inactivating mutations in cancer cell lines but not in primary tumours
Mutation analysis of CDP, TP53, and KRAS in uterine leiomyomas
Mutation analysis of CFTR gene by DGGE method in CF patients from West Ukraine
Mutation analysis of CTNNB1 (beta-catenin) and AXIN1, the components of Wnt pathway, in cervical carcinomas
Mutation analysis of Connexin 31 (GJB3) in sporadic non-syndromic hearing impairment
Mutation analysis of Crouzon syndrome and identification of one novel mutation in Taiwanese patients
Mutation analysis of DMBT1 in glioblastoma, medulloblastoma and oligodendroglial tumors
Mutation analysis of EP300 in colon, breast and ovarian carcinomas
Mutation analysis of Gaucher disease patients from Argentina: High prevalence of the RecNciI mutation
Mutation analysis of Gsalpha, adrenocorticotropin receptor and p53 genes in Japanese patients with adrenocortical neoplasms: Including a case of Gsalpha mutation
Mutation analysis of K-ras and beta-catenin genes related to O6-methylguanin-DNA methyltransferase and mismatch repair protein status in human gallbladder carcinoma
Mutation analysis of K-ras-2 in liver angiosarcoma and adjacent nonneoplastic liver tissue from patients occupationally exposed to vinyl chloride
Mutation analysis of MECP2 and clinical characterization in Korean patients with Rett syndrome
Mutation analysis of MLH1 and MSH2 genes performed by denaturing high-performance liquid chromatography
Mutation analysis of NTRK2 and NTRK3, encoding 2 tyrosine kinase receptors, in sporadic human medullary thyroid carcinoma reveals novel sequence variants
Mutation analysis of P73 and TP53 in Merkel cell carcinoma
Mutation analysis of PEX7 in 60 probands with rhizomelic chondrodysplasia punctata and functional correlations of genotype with phenotype
Mutation analysis of PTEN/MMAC 1 in sporadic thyroid tumors
Mutation analysis of PTEN/MMAC1 in acute myeloid leukemia
Mutation analysis of SLC7A9 in cystinuria patients in Sweden
Mutation analysis of SYNJ1: A possible candidate gene for chromosome 21q22-linked bipolar disorder
Mutation analysis of TP53 exons 5-8 by automated constant denaturant capillary electrophoresis
Mutation analysis of Wilson disease in Taiwan and description of six new mutations
Mutation analysis of a Mauritian hereditary breast cancer family reveals the BRCA2 6503deITT mutation previously found to recur in different ethnic populations
Mutation analysis of a family with hereditary hemorrhagic telangiectasia associated with hepatic arteriovenous malformation
Mutation analysis of a putative sialyltransferase gene, the SFRS2 splicing factor gene and the c-myb ET-locus in two families with hereditary neuralgic amyotrophy (HNA)
Mutation analysis of cadherin-4 reveals amino acid residues of EC1 important for the structure and function
Mutation analysis of codons 345 and 347 of rhodopsin gene in Indian retinitis pigmentosa patients
Mutation analysis of copper-transporting P-type adenosine triphosphatase (ATP7B) in human solid carcinomas
Mutation analysis of exon 9 of the LDL receptor gene in Thai subjects with primary hypercholesterolemia
Mutation analysis of gaucher disease using dot-blood samples on FTA(R) filter paper
Mutation analysis of hBUB1 in aneuploid HNSCC and lung cancer cell lines
Mutation analysis of hBUB1, human mitotic checkpoint gene in multiple carcinomas
Mutation analysis of human LEFTY A and LEFTY B genes in children with Ivemark syndrome
Mutation analysis of left-right axis determining genes in NOD and ICR, strains susceptible to maternal diabetes
Mutation analysis of mitotic checkpoint genes (hBUB1 and hBUBR1) and microsatellite instability in adult T-cell leukemia/lymphoma
Mutation analysis of oculopharyngeal muscular dystrophy in Hispanic American families
Mutation analysis of p53 in ovarian tumors by DHPLC
Mutation analysis of pertussis toxin promoter
Mutation analysis of phenylketonuria in Yamagata prefecture, Japan
Mutation analysis of replicative genes encoding the large subunits of DNA polymerase alpha and replication factors A and C in human sporadic colorectal cancers
Mutation analysis of synapsin III gene in schizophrenia
Mutation analysis of the ATP2A2 gene in Taiwanese patients with Darier's disease
Mutation analysis of the BCL10 gene in childhood solid malignancies
Mutation analysis of the BRCA1 gene in Malaysian breast cancer patients
Mutation analysis of the BRG1 gene in prostate cancer clinical samples
Mutation analysis of the Bcl 10 gene in hepatocellular carcinoma
Mutation analysis of the CACNA1A calcium channel subunit gene in 27 patients with sporadic hemiplegic migraine
Mutation analysis of the CDKN2A promoter in Australian melanoma families
Mutation analysis of the CHK2 gene in families with hereditary breast cancer
Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopia
Mutation analysis of the DNA-damage checkpoint gene CHK2 in myelodysplastic syndromes and acute myeloid leukemias
Mutation analysis of the EMX2 gene in Kallmann's syndrome
Mutation analysis of the FAS and TNFR apoptotic cascade genes in hematological malignancies
Mutation analysis of the Fanconi anaemia A gene in breast tumours with loss of heterozygosity at 16q24.3
Mutation analysis of the G4.5 gene in patients with isolated left ventricular noncompaction
Mutation analysis of the GCDH gene in Italian and Portuguese patients with glutaric aciduria type I
Mutation analysis of the GJB2 (connexin 26) gene by DGGE in Greek patients with sensorineural deafness
Mutation analysis of the MCM gene in Israeli patients with mut0 disease
Mutation analysis of the MEN1 gene in Belgian patients with multiple endocrine neoplasia type 1 and related diseases
Mutation analysis of the MEN1 tumour suppressor gene in malignant melanoma
Mutation analysis of the MPZ and PMP22 genes in Croatian patients
Mutation analysis of the N-methyl-D-aspartate receptor NR1 subunit gene (GRIN1) in schizophrenia
Mutation analysis of the NMDAR2B (GRIN2B) gene in schizophrenia
Mutation analysis of the PTEN/MMAC1 gene in Japanese patients with Cowden disease
Mutation analysis of the PTEN/MMAC1 gene in cancers of the digestive tract
Mutation analysis of the RPGR gene reveals novel mutations in south European patients with X-linked retinitis pigmentosa
Mutation analysis of the STK11/LKB1 gene and clinical characteristics of an Australian series of Peutz-Jeghers syndrome patients
Mutation analysis of the Smad3 gene in human ovarian cancers
Mutation analysis of the Smad6 and Smad7 gene in human ovarian cancers
Mutation analysis of the acid beta-glucosidase gene in a patient with type 3 Gaucher disease and neutralizing antibody to alglucerase
Mutation analysis of the calpastatin gene (CAST) in patients with Alzheimer's disease
Mutation analysis of the carbohydrate sulfotransferase gene in Vietnamese with macular corneal dystrophy
Mutation analysis of the cationic trypsinogen gene in patients with pancreatic cancer
Mutation analysis of the conserved motif of the ArdA antirestriction protein encoded by self-transmissible IncI plasmid ColIb-P9
Mutation analysis of the cystic fibrosis and cationic trypsinogen genes in patients with alcohol-related pancreatitis
Mutation analysis of the entire PKD1 gene: Genetic and diagnostic implications
Mutation analysis of the feedback inhibition site of aspartokinase III of Escherichia coli K-12 and its use in L-threonine production
Mutation analysis of the feedback inhibition site of phenylalanine-sensitive 3-deoxy-D-arabino-heptulosonate 7-phosphate synthase of Escherichia coli
Mutation analysis of the growth differentiation factor-9 and -9B genes in patients with premature ovarian failure and polycystic ovary syndrome
Mutation analysis of the hMTH1 gene in sporadic human ovarian cancer
Mutation analysis of the hamartin gene using denaturing high performance liquid chromatography
Mutation analysis of the human CYP3A4 gene 5' regulatory region: Population screening using non-radioactive SSCP
Mutation analysis of the human NR4A2 gene, an essential gene for midbrain dopaminergic neurogenesis, in schizophrenic patients
Mutation analysis of the human adipocyte-specific apM-1 gene
Mutation analysis of the inhibin alpha gene in a cohort of Italian women affected by ovarian failure
Mutation analysis of the inwardly rectifying K+ channels KCNJ6 (GIRK2) and KCNJ3 (GIRK1) in juvenile myoclonic epilepsy
Mutation analysis of the methyl-CpG-binding protein 2 gene (MECP2) in Rett patients with preserved speech
Mutation analysis of the non-muscle myosin light chain kinase (MLCK) deletion constructs on CV1 fibroblast contractile activity and proliferation
Mutation analysis of the p15 gene exon 2 in human primary hepatocarcinoma
Mutation analysis of the p51 gene and correlation between p53, p73, and p51 expressions in prostatic carcinoma
Mutation analysis of the p53 tumor suppressor gene using paraffin-embedded specimens of human transitional cell carcinomas by the direct sequencing method
Mutation analysis of the p73 gene in nonastrocytic brain tumours
Mutation analysis of the pRb pathway in 2',3'-dideoxycytidine- and 1,3-butadiene-induced mouse lymphomas
Mutation analysis of the potassium chloride cotransporter KCC3 (SLC12A6) in rolandic and idiopathic generalized epilepsy
Mutation analysis of the putative tumor suppressor gene PTEN/MMAC1 in cervical cancer
Mutation analysis of the putative tumor suppressor gene PTEN/MMAC1 in hepatocellular carcinoma
Mutation analysis of the retinoid X receptor beta, nuclear-related receptor 1, and peroxisome proliferator-activated receptor alpha genes in schizophrenia and alcohol dependence: Possible haplotype association of nuclear-related receptor 1 gene to alcohol dependence
Mutation analysis of the spastin gene (SPG4) in patients in Germany with autosomal dominant hereditary spastic paraplegia
Mutation analysis of transforming growth factor beta type II receptor, Smad2, Smad3 and Smad4 in esophageal squamous cell carcinoma
Mutation analysis of transforming growth factor beta type II receptor, Smad2, and Smad4 in hepatocellular carcinoma
Mutation analysis of type II gaucher disease in five Taiwanese children: Identification of two novel mutations
Mutation analysis of vinyl carbamate or urethane induced lung tumors in rasH2 transgenic mice
Mutation and DNA modification in Salmonella exposed to N-nitrosodimethylamine under UVA- and sunlight-irradiation
Mutation and VNTR-polymorphism analysis of phenylalanine hydroxylase gene
Mutation and allelic loss of the PTEN/MMAC1 gene in primary and metastatic melanoma biopsies
Mutation and altered expression of beta-catenin during gallbladder carcinogenesis
Mutation and association analysis of the 5' region of the dopamine D3 receptor gene in schizophrenia patients: Identification of the Ala38Thr polymorphism and suggested association between DRD3 haplotypes and schizophrenia
Mutation and association analysis of the Fyn kinase gene with alcoholism and schizophrenia
Mutation and deletion analysis of GFRalpha-1, encoding the co-receptor for the GDNF/RET complex, in human brain tumours
Mutation and expression analysis of human BUB1 and BUB1B in aneuploid breast cancer cell lines
Mutation and expression analysis of the AGO gene in cancer cell lines and primary gastric carcinomas
Mutation and expression analysis of the p73 gene in prostate cancer
Mutation and expression analysis of the putative prostate tumour-supressor gene PTEN
Mutation and expression of N233C-D506C of cellulase Cel6B from Thermobifida fusca in Escherichia coli
Mutation and expression of Nkx 2-5 gene in human simple congenital heart disease
Mutation and expression of nm23 - H1 gene in bladder carcinomas
Mutation and expression of p16 in human ovarian neoplasms
Mutation and expression of the DCC gene in human lung cancer
Mutation and expression of the metastasis suppressor gene KAI1 in esophageal squamous cell carcinoma
Mutation and expression of the p27KIP1 and p57KIP2 genes in human gastric cancer
Mutation and expression of the p51 gene in human lung cancer
Mutation and expression of the p53 gene during chemical hepatocarcinogenesis in F344 rats
Mutation and fermentation studies on S. laurentii
Mutation and functional analysis of IL-13 receptors in human malignant glioma cells
Mutation and functional analysis of the Aspergillus nidulans ammonium permease MeaA and evidence for interaction with itself and MepA
Mutation and haplotype analyses in 26 Spanish Sanfilippo syndrome type A patients: Possible single origin for 1091delC mutation
Mutation and methylation analysis of the transforming growth factor beta receptor II gene in polycythaemia vera
Mutation and methylation status of p53 gene promoter in human breast tumours
Mutation and overexpression of the transgene in ethylnitrosourea-induced tumors in mice carrying a human prototype c-Ha-ras gene
Mutation and recombination variability of vaccine polioviruses isolated in Belarus (1960-1999)
Mutation and selection of tobramycins producing strains
Mutation and sexual selection: A test using barn swallows from Chernobyl
Mutation and transcription analyses of the p63 gene in cervical carcinoma
Mutation and transcription analysis of transthyretin gene in Italian families with hereditary amyloidosis: A putative novel 'hot spot' in codon 47
Mutation at active site lysine 212 to arginine uncouples the glycosylase activity from the lyase activity of human endonuclease III
Mutation at codon 130 in hepatitis B virus (HBV) core region increases markedly during acute exacerbation of hepatitis in chronic HBV carriers
Mutation at codon 210 (V210I) of the prion protein gene in a North African patient with Creutzfeldt-Jakob disease
Mutation at minisatellite locus DYF155S1: Allele length mutation rate is affected by age of progenitor
Mutation at position - 12 of intron 45 (cfwdarwt) plays a prevalent role in the partial skipping of exon 46 from the transcript of allele alphaLELY in erythroid cells
Mutation at the acidic residue-rich domain of eukaryotic initiation factor 2 (eIF2alpha)-associated glycoprotein p67 increases the protection of eIF2alpha phosphorylation during heat shock
Mutation at the putative GABAA ion-channel gate reveals changes in allosteric modulation
Mutation breeding in hexaploid triticales: Desirable mutants
Mutation breeding in sorghum in Indonesia
Mutation breeding of high colistin producing strains
Mutation bursts at the yellow locus in a natural population of Drosophila melanogaster are associated with a hobo insertion
Mutation by deletion-insertion in BRCA-1 gene in three unrelated French breast/ovarian cancer families: Possible implication of a mobile element
Mutation causing von Willebrand's Disease in Scottish Terriers
Mutation detection and mutation databases
Mutation detection by TaqMan-allele specific amplification: Application to molecular diagnosis of glycogen storage disease type Ia and medium-chain acyl-CoA dehydrogenase deficiency
Mutation detection by denaturing DNA chromatography using fluorescently labeled polymerase chain reaction products
Mutation detection by pyrosequencing: Sequencing of exons 5-8 of the p53 tumor suppressor gene
Mutation detection by sequencing and TaqMan-allele specific amplification
Mutation detection by stacking hybridization on genosensor arrays
Mutation detection for exons 2 to 10 of the Polycystic Kidney Disease 1 (PKD1)-gene by DGGE
Mutation detection in KRAS exon 1 by constant denaturant capillary electrophoresis in 96 parallel capillaries
Mutation detection in the alpha-1 antitrypsin gene (PI) using denaturing gradient gel electrophoresis
Mutation detection in the aspartoacylase gene in 17 patients with Canavan disease: Four new mutations in the non-Jewish population
Mutation detection in the breast cancer gene BRCA1 using the protein truncation test
Mutation detection in the duplicated region of the polycystic kidney disease 1 (PKD1) gene in PKD1-linked Australian families
Mutation detection of DNA by reversed micelles
Mutation detection of immunoglobulin V-regions by DHPLC
Mutation detection of the human glucocorticoid receptor alpha gene area coding for the hormone-binding domain by denaturing gradient gel electrophoresis
Mutation detection using fluorescent enzyme mismatch cleavage with T4 endonuclease VII
Mutation distribution and CYP21/C4 locus variability in Brazilian families with the classical form of the 21-hydroxylase deficiency
Mutation effects of a conserved threonine (Thr243) of cytochrome P450nor on its structure and function
Mutation for pathogenicity of Magnaporthe grisea by Restriction Enzyme Mediated Integration (REMI)
Mutation frequencies of EXT1 and EXT2 in 43 Japanese families with hereditary multiple exostoses
Mutation frequency and chlorophyll mutations in parents and hybrid of cowpea following gamma irradiation
Mutation frequency and type during ageing in mouse seminiferous tubules
Mutation frequency in coding and non-coding repeat sequences in mismatch repair deficient cells derived from normal human tissue
Mutation frequency in the lacI gene of liver DNA from lambda/lacI transgenic mice following the interaction of PCBs with iron causing hepatic cancer and porphyria
Mutation frequency is reduced in the cerebellum of Big Blue(R) mice overexpressing a human wild type SOD1 gene
Mutation frequency of Familial Mediterranean Fever and evidence for a high carrier rate in the Turkish population
Mutation frequency of plasmid DNA and Escherichia coli following long-term space flight on Mir
Mutation identification DNA analysis system (MIDAS) for detection of known mutations
Mutation in Arabidopsis HIT 1 locus causing heat and osmotic hypersensitivity
Mutation in GDP-fucose synthesis genes of Sinorhizobium fredii alters nod factors and significantly decreases competititveness to nodulate soybeans
Mutation in TSC2 and activation of mammalian target of rapamycin signalling pathway in renal angiomyolipoma
Mutation in a calpain-like protease affects the posttranslational mannosylation of phosphatases in Aspergillus nidulans
Mutation in a protein kinase C phosphorylation site of the 5-HT1A receptor preferentially attenuates Ca2+ responses to partial as opposed to higher-efficacy 5-HT1A agonists
Mutation in a sex-determining gene in rainbow trout: Detection and genetic analysis
Mutation in a winged-helix DNA-binding motif causes atypical bare lymphocyte syndrome
Mutation in bcr/abl hybrid gene as a possible factor of tumor progression during CML
Mutation in bombesin receptor subtype-3 gene is not a major cause of obesity in the Japanese
Mutation in collagen gene induces cardiomyopathy in transgenic mice
Mutation in csrR global regulator reduces Streptococcus pyogenes internalization
Mutation in gene 5,10-methylentetrahydrofolatereductase in systemic lupus erythematosus and antiphospholipid syndrome
Mutation in hotfoot-4J mice results in retention of delta2 glutamate receptors in ER
Mutation in recR gene of Deinococcus radiodurans and possible involvement of its product in the repair of DNA interstrand cross-links
Mutation in rod PDE6 linked to congenital stationary night blindness impairs the enzyme inhibition by its gamma-subunit
Mutation in the ATP-binding site of BCR-ABL in a patient with chronic myeloid leukaemia with increasing resistance to STI571
Mutation in the CAV3 gene causes partial caveolin-3 deficiency and hyperCKemia
Mutation in the FGFR2 gene in a Taiwanese patient with Beare-Stevenson cutis gyrata syndrome
Mutation in the NDUFS4 gene of complex I abolishes cAMP-dependent activation of the complex in a child with fatal neurological syndrome
Mutation in the PAX6 gene in twenty patients with aniridia
Mutation in the PTEN/MMAC1 gene in archival low grade and high grade gliomas
Mutation in the Xanthomonas campestris xanA gene required for synthesis of xanthan and lipopolysaccharide drastically reduces the efficiency of bacteriophage variant phiL7 adsorption
Mutation in the beta-tubulin signature motif suppresses microtubule GTPase activity and dynamics, and slows mitosis
Mutation in the beta2m gene is not a frequent event in head and neck squamous cell carcinomas
Mutation in the betaA3/A1-crystallin encoding gene Cryba1 causes a dominant cataract in the mouse
Mutation in the cartilage-derived morphogenetic protein-1 (CDMP1) gene in a kindred affected with fibular hypoplasia and complex brachydactyly (DuPan syndrome)
Mutation in the caveolin-3 gene causes a peculiar form of distal myopathy
Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease
Mutation in the gene for bone morphogenetic protein receptor II as a cause of primary pulmonary hypertension in a large kindred
Mutation in the gene responsible for cystic fibrosis and predisposition to chronic rhinosinusitis in the general population
Mutation in the leucine-rich repeat of platelet glycoprotein Ibalpha results in defects in its interaction with immobilized von Willebrand factor under flow
Mutation in the methylenetetrahydrofolate reductase gene might be a risk factor for cerebrovascular disease in peripartum and under oral contraceptive use
Mutation in the neural cell adhesion molecule interferes with the differentiation of anterior pituitary secretory cells
Mutation in the ntrR gene, a member of the vap gene family, increases the symbiotic efficiency of Sinorhizobium meliloti
Mutation in the pssB-pssA intergenic region of Rhizobium leguminosarum bv. trifolii affects the surface polysaccharides synthesis and nitrogen fixation ability
Mutation in the zonadhesin-like domain of alpha-tectorin associated with autosomal dominant non-syndromic hearing loss
Mutation induced modulation of hydrogen bonding to P700 studied using FTIR difference spectroscopy
Mutation induction and RBE of low energy neutrons in V79 cells
Mutation induction by N-propyl-N-nitrosourea in eight Muta(R)Mouse organs
Mutation induction by different types of radiation at the Hprt locus
Mutation induction by mechanical irritation caused by uracil-induced urolithiasis in Big Blue(R) rats
Mutation induction with UVB in mouse skin epidermis is suppressed in acute high-dose exposure
Mutation landscapes
Mutation load in natural populations of the sensitive fern Onoclea sensibilis exposed to soil mutagens
Mutation load, functional overlap, and synthetic lethality in the evolution and treatment of cancer
Mutation nomenclature extensions and suggestions to describe complex mutations: A discussion
Mutation of ALMS1, a large gene with a tandem repeat encoding 47 amino acids, causes Alstrom syndrome
Mutation of APC gene in sporadic colorectal tumors
Mutation of BAD within the BH3 domain impairs its phosphorylation-mediated regulation
Mutation of BAX occurs infrequently in acquired immunodeficiency syndrome-related non-Hodgkin's lymphomas
Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D
Mutation of COOH-terminal lysines in overexpressed alphaB-crystallin abrogates ischemic protection in cardiomyocytes
Mutation of Celsr1 disrupts planar polarity of inner ear hair cells and causes severe neural tube defects in the mouse
Mutation of DNASE1 in people with systemic lupus erythematosus
Mutation of E2F2 in mice causes enhanced T lymphocyte proliferation, leading to the development of autoimmunity
Mutation of FKBP associated protein 48 (FAP48) at proline 219 disrupts the interaction with FKBP12 and FKBP52
Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy
Mutation of GCK gene of Chinese patients with late-onset Type 2 diabetes
Mutation of K-RAS protooncogene and loss of heterozygosity on 6q27 in serous and mucinous ovarian carcinomas
Mutation of KCNK5 or Kir3.2 potassium channels in mice does not change minimum