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Pattern of p53 Gene Mutations in Breast Cancers of Women of the Midwestern United States.
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- JNCI: Journal of the National Cancer Institute, 1992, v. 84, n. 4, p. 246, doi. 10.1093/jnci/84.4.246
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- Article
REPORTS.
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- JNCI: Journal of the National Cancer Institute, 1991, v. 83, n. 14, p. 1004, doi. 10.1093/jnci/83.14.1004
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- Article
Mutagenic and Recombinagenic Responses to Defective DNA Polymerase δ Are Facilitated by the Rev1 Protein in pol3-t Mutants of Saccharomyces cerevisiae.
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- Genetics, 2008, v. 179, n. 4, p. 1795, doi. 10.1534/genetics.108.089821
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- Article
Overexpression and mutations of p53 in metastatic malignant melanomas.
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- International Journal of Cancer, 1996, v. 67, n. 3, p. 313, doi. 10.1002/(SICI)1097-0215(19960729)67:3<313::AID-IJC1>3.0.CO;2-U
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- Article
Three Ways of Combining Genotyping and Resequencing in Case-Control Association Studies.
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- PLoS ONE, 2010, v. 5, n. 12, p. 1, doi. 10.1371/journal.pone.0014318
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- Article
Missense Mutations in the MEFV Gene Are Associated with Fibromyalgia Syndrome and Correlate with Elevated IL-1β Plasma Levels.
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- PLoS ONE, 2009, v. 4, n. 12, p. 1, doi. 10.1371/journal.pone.0008480
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- Article
Analysis of Cancer Mutation Signatures in Blood by a Novel Ultra-Sensitive Assay: Monitoring of Therapy or Recurrence in Non-Metastatic Breast Cancer.
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- PLoS ONE, 2009, v. 4, n. 9, p. 1, doi. 10.1371/journal.pone.0007220
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- Article
Evidence for X-Chromosomal Schizophrenia Associated with microRNA Alterations.
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- PLoS ONE, 2009, v. 4, n. 7, p. 1, doi. 10.1371/journal.pone.0006121
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- Article
Epidemiology of Doublet/Multiplet Mutations in Lung Cancers: Evidence that a Subset Arises by Chronocoordinate Events.
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- PLoS ONE, 2008, v. 3, n. 11, p. 1, doi. 10.1371/journal.pone.0003714
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- Article
A yeast antiviral protein, SKI8, shares a repeated amino acid sequence pattern with β-subunits of G proteins and several other proteins.
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- Yeast, 1993, v. 9, n. 1, p. 43, doi. 10.1002/yea.320090106
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- Article
Pyrophosphorolysis-activatable oligonucleotides may facilitate detection of rare alleles, mutation scanning and analysis of chromatin structures.
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- Nucleic Acids Research, 2002, v. 30, n. 2, p. 598, doi. 10.1093/nar/30.2.598
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- Article
Discrete mobility of single-stranded DNA in non-denaturing gel electrophoresis.
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- Nucleic Acids Research, 2000, v. 28, n. 4, p. 940, doi. 10.1093/nar/28.4.940
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- Article
Conversion Analysis for Mutation Detection in MLH1 and MSH2 in Patients With Colorectal Cancer.
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- JAMA: Journal of the American Medical Association, 2005, v. 293, n. 7, p. 799, doi. 10.1001/jama.293.7.799
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- Article
Tissue‐specific time courses of spontaneous mutation frequency and deviations in mutation pattern are observed in middle to late adulthood in Big Blue mice.
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- Environmental & Molecular Mutagenesis, 2005, v. 45, n. 5, p. 442
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- Article
Spontaneous mutation in Big Blue® mice from fetus to old age: Tissue-specific time courses of mutation frequency but similar mutation types.
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- Environmental & Molecular Mutagenesis, 2004, v. 43, n. 2, p. 110
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- Article
p53 As a mutagen test in breast cancer.
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- Environmental & Molecular Mutagenesis, 2002, v. 39, n. 2/3, p. 216, doi. 10.1002/em.10065
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- Article
Spontaneous microdeletions and microinsertions in a transgenic mouse mutation detection system: analysis of age, tissue, and sequence specificity.
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- Environmental & Molecular Mutagenesis, 2001, v. 37, n. 4, p. 311, doi. 10.1002/em.1038
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- Article
Spontaneous mutation frequency and pattern in Big Blue® mice fed a vitamin E-supplemented diet.
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- Environmental & Molecular Mutagenesis, 1999, v. 34, n. 2/3, p. 195, doi. 10.1002/(SICI)1098-2280(1999)34:2/3<195::AID-EM19>3.0.CO;2-I
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- Article
Tandem-base mutations occur in mouse liver and adipose tissue preferentially as G:C to T:A transversions and accumulate with age.
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- Environmental & Molecular Mutagenesis, 1999, v. 33, n. 4, p. 320, doi. 10.1002/(SICI)1098-2280(1999)33:4<320::AID-EM9>3.0.CO;2-S
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- Article
System issues: Spontaneous mutation in Big Blue® transgenic mice: Analysis of age, gender, and tissue type.
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- Environmental & Molecular Mutagenesis, 1996, v. 28, n. 4, p. 299, doi. 10.1002/(SICI)1098-2280(1996)28:4<299::AID-EM2>3.0.CO;2-7
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- Article
Mutational specificity: Mutation frequencies but not mutant frequencies in Big Blue® mice fit a Poisson distribution.
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- Environmental & Molecular Mutagenesis, 1996, v. 28, n. 4, p. 414, doi. 10.1002/(SICI)1098-2280(1996)28:4<414::AID-EM16>3.0.CO;2-I
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- Article
A prospective trial of midwest breast cancer patients: A p53 gene mutation is the most important predictor of adverse outcome.
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- International Journal of Cancer, 2000, v. 89, n. 1, p. 32, doi. 10.1002/(SICI)1097-0215(20000120)89:1<32::AID-IJC6>3.0.CO;2-G
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Database of somatic mutations in EGFR with analyses revealing indel hotspots but no smoking-associated signature.
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- 2007
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- Other
Detection of ultrarare somatic mutation in the human TP53 gene by bidirectional pyrophosphorolysis-activated polymerization allele-specific amplification.
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- Human Mutation, 2007, v. 28, n. 2, p. 131, doi. 10.1002/humu.20423
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- Article
Somatic microindels: analysis in mouse soma and comparison with the human germline.
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- Human Mutation, 2007, v. 28, n. 1, p. 69, doi. 10.1002/humu.20416
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- Article
Preferential occurrence of 1-2 microindels.
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- Human Mutation, 2006, v. 27, n. 1, p. 55, doi. 10.1002/humu.20260
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- Article
Increased risk of idiopathic chronic pancreatitis in cystic fibrosis carriers.
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- Human Mutation, 2005, v. 26, n. 4, p. 303, doi. 10.1002/humu.20232
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- Article
Detection of heterozygous deletions and duplications in the MECP2 gene in Rett syndrome by Robust Dosage PCR (RD-PCR).
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- Human Mutation, 2005, v. 25, n. 5, p. 505, doi. 10.1002/humu.9338
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- Article
Mutation rates in the dystrophin gene: A hotspot of mutation at a CpG dinucleotide.
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- Human Mutation, 2005, v. 25, n. 2, p. 177, doi. 10.1002/humu.20132
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- Article
Somatic microindels in human cancer: the insertions are highly error-prone and derive from nearby but not adjacent sense and antisense templates.
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- Human Molecular Genetics, 2008, v. 17, n. 18, p. 2910, doi. 10.1093/hmg/ddn190
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- Article
PAP: Detection of ultra rare mutations depends on P<sup>*</sup> oligonucleotides: 'Sleeping Beauties' awakened by the kiss of pyrophosphorolysis.
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- Human Mutation, 2004, v. 23, n. 5, p. 426, doi. 10.1002/humu.20036
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- Article
Comprehensive scanning of the ATM gene with DOVAM-S.
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- Human Mutation, 2003, v. 21, n. 2, p. 123, doi. 10.1002/humu.10158
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- Article
Mutations in the factor IX gene (F9) during the past 150 years have relative rates similar to ancient mutations.
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- Human Mutation, 2002, v. 19, n. 1, p. 49, doi. 10.1002/humu.10018
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- Article
Frequency of recent retrotransposition events in the human factor IX gene.
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- Human Mutation, 2001, v. 17, n. 6, p. 511, doi. 10.1002/humu.1134
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- Article
Factor IX mutations in South Africans and African Americans are compatible with primarily endogenous influences upon recent germline mutations.
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- Human Mutation, 2000, v. 16, n. 4, p. 371, doi. 10.1002/1098-1004(200010)16:4<371::AID-HUMU11>3.0.CO;2-P
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- Article
The human factor IX gene as germline mutagen test: Samples from mainland China have the putatively endogenous pattern of mutation.
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- Human Mutation, 2000, v. 16, n. 1, p. 31, doi. 10.1002/1098-1004(200007)16:1<31::AID-HUMU6>3.0.CO;2-I
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- Article
Novel hotspot detector software reveals a non-CpG hotspot of germline mutation in the factor IX gene ( F9) in Latin Americans.
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- Human Mutation, 2000, v. 16, n. 3, p. 203, doi. 10.1002/1098-1004(200009)16:3<203::AID-HUMU3>3.0.CO;2-1
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- Article
Nine independent F9 mutations in the Mexican hemophilia B population: Nonrandom recurrences of point mutation events in the human germline.
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- Human Mutation, 2000, v. 15, n. 1, p. 116, doi. 10.1002/(SICI)1098-1004(200001)15:1<116::AID-HUMU25>3.0.CO;2-N
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- Article
Deep intronic mutations are rarely a cause of hemophilia B.
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- Human Mutation, 1999, v. 14, n. 3, p. 267, doi. 10.1002/(SICI)1098-1004(1999)14:3<267::AID-HUMU11>3.0.CO;2-I
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- Article
Highly sensitive mutation screening by REF with low concentrations of urea: A blinded analysis of a 2-kb region of the p53 gene reveals two common haplotypes.
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- Human Mutation, 1999, v. 14, n. 2, p. 175, doi. 10.1002/(SICI)1098-1004(1999)14:2<175::AID-HUMU9>3.0.CO;2-3
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- Article
Reported in vivo splice-site mutations in the factor IX gene: Severity of splicing defects and a hypothesis for predicting deleterious splice donor mutations.
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- Human Mutation, 1999, v. 13, n. 3, p. 221, doi. 10.1002/(SICI)1098-1004(1999)13:3<221::AID-HUMU6>3.0.CO;2-U
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- Article
Germline mutations in Peruvian patients with hemophilia B: Pattern of mutation in AmerIndians is similar to the putative endogenous germline pattern.
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- Human Mutation, 1998, v. 11, n. 5, p. 372, doi. 10.1002/(SICI)1098-1004(1998)11:5<372::AID-HUMU4>3.0.CO;2-M
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- Article
SSCP analysis of long DNA fragments in low pH gel.
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- Human Mutation, 1997, v. 10, n. 5, p. 400, doi. 10.1002/(SICI)1098-1004(1997)10:5<400::AID-HUMU11>3.0.CO;2-3
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- Article
Mutations associated with hemophilia B in Turkish patients.
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- Human Mutation, 1997, v. 10, n. 1, p. 76, doi. 10.1002/(SICI)1098-1004(1997)10:1<76::AID-HUMU11>3.0.CO;2-X
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- Article
Database of mutations in the p53 and APC tumor suppressor genes designed to facilitate molecular epidemiological analyses.
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- Human Mutation, 1996, v. 7, n. 3, p. 202, doi. 10.1002/(SICI)1098-1004(1996)7:3<202::AID-HUMU4>3.0.CO;2-C
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- Article
Identification of mutations in four hemophilia B patients of Turkish origin, including a novel deletion of base 6411.
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- Human Mutation, 1994, v. 4, n. 2, p. 163, doi. 10.1002/humu.1380040214
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- Article
A tandem CC → TT transition in the p53 gene of a breast cancer.
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- Human Mutation, 1994, v. 4, n. 2, p. 158, doi. 10.1002/humu.1380040212
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- Article
Alu repeats in the human factor IX gene: The rate of polymorphism is not substantially elevated.
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- Human Mutation, 1993, v. 2, n. 6, p. 468, doi. 10.1002/humu.1380020607
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- Article
Does cancer kill the individual and save the species?
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- Human Mutation, 1994, v. 3, n. 2, p. 166, doi. 10.1002/humu.1380030214
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- Article
Deletions with inversions: Report of a mutation and review of the literature.
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- Human Mutation, 1993, v. 2, n. 1, p. 53, doi. 10.1002/humu.1380020110
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- Article