نتایج جستجو برای: 32 mutation

تعداد نتایج: 434226  

Journal: :The American Journal of The Medical Sciences 1861

Journal: :Cadernos de Tradução 2013

Journal: :Hereditary Cancer in Clinical Practice 2007
Joanne M McKinley Prue C Weideman Mark A Jenkins Michael L Friedlander John L Hopper Sue-Anne McLachlan Geoffrey J Lindeman kConFab Investigators Kelly-Anne Phillips

Men who carry mutations in BRCA1 or BRCA2 are at increased risk for prostate cancer. However the efficacy of prostate screening in this setting is uncertain and limited data exists on the uptake of prostate screening by mutation carriers. This study prospectively evaluated uptake of prostate cancer screening in a multi-institutional cohort of mutation carriers. Subjects were unaffected male BRC...

Journal: :The Journal of clinical endocrinology and metabolism 2002
Chanda T Moseley Primus E Mullis Melissa A Prince John A Phillips

Familial isolated GH deficiency type II (IGHD II) is caused, in some cases, by heterogeneous IVS3 mutations that affect GH mRNA splicing. We report here our finding an A-->G transition of the fifth base of exon 3 (E3+ 5 A-->G) in affected individuals from an IGHD II family. This mutation disrupts a (GAA)(n) exon splice enhancer (ESE) motif immediately following the weak IVS2 3' splice site. The...

2003

Temperature-sensitive (ts) mutants representative of a number of genes of phage T4 were crossed with rII mutants to allow isolation of ts, rII double-mutant recombinants. The rl mutations used were characterized as frameshift mutations primarily on the basis of their revertability by proflavine. For each ts, rII double mutant, the effect of the ts mutation on spontaneous reversion of the rII mu...

2014
Tomoko Ichiyanagi Kenji Ichiyanagi Ayako Ogawa Satomi Kuramochi-Miyagawa Toru Nakano Shinichiro Chuma Hiroyuki Sasaki Heiichiro Udono

HSP90, found in all kingdoms of life, is a major chaperone protein regulating many client proteins. We demonstrated that HSP90α, one of two paralogs duplicated in vertebrates, plays an important role in the biogenesis of fetal PIWI-interacting RNAs (piRNA), which act against the transposon activities, in mouse male germ cells. The knockout mutation of Hsp90α resulted in a large reduction in the...

Journal: :Molecular genetics & genomic medicine 2016
Jie Yang Kazuhiko Kawasaki Moses Lee Bryan M Reid Stephanie M Nunez Murim Choi Figen Seymen Mine Koruyucu Yelda Kasimoglu Ninna Estrella-Yuson Brent P J Lin James P Simmer Jan C-C Hu

Nonsyndromic dentin defects classified as type II dentin dysplasia and types II and III dentinogenesis imperfecta are caused by mutations in DSPP (dentin sialophosphoprotein). Most reported disease-causing DSPP mutations occur within the repetitive DPP (dentin phosphoprotein) coding sequence. We characterized the DPP sequences of five probands with inherited dentin defects using single molecule...

2013
Christophe Rosty Joanne P. Young Michael D. Walsh Mark Clendenning Kristy Sanderson Rhiannon J. Walters Susan Parry Mark A. Jenkins Aung Ko Win Melissa C. Southey John L. Hopper Graham G. Giles Elizabeth J. Williamson Dallas R. English Daniel D. Buchanan

Mutations in PIK3CA are present in 10 to 15% of colorectal carcinomas. We aimed to examine how PIK3CA mutations relate to other molecular alterations in colorectal carcinoma, to pathologic phenotype and survival. PIK3CA mutation testing was carried out using direct sequencing on 757 incident tumors from the Melbourne Collaborative Cohort Study. The status of O-6-methylguanine-DNA methyltransfer...

Journal: :Australasian Journal of Educational Technology 2016

Journal: :Revista Científica de FAREM-Estelí 2020

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