نتایج جستجو برای: point mutation

تعداد نتایج: 796715  

2006
Consuelo Junqueira Rodrigues Jin Hwan Yoo Aldo Junqueira Rodrigues

Groin hernias emerge at the myopectineal orifice of Fruchaud which is closed off by the fascia transversalis. Our previous studies showed structural and quantitative changes of the fascia transversalis elastic fibers of inguinal hernia patients and elderly people. The present study used single-strand conformation polymorphism (SSCP) elastin (analysis to investigate the 34 exons of the ELN gene ...

Journal: :EMBO reports 2000
J P Muyrers Y Zhang V Benes G Testa W Ansorge A F Stewart

Bacterial artificial chromosomes (BACs) offer many advantages for functional studies of large eukaryotic genes. To utilize the potential applications of BACs optimally, new approaches that allow rapid and precise engineering of these large molecules are required. Here, we describe a simple and flexible two-step approach based on ET recombination, which permits point mutations to be introduced i...

2005
Anthony S. Guerrero

The recent discovery of activating somatic mutations in cancer that correlate with phenotypes such as drug responsiveness, has generated renewed interest in the sequencing of genomes of tumor samples and cancer cancer cell lines with the goal of identifying the set of mutations that produce those phenotypes [1]. The two most popular strategies for discovering these events are array CGH [2], and...

2013
Karin S. Kassahn Oliver Holmes Katia Nones Ann-Marie Patch David K. Miller Angelika N. Christ Ivon Harliwong Timothy J. Bruxner Qinying Xu Matthew Anderson Scott Wood Conrad Leonard Darrin Taylor Felicity Newell Sarah Song Senel Idrisoglu Craig Nourse Ehsan Nourbakhsh Suzanne Manning Shivangi Wani Anita Steptoe Marina Pajic Mark J. Cowley Mark Pinese David K. Chang Anthony J. Gill Amber L. Johns Jianmin Wu Peter J. Wilson Lynn Fink Andrew V. Biankin Nicola Waddell Sean M. Grimmond John V. Pearson

Somatic mutation calling from next-generation sequencing data remains a challenge due to the difficulties of distinguishing true somatic events from artifacts arising from PCR, sequencing errors or mis-mapping. Tumor cellularity or purity, sub-clonality and copy number changes also confound the identification of true somatic events against a background of germline variants. We have developed a ...

2005
Lisa M. Davis Royal A. McGraw Jerry L. Ware Harold R. Roberts Darrel W. Stafford

Factor lX,, ,,,. is a variant factor IX molecule responsible for a clinically moderate form of hemophilia B. Twenty-five kilobases (kb) of the variant gene, including seven exons coding for the structural protein, were cloned and characterized. The restriction map and the arrangement of coding regions are identical to those of the normal gene. DNA sequence analysis of the coding regions reveale...

Journal: :Cancer research 1995
A Tamori S Nishiguchi T Kuroki N Koh K Kobayashi Y Yano S Otani

Ornithine decarboxylase (ODC) plays an important role in cell growth, and its activity is regulated by many mechanisms. The biochemical characteristics of ODC in malignant cells differ from those of ODC in normal cells. To determine whether novel changes occur in ODC in neoplastic tissue, we compared the nucleotide sequence of ODC cDNA obtained from human hepatoma tissue as determined by revers...

Journal: :Journal of neurophysiology 2012
Neal S Peachey Jillian N Pearring Pasano Bojang Matthew E Hirschtritt Gwen Sturgill-Short Thomas A Ray Takahisa Furukawa Chieko Koike Andrew F X Goldberg Yin Shen Maureen A McCall Scott Nawy Patsy M Nishina Ronald G Gregg

Mutations in TRPM1 are found in humans with an autosomal recessive form of complete congenital stationary night blindness (cCSNB). The Trpm1(-/-) mouse has been an important animal model for this condition. Here we report a new mouse mutant, tvrm27, identified in a chemical mutagenesis screen. Genetic mapping of the no b-wave electroretinogram (ERG) phenotype of tvrm27 localized the mutation to...

Journal: :PLoS Pathogens 2007
Laura B Goodman Arianna Loregian Gillian A Perkins Josie Nugent Elizabeth L Buckles Beatrice Mercorelli Julia H Kydd Giorgio Palù Ken C Smith Nikolaus Osterrieder Nicholas Davis-Poynter

Infection with equid herpesvirus type 1 (EHV-1) leads to respiratory disease, abortion, and neurologic disorders in horses. Molecular epidemiology studies have demonstrated that a single nucleotide polymorphism resulting in an amino acid variation of the EHV-1 DNA polymerase (N752/D752) is significantly associated with the neuropathogenic potential of naturally occurring strains. To test the hy...

2009
Dong Yeon Lee Tae-Joon Cho Hye Ran Lee Moon Seok Park Won Joon Yoo Chin Youb Chung In Ho Choi

Fibrodysplasia ossificans progressiva (FOP; OMIM 135100) is a rare but extremely disabling genetic disorder of the skeletal system, and is characterized by the progressive development of ectopic ossification of skeletal muscles and subsequent joint ankylosis. The c.617G>A; p.R206H point mutation in the activin A type I receptor (ACVR1) gene has been reported to be a causative mutation of FOP. I...

Journal: :Cancer research 1995
H S Goh J Yao D R Smith

We have examined the relationship between point mutation of the p53 tumor suppressor gene and survival in colorectal cancer patients. We found that patients with tumors harboring mutated p53 genes showed a significantly poorer prognosis than did those patients with genes without point mutations, and, moreover, patient response to postoperative therapies depended significantly on mutation status...

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