نتایج جستجو برای: germline mutation

تعداد نتایج: 300136  

2010
Silvia Cantara Serena Capuano Caterina Formichi Milena Pisu Marco Capezzone Furio Pacini

Thyroid cancer may have a familial predisposition but a specific germline alteration responsible for the disease has not been discovered yet. We have shown that familial papillary thyroid cancer (FPTC) patients have an imbalance in telomere-telomerase complex with short telomeres and increased telomerase activity. A germline mutation (A339V) in thyroid transcription factor-1 has been described ...

Journal: :Mutation research 2007
Karen L-A Burr Annemarie van Duyn-Goedhart Peter Hickenbotham Karen Monger Paul P W van Buul Yuri E Dubrova

Mutation rates at two expanded simple tandem repeat (ESTR) loci were studied in the germline of mismatch repair deficient Msh2 knock-out mice. Spontaneous mutation rates in homozygous Msh2(-/-) males were significantly higher than those in isogenic wild-type (Msh2(+/+)) and heterozygous (Msh2(+/-)) mice. In contrast, the irradiated Msh2(-/-) mice did not show any detectable increases in their m...

Journal: :Genetics 2006
Mattieu Bégin Daniel J Schoen

Little is known about the role of transposable element (TE) insertion in the production of mutations with mild effects on fitness, the class of mutations thought to be central to the evolution of many basic features of natural populations. We propagated mutation-accumulation (MA) lines of two RNAi-deficient strains of Caenorhabditis elegans that exhibit germline transposition. We show here that...

Journal: :Endocrine journal 2016
Claudia Scollo Marco Russo Laura De Gregorio Rosa Terranova Erika Mangione Carlotta Castoro Sebastiano Squatrito Gabriella Pellegriti

Pheochromocytoma (Pheo) is a chromaffin tumor arising from the adrenal medulla. The recent discovery of new germline mutations in RET, SDHA, SDHB, SDHC, SDHD, VHL, NF1, TMEM127, MAX genes, increased the rate of genetic disease from 10% to 28% in patients with apparently sporadic tumor. RET germline mutations cause multiple endocrine neoplasia type 2 syndrome (MEN 2A) characterized by complete p...

Journal: :Journal of medical genetics 1997
R Froissart I Maire V Bonnet T Levade D Bozon

Carrier detection in a mucopolysaccharidosis type II family (Hunter disease) allowed the identification of germline and somatic mosaicism in the patient's mother: the R443X mutation was found in a varying proportion in tested tissue (7% in leucocytes, lymphocytes, and lymphoblastoid cells, and 22% in fibroblasts). The proband's sister carries the at risk allele (determined by haplotype analysis...

2014
Nicola Brunetti-Pierri Maria Torrado Maria del Carmen Fernandez Ana Maria Tello Claudia L Arberas Antonella Cardinale Pasquale Piccolo Carlos A Bacino

Terminal osseous dysplasia with pigmentary defects (TODPD) is an X-linked dominant syndrome with distal limb anomalies, pigmentary skin defects, digital fibromas, and generalized bone involvement due to a recurrent mutation in the filamin A (FLNA) gene. We here report the mutation c.5217G>A in FLNA in three families with TODPD and we found possible germline and somatic mosaicism in two out of t...

Journal: :Clinical advances in hematology & oncology : H&O 2011
Srinath Sundararajan Aisha Ahmed Oscar B Goodman

The breast cancer susceptibility genes 1 (BRCA1) and 2 (BRCA2) are cellular proteins involved in DNA repair. They are normally expressed in the breast, ovaries, prostate, and other tissues. Their germline mutation is the cause of hereditary breast-ovarian cancer syndromes. BRCA mutation carriers are also susceptible to other cancers, notably prostate cancer. In this article, we review the role ...

2010
Emmanuelle Jeannot Lucille Mellottee Paulette Bioulac-Sage Charles Balabaud Jean-Yves Scoazec Jeanne Tran Van Nhieu Yannick Bacq Sophie Michalak David Buob Pierre Laurent-Puig Ivan Rusyn Jessica Zucman-Rossi

OBJECTIVE Maturity onset diabetes of the young type 3 (MODY3) is a consequence of heterozygous germline mutation in HNF1A. A subtype of hepatocellular adenoma (HCA) is also caused by biallelic somatic HNF1A mutations (H-HCA), and rare HCA may be related to MODY3. To better understand a relationship between the development of MODY3 and HCA, we compared both germline and somatic spectra of HNF1A ...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2011
Franck Bourdeaut Delphine Lequin Laurence Brugières Stéphanie Reynaud Christelle Dufour François Doz Nicolas André Jean-Louis Stephan Yves Pérel Odile Oberlin Daniel Orbach Christophe Bergeron Xavier Rialland Paul Fréneaux Dominique Ranchere Dominique Figarella-Branger Georges Audry Stéphanie Puget D Gareth Evans Joan Carles Ferreres Pinas Valeria Capra Véronique Mosseri Isabelle Coupier Marion Gauthier-Villars Gaëlle Pierron Olivier Delattre

PURPOSE Germline hSNF5/INI1 mutations are responsible for hereditary cases of rhabdoid tumors (RT) that constitute the rhabdoid predisposition syndrome (RPS). Our study provides the first precise overview of the prevalence of RPS within a large cohort of RT. EXPERIMENTAL DESIGN hSNF5/INI1 coding exons were investigated by sequencing and by multiplex ligation-dependent probe amplification. R...

Journal: :Cancer research 1996
L Xia W Shen F Ritacca A Mitri L Madlensky T Berk Z Cohen S Gallinger B Bapat

Germline mutations of the hMSH2 gene are responsible for many cases of hereditary nonpolyposis colorectal cancer. While screening for hMSH2 gene mutations in hereditary nonpolyposis colorectal cancer kindreds, we observed that a previously reported germline mutation is in fact a common, alternatively spliced variant in the population. Using RT-PCR and the protein truncation test, the hMSH2 exon...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید