نتایج جستجو برای: missense

تعداد نتایج: 12396  

Journal: :Current Opinion in Pharmacology 2017

Journal: :Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids 2014

2016
Kenta Yamamoto Jiguang Wang Lisa Sprinzen Jun Xu Christopher J Haddock Chen Li Brian J Lee Denis G Loredan Wenxia Jiang Alessandro Vindigni Dong Wang Raul Rabadan Shan Zha

Missense mutations in ATM kinase, a master regulator of DNA damage responses, are found in many cancers, but their impact on ATM function and implications for cancer therapy are largely unknown. Here we report that 72% of cancer-associated ATM mutations are missense mutations that are enriched around the kinase domain. Expression of kinase-dead ATM (Atm(KD/-)) is more oncogenic than loss of ATM...

2015
Irma Eloisa Monroy-Muñoz Nonanzit Pérez-Hernández José Manuel Rodríguez-Pérez José Esteban Muñoz-Medina Javier Angeles-Martínez José J García-Trejo Edgar Morales-Ríos Felipe Massó Juan Pablo Sandoval-Jones Jorge Cervantes-Salazar José Antonio García-Montes Juan Calderón-Colmenero Gilberto Vargas-Alarcón

BACKGROUND The relevance of TBX20 gene in heart development has been demonstrated in many animal models, but there are few works that try to elucidate the effect of TBX20 mutations in human congenital heart diseases. In these studies, all missense mutations associated with atrial septal defect (ASD) were found in the DNA-binding T-box domain, none in the transcriptional activator domain. METH...

Journal: :Cancer genetics and cytogenetics 2008
Léon Mutesa Geneviève Pierquin Nicolas Janin Karin Segers Caroline Thomée Massimo Provenzi Vincent Bours

Noonan syndrome (NS) is an autosomal dominant disorder characterized by short stature, typical craniofacial dysmorphism, skeletal anomalies, congenital heart defects, and predisposition to malignant tumors. In approximately 50% of cases, the disease is caused by missense mutations in the PTPN11 gene. To date, solid tumors, and particularly brain tumors and rhabdomyosarcomas, have been documente...

Journal: :Genetics 1981
J A Kinsey B S Hung

Forty-eight new mutations at the am locus of Neurospora crassa have been characterized. Nineteen mutations were induced by UV; of these, eight were missense, two were frameshifts, two were nonsense, three were deletions and four were unidentified. Twenty-nine mutations were induced with nitrous acid; of these, twenty-one were missense, three were frameshifts, one was nonsense, two were deletion...

Journal: :Journal of medical genetics 1995
G Lundin J Hashemi Y Floderus S Thunell E Sagen A Laegreid W Wassif T Peters M Anvret

We have detected four different mutations in the porphobilinogen deaminase (PBGD) gene in acute intermittent porphyria (AIP) families from England, Norway, and Sweden. A splicing mutation in the first position of intron 8 (Int8 + 1) was found in a family from England and a missense mutation in exon 12 (Glu250) was detected in a Norwegian family. Two mutations were identified in Swedish families...

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