نتایج جستجو برای: rare mutations

تعداد نتایج: 402573  

Journal: :The New England journal of medicine 2014
Jacy Crosby Gina M Peloso Paul L Auer David R Crosslin Nathan O Stitziel Leslie A Lange Yingchang Lu Zheng-zheng Tang He Zhang George Hindy Nicholas Masca Kathleen Stirrups Stavroula Kanoni Ron Do Goo Jun Youna Hu Hyun Min Kang Chenyi Xue Anuj Goel Martin Farrall Stefano Duga Pier Angelica Merlini Rosanna Asselta Domenico Girelli Oliviero Olivieri Nicola Martinelli Wu Yin Dermot Reilly Elizabeth Speliotes Caroline S Fox Kristian Hveem Oddgeir L Holmen Majid Nikpay Deborah N Farlow Themistocles L Assimes Nora Franceschini Jennifer Robinson Kari E North Lisa W Martin Mark DePristo Namrata Gupta Stefan A Escher Jan-Håkan Jansson Natalie Van Zuydam Colin N A Palmer Nicholas Wareham Werner Koch Thomas Meitinger Annette Peters Wolfgang Lieb Raimund Erbel Inke R Konig Jochen Kruppa Franziska Degenhardt Omri Gottesman Erwin P Bottinger Christopher J O'Donnell Bruce M Psaty Christie M Ballantyne Goncalo Abecasis Jose M Ordovas Olle Melander Hugh Watkins Marju Orho-Melander Diego Ardissino Ruth J F Loos Ruth McPherson Cristen J Willer Jeanette Erdmann Alistair S Hall Nilesh J Samani Panos Deloukas Heribert Schunkert James G Wilson Charles Kooperberg Stephen S Rich Russell P Tracy Dan-Yu Lin David Altshuler Stacey Gabriel Deborah A Nickerson Gail P Jarvik L Adrienne Cupples Alex P Reiner Eric Boerwinkle Sekar Kathiresan

BACKGROUND Plasma triglyceride levels are heritable and are correlated with the risk of coronary heart disease. Sequencing of the protein-coding regions of the human genome (the exome) has the potential to identify rare mutations that have a large effect on phenotype. METHODS We sequenced the protein-coding regions of 18,666 genes in each of 3734 participants of European or African ancestry i...

Journal: :iranian journal of medical sciences 0
mohammad miryounesi genomic research center, shahid beheshti university of medical sciences, tehran, iran; soudeh ghafouri-fard department of medical genetics, shahid beheshti university of medical sciences, tehran, iran; majid fardaei department of medical genetics, shiraz university of medical sciences, shiraz, iran

congenital recessive myotonia is a rare genetic disorder caused by mutations in clcn1, which codes for the main skeletal muscle chloride channel clc-1. more than 120 mutations have been found in this gene. the main feature of this disorder is muscle membrane hyperexcitability. here, we report a 59-year male patient suffering from congenital myotonia. he had transient generalized myotonia, which...

Journal: :international journal of pediatrics 0
masoud dehghan tezerjani reproductive and genetic unit, yazd research and clinical center for infertility, shahid sadoughi university of medical sciences, yazd, iran mohammad yahya vahidi mehrjardi medical genetic research center, shahid sadoughi university of medical sciences, yazd, iran seyed mehdi kalantar reproductive and genetic unit, yazd research and clinical center for infertility, shahid sadoughi university of medical sciences, yazd, iran mohammadreza dehghani medical genetic research center, shahid sadoughi university of medical sciences, yazd, iran

neonatal diabetes mellitus (ndm) is a rare kind of diabetes characterized by hyperglycemia and low levels of insulin. clinically, it is categorized into two main types: transient ndm (tndm) and permanent ndm (pndm). these types are diagnosed based on duration of insulin dependence early in the disease. in tndm, diabetes begins in the first few weeks of life with remission in a few months. howev...

Premature ovarian failure (POF) is a heterogeneous disorder, defined as menopause under age 40 years. The prevalence is 1%; POF before age 30 years is much less common. Chromosomal causes have long been recognized - visible deletions of the X chromosome, 45,X/46,XX mosaicism, and autosomal rearrangements (balanced translocations). Toxins or iatrogenic causes (e.g., chemotherapeutic agents) are ...

2015
Ron Do Nathan O. Stitziel Hong-Hee Won Anders Berg Jørgensen Stefano Duga Pier Angelica Merlini Adam Kiezun Martin Farrall Anuj Goel Or Zuk Illaria Guella Rosanna Asselta Leslie A. Lange Gina M. Peloso Paul L. Auer Domenico Girelli Nicola Martinelli Deborah N. Farlow Mark A. DePristo Robert Roberts Alexander F.R. Stewart Danish Saleheen John Danesh Stephen E. Epstein Suthesh Sivapalaratnam G. Kees Hovingh John J. Kastelein Nilesh J. Samani Heribert Schunkert Jeanette Erdmann Svati H. Shah William E. Kraus Robert Davies Majid Nikpay Christopher T. Johansen Jian Wang Robert A. Hegele Eliana Hechter Winfried Marz Marcus E. Kleber Jie Huang Andrew D. Johnson Mingyao Li Greg L. Burke Myron Gross Yongmei Liu Themistocles L. Assimes Gerardo Heiss Ethan M. Lange Aaron R. Folsom Herman A. Taylor Oliviero Olivieri Anders Hamsten Robert Clarke Dermot F. Reilly Wu Yin Manuel A. Rivas Peter Donnelly Jacques E. Rossouw Bruce M. Psaty David M. Herrington James G. Wilson Stephen S. Rich Michael J. Bamshad Russell P. Tracy L. Adrienne Cupples Daniel J. Rader Muredach P. Reilly John A. Spertus Sharon Cresci Jaana Hartiala W.H. Wilson Tang Stanley L. Hazen Hooman Allayee Alex P. Reiner Christopher S. Carlson Charles Kooperberg Rebecca D. Jackson Eric Boerwinkle Eric S. Lander Stephen M. Schwartz David S. Siscovick Ruth McPherson Anne Tybjaerg-Hansen Goncalo R. Abecasis Hugh Watkins Deborah A. Nickerson Diego Ardissino Shamil R. Sunyaev Christopher J. O’Donnell David Altshuler Stacey Gabriel Sekar Kathiresan

Myocardial infarction (MI), a leading cause of death around the world, displays a complex pattern of inheritance1,2. When MI occurs early in life, the role of inheritance is substantially greater1. Previously, rare mutations in low-density lipoprotein (LDL) genes have been shown to contribute to MI risk in individual families3–8 whereas common variants at more than 45 loci have been associated ...

Journal: :Pathology 2021

Desmoid tumours are rare soft tissue tumours. The a locally invasive monoclonal fibroblastic proliferation leading to variable clinical course. Abnormal functioning of the Wnt/APC/Beta catenin pathway accounts for large proportion desmoid There currently two genetic subtypes: sporadic resulting from somatic CTNNB1 mutations in exon 3 and associated with germline pathogenic variants APC. APC tho...

2013
Sylvie Bannwarth Vincent Procaccio Anne Sophie Lebre Claude Jardel Annabelle Chaussenot Claire Hoarau Hassani Maoulida Nathanaël Charrier Xiaowu Gai Hongbo M Xie Marc Ferre Konstantina Fragaki Gaëlle Hardy Bénédicte Mousson de Camaret Sandrine Marlin Claire Marie Dhaenens Abdelhamid Slama Christophe Rocher Jean Paul Bonnefont Agnès Rötig Nadia Aoutil Mylène Gilleron Valérie Desquiret-Dumas Pascal Reynier Jennifer Ceresuela Laurence Jonard Aurore Devos Caroline Espil-Taris Delphine Martinez Pauline Gaignard Kim-Hanh Le Quan Sang Patrizia Amati-Bonneau Marni J Falk Catherine Florentz Brigitte Chabrol Isabelle Durand-Zaleski Véronique Paquis-Flucklinger

BACKGROUND Mitochondrial DNA (mtDNA) diseases are rare disorders whose prevalence is estimated around 1 in 5000. Patients are usually tested only for deletions and for common mutations of mtDNA which account for 5-40% of cases, depending on the study. However, the prevalence of rare mtDNA mutations is not known. METHODS We analysed the whole mtDNA in a cohort of 743 patients suspected of mani...

Journal: :medical journal of islamic republic of iran 0
amir mehrgou department of medical genetics and molecular biology, school of medicine, iran university of medical sciences, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی ایران (iran university of medical sciences) mansoureh akouchekian department of medical genetics and molecular biology, school of medicine, iran university of medical sciences, tehran, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی ایران (iran university of medical sciences)

many factors including genetic, environmental, and acquired are involved in breast cancer development across various societies. among all of these factors in families with a history of breast cancer throughout several generations, genetics, like predisposing genes to develop this disease, should be considered more. early detection of mutation carriers in these genes, in turn, can play an import...

Journal: :iranian journal of public health 0
n saleh-gohari mr bazrafshani

background: mutations in β -globin gene may result in β-thalassemia major, which is one of the most common genetic dis­or­ders in iran and some other countries. knowing the beta-globin mutation spectrum improves the efficiency of prenatal diagno­sis in the affected fetuses (major β-thalassemia) of heterozygote couples. methods: couples with high hemoglobin a 2 and low mean corpuscular volume we...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید