نتایج جستجو برای: chromosome 10q

تعداد نتایج: 119424  

Journal: :Diabetes 2007
Donna M Lehman Kelly J Hunt Robin J Leach Jeanette Hamlington Rector Arya Hanna E Abboud Ravindranath Duggirala John Blangero Harald H H Göring Michael P Stern

TCF7L2 acts as both a repressor and transactivator of genes, as directed by the Wnt signaling pathway. Recently, several highly correlated sequence variants located within a haplotype block of the TCF7L2 gene were observed to associate with type 2 diabetes in three Caucasian cohorts. We previously reported linkage of type 2 diabetes in the San Antonio Family Diabetes Study (SAFADS) cohort consi...

2015
Chinyere Ibeawuchi Hartmut Schmidt Reinhard Voss Ulf Titze Mahmoud Abbas Joerg Neumann Elke Eltze Agnes Marije Hoogland Guido Jenster Burkhard Brandt Axel Semjonow

The multifocal nature of prostate cancer (PCa) creates a challenge to patients' outcome prediction and their clinical management. An approach that scrutinizes every cancer focus is needed in order to generate a comprehensive evaluation of the disease, and by correlating to patients' clinico-pathological information, specific prognostic biomarker can be identified. Our study utilized the Affymet...

Journal: :Proceedings of the National Academy of Sciences 1990

Journal: :Cancer research 2002
Maria Pik Wong Wah Kit Lam Elaine Wang Shui Wah Chiu Chi Leung Lam Lap Ping Chung

Lung cancer development in nonsmokers, particularly in females, has long been observed,but the genetic pathways of oncogenesis are still unclear. The purpose of this study was to identify important targets of chromosomal alteration involved in non-tobacco-related adenocarcinomas of lung. In this study, loci of recurrent allelic imbalance (AI) were identified by microsatellite analysis, focusing...

Journal: :American journal of medical genetics 1999
B J Keats D P Corey

Mutations in the gene (MYO7A) encoding myosin-VIIa, a member of the large superfamily of myosin motor proteins that move on cytoplasmic actin filaments, and in the USH2A gene, which encodes a novel protein resembling an extracellular matrix protein or a cell adhesion molecule, both cause Usher syndrome (USH), a clinically heterogeneous autosomal recessive disorder comprising hearing and visual ...

Journal: :Human molecular genetics 2007
Akinori Miyashita Hiroyuki Arai Takashi Asada Masaki Imagawa Etsuro Matsubara Mikio Shoji Susumu Higuchi Katsuya Urakami Akiyoshi Kakita Hitoshi Takahashi Shinichi Toyabe Kohei Akazawa Ichiro Kanazawa Yasuo Ihara Ryozo Kuwano

Alzheimer's disease (AD), the most common form of dementia in the elderly, was found to exhibit a trend toward a higher risk in females than in males through epidemiological studies. Therefore, we hypothesized that gender-related genetic risks could exist. To reveal the ones for late-onset AD (LOAD), we extended our previous genetic work on chromosome 10q (genomic region, 60-107 Mb), and single...

Journal: :Diabetes 2004
Harvest F Gu Suad Efendic Sofia Nordman Claes-Göran Ostenson Kerstin Brismar Anthony J Brookes Jonathan A Prince

Insulin-degrading enzyme (IDE) plays a principal role in the proteolysis of several peptides in addition to insulin and is encoded by IDE, which resides in a region of chromosome 10q that is linked to type 2 diabetes. Two recent studies presented genetic association data on IDE and type 2 diabetes (one positive and the other negative), but neither explored the fundamental question of whether po...

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