نتایج جستجو برای: 10q

تعداد نتایج: 340  

Journal: :Diabetes 2004
Marcus G Pezzolesi Moonsuk Nam Terumasa Nagase Tomasz Klupa Jonathon S Dunn Wojciech M Mlynarski Stephen S Rich James H Warram Andrzej S Krolewski

In a panel of large Caucasian pedigrees, we genotyped markers in eight chromosomal regions previously reported as supporting linkage with type 2 diabetes. We previously reported significant linkage on chromosome 20q (maximum logarithm of odds score [MLS] = 2.79) in this panel. In the present analysis, candidate regions on 1q, 2q, 3q, 5q, 9q, and 10q yielded little evidence for linkage; a region...

2000

EDITOR—Duplication of proximal segments of the long arm of chromosome 10 is rare and results in a pattern of malformations and dysmorphic features that are distinct from those of the more common distal 10q trisomy syndrome. To our knowledge, only nine patients with proximal 10q trisomy have been documented. Well defined clinical features of proximal 10q trisomy syndrome are growth and developme...

Journal: :Human molecular genetics 2003
Yi-Ju Li Sofia A Oliveira Puting Xu Eden R Martin Judith E Stenger Clemens R Scherzer Michael A Hauser William K Scott Gary W Small Martha A Nance Ray L Watts Jean P Hubble William C Koller Rajesh Pahwa Mathew B Stern Bradley C Hiner Joseph Jankovic Christopher G Goetz Frank Mastaglia Lefkos T Middleton Allen D Roses Ann M Saunders Donald E Schmechel Steven R Gullans Jonathan L Haines John R Gilbert Jeffery M Vance Margaret A Pericak-Vance Christine Hulette Kathleen A Welsh-Bohmer

We previously reported genetic linkage of loci controlling age-at-onset in Alzheimer disease (AD) and Parkinson's disease (PD) to a 15 cM region on chromosome 10q. Given the large number of genes in this initial starting region, we applied the process of 'genomic convergence' to prioritize and reduce the number of candidate genes for further analysis. As our second convergence factor we perform...

Journal: :Cancer research 1997
P Cairns K Okami S Halachmi N Halachmi M Esteller J G Herman J Jen W B Isaacs G S Bova D Sidransky

Sporadic prostate carcinoma is the most common male cancer in the Western world, yet many of the major genetic events involved in the progression of this often fatal cancer remain to be elucidated. Numerous cytogenetic and allelotype studies have reported frequent loss of heterozygosity on chromosomal arm 10q in sporadic prostate cancer. Deletion mapping studies have unambiguously identified a ...

Journal: :Cancer research 2002
Eric C Burton Kathleen R Lamborn Burt G Feuerstein Michael Prados James Scott Peter Forsyth Sandra Passe Robert B Jenkins Ken D Aldape

Glioblastoma (GBM) remains a highly lethal neoplasm, refractory to current therapies. The molecular genetic aberrations most closely related to clinical aggressiveness in GBM have been difficult to identify, perhaps due in part to the short survival range observed in cohorts of GBM patients. To address this, we characterized 39 tumors from rare patients (2-5% of all GBM cases) who experienced l...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1987
J Kagan J Finan J Letofsky E C Besa P C Nowell C M Croce

Human leukemic T cells carrying a t(10;14)(q24;q11) chromosome translocation were fused with mouse leukemic T cells, and the hybrids were examined for genetic markers of human chromosomes 10 and 14. Hybrids containing the human 10q+ chromosome had the human genes for terminal deoxynucleotidyltransferase that has been mapped at 10q23-q25 and for C alpha [the constant region of TCRA (the alpha-ch...

Journal: :Cancer research 1996
E Healy C E Belgaid M Takata A Vahlquist I Rehman H Rigby J L Rees

A multistep genetic model of tumorigenesis, based on genetic alterations in benign and primary malignant lesions, has been proposed for neoplasms such as colonic carcinoma. However, evidence for a similar genetic progression in melanoma has relied heavily on findings in cultured lesions or metastases. We have investigated every autosomal arm for loss of heterozygosity in 41 primary cutaneous me...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2001
J R Kelsoe M A Spence E Loetscher M Foguet A D Sadovnick R A Remick P Flodman J Khristich Z Mroczkowski-Parker J L Brown D Masser S Ungerleider M H Rapaport W L Wishart H Luebbert

Bipolar disorder or manic depressive illness is a major psychiatric disorder that is characterized by fluctuation between two abnormal mood states. Mania is accompanied by symptoms of euphoria, irritability, or excitation, whereas depression is associated with low mood and decreased motivation and energy. The etiology is currently unknown; however, numerous family, twin, and adoption studies ha...

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