نتایج جستجو برای: chromosome 5q21

تعداد نتایج: 119353  

Journal: :Cancer research 1994
S Hosoe K Ueno Y Shigedo I Tachibana T Osaki T Kumagai Y Tanio I Kawase Y Nakamura T Kishimoto

We have examined the deletion of the long arm of chromosome 5 (5q) in 59 cases of advanced lung cancer [39 cases of small cell lung cancer (SCLC), 20 cases of non-SCLC] using 12 restriction fragment length polymorphism markers on 5q. Of 59 lung cancer cases, 48 (81%) exhibited deletion at any portion of the 5q locus (loci). Such a high frequency of 5q deletion has not been reported in surgicall...

2015
Christoph Burdelski Christian Strauss Maria Christina Tsourlakis Martina Kluth Claudia Hube-Magg Nathaniel Melling Patrick Lebok Sarah Minner Christina Koop Markus Graefen Hans Heinzer Corinna Wittmer Till Krech Guido Sauter Waldemar Wilczak Ronald Simon Thorsten Schlomm Stefan Steurer

Thymidylate synthase (TYMS) plays a role in DNA synthesis and is a target for 5-fluorouracil. In this study TYMS was analyzed by immunohistochemistry on a tissue microarray containing 11,152 prostate cancers. TYMS expression was higher in neoplastic than in normal prostate epithelium and was detectable in 72.9% of 10,223 interpretable cancers. It was considered strong in 21.9%, moderate in 33.4...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2002
O M Sieber H Lamlum M D Crabtree A J Rowan E Barclay L Lipton S Hodgson H J W Thomas K Neale R K S Phillips S M Farrington M G Dunlop H J Mueller M L Bisgaard S Bulow P Fidalgo C Albuquerque M I Scarano W Bodmer I P M Tomlinson K Heinimann

Familial adenomatous polyposis (FAP) is a dominantly inherited colorectal tumor predisposition that results from germ-line mutations in the APC gene (chromosome 5q21). FAP shows substantial phenotypic variability: classical polyposis patients develop more than 100 colorectal adenomas, whereas those with attenuated polyposis (AAPC) have fewer than 100 adenomas. A further group of individuals, so...

Journal: :International journal of oncology 2006
G A Balogh I H Russo B R Balsara J Russo

Breast cancer is the most frequent malignancy in women. It is well recognized that tumorigenesis is a multistep process resulting from the accumulation of sequential genetic alterations. In breast cancers LOH has been described on one or both arms of multiple chromosomes. Comparative genomic hybridization (CGH) analysis was performed to identify chromosomal imbalances in the breast epithelial c...

Journal: :Carcinogenesis 2006
Liping Luo Gong-Qing Shen Karen A Stiffler Qing K Wang Thomas G Pretlow Theresa P Pretlow

Aberrant crypt foci (ACF), the earliest neoplastic lesions of the colon, have genetic and epigenetic alterations. Loss of heterozygosity (LOH) of tumor suppressor gene loci is seen in most colon cancers, but it is not known how early in tumorigenesis this takes place. Nine microsatellite markers close to specific genes, that is, APC (5q21), PTPRJ (11p11), p53 (17p13) and DCC (18q21), were analy...

Journal: :Cancer research 2013
Lia Burkhardt Sarah Fuchs Antje Krohn Sawinee Masser Malte Mader Martina Kluth Frederik Bachmann Hartwig Huland Thomas Steuber Markus Graefen Thorsten Schlomm Sarah Minner Guido Sauter Hüseyin Sirma Ronald Simon

Deletions involving the chromosomal band 5q21 are among the most frequent alterations in prostate cancer. Using single-nucleotide polymorphism (SNP) arrays, we mapped a 1.3 megabase minimally deleted region including only the repulsive guidance molecule B (RGMB) and chromodomain helicase DNA-binding protein 1 (CHD1) genes. Functional analyses showed that CHD1 is an essential tumor suppressor. F...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2004
Tsuyoshi Mikkaichi Takehiro Suzuki Tohru Onogawa Masayuki Tanemoto Hiroya Mizutamari Masahiro Okada Tatsuji Chaki Satohiro Masuda Taro Tokui Nobuaki Eto Michiaki Abe Fumitoshi Satoh Michiaki Unno Takanori Hishinuma Ken-Ichi Inui Sadayoshi Ito Junichi Goto Takaaki Abe

Digoxin, which is one of the most commonly prescribed drugs for the treatment of heart failure, is mainly eliminated from the circulation by the kidney. P-glycoprotein is well characterized as a digoxin pump at the apical membrane of the nephron. However, little is known about the transport mechanism at the basolateral membrane. We have isolated an organic anion transporter (OATP4C1) from human...

Journal: :Journal of medical genetics 2005
N Craddock M C O'Donovan M J Owen

Much work has been done to identify susceptibility genes in schizophrenia and bipolar disorder. Several well established linkages have emerged in schizophrenia. Strongly supported regions are 6p24-22, 1q21-22, and 13q32-34, while other promising regions include 8p21-22, 6q16-25, 22q11-12, 5q21-q33, 10p15-p11, and 1q42. Genomic regions of interest in bipolar disorder include 6q16-q22, 12q23-q24,...

2014
Adrianna D’Mello Ramesh B. Deshpande Devendra Desai Sudeep R. Shah

A 30-year-old female, with no significant family history, came with complaints of intermittent, colicky abdominal pain and abdominal distension of 5 months duration, with significant weight loss. CT abdomen showed multiple polypoidal lesions in the colon. Colonoscopy revealed multiple polyps carpeting the entire colon (Fig. 1A); biopsy of which revealed adenomatous polyps. The patient underwent...

Journal: :Arteriosclerosis, thrombosis, and vascular biology 2013
Alex P Reiner Ethan M Lange Nancy S Jenny Paulo H M Chaves Jaclyn Ellis Jin Li Jeremy Walston Leslie A Lange Mary Cushman Russell P Tracy

OBJECTIVE CD14 is a glycosylphosphotidylinositol-anchored membrane glycoprotein expressed on neutrophils and monocytes/macrophages that also circulates as a soluble form (sCD14). Despite the well-recognized role of CD14 in inflammation, relatively little is known about the genetic determinants of sCD14 or the relationship of sCD14 to vascular- and aging-related phenotypes. METHODS AND RESULTS...

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