نتایج جستجو برای: chromosome 5q21

تعداد نتایج: 119353  

2014
Stefano La Rosa Daniela Furlan Francesca Franzi Paolo Battaglia Milo Frattini Elena Zanellato Alessandro Marando Nora Sahnane Mario Turri-Zanoni Paolo Castelnuovo Carlo Capella

Sinonasal intestinal-type adenocarcinomas (ITACs) are rare neoplasms histologically resembling intestinal adenocarcinomas. Although a neuroendocrine differentiation in ITACs has been described, true mixed exocrine-neuroendocrine carcinomas, neoplasms in which each component represents at least 30 % of the lesion, are extremely rare and their molecular alterations are largely unknown. We describ...

Journal: :Endocrine-related cancer 2003
P D Leotlela A Jauch H Holtgreve-Grez R V Thakker

Neuroendocrine tumours (NETs) originate in tissues that contain cells derived from the embryonic neural crest, neuroectoderm and endoderm. Thus, NETs occur at many sites in the body, although the majority occur within the gastro-entero-pancreatic axis and can be subdivided into those of foregut, midgut and hindgut origin. Amongst these, only those of midgut origin are generally argentaffin posi...

Journal: :Cancer research 1995
L Thiberville P Payne J Vielkinds J LeRiche D Horsman G Nouvet B Palcic S Lam

Human bronchial carcinoma is thought to develop through progressive stages from basal cell hyperplasia to squamous metaplasia, dysplasia, carcinoma in situ, and finally invasive cancer. In this study, we used tissue microdissection to examine loss of heterozygosity of chromosomes 3p21, 5q21, and 9p21 at each stage of the epithelial progression to invasive cancers. Forty-eight premalignant/malig...

Journal: :Biological psychiatry 2013
Karin Hek Ayse Demirkan Jari Lahti Antonio Terracciano Alexander Teumer Marilyn C Cornelis Najaf Amin Erin Bakshis Jens Baumert Jingzhong Ding Yongmei Liu Kristin Marciante Osorio Meirelles Michael A Nalls Yan V Sun Nicole Vogelzangs Lei Yu Stefania Bandinelli Emelia J Benjamin David A Bennett Dorret Boomsma Alessandra Cannas Laura H Coker Eco de Geus Philip L De Jager Ana V Diez-Roux Shaun Purcell Frank B Hu Eric B Rimma David J Hunter Majken K Jensen Gary Curhan Kenneth Rice Alan D Penman Jerome I Rotter Nona Sotoodehnia Rebecca Emeny Johan G Eriksson Denis A Evans Luigi Ferrucci Myriam Fornage Vilmundur Gudnason Albert Hofman Thomas Illig Sharon Kardia Margaret Kelly-Hayes Karestan Koenen Peter Kraft Maris Kuningas Joseph M Massaro David Melzer Antonella Mulas Cornelis L Mulder Anna Murray Ben A Oostra Aarno Palotie Brenda Penninx Astrid Petersmann Luke C Pilling Bruce Psaty Rajesh Rawal Eric M Reiman Andrea Schulz Joshua M Shulman Andrew B Singleton Albert V Smith Angelina R Sutin André G Uitterlinden Henry Völzke Elisabeth Widen Kristine Yaffe Alan B Zonderman Francesco Cucca Tamara Harris Karl-Heinz Ladwig David J Llewellyn Katri Räikkönen Toshiko Tanaka Cornelia M van Duijn Hans J Grabe Lenore J Launer Kathryn L Lunetta Thomas H Mosley Anne B Newman Henning Tiemeier Joanne Murabito

BACKGROUND Depression is a heritable trait that exists on a continuum of varying severity and duration. Yet, the search for genetic variants associated with depression has had few successes. We exploit the entire continuum of depression to find common variants for depressive symptoms. METHODS In this genome-wide association study, we combined the results of 17 population-based studies assessi...

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

The transcription factor SOX9 plays a crucial role in normal prostate development and has been suggested to drive prostate carcinogenesis in concert with PTEN inactivation. To evaluate the clinical impact of SOX9 and its relationship with key genomic alterations in prostate cancer, SOX9 expression was analyzed by immunohistochemistry on a tissue microarray containing 11,152 prostate cancers. Da...

1991
Ryoji Morita Susumu Saito Jiro Ishikawa Osamu Ogawa Osamu Yoshida Kazuhiro Yamakawa Yusuke Nakamura

Relatively frequent losses of heterozygosity on chromosomes 5q, 6q, and lOq, in addition to loss of heterozygosity on the short arm of chromosome 3, have been observed in renal cell carcinomas. As the first step toward isolation of tumor suppressor genes on these three chromo somal arms, we used six restriction fragment length polymorphism markers for 5q, nine for 6q, and eight for lOq to ident...

پایان نامه :وزارت بهداشت، درمان و آموزش پزشکی - دانشگاه علوم پزشکی و خدمات بهداشتی درمانی استان کرمانشاه 1370

cml in breif cml is characterized by the proliferation of large numbers of immature wbc in the blood and bone marrow. in most of the patients , it is a clonal disorder in which all cell lines, express the philadelphia chromosome)q/22 translocation(it accounts for 20 of all leukemias and most cases occur over 25 yrs of age. the disease usually begins insidiously,but symptoms referable to anemia ...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2015
Christoph Burdelski Viktor Reiswich Claudia Hube-Magg Martina Kluth Sarah Minner Christina Koop Markus Graefen Hans Heinzer Maria Christina Tsourlakis Corinna Wittmer Hartwig Huland Ronald Simon Thorsten Schlomm Guido Sauter Stefan Steurer

PURPOSE Sequestosome 1 (p62) is a multifunctional adapter protein accumulating in autophagy-defective cells. EXPERIMENTAL DESIGN To evaluate the clinical impact and relationship with key genomic alterations in prostate cancer, p62 protein levels were analyzed by immunohistochemistry on a tissue microarray containing 12,427 prostate cancers. Data on ERG status and deletions of PTEN, 3p13, 5q21...

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