نتایج جستجو برای: q12

تعداد نتایج: 725  

Journal: :Journal of medical genetics 1993
W P Robinson J Wagstaff F Bernasconi C Baccichetti L Artifoni E Franzoni L Suslak L Y Shih H Aviv A A Schinzel

A patient with Angelman syndrome and a 46,XY/47,XY,+inv dup(15)(pter-->q11: q11-->pter) karyotype and a patient with Prader-Willi syndrome and a 46,XY/47,XY,+inv dup(15)(pter-->q12: q12-->pter) karyotype were investigated with molecular markers along chromosome 15. Paternal uniparental isodisomy was found for all informative markers in the first case which indicates that this, rather than the p...

Journal: :Annals of clinical and laboratory science 1994
H F Mark D R Gnepp P Nigri W Campbell Y Mark

The limiting factors in conventional cytogenetic analysis of cell culture, especially of solid tumors, include insufficient metaphases, overgrowth of abnormal mitotic cells by normal cells, and suboptimal quality of harvesting and banding. Despite the availability of numerous protocols to induce G-banding, as well as Q-, R-, and C-banding, occasions still arise in which the analysis is severely...

2016
Sarah Hackman Richard D Hammer Lester Layfield

Malignant mesotheliomas are generally classified into epithelioid, sarcomatoid, desmoplastic, and biphasic types with rare reports of a small cell form. These small cell variants display some morphologic overlap with desmoplastic small round cell tumors (DSRCTs) which generally occur within the abdominal cavity of young males and are defined by a characteristic t(11;22)(p13;q12) translocation. ...

Journal: :Cancer research 2004
Wei Xiong Zhao Yang Zeng Jia Hui Xia Kun Xia Shou Rong Shen Xiao Ling Li Dong Xu Hu Chen Tan Juan Juan Xiang Jie Zhou Hao Deng Song Qing Fan Wei Fang Li Rong Wang Ming Zhou Shi Guo Zhu Hong Bin Lü Jun Qian Bi Cheng Zhang Jie Ru Wang Jian Ma Bing Yi Xiao He Huang Qiu Hong Zhang Yan Hong Zhou Xiao Min Luo Hou De Zhou Yi Xin Yang He Ping Dai Guo Yin Feng Qian Pan Ling Qian Wu Lin He Gui Yuan Li

Nasopharyngeal carcinoma (NPC) poses one of the serious health problems in southern Chinese, with an incidence rate ranging from 15 to 50/100,000. Chromosome translocation t(1;3) and frequent loss of heterogeneity on short arms of chromosome 3 and 9 have been reported to be associated with NPC, and a genome-wide scan identified an NPC susceptibility locus on chromosome 4p15.1-q12 recently. In o...

Journal: :Journal of medical genetics 1997
H R Davies I A Hughes M O Savage C A Quigley M Trifiro L Pinsky T R Brown M N Patterson

We present data to suggest the existence of a mental retardation (MR) locus at Xq11.2-q12 between DXS1 and DXS905, identified in two subjects with complete androgen insensitivity syndrome (CAIS) and MR. Androgen insensitivity syndrome is a disorder of male sexual differentiation caused by a defect in the androgen receptor (AR) gene (Xq11-q12). Two subjects with CAIS resulting from a complete de...

Journal: :American Economic Journal: Economic Policy 2021

This paper examines how subsistence farmers respond to extreme heat. Using microdata from Peruvian households, we find that high temperatures reduce agricultural productivity, increase area planted, and change crop mix. These findings are consistent with using input adjustments as a short-term mechanism attenuate the effect of heat on output. response seems complement other coping strategies, s...

Journal: :The American Economic Review 2021

Can targeting information to network-central farmers induce more adoption of a new agricultural technology? By combining social network data and field experiment in 200 villages Malawi, we find that central is important spur the diffusion process. We also provide evidence one explanation for why centrality matters: process governed by complex contagion. Our results are consistent with model whi...

Journal: :Genes, chromosomes & cancer 2001
M D Odero K Carlson M J Calasanz I Lahortiga V Chinwalla J D Rowley

TEL/ETV6 is the first transcription factor identified that is specifically required for hematopoiesis within the bone marrow. This gene has been found to have multiple fusion partners; 35 different chromosome bands have been involved in ETV6 translocations, of which 13 have been cloned. To identify additional ETV6 partner genes and to characterize the chromosomal abnormalities more fully, we st...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2004
Jing Chen Daniel J Deangelo Jeffery L Kutok Ifor R Williams Benjamin H Lee Martha Wadleigh Nicole Duclos Sarah Cohen Jennifer Adelsperger Rachel Okabe Allison Coburn Ilene Galinsky Brian Huntly Pamela S Cohen Thomas Meyer Doriano Fabbro Johannes Roesel Lolita Banerji James D Griffin Sheng Xiao Jonathan A Fletcher Richard M Stone D Gary Gilliland

Human stem cell leukemia-lymphoma syndrome usually presents itself as a myeloproliferative disorder (MPD) that evolves to acute myeloid leukemia and/or lymphoma. The syndrome associated with t(8;13)(p11;q12) results in expression of the ZNF198-fibroblast growth factor receptor (FGFR) 1 fusion tyrosine kinase. Current empirically derived cytotoxic chemotherapy is inadequate for treatment of this...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2004
Sudha K Iyengar Barbara E K Klein Ronald Klein Gyungah Jun James H Schick Christopher Millard Rachel Liptak Karlie Russo Kristine E Lee Robert C Elston

Age-related cataracts are one of the leading causes of visual impairment and blindness among the elderly worldwide. Among age-related cataracts, cortical opacities rank as the second most common type; however, little is known about their molecular pathogenesis or genetics. To identify susceptibility loci for cortical cataracts, we genotyped a subset of families (102 families; n = 224 sib pairs)...

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