Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Diem Dao"'
Autor:
Tran, Nguyen, Trang, Pham, Loc, Phan, Gary, Mize, Amy, Trang, Diem, Dao, Anh, Le, Robert, Gish, William M, Lee, Dung, Do, Hong K, Tang, Hai T, Phan, Binh T, Nguyen, Doan Y, Dao
Publikováno v:
Clin Liver Dis (Hoboken)
Content available: Audio Recording.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59bab937f08f4c0ea941ff64589175fd
https://doi.org/10.1002/cld.1186
https://doi.org/10.1002/cld.1186
Autor:
Trang Thi Diem Dao
Publikováno v:
Science & Technology Development Journal - Social Sciences & Humanities. 1:73-79
Literary Tourism (Literature Tourism / Literature Journey) concept is no stranger to travel organizations in the world. In Asia alone, forms of literary travel are often incorporated into tour programs such as visiting a writer’s homeland, visiting
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bef860157edf815d0937c525fb1961f9
https://doi.org/10.32508/stdjssh.v1ix3.453
https://doi.org/10.32508/stdjssh.v1ix3.453
Publikováno v:
Developmental Biology. 304:735-744
Flk1 is the major receptor for VEGF on endothelial cells. During embryogenesis, flk1 is required for both vasculogenesis and angiogenesis and abnormally elevated flk1 expression is often associated with pathological conditions in adults. While the bi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9582cd18ae6168f64d579972decb664
https://doi.org/10.1016/j.ydbio.2007.01.023
https://doi.org/10.1016/j.ydbio.2007.01.023
Autor:
Dale Frank, Robert J. Vosatka, Colum P. Walsh, Naifeng Qian, Diem Dao, Benjamin Tycko, Denise S. O'Keefe
Publikováno v:
Human Molecular Genetics. 7:597-608
Human chromosome 11p15.5 and distal mouse chromosome 7 include a megabase-scale chromosomal domain with multiple genes subject to parental imprinting. Here we describe mouse and human versions of a novel imprinted gene, IMPT1 , which lies between IPL
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf0a4753440e235a6292924b5887a66b
https://doi.org/10.1093/hmg/7.4.597
https://doi.org/10.1093/hmg/7.4.597
Autor:
Long Zhao, Qing Wang, Benjamin Tycko, Denise S. O'Keefe, Mark T. Keating, Naifeng Qian, Dale Frank, Colum P. Walsh, Diem Dao, Luwa Yuan
Publikováno v:
Human Molecular Genetics. 6:2021-2029
We searched for novel imprinted genes in a region of human chromosome 11p15.5, which contains several known imprinted genes. Here we describe the cloning and characterization of the IPL ( I mprinted in P lacenta and L iver) gene, which shows tissue-s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e770d41ee885a4cd91684d99df2d095
https://doi.org/10.1093/hmg/6.12.2021
https://doi.org/10.1093/hmg/6.12.2021
Autor:
Kwame Anyane-Yeboa, Long Zhao, Dorothy Warburton, Rhonda Sanderson, Diem Dao, Benjamin Tycko, Denise S. O'Keefe, Lawrence M. Weiss
Publikováno v:
The American Journal of Human Genetics. 61:295-303
Summary The Beckwith-Wiedemann syndrome (BWS) is marked by fetal organ overgrowth and conveys a predisposition to certain childhood tumors, including Wilms tumor (WT). The genetics of BWS have implicated a gene that maps to chromosome 11p15 and is pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e2b4f063c31fc8ed1fea913081afff28
https://doi.org/10.1086/514854
https://doi.org/10.1086/514854
Publikováno v:
The Journal of cardiovascular nursing. 21(3)
BACKGROUND AND RESEARCH OBJECTIVE Patients with mechanical heart valves must follow lifelong warfarin therapy. Warfarin, however, is a difficult drug to manage because it has a narrow therapeutic window and potentially serious side effects. Successfu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dba83bb4b631422d0736e3a7cc772173
https://pubmed.ncbi.nlm.nih.gov/16699355
https://pubmed.ncbi.nlm.nih.gov/16699355
Publikováno v:
Gene. 318
Skeletal muscle differentiation has been shown to be dependent on the expression of Rb and p300. We recently cloned a novel inhibitor of muscle differentiation called EID-1, which interacted with both of these factors. In a database search for relate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b42f2eb78fe6d7d3343a4f1f25dc627a
https://pubmed.ncbi.nlm.nih.gov/14585496
https://pubmed.ncbi.nlm.nih.gov/14585496
Autor:
Benjamin Tycko, Colum P. Walsh, Perry Nisen, Terrence Hensle, Lin Feng, Luwa Yuan, Dmitri Gorelov, Diem Dao, Darrell J. Yamashiro, Timothy H. Bestor
Publikováno v:
Human molecular genetics. 8(7)
WT2 is defined by maternal-specific loss of heterozygosity (LOH) on chromosome 11p15.5 in Wilms' tumors (WTs). The imprinted H19 gene, in this region, is silenced and hypermethylated in most WTs, and this is linked to pathological biallelic expressio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::739572f9d2035cd1795b7b24c57927c8
https://pubmed.ncbi.nlm.nih.gov/10369881
https://pubmed.ncbi.nlm.nih.gov/10369881