Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Wozhan Tang"'
Autor:
Cherie H. Dunphy, Wozhan Tang
Publikováno v:
Leukemia & Lymphoma. 49:75-80
Non-Hodgkin lymphomas (NHLs) are often characterized by specific cytogenetic abnormalities. We evaluate the utility of routine cytogenetic studies in 261 "lymphoma work-ups". These include 4 non-hematolymphoid malignancies and 257 hematolymphoid proc
Publikováno v:
Biochemical and Biophysical Research Communications. 209:40-46
A λgt11 cDNA library was constructed from poly-A rich RNA prepared from circulating murine yolk sac derived nucleated erythroblasts, on day 9 of gestation. In addition to the embryonic globin genes, this library was found to contain clones for the h
Publikováno v:
Blood. 81:1636-1640
A 10-year-old Danish girl with congenital anemia is described. At birth, she had severe anemia and erythroblastosis and was transfused a number of times during the first year. The need for transfusions has since declined steadily. Her reticulocyte co
Autor:
Barry Eng, Stephen A. Liebhaber, Wozhan Tang, M. Albitar, Margie Patterson, John S. Waye, D. R. Higgs, Hong-yuan Luo, David H.K. Chui
Publikováno v:
Blood. 80:517-522
zeta-Globin chain expression in carriers of a number of deletional alpha-thalassemias is investigated by radioimmunoassay. In a few cases, zeta-globin mRNAs are also studied. zeta-Globin chains are detected in (--SEA/), (--MED/), and (--SPAN/) deleti
Acute liver failure (ALF) is a medical emergency requiring immediate evaluation for liver transplantation. We describe an unusual case of a patient who presented with ascites, jaundice, and encephalopathy and was found to have ALF due to natural kill
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afeef3e49f673f48a19270c65271da40
https://europepmc.org/articles/PMC4087729/
https://europepmc.org/articles/PMC4087729/
Autor:
Wozhan, Tang, Sharon L, Wenger
Publikováno v:
Journal of the Association of Genetic Technologists. 31(4)
Pallister-Killian syndrome is a chromosomal mosaic syndrome with a normal and an isochromosome 12p cell line, the latter rarely seen in peripheral blood. The isochromosome 12p cell line decreases with serial passages of fibroblasts in vitro and with
Publikováno v:
The Lancet. 342:1145-1147
The gene frequency for (SEA/) deletional α-thalassaemia is high in Southeast Asian populations. We report a simple immunocytological test that is higly sensitive and specific for the detection of adult carriers of the (SEA/) deletion. We prospective
Autor:
Wozhan Tang, Luanne L. Peters, Xiao-Dong Han, Peter M. C. Wong, Yong-Hong Lai, David H.K. Chui
Publikováno v:
Mammalian genome : official journal of the International Mammalian Genome Society. 8(9)
Publikováno v:
Journal of interferon research. 12(4)
Treatment of human K-562 erythroleukemia cells with interferon-alpha (IFN-alpha) resulted in a six-fold increase in the production of epsilon-globin, a component of embryonic hemoglobin, but in a two-fold or less augmentation of the production of oth
Publikováno v:
American Journal of Medical Genetics. :328-328