Zobrazeno 1 - 10
of 380
pro vyhledávání: '"Sl Thein"'
Publikováno v:
Hematology, Transfusion and Cell Therapy. 44:S12-S13
Autor:
Stephan Menzel, Rooks H, Zelenika D, Sn, Mtatiro, Gnanakulasekaran A, Drasar E, Cox S, Liu L, Masood M, Silver N, Garner C, Vasavda N, Howard J, Makani J, Adekile A, Pace B, Spector T, Farrall M, Lathrop M, Sl, Thein
Publikováno v:
Menzel, S; Rooks, H; Zelenika, D; Mtatiro, SN; Gnanakulasekaran, A; Drasar, E; et al.(2014). Global Genetic Architecture of an Erythroid Quantitative Trait Locus, HMIP-2. Annals of Human Genetics. doi: 10.1111/ahg.12077. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/5gq115v8
Europe PubMed Central
Europe PubMed Central
HMIP-2 is a human quantitative trait locus affecting peripheral numbers, size and hemoglobin composition of red blood cells, with a marked effect on the persistence of the fetal form of hemoglobin, HbF, in adults. The locus consists of multiple commo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::4ac73c328e534204ad514d28fc584d1f
http://www.escholarship.org/uc/item/5gq115v8
http://www.escholarship.org/uc/item/5gq115v8
Autor:
David Neil Cooper, J. Emmerich, Sl Thein, M. Boisclair, D W Perry, R. J. Olds, M. Aiach, V. Chowdhury, Morris A. Blajchman, David A. Lane
Publikováno v:
Scopus-Elsevier
Publikováno v:
Blood. 81:861-863
Publikováno v:
Blood. 79:2801-2803
Publikováno v:
Blood. 77:2791-2793
Autor:
Hh, Boven, Rj, Olds, Sl, Thein, Ph, Reitsma, Da, Lane, Briët E, Jan P Vandenbroucke, Fr, Rosendaal
Publikováno v:
Europe PubMed Central
We studied the molecular basis and genetic heterogeneity of hereditary antithrombin (III) deficiency in nine Dutch families. Polymerase chain reaction (PCR) amplification and direct sequencing of all antithrombin gene exons and flanking intronic regi
Publikováno v:
Blood. 83(6)
A considerable number of deletions of variable size and position that involve the beta-globin gene complex on chromosome 11 are associated with the clinical entities of hereditary persistence of fetal hemoglobin (HPFH) and delta beta thalassemia. Spe
Publikováno v:
Europe PubMed Central
"Heterocellular hereditary persistence of fetal hemoglobin" (HPFH) is the term used to describe the genetically determined persistence of fetal hemoglobin (Hb F) production into adult life, in the absence of any related hematological disorder. Wherea
Publikováno v:
Blood. 82(3)
An inherited hypochromic microcytic anemia transmitted in an autosomal manner has been observed in three generations of an English family. Affected members had the hallmarks of heterozygous beta-thalassemia, ie, elevated levels of hemoglobin A2 and i