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Rhnull disease相关文献:
[RHnull disease].
Hrubisko M, Fábryová L, Lipsic T.
Vnitr Lek. 1974 Jul;20(6):555-62.
PMID:4210818
Rhnull disease: the amorph type results from a novel double mutation in RhCe gene on D-negative background.
Huang CH, Chen Y, Reid ME, Seidl C.
Blood. 1998 Jul 15;92(2):664-71.
PMID:9657769
Rh50 glycoprotein gene and rhnull disease: a silent splice donor is trans to a Gly279-->Glu missense mutation in the conserved transmembrane segment.
Huang CH, Liu Z, Cheng G, Chen Y.
Blood. 1998 Sep 1;92(5):1776-84.
PMID:9716608
Rhnull red cells and pregnancy.
Gibbs BJ, Moores P.
Vox Sang. 1983;45(1):83-6. doi: 10.1111/j.1423-0410.1983.tb04127.x.
PMID:6410586
Identification of a cell-surface antigen produced by a gene on human chromosome 3 (cen-q22) and not expressed by Rhnull cells.
Miller YE, Daniels GL, Jones C, Palmer DK.
Am J Hum Genet. 1987 Dec;41(6):1061-70.
PMID:3120581
A new Rhnull allele in francophone Quebecers.
St-Louis M, Éthier C, Perreault J, Lavoie J.
Transfusion. 2015 Jun;55(6 Pt 2):1580-1. doi: 10.1111/trf.12887. Epub 2014 Oct 9.
PMID:25296744
Rhnull blood group caused by novel base deletion and comprehensive pedigree analysis.
Xiaoli Z, Xi Q, Hongjun G, Ziqing Z, Yuxuan S, Yi Q, Anming L, Jianfeng Z, Yayun S, Junling H, Lingbao G.
Int Immunopharmacol. 2025 Feb 6;147:113993. doi: 10.1016/j.intimp.2024.113993. Epub 2025 Jan 3.
PMID:39755105
Phosphatidylserine transport in Rhnull erythrocytes.
Smith RE, Daleke DL.
Blood. 1990 Sep 1;76(5):1021-7.
PMID:2118395
Short duplication within the RHCE gene associated with an in cis deleted RHD causing a Rhnull amorph phenotype in an immunized pregnant woman with anti-Rh29.
Silvy M, Beley S, Peyrard T, Ouchari M, Abdelkefi S, Jemni Yacoub S, Chiaroni J, Bailly P.
Transfusion. 2015 Jun;55(6 Pt 2):1407-10. doi: 10.1111/trf.12937. Epub 2014 Nov 21.
PMID:25413218
NLRP3 Inflammasome Activation Regulates Aged RBC Clearance.
Qin L, Fengyong Z, Jiamin Z, Qixiu Y, Geming L, Rongwei X, Ziyan Z.
Inflammation. 2018 Aug;41(4):1361-1371. doi: 10.1007/s10753-018-0784-9.
PMID:29680907
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