Molecular Basis of the Kell-null Phenotype-Reference-Cited by-同舟云学术

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Molecular Basis of the Kell-null Phenotype

Published:2001-03 Issue:13 Volume:276 Page:10247-10252
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Yu Lung-Chih,Twu Yuh-Ching,Chang Ching-Yi,Lin Marie

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference39 articles.

1. IN-VIVO ISOSENSITISATION OF RED CELLS IN BABIES WITH HÆMOLYTIC DISEASE

2. Blood Cell Biochemistry;Redman,1995

3. Human Blood Groups;Daniels,1995

4. The Blood Group Antigen FactsBook;Reid,1997

Cited by 41 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Chronic granulomatous disease associated with Duchenne muscular dystrophy caused by Xp21.1 contiguous gene deletion syndrome: Case report and literature review;Frontiers in Genetics;2023-01-13

2. Rare Blood Groups in ABO, Rh, Kell Systems – Biological and Clinical Significance;PRILOZI;2022-07-01

3. A novel KEL null allele with c.223+1g>t leads to the absence of the Kp b antigen in a First Nation donor;Transfusion;2021-07-26

4. First report of a KELnull phenotype in Peru and a lesson of invisible genetic disparity;Transfusion and Apheresis Science;2019-08

5. Blood Donation During Pregnancy Due to Anti-Ku Hemolytic Disease of the Fetus and Newborn;Laboratory Medicine;2019-05-15

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