Mutations of theKLF1gene detected in Japanese with the In(Lu) phenotype-Reference-Cited by-同舟云学术

Mutations of theKLF1gene detected in Japanese with the In(Lu) phenotype

Published:2017-02-14 Issue:4 Volume:57 Page:1072-1077
ISSN:0041-1132
Container-title:Transfusion
language:en
Short-container-title:EDITORIAL

Author:

Kawai Miho¹,Obara Kumi¹,Onodera Takayuki¹,Enomoto Takayuki¹,Ogasawara Kenichi²,Tsuneyama Hatsue²³,Uchikawa Makoto³,Inaba Shoichi¹

Affiliation:

1. Japanese Red Cross Kanto-Koshinetsu Block Saitama Blood Center; Saitama Japan

2. Japanese Red Cross Central Blood Institute; Tokyo Japan

3. Japanese Red Cross Kanto-Koshinetsu Block Blood Center; Tokyo Japan

Publisher

Wiley

Subject

Hematology,Immunology,Immunology and Allergy

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/trf.13990/fullpdf

Reference21 articles.

1. The Lutheran blood group glycoprotein, another member of the immunoglobulin superfamily, is widely expressed in human tissues and is developmentally regulated in human liver;Parsons;Proc Natl Acad Sci U S A,1995

2. Molecular cloning of the B-CAM cell surface glycoprotein of epithelial cancers: a novel member of the immunoglobulin superfamily;Campbell;Cancer Res,1994

3. Different inactivating mutations in the LU genes of three individuals with the Lutheran-null phenotype;Crew;Transfusion,2007

4. An example of Lutheran-null phenotype in a Japanese individual with 27-kb deletion from intron 2 of the LU genes [abstract];Ogasawara;Transfusion,2008

5. A novel example of the recessive Lutheran-null phenotype: a serological and molecular study [abstract];Crew;Transfus Med,2009

Cited by 13 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. Modeling primitive and definitive erythropoiesis with induced pluripotent stem cells;Blood Advances;2024-03-15

2. Targeted next-generation sequencing and long-read HiFi sequencing provide novel insights into clinically significant KLF1 variants;BMC Genomics;2024-03-01

3. Molecular and haematological characterisation of haemolytic anaemia associated with biallelic KLF1 mutations: a case series;Journal of Clinical Pathology;2023-07-28

4. Identification of Lutheran Blood Groups and Genetic Variants within KLF1 among Thai Blood Donors;Transfusion Medicine and Hemotherapy;2023

5. Novel variants in Krueppel like factor 1 that cause persistence of fetal hemoglobin in In(Lu) individuals;Scientific Reports;2021-09-17