Literature DB >> 9108434

Both paroxysmal nocturnal hemoglobinuria (PNH) type II cells and PNH type III cells can arise from different point mutations involving the same codon of the PIG-A gene.

S Rollinson, S Richards, D Norfolk, K Bibi, G Morgan, P Hillmen.   

Abstract

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Year:  1997        PMID： 9108434

Source DB:  PubMed          Journal:  Blood        ISSN： 0006-4971            Impact factor:   22.113


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  4 in total

1.  Impaired growth and elevated fas receptor expression in PIGA(+) stem cells in primary paroxysmal nocturnal hemoglobinuria.

Authors:  R Chen; S Nagarajan; G M Prince; U Maheshwari; L W Terstappen; D R Kaplan; S L Gerson; J M Albert; D E Dunn; H M Lazarus; M E Medof
Journal:  J Clin Invest       Date:  2000-09       Impact factor: 14.808

2.  Deep sequencing reveals stepwise mutation acquisition in paroxysmal nocturnal hemoglobinuria.

Authors:  Wenyi Shen; Michael J Clemente; Naoko Hosono; Kenichi Yoshida; Bartlomiej Przychodzen; Tetsuichi Yoshizato; Yuichi Shiraishi; Satoru Miyano; Seishi Ogawa; Jaroslaw P Maciejewski; Hideki Makishima
Journal:  J Clin Invest       Date:  2014-09-17       Impact factor: 14.808

3.  [The progress of molecular genetics in bone marrow failure].

Authors:  C X Liu; F K Zhang
Journal:  Zhonghua Xue Ye Xue Za Zhi       Date:  2017-01-14

4.  Bone Marrow as a Source of Cells for Paroxysmal Nocturnal Hemoglobinuria Detection.

Authors:  Alina E Dulau-Florea; Neal S Young; Irina Maric; Katherine R Calvo; Cynthia E Dunbar; Danielle M Townsley; Thomas Winkler; Mariela Monreal; Chunjie Jiang; Elaine K Jordan; Raul C Braylan
Journal:  Am J Clin Pathol       Date:  2018-07-31       Impact factor: 2.493
  4 in total

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