تقرير
NF-E2 mutation as a novel cause for inherited thrombocytopenia.
العنوان: | NF-E2 mutation as a novel cause for inherited thrombocytopenia. |
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المؤلفون: | Luk ADW; Department of Paediatrics and Adolescent Medicine, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong, China., Yang X; Department of Paediatrics and Adolescent Medicine, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong, China., Alcasabas AP; Section of Pediatric Hematology-Oncology, University of the Philippines - Philippine General Hospital, Manila, Philippines., Hao RC; Section of Allergy and Immunology, University of the Philippines - Philippine General Hospital, Manila, Philippines., Chan KW; Department of Paediatrics and Adolescent Medicine, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong, China., Lee PP; Department of Paediatrics and Adolescent Medicine, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong, China.; The Hong Kong Children's Hospital, Hong Kong, China., Yang J; Department of Paediatrics and Adolescent Medicine, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong, China., Chan GC; Department of Paediatrics and Adolescent Medicine, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong, China.; The Hong Kong Children's Hospital, Hong Kong, China., So JC; The Hong Kong Children's Hospital, Hong Kong, China., Yang W; Department of Paediatrics and Adolescent Medicine, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong, China., Lau YL; Department of Paediatrics and Adolescent Medicine, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong, China.; The Hong Kong Children's Hospital, Hong Kong, China. |
المصدر: | British journal of haematology [Br J Haematol] 2020 Apr; Vol. 189 (2), pp. e41-e44. Date of Electronic Publication: 2020 Jan 17. |
نوع المنشور: | Case Reports; Letter |
اللغة: | English |
بيانات الدورية: | Publisher: Wiley-Blackwell Country of Publication: England NLM ID: 0372544 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1365-2141 (Electronic) Linking ISSN: 00071048 NLM ISO Abbreviation: Br J Haematol Subsets: MEDLINE |
أسماء مطبوعة: | Publication: Oxford : Wiley-Blackwell Original Publication: Oxford : Blackwell Scientific Publications |
مواضيع طبية MeSH: | NF-E2 Transcription Factor, p45 Subunit/*adverse effects , Thrombocytopenia/*genetics, Humans ; Infant, Newborn ; Male ; Mutation |
References: | Cell. 1995 Jun 2;81(5):695-704. (PMID: 7774011) Front Cardiovasc Med. 2019 Jun 19;6:80. (PMID: 31275945) J Clin Immunol. 2009 Jul;29(4):490-500. (PMID: 19308710) Blood. 1999 Nov 1;94(9):3037-47. (PMID: 10556187) Leukemia. 2002 Sep;16(9):1773-81. (PMID: 12200693) Ann N Y Acad Sci. 2011 Nov;1238:33-41. (PMID: 22129051) Blood. 2010 Jan 21;115(3):677-86. (PMID: 19901266) J Exp Med. 2014 Oct 20;211(11):2137-49. (PMID: 25311508) PLoS One. 2012;7(10):e46688. (PMID: 23056405) J Exp Med. 2013 May 6;210(5):1003-19. (PMID: 23589569) Genome Biol. 2012 Feb 09;13(2):R9. (PMID: 22322200) Mol Cell Biol. 2005 Dec;25(23):10365-78. (PMID: 16287851) Blood. 2001 Apr 1;97(7):2151-8. (PMID: 11264184) Blood. 2003 Dec 1;102(12):3970-9. (PMID: 12907454) Blood. 2019 Dec 5;134(23):2070-2081. (PMID: 31217188) Proc Natl Acad Sci U S A. 1995 Sep 12;92(19):8690-4. (PMID: 7567998) Blood. 2007 Feb 15;109(4):1451-9. (PMID: 17047147) Blood. 2000 Aug 15;96(4):1366-73. (PMID: 10942379) |
المشرفين على المادة: | 0 (NF-E2 Transcription Factor, p45 Subunit) |
تواريخ الأحداث: | Date Created: 20200118 Date Completed: 20201204 Latest Revision: 20201214 |
رمز التحديث: | 20221213 |
مُعرف محوري في PubMed: | PMC7187305 |
DOI: | 10.1111/bjh.16438 |
PMID: | 31951293 |
قاعدة البيانات: | MEDLINE |
تدمد: | 1365-2141 |
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DOI: | 10.1111/bjh.16438 |