遗传性球形红细胞增多症与UGT1A1基因启动子区域的(TA)nTAA多态性——不同临床类型血浆胆红素水平的比较 - Suppr

Hereditary spherocytosis and the (TA)nTAA polymorphism of UGT1A1 gene promoter region--a comparison of the bilirubin plasmatic levels in the different clinical forms.

作者信息

Rocha Susana, Costa Elísio, Ferreira Fátima, Cleto Esmeralda, Barbot José, Rocha-Pereira Petronila, Quintanilha Alexandre, Belo Luís, Santos-Silva Alice

出版信息

Blood Cells Mol Dis. 2010 Mar-Apr;44(2):117-9. doi: 10.1016/j.bcmd.2009.10.012.

DOI:10.1016/j.bcmd.2009.10.012

PMID:19931474

Abstract

摘要

相似文献

Hereditary spherocytosis and the (TA)nTAA polymorphism of UGT1A1 gene promoter region--a comparison of the bilirubin plasmatic levels in the different clinical forms.

Blood Cells Mol Dis. 2010 Mar-Apr;44(2):117-9. doi: 10.1016/j.bcmd.2009.10.012.

Kernicterus associated with hereditary spherocytosis and UGT1A1 promoter polymorphism.

Biol Neonate. 2006;90(4):243-6. doi: 10.1159/000093668. Epub 2006 May 30.

Coinheritance of Gilbert syndrome increases the risk for developing gallstones in patients with hereditary spherocytosis.

Blood. 1999 Oct 1;94(7):2259-62.

Gilbert Syndrome with Concomitant Hereditary Spherocytosis Presenting with Moderate Unconjugated Hyperbilirubinemia.

Intern Med. 2017;56(6):661-664. doi: 10.2169/internalmedicine.56.7362. Epub 2017 Mar 17.

Impact of UGT1A1 gene variants on total bilirubin levels in Gilbert syndrome patients and in healthy subjects.

Blood Cells Mol Dis. 2012 Mar 15;48(3):166-72. doi: 10.1016/j.bcmd.2012.01.004. Epub 2012 Feb 9.

A Novel SPTA1 Mutation in a Patient with Hereditary Spherocytosis without a Family History and Coexisting Gilbert's Syndrome.

Intern Med. 2023 Jan 1;62(1):107-111. doi: 10.2169/internalmedicine.9478-22. Epub 2022 May 31.

Gilbert syndrome associated with beta-thalassemia.

Pediatr Hematol Oncol. 2001 Dec;18(8):477-84. doi: 10.1080/088800101753328439.

A case of concomitant Gilbert's syndrome and hereditary spherocytosis.

Korean J Hepatol. 2010 Sep;16(3):321-4. doi: 10.3350/kjhep.2010.16.3.321.

Role of co-inherited Gilbert syndrome on hyperbilirubinemia in Indian beta thalassemia patients.

Hematology. 2014 Oct;19(7):388-92. doi: 10.1179/1607845413Y.0000000142. Epub 2013 Nov 30.

Gilbert syndrome increasing unconjugated hyperbilirubinemia in a child with hereditary spherocytosis.

J Pediatr Hematol Oncol. 2012 Jan;34(1):54-6. doi: 10.1097/MPH.0b013e318228fdd1.

引用本文的文献

Body fat percentage is a major determinant of total bilirubin independently of UGT1A1*28 polymorphism in young obese.

PLoS One. 2014 Jun 5;9(6):e98467. doi: 10.1371/journal.pone.0098467. eCollection 2014.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验

Hereditary spherocytosis and the (TA)nTAA polymorphism of UGT1A1 gene promoter region--a comparison of the bilirubin plasmatic levels in the different clinical forms.

作者信息

Rocha Susana, Costa Elísio, Ferreira Fátima, Cleto Esmeralda, Barbot José, Rocha-Pereira Petronila, Quintanilha Alexandre, Belo Luís, Santos-Silva Alice

出版信息

Blood Cells Mol Dis. 2010 Mar-Apr;44(2):117-9. doi: 10.1016/j.bcmd.2009.10.012.

DOI:10.1016/j.bcmd.2009.10.012

PMID:19931474

Abstract

摘要

相似文献

Hereditary spherocytosis and the (TA)nTAA polymorphism of UGT1A1 gene promoter region--a comparison of the bilirubin plasmatic levels in the different clinical forms.

Blood Cells Mol Dis. 2010 Mar-Apr;44(2):117-9. doi: 10.1016/j.bcmd.2009.10.012.

Kernicterus associated with hereditary spherocytosis and UGT1A1 promoter polymorphism.

Biol Neonate. 2006;90(4):243-6. doi: 10.1159/000093668. Epub 2006 May 30.

Coinheritance of Gilbert syndrome increases the risk for developing gallstones in patients with hereditary spherocytosis.

Blood. 1999 Oct 1;94(7):2259-62.

Gilbert Syndrome with Concomitant Hereditary Spherocytosis Presenting with Moderate Unconjugated Hyperbilirubinemia.

Intern Med. 2017;56(6):661-664. doi: 10.2169/internalmedicine.56.7362. Epub 2017 Mar 17.

Impact of UGT1A1 gene variants on total bilirubin levels in Gilbert syndrome patients and in healthy subjects.

Blood Cells Mol Dis. 2012 Mar 15;48(3):166-72. doi: 10.1016/j.bcmd.2012.01.004. Epub 2012 Feb 9.

A Novel SPTA1 Mutation in a Patient with Hereditary Spherocytosis without a Family History and Coexisting Gilbert's Syndrome.

Intern Med. 2023 Jan 1;62(1):107-111. doi: 10.2169/internalmedicine.9478-22. Epub 2022 May 31.

Gilbert syndrome associated with beta-thalassemia.

Pediatr Hematol Oncol. 2001 Dec;18(8):477-84. doi: 10.1080/088800101753328439.

A case of concomitant Gilbert's syndrome and hereditary spherocytosis.

Korean J Hepatol. 2010 Sep;16(3):321-4. doi: 10.3350/kjhep.2010.16.3.321.

Role of co-inherited Gilbert syndrome on hyperbilirubinemia in Indian beta thalassemia patients.

Hematology. 2014 Oct;19(7):388-92. doi: 10.1179/1607845413Y.0000000142. Epub 2013 Nov 30.

Gilbert syndrome increasing unconjugated hyperbilirubinemia in a child with hereditary spherocytosis.

J Pediatr Hematol Oncol. 2012 Jan;34(1):54-6. doi: 10.1097/MPH.0b013e318228fdd1.

引用本文的文献

Body fat percentage is a major determinant of total bilirubin independently of UGT1A1*28 polymorphism in young obese.

PLoS One. 2014 Jun 5;9(6):e98467. doi: 10.1371/journal.pone.0098467. eCollection 2014.

Hereditary spherocytosis and the (TA)nTAA polymorphism of UGT1A1 gene promoter region--a comparison of the bilirubin plasmatic levels in the different clinical forms.

作者信息

出版信息

相似文献

引用本文的文献

文献AI研究员

用中文搜PubMed

文档翻译

Suppr 超能文献

Hereditary spherocytosis and the (TA)nTAA polymorphism of UGT1A1 gene promoter region--a comparison of the bilirubin plasmatic levels in the different clinical forms.

作者信息

出版信息

相似文献

引用本文的文献