187 related articles for article (PubMed ID: 33187473)
1. Novel nonsense mutation p. Gln264Ter in the ANK1 confirms causative role for hereditary spherocytosis: a case report.
Chai S; Jiao R; Sun X; Fu P; Zhao Q; Sang M
BMC Med Genet; 2020 Nov; 21(1):223. PubMed ID: 33187473
[TBL] [Abstract][Full Text] [Related]
2. Identification of a de novo ANK1 mutation in a Chinese family with hereditary spherocytosis.
Guan H; Liang X; Zhang R; Wang H; Liu W; Zhang R; Yang J; Liu S
Hematology; 2018 Jul; 23(6):357-361. PubMed ID: 29099659
[TBL] [Abstract][Full Text] [Related]
3. Identification of a novel p.Q1772X ANK1 mutation in a Korean family with hereditary spherocytosis.
Han JH; Kim S; Jang H; Kim SW; Lee MG; Koh H; Lee JH
PLoS One; 2015; 10(6):e0131251. PubMed ID: 26107955
[TBL] [Abstract][Full Text] [Related]
4. Targeted next-generation sequencing identified a novel
Sun Q; Xie Y; Wu P; Li S; Hua Y; Lu X; Zhao W
Hematology; 2019 Dec; 24(1):583-587. PubMed ID: 31390973
[No Abstract] [Full Text] [Related]
5. Spectrum of Ankyrin Mutations in Hereditary Spherocytosis: A Case Report and Review of the Literature.
Luo Y; Li Z; Huang L; Tian J; Xiong M; Yang Z
Acta Haematol; 2018; 140(2):77-86. PubMed ID: 30227413
[TBL] [Abstract][Full Text] [Related]
6. Exome sequencing confirms molecular diagnoses in 38 Chinese families with hereditary spherocytosis.
Wang R; Yang S; Xu M; Huang J; Liu H; Gu W; Zhang X
Sci China Life Sci; 2018 Aug; 61(8):947-953. PubMed ID: 29572776
[TBL] [Abstract][Full Text] [Related]
7. A Novel ANK1 Mutation in a Neonatal Hereditary Spherocytosis Case: Diagnostic Challenges and Familial Genetic Analysis.
Li J; Guo H; Zhu Z; Sun J
Acta Haematol; 2022; 145(6):575-581. PubMed ID: 35817016
[TBL] [Abstract][Full Text] [Related]
8. Clinical and genetic diagnosis for 26 paitents with hereditary spherocytosis.
Bai L; Zheng L; Li B; Huang H; Shi X; Yi Y
Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2023 Apr; 48(4):565-574. PubMed ID: 37385619
[TBL] [Abstract][Full Text] [Related]
9. Two novel ANK1 loss-of-function mutations in Chinese families with hereditary spherocytosis.
Hao L; Li S; Ma D; Chen S; Zhang B; Xiao D; Zhang J; Jiang N; Jiang S; Ma J
J Cell Mol Med; 2019 Jun; 23(6):4454-4463. PubMed ID: 31016877
[TBL] [Abstract][Full Text] [Related]
10. Identification of new mutations in patients with hereditary spherocytosis by next-generation sequencing.
Qin L; Nie Y; Zhang H; Chen L; Zhang D; Lin Y; Ru K
J Hum Genet; 2020 Apr; 65(4):427-434. PubMed ID: 31980736
[TBL] [Abstract][Full Text] [Related]
11. Identification of a novel ANK1 mutation in hereditary spherocytosis co-existing with BWS.
Zhang Q; Zhang C; Wang Y; Hao S; Shi J; Feng X; Zheng L; Wang X; Xue C; Zhou B; Liu F; Zhao F; Li X; Deng L; Hou J; Meng Z
Mol Genet Genomic Med; 2022 Apr; 10(4):e1903. PubMed ID: 35218326
[TBL] [Abstract][Full Text] [Related]
12. Mutational characteristics of ANK1 and SPTB genes in hereditary spherocytosis.
Park J; Jeong DC; Yoo J; Jang W; Chae H; Kim J; Kwon A; Choi H; Lee JW; Chung NG; Kim M; Kim Y
Clin Genet; 2016 Jul; 90(1):69-78. PubMed ID: 26830532
[TBL] [Abstract][Full Text] [Related]
13. Targeted next-generation sequencing identifies novel deleterious variants in ANK1 gene causing severe hereditary spherocytosis in Indian patients: expanding the molecular and clinical spectrum.
More TA; Devendra R; Dongerdiye R; Warang P; Kedar P
Mol Genet Genomics; 2023 Mar; 298(2):427-439. PubMed ID: 36598564
[TBL] [Abstract][Full Text] [Related]
14. De novo variations of ANK1 gene caused hereditary spherocytosis in two Chinese children by affecting pre-mRNA splicing.
Wang Y; Huang L; Zhu Y; An X; Li J; Zhen J; Yu J
BMC Pediatr; 2023 Jan; 23(1):23. PubMed ID: 36647015
[TBL] [Abstract][Full Text] [Related]
15. Identification of a novel ANK1 mutation in a Chinese family with hereditary spherocytosis: A case report.
Zhu X; Peng M; Yin Y; Zhang Y; Zheng D; Peng Z; Cheng J; Yang S; Wang J
Exp Ther Med; 2023 Jan; 25(1):4. PubMed ID: 36561627
[TBL] [Abstract][Full Text] [Related]
16. A Novel
Jang W; Kim SK; Nahm CH; Choi JW; Kim JJ; Moon Y
Ann Clin Lab Sci; 2021 Jan; 51(1):136-139. PubMed ID: 33653793
[TBL] [Abstract][Full Text] [Related]
17. A novel ENU-generated truncation mutation lacking the spectrin-binding and C-terminal regulatory domains of Ank1 models severe hemolytic hereditary spherocytosis.
Hughes MR; Anderson N; Maltby S; Wong J; Berberovic Z; Birkenmeier CS; Haddon DJ; Garcha K; Flenniken A; Osborne LR; Adamson SL; Rossant J; Peters LL; Minden MD; Paulson RF; Wang C; Barber DL; McNagny KM; Stanford WL
Exp Hematol; 2011 Mar; 39(3):305-20, 320.e1-2. PubMed ID: 21193012
[TBL] [Abstract][Full Text] [Related]
18. [Identification of a novel ANK1 gene mutation in a newborn with hereditary spherocytosis].
Jiang M; Lu J; Zhong Y; Wang Y; Yang C
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Feb; 33(1):44-7. PubMed ID: 26829732
[TBL] [Abstract][Full Text] [Related]
19. A de novo ANK1 mutation associated to hereditary spherocytosis: a case report.
Huang TL; Sang BH; Lei QL; Song CY; Lin YB; Lv Y; Yang CH; Li N; Yang YH; Zhang XW; Tian X
BMC Pediatr; 2019 Feb; 19(1):62. PubMed ID: 30777044
[TBL] [Abstract][Full Text] [Related]
20. Identification of a De Novoc.1000delA ANK1 mutation associated to hereditary spherocytosis in a neonate with Coombs-negative hemolytic jaundice-case reports and review of the literature.
Xie L; Xing Z; Li C; Liu SX; Wen FQ
BMC Med Genomics; 2021 Mar; 14(1):77. PubMed ID: 33706756
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
