213 related articles for article (PubMed ID: 31014431)
1. [Clinical characteristics and genetic analysis of hereditary spherocytosis caused by mutations of ANK1 and SPTB genes].
Gong J; He XL; Zou RY; Chen KK; You YL; Zou H; Tian X; Zhu CG
Zhongguo Dang Dai Er Ke Za Zhi; 2019 Apr; 21(4):370-374. PubMed ID: 31014431
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. 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]
6. Molecular diagnosis of hereditary spherocytosis by multi-gene target sequencing in Korea: matching with osmotic fragility test and presence of spherocyte.
Choi HS; Choi Q; Kim JA; Im KO; Park SN; Park Y; Shin HY; Kang HJ; Kook H; Kim SY; Kim SJ; Kim I; Kim JY; Kim H; Park KD; Park KB; Park M; Park SK; Park ES; Park JA; Park JE; Park JK; Baek HJ; Seo JH; Shim YJ; Ahn HS; Yoo KH; Yoon HS; Won YW; Lee KS; Lee KC; Lee MJ; Lee SA; Lee JA; Lee JM; Lee JH; Lee JW; Lim YT; Jung HJ; Chueh HW; Choi EJ; Jung HL; Kim JH; Lee DS;
Orphanet J Rare Dis; 2019 May; 14(1):114. PubMed ID: 31122244
[TBL] [Abstract][Full Text] [Related]
7. Genotype-degree of hemolysis correlation in hereditary spherocytosis.
Shi Y; Li Y; Yang X; Li X; Peng G; Zhao X; Liu X; Zhao Y; Hu J; Hu X; Zhang B; Zhou K; Yang Y; Xiong Y; Li J; Fan H; Yang W; Ye L; Jing L; Zhang L; Zhang F
BMC Genomics; 2023 Jun; 24(1):304. PubMed ID: 37280519
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Whole exome sequencing identified a novel mutation (p.Ala1884Pro) of β-spectrin in a Chinese family with hereditary spherocytosis.
Fan LL; Liu JS; Huang H; Du R; Xiang R
J Gene Med; 2019 Feb; 21(2-3):e3073. PubMed ID: 30690801
[TBL] [Abstract][Full Text] [Related]
10. Mutational Characteristics of Causative Genes in Chinese Hereditary Spherocytosis Patients: a Report on Fourteen Cases and a Review of the Literature.
Wang D; Song L; Shen L; Zhang K; Lv Y; Gao M; Ma J; Wan Y; Gai Z; Liu Y
Front Pharmacol; 2021; 12():644352. PubMed ID: 34335240
[No Abstract] [Full Text] [Related]
11. Deciphering molecular heterogeneity of Indian families with hereditary spherocytosis using targeted next-generation sequencing: First South Asian study.
Aggarwal A; Jamwal M; Sharma P; Sachdeva MUS; Bansal D; Malhotra P; Das R
Br J Haematol; 2020 Mar; 188(5):784-795. PubMed ID: 31602632
[TBL] [Abstract][Full Text] [Related]
12. Clinical manifestation and phenotypic analysis of novel gene mutation in 28 Chinese children with hereditary spherocytosis.
Xie F; Lei L; Cai B; Gan L; Gao Y; Liu X; Zhou L; Jiang J
Mol Genet Genomic Med; 2021 Apr; 9(4):e1577. PubMed ID: 33620149
[TBL] [Abstract][Full Text] [Related]
13. Hereditary spherocytosis caused by copy number variation in SPTB gene identified through targeted next-generation sequencing.
Jang W; Kim J; Chae H; Kim M; Koh KN; Park CJ; Kim Y
Int J Hematol; 2019 Aug; 110(2):250-254. PubMed ID: 30903564
[TBL] [Abstract][Full Text] [Related]
14. A previously unrecognized Ankyrin-1 mutation associated with Hereditary Spherocytosis in an Italian family.
Lazzareschi I; Curatola A; Pedicelli C; Castiglia D; Buonsenso D; Gatto A; Attinà G; Valentini P
Eur J Haematol; 2019 Nov; 103(5):523-526. PubMed ID: 31400153
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. A clinical and experimental study of adult hereditary spherocytosis in the Chinese population.
Xue J; He Q; Xie XJ; Su AL; Cao SB
Kaohsiung J Med Sci; 2020 Jul; 36(7):552-560. PubMed ID: 32133777
[TBL] [Abstract][Full Text] [Related]
17. An
Wang X; Mao L; Shen N; Peng J; Zhu Y; Hu Q; Lu Y
Oncotarget; 2017 Dec; 8(68):113282-113286. PubMed ID: 29348906
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. A novel
Liu Y; Zheng J; Song L; Fang Y; Sun C; Li N; Liu G; Shu J
Exp Ther Med; 2020 Oct; 20(4):3253-3259. PubMed ID: 32855695
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
