145 related articles for article (PubMed ID: 37890331)
21. Clinical Characterization of Alagille Syndrome in Patients with Cholestatic Liver Disease.
Semenova N; Kamenets E; Annenkova E; Marakhonov A; Gusarova E; Demina N; Guseva D; Anisimova I; Degtyareva A; Taran N; Strokova T; Zakharova E
Int J Mol Sci; 2023 Jul; 24(14):. PubMed ID: 37511516
[TBL] [Abstract][Full Text] [Related]
22. Novel JAG1 variants leading to Alagille syndrome in two Chinese cases.
Feng X; Ping J; Gao S; Han D; Song W; Li X; Tao Y; Wang L
Sci Rep; 2024 Jan; 14(1):1812. PubMed ID: 38245625
[TBL] [Abstract][Full Text] [Related]
23. Alagille syndrome: understanding the genotype-phenotype relationship and its potential therapeutic impact.
Halma J; Lin HC
Expert Rev Gastroenterol Hepatol; 2023; 17(9):883-892. PubMed ID: 37668532
[TBL] [Abstract][Full Text] [Related]
24. Sox9 Is a Modifier of the Liver Disease Severity in a Mouse Model of Alagille Syndrome.
Adams JM; Huppert KA; Castro EC; Lopez MF; Niknejad N; Subramanian S; Zarrin-Khameh N; Finegold MJ; Huppert SS; Jafar-Nejad H
Hepatology; 2020 Apr; 71(4):1331-1349. PubMed ID: 31469182
[TBL] [Abstract][Full Text] [Related]
25. Alagille syndrome: an uncommon cause of intrahepatic cholestasis in adults.
Zhang W; Zhao X; Huang J; Ou X; Jia J
Rev Esp Enferm Dig; 2019 Apr; 111(4):323-326. PubMed ID: 30746957
[TBL] [Abstract][Full Text] [Related]
26. [Clinical features and gene mutation analysis of patients with Alagille syndrome].
Liu XG; Wei HJ; Liu P; Liu X; Tang L; Yang Y; Li YR
Zhonghua Yi Xue Za Zhi; 2021 Aug; 101(31):2454-2459. PubMed ID: 34399559
[No Abstract] [Full Text] [Related]
27. Alagille syndrome: pathogenesis, diagnosis and management.
Turnpenny PD; Ellard S
Eur J Hum Genet; 2012 Mar; 20(3):251-7. PubMed ID: 21934706
[TBL] [Abstract][Full Text] [Related]
28. ASO silencing of a glycosyltransferase, Poglut1 , improves the liver phenotypes in mouse models of Alagille syndrome.
Niknejad N; Fox D; Burwinkel JL; Zarrin-Khameh N; Cho S; Soriano A; Cast AE; Lopez MF; Huppert KA; Rigo F; Huppert SS; Jafar-Nejad P; Jafar-Nejad H
Hepatology; 2023 Nov; 78(5):1337-1351. PubMed ID: 37021797
[TBL] [Abstract][Full Text] [Related]
29. Premature senescence of the liver in Alagille patients.
Jannone G; de Magnée C; Tambucci R; Evraerts J; Ravau J; Najimi M; Sokal EM
PLoS One; 2023; 18(4):e0285019. PubMed ID: 37099537
[TBL] [Abstract][Full Text] [Related]
30. [Alagille syndrome associated to JAG1 gene deletion. An unusual etiology].
Avila-Jaque D; Díaz C; Pardo R
Andes Pediatr; 2024 Apr; 95(2):196-201. PubMed ID: 38801368
[TBL] [Abstract][Full Text] [Related]
31. An Atypical Presentation of Alagille Syndrome.
Wu KY; Treece AL; Russo PA; Wen JW
Pediatr Dev Pathol; 2018; 21(1):79-83. PubMed ID: 29187043
[TBL] [Abstract][Full Text] [Related]
32. Alagille Syndrome: Current Understanding of Pathogenesis, and Challenges in Diagnosis and Management.
Ayoub MD; Kamath BM
Clin Liver Dis; 2022 Aug; 26(3):355-370. PubMed ID: 35868679
[TBL] [Abstract][Full Text] [Related]
33. Isolated aneurysmal disease as an underestimated finding in individuals with JAG1 pathogenic variants.
Rodrigues Bento J; Krebsová A; Van Gucht I; Valdivia Callejon I; Van Berendoncks A; Votypka P; Luyckx I; Peldova P; Laga S; Havelka M; Van Laer L; Trunecka P; Boeckx N; Verstraeten A; Macek M; Meester JAN; Loeys B
Hum Mutat; 2022 Dec; 43(12):1824-1828. PubMed ID: 35819173
[TBL] [Abstract][Full Text] [Related]
34. Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 20p (20p12-p13) encompassing JAG1 and a literature review of prenatal diagnosis of Alagille syndrome.
Chen CP; Yin CS; Wang LK; Chern SR; Chen SW; Lai ST; Wu PS; Chen WL; Wang W
Taiwan J Obstet Gynecol; 2017 Jun; 56(3):390-393. PubMed ID: 28600057
[TBL] [Abstract][Full Text] [Related]
35. Alagille Syndrome.
Mitchell E; Gilbert M; Loomes KM
Clin Liver Dis; 2018 Nov; 22(4):625-641. PubMed ID: 30266153
[TBL] [Abstract][Full Text] [Related]
36. Defining pathogenicity of NOTCH2 variants for diagnosis of Alagille syndrome type 2 using a large cohort of patients.
Li ZD; Abuduxikuer K; Wang L; Hao CZ; Zhang J; Wang MX; Li LT; Qiu YL; Xie XB; Lu Y; Wang JS
Liver Int; 2022 Aug; 42(8):1836-1848. PubMed ID: 35567760
[TBL] [Abstract][Full Text] [Related]
37. JAG1 loss‑of‑function mutations contributed to Alagille syndrome in two Chinese families.
Zhang E; Xu Y; Yu Y; Chen S; Yu Y; Sun K
Mol Med Rep; 2018 Aug; 18(2):2356-2364. PubMed ID: 29956768
[TBL] [Abstract][Full Text] [Related]
38. Regenerative failure of intrahepatic biliary cells in Alagille syndrome rescued by elevated Jagged/Notch/Sox9 signaling.
Zhao C; Matalonga J; Lancman JJ; Liu L; Xiao C; Kumar S; Gates KP; He J; Graves A; Huisken J; Azuma M; Lu Z; Chen C; Ding BS; Dong PDS
Proc Natl Acad Sci U S A; 2022 Dec; 119(50):e2201097119. PubMed ID: 36469766
[TBL] [Abstract][Full Text] [Related]
39. A novel JAG1 frameshift variant causing Alagille syndrome with incomplete penetrance.
Yang Y; Wang H
Clin Biochem; 2022 Jun; 104():19-21. PubMed ID: 35151641
[TBL] [Abstract][Full Text] [Related]
40. [Identification of a novel JAG1 mutation in a family affected by Alagille syndrome].
Cheng Y; Zhao ST; Guo L; Deng M; Zhou Q; Song YZ
Zhongguo Dang Dai Er Ke Za Zhi; 2016 Nov; 18(11):1130-1135. PubMed ID: 27817779
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
