216 related articles for article (PubMed ID: 24391948)
21. Analysis of JAG1 gene variant in Chinese patients with Alagille syndrome.
Wang H; Wang X; Li Q; Chen S; Liu L; Wei Z; Wang L; Liu Y; Zhao X; He L; Wang J; Xing Q
Gene; 2012 May; 499(1):191-3. PubMed ID: 22405927
[TBL] [Abstract][Full Text] [Related]
22. Oxidative stress-induced apoptosis in two patients with Alagille syndrome.
Radi E; Formichi P; Di Maio G; Battisti C; Federico A
J Neurol Sci; 2011 Sep; 308(1-2):49-56. PubMed ID: 21714972
[TBL] [Abstract][Full Text] [Related]
23. Conditional JAG1 mutation shows the developing heart is more sensitive than developing liver to JAG1 dosage.
Lu F; Morrissette JJ; Spinner NB
Am J Hum Genet; 2003 Apr; 72(4):1065-70. PubMed ID: 12649809
[TBL] [Abstract][Full Text] [Related]
24. JAG1 mutations are found in approximately one third of patients presenting with only one or two clinical features of Alagille syndrome.
Guegan K; Stals K; Day M; Turnpenny P; Ellard S
Clin Genet; 2012 Jul; 82(1):33-40. PubMed ID: 21752016
[TBL] [Abstract][Full Text] [Related]
25. PKCδ is required for Jagged-1 induction of human mesenchymal stem cell osteogenic differentiation.
Zhu F; Sweetwyne MT; Hankenson KD
Stem Cells; 2013 Jun; 31(6):1181-92. PubMed ID: 23404789
[TBL] [Abstract][Full Text] [Related]
26. Jagged-mediated development and disease: Mechanistic insights and therapeutic implications for Alagille syndrome.
Mašek J; Andersson ER
Curr Opin Cell Biol; 2024 Feb; 86():102302. PubMed ID: 38194749
[TBL] [Abstract][Full Text] [Related]
27. The DSL domain in mutant JAG1 ligand is essential for the severity of the liver defect in Alagille syndrome.
Yuan ZR; Okaniwa M; Nagata I; Tazawa Y; Ito M; Kawarazaki H; Inomata Y; Okano S; Yoshida T; Kobayashi N; Kohsaka T
Clin Genet; 2001 May; 59(5):330-7. PubMed ID: 11359464
[TBL] [Abstract][Full Text] [Related]
28. Variable expression of Alagille syndrome in a family with a new JAG1 gene mutation.
Ziesenitz VC; Loukanov T; Gläser C; Gorenflo M
Cardiol Young; 2016 Jan; 26(1):164-7. PubMed ID: 25613755
[TBL] [Abstract][Full Text] [Related]
29. Ozzy, a Jag1 vestibular mouse mutant, displays characteristics of Alagille syndrome.
Vrijens K; Thys S; De Jeu MT; Postnov AA; Pfister M; Cox L; Zwijsen A; Van Hoof V; Mueller M; De Clerck NM; De Zeeuw CI; Van Camp G; Van Laer L
Neurobiol Dis; 2006 Oct; 24(1):28-40. PubMed ID: 16875832
[TBL] [Abstract][Full Text] [Related]
30. Alagille Syndrome Mimicking Biliary Atresia in Early Infancy.
Dědič T; Jirsa M; Keil R; Rygl M; Šnajdauf J; Kotalová R
PLoS One; 2015; 10(11):e0143939. PubMed ID: 26618708
[TBL] [Abstract][Full Text] [Related]
31. JAG1 Mutation Spectrum and Origin in Chinese Children with Clinical Features of Alagille Syndrome.
Li L; Dong J; Wang X; Guo H; Wang H; Zhao J; Qiu Y; Abuduxikuer K; Wang J
PLoS One; 2015; 10(6):e0130355. PubMed ID: 26076142
[TBL] [Abstract][Full Text] [Related]
32. Alagille syndrome and nephroblastoma: Unusual coincidence of two rare disorders.
Bourdeaut F; Guiochon-Mantel A; Fabre M; Martelli H; Patte C; Porta G; Bernard O; Delattre O; Jacquemin E
Pediatr Blood Cancer; 2008 Apr; 50(4):908-11. PubMed ID: 17584876
[TBL] [Abstract][Full Text] [Related]
33. Notch signaling in bile duct development: new insights raise new questions.
Lemaigre FP
Hepatology; 2008 Aug; 48(2):358-60. PubMed ID: 18666255
[No Abstract] [Full Text] [Related]
34. Alagille syndrome and the Jagged1 gene.
Piccoli DA; Spinner NB
Semin Liver Dis; 2001 Nov; 21(4):525-34. PubMed ID: 11745040
[TBL] [Abstract][Full Text] [Related]
35. JAGGED1 expression in human embryos: correlation with the Alagille syndrome phenotype.
Jones EA; Clement-Jones M; Wilson DI
J Med Genet; 2000 Sep; 37(9):658-62. PubMed ID: 10978356
[TBL] [Abstract][Full Text] [Related]
36. A novel JAG1 mutation in a patient with Alagille's syndrome.
Wang Y; Yu Y; Wang J; Tsuei SH; Zaho L; Fu Q
Pathology; 2010; 42(5):496-8. PubMed ID: 20632836
[No Abstract] [Full Text] [Related]
37. Clinical and molecular genetics of Alagille syndrome.
Krantz ID; Piccoli DA; Spinner NB
Curr Opin Pediatr; 1999 Dec; 11(6):558-64. PubMed ID: 10590916
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. Alagille syndrome in a Vietnamese cohort: mutation analysis and assessment of facial features.
Lin HC; Le Hoang P; Hutchinson A; Chao G; Gerfen J; Loomes KM; Krantz I; Kamath BM; Spinner NB
Am J Med Genet A; 2012 May; 158A(5):1005-13. PubMed ID: 22488849
[TBL] [Abstract][Full Text] [Related]
40. Mutation analysis of Jagged1 (JAG1) in Alagille syndrome patients.
Colliton RP; Bason L; Lu FM; Piccoli DA; Krantz ID; Spinner NB
Hum Mutat; 2001 Feb; 17(2):151-2. PubMed ID: 11180599
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]