197 related articles for article (PubMed ID: 26760175)
1. JAG1 Loss-Of-Function Variations as a Novel Predisposing Event in the Pathogenesis of Congenital Thyroid Defects.
de Filippis T; Marelli F; Nebbia G; Porazzi P; Corbetta S; Fugazzola L; Gastaldi R; Vigone MC; Biffanti R; Frizziero D; Mandarà L; Prontera P; Salerno M; Maghnie M; Tiso N; Radetti G; Weber G; Persani L
J Clin Endocrinol Metab; 2016 Mar; 101(3):861-70. PubMed ID: 26760175
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Jagged1 (JAG1): Structure, expression, and disease associations.
Grochowski CM; Loomes KM; Spinner NB
Gene; 2016 Jan; 576(1 Pt 3):381-4. PubMed ID: 26548814
[TBL] [Abstract][Full Text] [Related]
4. Disruptions of global and JAGGED1-mediated notch signaling affect thyroid morphogenesis in the zebrafish.
Porazzi P; Marelli F; Benato F; de Filippis T; Calebiro D; Argenton F; Tiso N; Persani L
Endocrinology; 2012 Nov; 153(11):5645-58. PubMed ID: 23008514
[TBL] [Abstract][Full Text] [Related]
5. A mouse model of Alagille syndrome: Notch2 as a genetic modifier of Jag1 haploinsufficiency.
McCright B; Lozier J; Gridley T
Development; 2002 Feb; 129(4):1075-82. PubMed ID: 11861489
[TBL] [Abstract][Full Text] [Related]
6. Human Jagged 1 mutants cause liver defect in Alagille syndrome by overexpression of hepatocyte growth factor.
Yuan ZR; Kobayashi N; Kohsaka T
J Mol Biol; 2006 Feb; 356(3):559-68. PubMed ID: 16403414
[TBL] [Abstract][Full Text] [Related]
7. Bile duct proliferation in Jag1/fringe heterozygous mice identifies candidate modifiers of the Alagille syndrome hepatic phenotype.
Ryan MJ; Bales C; Nelson A; Gonzalez DM; Underkoffler L; Segalov M; Wilson-Rawls J; Cole SE; Moran JL; Russo P; Spinner NB; Kusumi K; Loomes KM
Hepatology; 2008 Dec; 48(6):1989-97. PubMed ID: 19026002
[TBL] [Abstract][Full Text] [Related]
8. Novel human pathological mutations. Gene symbol: JAG1. Disease: Alagille syndrome.
Marchetti D; Iascone MR; Pezzoli L
Hum Genet; 2009 Aug; 126(2):345. PubMed ID: 19694043
[No Abstract] [Full Text] [Related]
9. Endothelial deletion of murine Jag1 leads to valve calcification and congenital heart defects associated with Alagille syndrome.
Hofmann JJ; Briot A; Enciso J; Zovein AC; Ren S; Zhang ZW; Radtke F; Simons M; Wang Y; Iruela-Arispe ML
Development; 2012 Dec; 139(23):4449-60. PubMed ID: 23095891
[TBL] [Abstract][Full Text] [Related]
10. Novel human pathological mutations. Gene symbol: JAG1. Disease: Alagille syndrome.
Marchetti D; Iascone MR; Pezzoli L
Hum Genet; 2009 Aug; 126(2):349. PubMed ID: 19694053
[No Abstract] [Full Text] [Related]
11. JAG1 mutation in a patient with deletion 22q11.2 syndrome and tetralogy of Fallot.
Digilio MC; Luca AD; Lepri F; Guida V; Ferese R; Dentici ML; Angioni A; Marino B; Dallapiccola B
Am J Med Genet A; 2013 Dec; 161A(12):3133-6. PubMed ID: 23956173
[TBL] [Abstract][Full Text] [Related]
12. Gene symbol: JAG1. Disease: Alagille syndrome.
Conidi ME; Michelucci A; Maggiore G; Simi P
Hum Genet; 2008 Oct; 124(3):322. PubMed ID: 18846681
[No Abstract] [Full Text] [Related]
13. 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]
14. 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]
15. Gene symbol: JAG1. Disease: Alagille syndrome.
Conidi ME; Michelucci A; Maggiore G; Simi P
Hum Genet; 2008 Oct; 124(3):321-2. PubMed ID: 18846680
[No Abstract] [Full Text] [Related]
16. Novel human pathological mutations. Gene symbol: JAG1. Disease: Alagille syndrome.
Marchetti D; Iascone MR; Pezzoli L
Hum Genet; 2009 Aug; 126(2):347-8. PubMed ID: 19694049
[No Abstract] [Full Text] [Related]
17. Novel human pathological mutations. Gene symbol: JAG1. Disease: Alagille syndrome.
Marchetti D; Iascone MR; Pezzoli L
Hum Genet; 2009 Aug; 126(2):350-1. PubMed ID: 19694056
[No Abstract] [Full Text] [Related]
18. Novel human pathological mutations. Gene symbol: JAG1. Disease: Alagille syndrome.
Marchetti D; Iascone MR; Pezzoli L
Hum Genet; 2009 Aug; 126(2):347. PubMed ID: 19694048
[No Abstract] [Full Text] [Related]
19. Novel human pathological mutations. Gene symbol: JAG1. Disease: Alagille syndrome.
Marchetti D; Iascone MR; Pezzoli L
Hum Genet; 2009 Aug; 126(2):345-6. PubMed ID: 19694044
[No Abstract] [Full Text] [Related]
20. 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]
[Next] [New Search]
