BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

226 related articles for article (PubMed ID: 28090565)

  • 1.
    Tsai EA; Gilbert MA; Grochowski CM; Underkoffler LA; Meng H; Zhang X; Wang MM; Shitaye H; Hankenson KD; Piccoli D; Lin H; Kamath BM; Devoto M; Spinner NB; Loomes KM
    Cell Mol Gastroenterol Hepatol; 2016 Sep; 2(5):663-675.e2. PubMed ID: 28090565
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mouse Model of Alagille Syndrome and Mechanisms of Jagged1 Missense Mutations.
    Andersson ER; Chivukula IV; Hankeova S; Sjöqvist M; Tsoi YL; Ramsköld D; Masek J; Elmansuri A; Hoogendoorn A; Vazquez E; Storvall H; Netušilová J; Huch M; Fischler B; Ellis E; Contreras A; Nemeth A; Chien KC; Clevers H; Sandberg R; Bryja V; Lendahl U
    Gastroenterology; 2018 Mar; 154(4):1080-1095. PubMed ID: 29162437
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. NOTCH2 mutations in Alagille syndrome.
    Kamath BM; Bauer RC; Loomes KM; Chao G; Gerfen J; Hutchinson A; Hardikar W; Hirschfield G; Jara P; Krantz ID; Lapunzina P; Leonard L; Ling S; Ng VL; Hoang PL; Piccoli DA; Spinner NB
    J Med Genet; 2012 Feb; 49(2):138-44. PubMed ID: 22209762
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Two Novel Mutations in the
    Prochazková D; Borská R; Fajkusová L; Konečná P; Hloušková E; Pavlovský Z; Slabý O; Pospíšilová Š
    Diagnostics (Basel); 2021 May; 11(6):. PubMed ID: 34071626
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Alagille syndrome caused by NOTCH2 mutation presented atypical pathological changes.
    ShenTu Y; Mi X; Tang D; Jiang Y; Gao L; Ma X; Zhou B; Yang W; Shi J; Lan D; Chen G; Gong L
    Clin Chim Acta; 2021 Oct; 521():258-263. PubMed ID: 34332988
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A case of Alagille syndrome presenting with chronic cholestasis in an adult.
    Kim J; Yang B; Paik N; Choe YH; Paik YH
    Clin Mol Hepatol; 2017 Sep; 23(3):260-264. PubMed ID: 28683534
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clinical features, outcomes, and genetic analysis in Korean children with Alagille syndrome.
    Cho JM; Oh SH; Kim HJ; Kim JS; Kim KM; Kim GH; Yu E; Lee BH; Yoo HW
    Pediatr Int; 2015 Aug; 57(4):552-7. PubMed ID: 25676721
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Microarray data reveal relationship between Jag1 and Ddr1 in mouse liver.
    Underkoffler LA; Carr E; Nelson A; Ryan MJ; Schulz R; Loomes KM
    PLoS One; 2013; 8(12):e84383. PubMed ID: 24391948
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Not only Alagille syndrome. Syndromic paucity of interlobular bile ducts secondary to HNF1β deficiency: a case report and literature review.
    Pinon M; Carboni M; Colavito D; Cisarò F; Peruzzi L; Pizzol A; Calosso G; David E; Calvo PL
    Ital J Pediatr; 2019 Feb; 45(1):27. PubMed ID: 30791938
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Notch signaling regulates bile duct morphogenesis in mice.
    Lozier J; McCright B; Gridley T
    PLoS One; 2008 Mar; 3(3):e1851. PubMed ID: 18365007
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. Pathogenic Novel Heterozygous Variant c.1076c>T p. (Ser359Phe) chr1: 120512166 in NOTCH2 Gene, Type 2 Alagille Syndrome Causing Neonatal Cholestasis: A Case Report.
    Uddin MS; Al Fulayyih S; Al Denaini FF; Al Hatlani MM
    Am J Case Rep; 2022 Oct; 23():e935840. PubMed ID: 36201396
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Polymorphism analysis and new JAG1 gene mutations of Alagille syndrome in Mexican population.
    Vázquez-Martínez ER; Varela-Fascinetto G; García-Delgado C; Rodríguez-Espino BA; Sánchez-Boiso A; Valencia-Mayoral P; Heller-Rosseau S; Pelcastre-Luna EL; Zenteno JC; Cerbón M; Morán-Barroso VF
    Meta Gene; 2014 Dec; 2():32-40. PubMed ID: 25606387
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Alagille syndrome and non-syndromic paucity of the intrahepatic bile ducts.
    Gilbert MA; Loomes KM
    Transl Gastroenterol Hepatol; 2021; 6():22. PubMed ID: 33824926
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Alagille Syndrome: A Focused Review on Clinical Features, Genetics, and Treatment.
    Kohut TJ; Gilbert MA; Loomes KM
    Semin Liver Dis; 2021 Nov; 41(4):525-537. PubMed ID: 34215014
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 12.