These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

209 related articles for article (PubMed ID: 33029133)

  • 1. Tufting Enteropathy: A Review of Clinical and Histological Presentation, Etiology, Management, and Outcome.
    Cai C; Chen Y; Chen X; Ji F
    Gastroenterol Res Pract; 2020; 2020():5608069. PubMed ID: 33029133
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic characterization of congenital tufting enteropathy: epcam associated phenotype and involvement of SPINT2 in the syndromic form.
    Salomon J; Goulet O; Canioni D; Brousse N; Lemale J; Tounian P; Coulomb A; Marinier E; Hugot JP; Ruemmele F; Dufier JL; Roche O; Bodemer C; Colomb V; Talbotec C; Lacaille F; Campeotto F; Cerf-Bensussan N; Janecke AR; Mueller T; Koletzko S; Bonnefont JP; Lyonnet S; Munnich A; Poirier F; Smahi A
    Hum Genet; 2014 Mar; 133(3):299-310. PubMed ID: 24142340
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Homozygous Missense Epithelial Cell Adhesion Molecule Variant in a Patient with Congenital Tufting Enteropathy and Literature Review.
    Güvenoğlu M; Şimşek-Kiper PÖ; Koşukcu C; Taskiran EZ; Saltık-Temizel İN; Gucer S; Utine E; Boduroğlu K
    Pediatr Gastroenterol Hepatol Nutr; 2022 Nov; 25(6):441-452. PubMed ID: 36451688
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Congenital Tufting Enteropathy, a Rare Cause of Diarrhea and Malnourishment in Arab Child with Genetic and Histopathology Investigations.
    Alkhalifa S; Darwish A; Awadh M; Alkhalifa SM; Darwish A
    Case Rep Pediatr; 2023; 2023():6301065. PubMed ID: 36743443
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic analysis of Italian patients with congenital tufting enteropathy.
    d'Apolito M; Pisanelli D; Faletra F; Giardino I; Gigante M; Pettoello-Mantovani M; Goulet O; Gasparini P; Campanozzi A
    World J Pediatr; 2016 May; 12(2):219-24. PubMed ID: 26684320
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Congenital Tufting Enteropathy: Biology, Pathogenesis and Mechanisms.
    Das B; Sivagnanam M
    J Clin Med; 2020 Dec; 10(1):. PubMed ID: 33374714
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Matriptase drives early-onset intestinal failure in a mouse model of congenital tufting enteropathy.
    Szabo R; Callies LK; Bugge TH
    Development; 2019 Nov; 146(22):. PubMed ID: 31628112
    [TBL] [Abstract][Full Text] [Related]  

  • 8. New mutation in
    Zhou YQ; Wu GS; Kong YM; Zhang XY; Wang CL
    World J Clin Cases; 2020 Oct; 8(20):4975-4980. PubMed ID: 33195669
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Enteroids expressing a disease-associated mutant of EpCAM are a model for congenital tufting enteropathy.
    Das B; Okamoto K; Rabalais J; Kozan PA; Marchelletta RR; McGeough MD; Durali N; Go M; Barrett KE; Das S; Sivagnanam M
    Am J Physiol Gastrointest Liver Physiol; 2019 Nov; 317(5):G580-G591. PubMed ID: 31433211
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Novel Mutations in EPCAM Cause Congenital Tufting Enteropathy.
    Tang W; Huang T; Xu Z; Huang Y
    J Clin Gastroenterol; 2018 Jan; 52(1):e1-e6. PubMed ID: 27875355
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Biallelic variants of the first Kunitz domain of SPINT2 cause a non-syndromic form of congenital diarrhea and tufting enteropathy.
    Al Rawahi Y; Al Sunaidi O; Al-Masqari M; Al Jamei A; Rahamtalla D; Al-Maawali A
    Am J Med Genet A; 2024 Mar; 194(3):e63474. PubMed ID: 37960980
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Tufting Enteropathy with EpCAM Mutations in Two Siblings.
    Ko JS; Seo JK; Shim JO; Hwang SH; Park HS; Kang GH
    Gut Liver; 2010 Sep; 4(3):407-10. PubMed ID: 20981223
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Aberrant Epithelial Differentiation Contributes to Pathogenesis in a Murine Model of Congenital Tufting Enteropathy.
    Das B; Okamoto K; Rabalais J; Young JA; Barrett KE; Sivagnanam M
    Cell Mol Gastroenterol Hepatol; 2021; 12(4):1353-1371. PubMed ID: 34198013
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Early-onset tufting enteropathy in HAI-2-deficient mice is independent of matriptase-mediated cleavage of EpCAM.
    Szabo R; Kawaguchi M; Kataoka H; Bugge TH
    Development; 2023 Sep; 150(17):. PubMed ID: 37539662
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Superficial punctate keratitis and conjunctival erosions associated with congenital tufting enteropathy.
    Roche O; Putterman M; Salomon J; Lacaille F; Brousse N; Goulet O; Dufier JL
    Am J Ophthalmol; 2010 Jul; 150(1):116-121.e1. PubMed ID: 20447614
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of EpCAM as the gene for congenital tufting enteropathy.
    Sivagnanam M; Mueller JL; Lee H; Chen Z; Nelson SF; Turner D; Zlotkin SH; Pencharz PB; Ngan BY; Libiger O; Schork NJ; Lavine JE; Taylor S; Newbury RO; Kolodner RD; Hoffman HM
    Gastroenterology; 2008 Aug; 135(2):429-37. PubMed ID: 18572020
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Kocuria kristinae-caused sepsis in an infant with congenital tufting enteropathy.
    Aydin M; Ganschow R; Jankofsky M
    Turk J Pediatr; 2017; 59(1):93-96. PubMed ID: 29168373
    [TBL] [Abstract][Full Text] [Related]  

  • 18. mTrop1/Epcam knockout mice develop congenital tufting enteropathy through dysregulation of intestinal E-cadherin/β-catenin.
    Guerra E; Lattanzio R; La Sorda R; Dini F; Tiboni GM; Piantelli M; Alberti S
    PLoS One; 2012; 7(11):e49302. PubMed ID: 23209569
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A rare cause of congenital diarrhea in a Turkish newborn: tufting enteropathy.
    Kahvecioğlu D; Yıldız D; Kılıç A; İnce-Alkan B; Erdeve Ö; Kuloğlu Z; Atasay B; Ensari A; Yılmaz R; Arsan S
    Turk J Pediatr; 2014; 56(4):440-3. PubMed ID: 25818968
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Tufting enteropathy: a rare anatomical cause of small bowel diarrhoea in infants with mild or no villous abnormality.
    Das P; Malik R; Kaul S; Makharia GK
    Gastroenterol Hepatol Bed Bench; 2023; 16(2):225-229. PubMed ID: 37554749
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.