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Journal Abstract Search

174 related items for PubMed ID: 26686525

  • 21. A case report of Hennekam syndrome with a mutation in the CCBE1 gene.
    Durak T, Karaer D, Karaer K.
    Clin Dysmorphol; 2024 Apr 01; 33(2):87-89. PubMed ID: 38441203
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  • 22. Mutations in CCBE1 cause generalized lymph vessel dysplasia in humans.
    Alders M, Hogan BM, Gjini E, Salehi F, Al-Gazali L, Hennekam EA, Holmberg EE, Mannens MM, Mulder MF, Offerhaus GJ, Prescott TE, Schroor EJ, Verheij JB, Witte M, Zwijnenburg PJ, Vikkula M, Schulte-Merker S, Hennekam RC.
    Nat Genet; 2009 Dec 01; 41(12):1272-4. PubMed ID: 19935664
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  • 23. Hennekam syndrome: an uncommon cause of chylous ascites and intestinal lymphangiectasia in the tropics.
    Menon J, Venkatesh V, Thirunavukkarasu B, Lal SB.
    BMJ Case Rep; 2019 Jul 19; 12(7):. PubMed ID: 31326900
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  • 25. CCBE1 enhances lymphangiogenesis via A disintegrin and metalloprotease with thrombospondin motifs-3-mediated vascular endothelial growth factor-C activation.
    Jeltsch M, Jha SK, Tvorogov D, Anisimov A, Leppänen VM, Holopainen T, Kivelä R, Ortega S, Kärpanen T, Alitalo K.
    Circulation; 2014 May 13; 129(19):1962-71. PubMed ID: 24552833
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  • 28. A homozygous variant in growth and differentiation factor 2 (GDF2) may cause lymphatic dysplasia with hydrothorax and nonimmune hydrops fetalis.
    Aukema SM, Ten Brinke GA, Timens W, Vos YJ, Accord RE, Kraft KE, Santing MJ, Morssink LP, Streefland E, van Diemen CC, Vrijlandt EJ, Hulzebos CV, Kerstjens-Frederikse WS.
    Am J Med Genet A; 2020 Sep 13; 182(9):2152-2160. PubMed ID: 32618121
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  • 29. Expansion of the phenotype in Hennekam syndrome: a case with new manifestations.
    Angle B, Hersh JH.
    Am J Med Genet; 1997 Aug 08; 71(2):211-4. PubMed ID: 9217224
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  • 35. Possible biallelic inheritance in TIE1 in a family with congenital lymphedema, intestinal lymphangiectasia and cutis aplasia.
    Abu Shtaya A, Sukenik-Halevy R, Bazak L, Lidzbarsky GA, Gonzaga-Jauregui C, Lagovsky I, Goldberg Y, Basel-Salmon L.
    Clin Genet; 2023 Aug 08; 104(2):275-276. PubMed ID: 37096293
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  • 36. Intestinal Lymphangiestasia With Hennekam Syndrome.
    Viswanathan P, Novak I.
    J Pediatr Gastroenterol Nutr; 2017 Dec 08; 65(6):e133. PubMed ID: 26863383
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  • 37. The regulatory role of SLP-2 and mechanism on CCBE1 gene expression in rectal carcinoma and adjacent lymphatic tube tissues.
    Guo RL, Wang XR, Wang QG, Li Z, Lu X, Miao RZ, Chang H.
    Eur Rev Med Pharmacol Sci; 2018 Jan 08; 22(1):87-94. PubMed ID: 29364474
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  • 39. Ccbe1 expression marks the cardiac and lymphatic progenitor lineages during early stages of mouse development.
    Facucho-Oliveira J, Bento M, Belo JA.
    Int J Dev Biol; 2011 Jan 08; 55(10-12):1007-14. PubMed ID: 22252499
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