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Journal Abstract Search

162 related items for PubMed ID: 26285796

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  • 3. Mutations in the leukemia inhibitory factor receptor (LIFR) gene and Lifr deficiency cause urinary tract malformations.
    Kosfeld A, Brand F, Weiss AC, Kreuzer M, Goerk M, Martens H, Schubert S, Schäfer AK, Riehmer V, Hennies I, Bräsen JH, Pape L, Amann K, Krogvold L, Bjerre A, Daniel C, Kispert A, Haffner D, Weber RG.
    Hum Mol Genet; 2017 May 01; 26(9):1716-1731. PubMed ID: 28334964
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  • 4. Mutations in LIFR rewire the JAK/STAT signaling pathway: A study unveiling mechanistic details of Stüve-Wiedemann syndrome.
    Paul I, Roy A, Chakrabarti D, Nandi C, Ray S.
    Comput Biol Med; 2024 Sep 01; 179():108797. PubMed ID: 38968765
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  • 8. Long-term follow-up in Stuve-Wiedemann syndrome: a clinical report.
    Gaspar IM, Saldanha T, Cabral P, Vilhena MM, Tuna M, Costa C, Dagoneau N, Daire VC, Hennekam RC.
    Am J Med Genet A; 2008 Jul 01; 146A(13):1748-53. PubMed ID: 18546280
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  • 20. Skoura - a genetic island for congenital insensitivity to pain and anhidrosis among Moroccan Jews, as determined by a novel mutation in the NTRK1 gene.
    Suriu C, Khayat M, Weiler M, Kfir N, Cohen C, Zinger A, Aslanidis C, Schmitz G, Falik-Zaccai TC.
    Clin Genet; 2009 Mar 01; 75(3):230-6. PubMed ID: 19250380
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