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Results 1 - 10 of 35 for nbs
  1. NBN gene 
    ... ATV Cell cycle regulatory protein p95 NBN_HUMAN NBS NBS1 Nijmegen breakage syndrome 1 p95 protein of ... is modulated by the amount of a variant NBS protein. Carcinogenesis. 2007 Jan;28(1):107-11. ...
    https://medlineplus.gov/genetics/gene/nbn - Genetics
  2. SP110 gene 
    The SP110 gene provides instructions for making a protein called SP110 nuclear body protein, which is a component of cellular structures called nuclear bodies. ...
    https://medlineplus.gov/genetics/gene/sp110 - Genetics
  3. JAG1 gene 
    ... L, Lu FM, Piccoli DA, Krantz ID, Spinner NB. Mutation analysis of Jagged1 (JAG1) in Alagille syndrome ... BM, Bason L, Piccoli DA, Krantz ID, Spinner NB. Consequences of JAG1 mutations. J Med Genet. 2003 ...
    https://medlineplus.gov/genetics/gene/jag1 - Genetics
  4. PML gene 
    ... of a cell called PML nuclear bodies (PML-NBs). In the PML-NBs, the PML protein interacts with other proteins that ... Researchers believe that the structure of the PML-NBs is required for blocking proliferation and inducing apoptosis. ...
    https://medlineplus.gov/genetics/gene/pml - Genetics
  5. CNBP gene 
    ... P, Aguero TH, Borgognone M, Aybar MJ, Calcaterra NB. Dissecting CNBP, a zinc-finger protein required for ... Citation on PubMed Armas P, Nasif S, Calcaterra NB. Cellular nucleic acid binding protein binds G-rich ...
    https://medlineplus.gov/genetics/gene/cnbp - Genetics
  6. NOTCH2 gene 
    ... PA, Pai A, Krantz ID, Piccoli DA, Spinner NB. NOTCH2 mutations cause Alagille syndrome, a heterogeneous disorder ... on PubMed Central Penton AL, Leonard LD, Spinner NB. Notch signaling in human development and disease. Semin ...
    https://medlineplus.gov/genetics/gene/notch2 - Genetics
  7. HSPB8 gene 
    ... PubMed Datskevich PN, Nefedova VV, Sudnitsyna MV, Gusev NB. Mutations of small heat shock proteins and human ... VV, Muranova LK, Sudnitsyna MV, Ryzhavskaya AS, Gusev NB. Small Heat Shock Proteins and Distal Hereditary Neuropathies. ...
    https://medlineplus.gov/genetics/gene/hspb8 - Genetics
  8. BIN1 gene 
    ... J, Faure J, Weis J, Mandel JL, Romero NB, Laporte J. Adult-onset autosomal dominant centronuclear myopathy ... Epub 2007 Aug 5. Citation on PubMed Romero NB. Centronuclear myopathies: a widening concept. Neuromuscul Disord. 2010 ...
    https://medlineplus.gov/genetics/gene/bin1 - Genetics
  9. ACTA1 gene 
    ... K, Gejman R, Diaz J, Santorelli FM, Romero NB, Bertini E, Bevilacqua JA. Muscle magnetic resonance imaging ... KR, Clement S, Barois A, Muntoni F, Romero NB, Laing NG. Nemaline myopathy caused by absence of ...
    https://medlineplus.gov/genetics/gene/acta1 - Genetics
  10. SELENON gene 
    ... G, Rederstorff M, Krol A, Lescure A, Romero NB, Guicheney P, Allamand V. Satellite cell loss and ... H, Straub V, Villanova M, Leroy JP, Romero NB, Martin JJ, Muntoni F, Voit T, Estournet B, ...
    https://medlineplus.gov/genetics/gene/selenon - Genetics
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