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Results 1 - 10 of 72 for Identifying
  1. IL23R gene 
    ... NK) cells, monocytes, and dendritic cells. These cells identify foreign substances and defend the body against infection ... DL, Cho JH. A genome-wide association study identifies IL23R as an inflammatory bowel disease gene. Science. ...
    https://medlineplus.gov/genetics/gene/il23r - Genetics
  2. MEGF8 gene 
    ... SJ, Wilkie AO. Mutations in multidomain protein MEGF8 identify a Carpenter syndrome subtype associated with defective lateralization. ... PJ, Pennacchio LA, Lo CW. Massively parallel sequencing identifies the gene Megf8 with ENU-induced mutation causing ...
    https://medlineplus.gov/genetics/gene/megf8 - Genetics
  3. ATG16L1 gene 
    ... A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1. ... Daly MJ, Brant SR. Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates ...
    https://medlineplus.gov/genetics/gene/atg16l1 - Genetics
  4. EYA1 gene 
    ... gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene family. Nat Genet. 1997 Feb; ... Semina EV. Whole exome sequencing in dominant cataract identifies a new causative factor, CRYBA2, and a variety ...
    https://medlineplus.gov/genetics/gene/eya1 - Genetics
  5. NBEAL2 gene 
    ... Rendon A, Nurden P, Ouwehand WH. Exome sequencing identifies NBEAL2 as the causative gene for gray platelet ...
    https://medlineplus.gov/genetics/gene/nbeal2 - Genetics
  6. PTPN22 gene 
    ... immune system cells called T cells. T cells identify foreign substances and defend the body against infection. ...
    https://medlineplus.gov/genetics/gene/ptpn22 - Genetics
  7. RMRP gene 
    ... incapacitating mutations in patients with extreme short stature identify RNA-processing endoribonuclease RMRP as an essential cell ...
    https://medlineplus.gov/genetics/gene/rmrp - Genetics
  8. CLCF1 gene 
    ... Ruben S, Alderson RF. Computational EST database analysis identifies a novel member of the neuropoietic cytokine family. ...
    https://medlineplus.gov/genetics/gene/clcf1 - Genetics
  9. UROS gene 
    ... III synthase mutations related to congenital erythropoietic porphyria identify a key helix for protein stability. Biochemistry. 2009 ...
    https://medlineplus.gov/genetics/gene/uros - Genetics
  10. CPOX gene 
    ... patients demonstrates absence of genotype-phenotype correlation and identifies relationship between hereditary coproporphyria and harderoporphyria. Am J ...
    https://medlineplus.gov/genetics/gene/cpox - Genetics
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