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Results 1 - 10 of 26 for Cutting
  1. CLN10 disease 
    ... act as protease enzymes, which modify proteins by cutting them apart. Cathepsin D is found in many ... digest and recycle different types of molecules. By cutting proteins apart, cathepsin D can break down certain ...
    https://medlineplus.gov/genetics/condition/cln10-disease - Genetics
  2. CTSD gene 
    ... act as protease enzymes, which modify proteins by cutting them apart. Cathepsin D is found in many ... digest and recycle different types of molecules. By cutting proteins apart, cathepsin D can break down certain ...
    https://medlineplus.gov/genetics/gene/ctsd - Genetics
  3. Hashimoto's disease 
    ... on PubMed Eschler DC, Hasham A, Tomer Y. Cutting edge: the etiology of autoimmune thyroid diseases. Clin ...
    https://medlineplus.gov/genetics/condition/hashimotos-disease - Genetics
  4. PTPN22 gene 
    ... Zhang X, Zhang ZY, Funk A, Buckner JH. Cutting edge: the PTPN22 allelic variant associated with autoimmunity ...
    https://medlineplus.gov/genetics/gene/ptpn22 - Genetics
  5. ABCD1 gene 
    ... HR, van Geel BM, Boehm CD, Raymond GV, Cutting GR, Wanders RJ, Moser HW. ABCD1 mutations and ...
    https://medlineplus.gov/genetics/gene/abcd1 - Genetics
  6. PRSS1 gene 
    ... form called trypsin. Trypsin aids in digestion by cutting protein chains at the protein building blocks (amino ...
    https://medlineplus.gov/genetics/gene/prss1 - Genetics
  7. MECP2 gene 
    ... serve as genetic blueprints for making proteins. By cutting and rearranging mRNA molecules in different ways, the ...
    https://medlineplus.gov/genetics/gene/mecp2 - Genetics
  8. CFTR gene 
    ... x. Citation on PubMed Deignan JL, Astbury C, Cutting GR, Del Gaudio D, Gregg AR, Grody WW, ...
    https://medlineplus.gov/genetics/gene/cftr - Genetics
  9. Neurofibromatosis type 1 
    ... TM, Materek A, Abel J, O'Donnell M, Cutting LE. Cognitive profile of neurofibromatosis type 1. Semin ...
    https://medlineplus.gov/genetics/condition/neurofibromatosis-type-1 - Genetics
  10. X-linked adrenoleukodystrophy 
    ... HR, van Geel BM, Boehm CD, Raymond GV, Cutting GR, Wanders RJ, Moser HW. ABCD1 mutations and ...
    https://medlineplus.gov/.../condition/x-linked-adrenoleukodystrophy - Genetics
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