• Thumbnail for Fanconi anemia
    originally described this disorder, Guido Fanconi. Some forms of Fanconi anemia, such as those of complementation group D1, N, and S, are embryonically lethal...
    37 KB (4,140 words) - 20:00, 18 November 2024
  • Thumbnail for Fanconi anemia, complementation group C
    characteristic of Fanconi anemia patients. Both male and female FANCC mutant mice have reduced numbers of germ cells. Fanconi anemia, complementation group C has been...
    20 KB (2,397 words) - 04:25, 19 February 2024
  • Thumbnail for FANCE
    Fanconi anemia, complementation group E protein is a protein that in humans is encoded by the FANCE gene. The Fanconi anemia complementation group (FANC)...
    18 KB (2,255 words) - 16:34, 12 June 2024
  • FAC (section Advocacy groups)
    mechanical construction set Familial amyloid cardiomyopathy Fanconi anemia, complementation group C Faisceaux algébriques cohérents, a mathematics paper sometimes...
    3 KB (334 words) - 16:08, 19 February 2024
  • Thumbnail for PALB2
    (also known as FANCN), similar to biallelic BRCA2 mutations, cause Fanconi anemia. Mutations in this gene have been associated with an increased risk...
    18 KB (1,567 words) - 01:04, 10 March 2024
  • Thumbnail for FANCA
    Fanconi anaemia, complementation group A, also known as FAA, FACA and FANCA, is a protein which in humans is encoded by the FANCA gene. It belongs to the...
    38 KB (4,760 words) - 00:26, 4 January 2024
  • Thumbnail for FANCF
    Fanconi anemia group F protein is a protein that in humans is encoded by the FANCF gene. FANCF has been shown to interact with Fanconi anemia, complementation...
    20 KB (2,441 words) - 21:11, 2 December 2023
  • FACC may refer to: Fanconi anemia, complementation group C, a protein that delays the onset of apoptosis and promotes homologous recombination repair...
    426 bytes (83 words) - 21:46, 17 May 2024
  • Thumbnail for GSTP1
    other diseases. GSTP1 has been shown to interact with Fanconi anemia, complementation group C and MAPK8. GST-Pi is expressed in many human tissues, particularly...
    5 KB (628 words) - 00:29, 4 March 2023
  • Thumbnail for FANCB
    Fanconi anemia group B protein is a protein that in humans is encoded by the FANCB gene. The Fanconi anemia complementation group (FANC) currently includes...
    8 KB (1,025 words) - 05:56, 4 January 2024
  • Thumbnail for STAT1
    W, Diaz J, Faulkner GR, Reifsteck C, Olson S, Bagby GC (September 2001). "The Fanconi anemia complementation group C gene product: structural evidence...
    31 KB (3,702 words) - 10:57, 15 July 2024
  • Thumbnail for BRIP1
    Fanconi anemia group J protein is a protein that in humans is encoded by the BRCA1-interacting protein 1 (BRIP1) gene. The protein encoded by this gene...
    13 KB (1,537 words) - 16:59, 27 August 2024
  • Thumbnail for Xeroderma pigmentosum
    infantile lethal cerebro-oculo-facio-skeletal syndrome. There are seven complementation groups, plus one variant form: There is no cure for the disorder; all treatment...
    30 KB (3,013 words) - 19:58, 29 October 2024
  • Thumbnail for FANCD2
    Fanconi anemia group D2 protein is a protein that in humans is encoded by the FANCD2 gene. The Fanconi anemia complementation group (FANC) currently includes...
    24 KB (2,547 words) - 15:10, 19 September 2024
  • hemoglobinuria (PCH) or Donath–Landsteiner hemolytic anemia (DLHA) is an autoimmune hemolytic anemia featured by complement-mediated intravascular hemolysis after cold...
    36 KB (3,861 words) - 18:53, 30 October 2024
  • Thumbnail for FANCM
    Fanconi anemia, complementation group M, also known as FANCM is a human gene. It is an emerging target in cancer therapy, in particular cancers with specific...
    19 KB (1,914 words) - 04:28, 19 June 2024
  • Thumbnail for FANCG
    FANCG gene is responsible for complementation group G. The clinical phenotype of all Fanconi anemia (FA) complementation groups is similar. This phenotype...
    21 KB (2,456 words) - 00:57, 27 January 2024
  • Thumbnail for FANCI
    Fanconi anemia, complementation group I (FANCI) also known as KIAA1794, is a protein which in humans is encoded by the FANCI gene. Mutations in the FANCI...
    13 KB (1,343 words) - 05:21, 6 July 2024
  • Thumbnail for Double-strand break repair model
    double-strand breaks. DNA double-strand damages activate the Fanconi anemia core complex (FANCA/B/C/E/F/G/L/M). The FA core complex monoubiquitinates the downstream...
    36 KB (4,324 words) - 17:45, 17 October 2024
  • Thumbnail for ERCC4
    with ERCC4 mutations have been classified as belonging to Fanconi anemia complementation group Q (FANCQ). ERCC4 (XPF) is normally expressed at a high level...
    27 KB (3,315 words) - 00:33, 27 January 2024
  • Thumbnail for Hereditary breast–ovarian cancer syndrome
    Fanconi Anemia; biallelic mutations of BRCA1 lead to Fanconi anemia complementation group S, and biallelic mutations of BRCA2 lead to complementation...
    11 KB (1,135 words) - 17:29, 17 September 2024
  • Thumbnail for SPTAN1
    SPTAN1 has been shown to interact with: Abl gene, FANCA, Fanconi anemia, complementation group C, GRIA2, Plectin, SHANK1, and Vimentin. Sjögren's syndrome...
    23 KB (2,717 words) - 09:07, 8 November 2023
  • heterogeneous-nuclear ribonucleoprotein group a-b MeSH D12.776.664.962.500.500.200 – heterogeneous-nuclear ribonucleoprotein group c MeSH D12.776.664.962.500.500...
    133 KB (7,397 words) - 16:43, 9 February 2024
  • Thumbnail for Microtia
    junctional 6, with pyloric atresia Fanconi anemia complementation group F Fanconi anemia complementation group L Fine-Lubinsky syndrome Gaucher disease...
    27 KB (3,078 words) - 22:50, 14 June 2024
  • Thumbnail for Micrognathism
    impaired intellectual development and dysmorphic features Fanconi anemia complementation groups L and P Faundes-Banka syndrome Feingold syndrome type 1...
    14 KB (1,343 words) - 23:07, 16 October 2024
  • Thumbnail for Science and technology in Canada
    S2CID 4222070. Strathdee, C.A.; Gavish, H.; Shannon, W.; Buchwald, M. (1992). "Cloning of cDNAs for Fanconi's anemia by functional complementation". Nature. 356 (6372):...
    14 KB (1,476 words) - 09:08, 22 November 2024
  • Thumbnail for ZBTB32
    protein (PLZP) Zbtb32 has been shown to interact with: Fanconi anemia complementation group C (Fancc) Thioredoxin interacting protein (Txnip), but the...
    13 KB (1,644 words) - 15:10, 29 April 2024
  • disorder of the skin and bone marrow in some ways resembling progeria Fanconi anemia, a rare genetic defect in a cluster of proteins responsible for DNA...
    74 KB (8,734 words) - 13:28, 2 November 2024
  • Thumbnail for Canada
    1038/235271b0. Strathdee, C.A.; Gavish, H.; Shannon, W.; Buchwald, M. (1992). "Cloning of cDNAs for Fanconi's anemia by functional complementation". Nature. 356 (6372):...
    275 KB (23,673 words) - 13:48, 16 November 2024
  • Competence factor Competent Complementarity genes Complementary DNA Complementation Complementation test Complete linkage Complex trait Component of fitness Composite...
    33 KB (2,517 words) - 18:31, 3 September 2024