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Results 1 - 10 of 111 for fa
  1. FANCA gene 
    ... a cell process known as the Fanconi anemia (FA) pathway. The FA pathway is turned on (activated) when the process ... replication, is blocked due to DNA damage. The FA pathway is particularly responsive to a certain type ...
    https://medlineplus.gov/genetics/gene/fanca - Genetics
  2. FANCG gene 
    ... a cell process known as the Fanconi anemia (FA) pathway. The FA pathway is turned on (activated) when the process ... replication, is blocked due to DNA damage. The FA pathway is particularly responsive to a certain type ...
    https://medlineplus.gov/genetics/gene/fancg - Genetics
  3. FANCC gene 
    ... a cell process known as the Fanconi anemia (FA) pathway. The FA pathway is turned on (activated) when the process ... replication, is blocked due to DNA damage. The FA pathway is particularly responsive to a certain type ...
    https://medlineplus.gov/genetics/gene/fancc - Genetics
  4. Friedreich ataxia 
    ... not show signs and symptoms of the condition. FA FRDA Friedreich spinocerebellar ataxia Friedrich's ataxia Genetic ...
    https://medlineplus.gov/genetics/condition/friedreich-ataxia - Genetics
  5. FXN gene 
    ... Friedreich ataxia. More About This Health Condition CyaY FA FARR FRDA FRDA_HUMAN Friedreich ataxia MGC57199 X25 ...
    https://medlineplus.gov/genetics/gene/fxn - Genetics
  6. BRCA2 gene 
    The BRCA2 gene provides instructions for making a protein that acts as a tumor suppressor. Tumor suppressor proteins help prevent cells from growing and ...
    https://medlineplus.gov/genetics/gene/brca2 - Genetics
  7. Fanconi anemia 
    ... involved in a cell process known as the FA pathway. The FA pathway is turned on (activated) when the process ... replication, is blocked due to DNA damage. The FA pathway sends certain proteins to the area of ...
    https://medlineplus.gov/genetics/condition/fanconi-anemia - Genetics
  8. X-linked infantile nystagmus 
    ... S, Arveiler B, Montoliu L, Engle EC, Proudlock FA, Nishad G, Pani P, Varma G, Gottlob I, ... EO, Jain S, Thomas S, Shah N, Proudlock FA, Thompson JR, McLean RJ, Degg C, Woodruff G, ...
    https://medlineplus.gov/.../condition/x-linked-infantile-nystagmus - Genetics
  9. RAB18 deficiency 
    ... JR, Gissen P, Muller F, Maher ER, Barr FA, Aligianis IA. Loss-of-function mutations in RAB18 ... R, Carpanini S, Aligianis I, Handley MT, Barr FA. Rab18 and a Rab18 GEF complex are required ...
    https://medlineplus.gov/genetics/condition/rab18-deficiency - Genetics
  10. TBC1D20 gene 
    ... R, Carpanini S, Aligianis I, Handley MT, Barr FA. Rab18 and a Rab18 GEF complex are required ... S, Stephens DJ, Preisinger C, Fuchs E, Barr FA. Analysis of GTPase-activating proteins: Rab1 and Rab43 ...
    https://medlineplus.gov/genetics/gene/tbc1d20 - Genetics
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