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Results 1 - 10 of 48 for Action study
  1. COL4A5 gene 
    ... 195 families: a "European Community Alport Syndrome Concerted Action" study. J Am Soc Nephrol. 2003 Oct;14(10): ...
    https://medlineplus.gov/genetics/gene/col4a5 - Genetics
  2. Alport syndrome 
    ... 195 families: a "European Community Alport Syndrome Concerted Action" study. J Am Soc Nephrol. 2003 Oct;14(10): ...
    https://medlineplus.gov/genetics/condition/alport-syndrome - Genetics
  3. HPSE2 gene 
    ... heparanase 2 enzyme is not well understood, but studies suggest that it may block the action of heparanase 1. MedlinePlus Genetics provides information about ...
    https://medlineplus.gov/genetics/gene/hpse2 - Genetics
  4. FOXN1 gene 
    ... of other genes. On the basis of this action, the FOXN1 protein is called a transcription factor.The FOXN1 protein is important for development of the skin, hair, nails, and immune system. Studies suggest that this protein helps guide the formation ...
    https://medlineplus.gov/genetics/gene/foxn1 - Genetics
  5. Chromosome 5 
    ... with del(5q) myelodysplastic syndromes: linking mechanism of action to clinical ... KJ, Gawne-Cain M; DDD study; Magee AC, Turnpenny PD, Baralle D. Whole exome ...
    https://medlineplus.gov/genetics/chromosome/5 - Genetics
  6. Fragile X-associated tremor/ataxia syndrome 
    ... which is the ability to plan and implement actions and develop problem-solving ... Studies show that approximately 1 in 450 males has ...
    https://medlineplus.gov/...agile-x-associated-tremor-ataxia-syndrome - Genetics
  7. APTX gene 
    ... with oculomotor apraxia type 1: clinical and genetic studies. Brain. 2003 Dec;126(Pt 12):2761-72. doi: 10.1093/brain/awg283. Epub 2003 Sep 23. Citation on PubMed Rass U, Ahel I, West SC. Actions of aprataxin in multiple DNA repair pathways. J ...
    https://medlineplus.gov/genetics/gene/aptx - Genetics
  8. FOXC1 gene 
    ... of other genes. On the basis of this action, the FOXC1 protein is called a ... the eye (the cornea). Studies suggest that the FOXC1 protein may also have ...
    https://medlineplus.gov/genetics/gene/foxc1 - Genetics
  9. SCN1A gene 
    ... DNA building block (nucleotide) in the SCN1A gene. Studies suggest that this polymorphism is associated with the ... associated with familial hemiplegic migraine: genetic and functional studies. Mutation in brief #957. Online. Hum Mutat. 2007 ...
    https://medlineplus.gov/genetics/gene/scn1a - Genetics
  10. Essential tremor 
    ... but is most common in older adults. Some studies have suggested that people with essential tremor have ...
    https://medlineplus.gov/genetics/condition/essential-tremor - Genetics
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