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Results 1 - 10 of 72 for slow
  1. PRPH2 gene 
    ... by PRPH2 gene mutations, retinitis pigmentosa involves a slow degeneration of photoreceptor cells, leading to progressive vision ... of retinal abnormalities. CACD2 peripherin 2 (retinal degeneration, slow) peripherin 2, homolog of mouse peripherin, photoreceptor type ...
    https://medlineplus.gov/genetics/gene/prph2 - Genetics
  2. ATP2A2 gene 
    ... Health Condition AT2A2_HUMAN ATP2B ATPase, Ca++ dependent, slow-twitch, cardiac muscle-2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 calcium-transporting ATPase sarcoplasmic reticulum type, ...
    https://medlineplus.gov/genetics/gene/atp2a2 - Genetics
  3. TPM3 gene 
    ... gene provides instructions for making a protein called slow muscle alpha (α)-tropomyosin, which is part of ... proteins play a role in controlling cell shape.Slow muscle α-tropomyosin is found in skeletal muscles, ...
    https://medlineplus.gov/genetics/gene/tpm3 - Genetics
  4. MYH7 gene 
    ... Type I fibers, which are also known as slow-twitch fibers, are one of two types of ... MGC138376 MGC138378 MPD1 MYH7_HUMAN MyHC-beta myhc-slow MYHCB myosin heavy chain (AA 1-96) Myosin ...
    https://medlineplus.gov/genetics/gene/myh7 - Genetics
  5. GRIN2A gene 
    ... also appear to play a role during deep (slow-wave) sleep.The GluN2A subunit of NMDA receptors ... abnormal electrical activity in the brain, usually during slow-wave sleep; a loss of speech and language ...
    https://medlineplus.gov/genetics/gene/grin2a - Genetics
  6. KCNE1 gene 
    ... delayed rectifier potassium channel subunit IsK IKs producing slow voltage-gated potassium channel beta subunit Mink ISK ...
    https://medlineplus.gov/genetics/gene/kcne1 - Genetics
  7. KCNQ1 gene 
    ... variation in the KCNQ1 gene. ATFB1 IKs producing slow voltage-gated potassium channel alpha subunit KvLQT1 JLNS1 ...
    https://medlineplus.gov/genetics/gene/kcnq1 - Genetics
  8. MYBPC1 gene 
    ... the MYBPC1 gene, which is known as the slow skeletal isoform, is found primarily in skeletal muscles.The slow isoform of myosin binding protein C is active ...
    https://medlineplus.gov/genetics/gene/mybpc1 - Genetics
  9. DCTN1 gene 
    ... as parkinsonism, psychiatric changes, weight loss, and abnormally slow breathing (hypoventilation).Most of the mutations that cause ... a reduced ability to transport materials within cells. Slow or abnormal transport of materials needed for the ...
    https://medlineplus.gov/genetics/gene/dctn1 - Genetics
  10. F5 gene 
    ... cutting (cleaving) it at specific sites. This inactivation slows down the clotting process and prevents clots from ... coagulation factor V, the factor V Leiden variant slows the rate at which APC inactivates this factor. ...
    https://medlineplus.gov/genetics/gene/f5 - Genetics
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