Skip to search formSkip to main content
You are currently offline. Some features of the site may not work correctly.

MYOF gene

Known as: FER-1, C. ELEGANS, HOMOLOG-LIKE 3, KIAA1207, fer-1-like family member 3 
 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
The muscular dystrophy protein dysferlin plays a key role in the calcium-activated vesicle fusion of membrane repair. This study… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Is this relevant?
Highly Cited
2012
Highly Cited
2012
Follicular lymphoma is a monoclonal B-cell malignancy with each patient's tumor expressing a unique cell surface immunoglobulin… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Is this relevant?
Highly Cited
2012
Highly Cited
2012
Mutations in the dysferlin gene are the cause of Limb-girdle Muscular Dystrophy type 2B and Miyoshi Myopathy. The dysferlin… Expand
  • figure 1
  • figure 2
Is this relevant?
Highly Cited
2011
Highly Cited
2011
Myoferlin (MYOF) is a member of the evolutionarily conserved ferlin family of proteins, noted for their role in a variety of… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 4
Is this relevant?
Highly Cited
2010
Highly Cited
2010
Insulin‐like growth factor (IGF) is a potent stimulus of muscle growth. Myoferlin is a membraneassociated protein important for… Expand
Is this relevant?
Highly Cited
2007
Highly Cited
2007
Myoferlin and dysferlin are members of the ferlin family of membrane proteins. Recent studies have shown that mutation or genetic… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Is this relevant?
Highly Cited
2005
Highly Cited
2005
Muscle growth occurs during embryonic development and continues in adult life as regeneration. During embryonic muscle growth and… Expand
  • figure 1
  • figure 3
  • figure 2
  • figure 4
  • figure 5
Is this relevant?
Highly Cited
2002
Highly Cited
2002
Mutations in dysferlin, a novel membrane protein of unknown function, lead to muscular dystrophy. Myoferlin is highly homologous… Expand
Is this relevant?
Highly Cited
2000
Highly Cited
2000
We have recently reported that OTOF underlies an autosomal recessive form of prelingual sensorineural deafness, DFNB9. The… Expand
Is this relevant?
Highly Cited
2000
Highly Cited
2000
Dysferlin, the gene product of the limb girdle muscular dystrophy (LGMD) 2B locus, encodes a membrane-associated protein with… Expand
  • figure 1
  • figure 2
  • figure 2
  • figure 3
  • figure 4
Is this relevant?