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Plos One
|
January 30, 2013
ACTN3 allele frequency in humans covaries with global latitudinal gradient
Scott M Friedlander, Amanda L Herrmann, Daniel P Lowry, et al.
Disability and Rehabilitation
|
June 24, 2021
Development of clinical practice guidelines for allied health and nursing assessment and management of Duchenne muscular dystrophy
Z E Davidson, P Bray, K Rose, et al.
Journal of Genetic Counseling
|
April 21, 2015
The Impact of Neurofibromatosis Type 1 on the Health and Wellbeing of Australian Adults
Hilda A Crawford, Belinda Barton, Meredith J Wilson, et al.
American Journal of Human Genetics
|
September 16, 1999
A novel syndrome of episodic muscle weakness maps to xp22.3
M M Ryan, P Taylor, J A Donald, et al.
The Journal of Pediatrics
|
June 1, 1995
Neonatal-onset propionic acidemia: neurologic and developmental profiles, and implications for management
K N North, M S Korson, Y R Gopal, et al.
Scientific Reports
|
September 5, 2019
A "human knockout" model to investigate the influence of the α-actinin-3 protein on exercise-induced mitochondrial adaptations
I D Papadimitriou, N Eynon, X Yan, et al.
Plos Genetics
|
January 16, 2015
Altered Ca2+ kinetics associated with α-actinin-3 deficiency may explain positive selection for ACTN3 null allele in human evolution
Stewart I Head, Stephen Chan, Peter J Houweling, et al.
The Journal of Thoracic and Cardiovascular Surgery
|
July 7, 2009
Dysfunction induced by ischemia versus edema: does edema matter?
Tanya L Butler, Jonathan R Egan, Fabian G Graf, et al.
Journal of Medical Genetics
|
September 2, 2000
Cockayne syndrome associated with low CSF 5-hydroxyindole acetic acid levels
C J Ellaway, A Duggins, V S Fung, et al.
Neuromuscular Disorders : NMD
|
June 18, 2010
Evidence for a dominant negative disease mechanism in cap myopathy due to TPM3
Leigh B Waddell, Michaela Kreissl, Andrew Kornberg, et al.
Page
of 34
Search research articles
Search
Showing results (171-180 of 333) with videos related to
Sort By:
Page
of 34
Plos One
|
January 30, 2013
ACTN3 allele frequency in humans covaries with global latitudinal gradient
Scott M Friedlander, Amanda L Herrmann, Daniel P Lowry, et al.
Disability and Rehabilitation
|
June 24, 2021
Development of clinical practice guidelines for allied health and nursing assessment and management of Duchenne muscular dystrophy
Z E Davidson, P Bray, K Rose, et al.
Journal of Genetic Counseling
|
April 21, 2015
The Impact of Neurofibromatosis Type 1 on the Health and Wellbeing of Australian Adults
Hilda A Crawford, Belinda Barton, Meredith J Wilson, et al.
American Journal of Human Genetics
|
September 16, 1999
A novel syndrome of episodic muscle weakness maps to xp22.3
M M Ryan, P Taylor, J A Donald, et al.
The Journal of Pediatrics
|
June 1, 1995
Neonatal-onset propionic acidemia: neurologic and developmental profiles, and implications for management
K N North, M S Korson, Y R Gopal, et al.
Scientific Reports
|
September 5, 2019
A "human knockout" model to investigate the influence of the α-actinin-3 protein on exercise-induced mitochondrial adaptations
I D Papadimitriou, N Eynon, X Yan, et al.
Plos Genetics
|
January 16, 2015
Altered Ca2+ kinetics associated with α-actinin-3 deficiency may explain positive selection for ACTN3 null allele in human evolution
Stewart I Head, Stephen Chan, Peter J Houweling, et al.
The Journal of Thoracic and Cardiovascular Surgery
|
July 7, 2009
Dysfunction induced by ischemia versus edema: does edema matter?
Tanya L Butler, Jonathan R Egan, Fabian G Graf, et al.
Journal of Medical Genetics
|
September 2, 2000
Cockayne syndrome associated with low CSF 5-hydroxyindole acetic acid levels
C J Ellaway, A Duggins, V S Fung, et al.
Neuromuscular Disorders : NMD
|
June 18, 2010
Evidence for a dominant negative disease mechanism in cap myopathy due to TPM3
Leigh B Waddell, Michaela Kreissl, Andrew Kornberg, et al.
Page
of 34