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Nature
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November 4, 1982
Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy
J M Murray, K E Davies, P S Harper, et al.
Clinical Genetics
|
April 1, 1981
Huntington's Chorea in South Wales. A genetic and epidemiological study
D A Walker, P S Harper, C E Wells, et al.
American Journal of Medical Genetics
|
August 1, 1992
Five years experience of predictive testing for myotonic dystrophy using linked DNA markers
W Reardon, J L Floyd, J Myring, et al.
Neuromuscular Disorders : NMD
|
January 1, 1992
Molecular analysis for the myotonic dystrophy mutation in neuromuscular disorders
J C MacMillan, J Myring, H G Harley, et al.
American Journal of Dentistry
|
January 5, 2002
Caries inhibition efficacy of an antiplaque/antigingivitis dentifrice
D Yu, S K Pearson, W H Bowen, et al.
Basic Research in Cardiology
|
September 1, 1993
Inhibition of Na+/H+ exchange preserves viability, restores mechanical function, and prevents the pH paradox in reperfusion injury to rat neonatal myocytes
I S Harper, J M Bond, E Chacon, et al.
Molecular Pharmacology
|
July 1, 1999
The staurosporine-like compound L-753,000 (NB-506) potentiates the neurotrophic effects of neurotrophin-3 by acting selectively at the TrkA receptor
S Pollack, L Young, J Bilsland, et al.
Basic Research in Cardiology
|
January 1, 1987
Ultrastructural observations on the effects of different substrates on ischaemic contracture in global subtotal ischaemia in the rat heart
E van der Merwe, I S Harper, P Owen, et al.
Radiology
|
November 1, 1985
MR imaging of calcified intracranial lesions
B A Holland, W Kucharczyk, M Brant-Zawadzki, et al.
Lancet (London, England)
|
November 24, 1990
DNA marker applicable to presymptomatic and prenatal diagnosis of facioscapulohumeral disease
M Upadhyaya, P W Lunt, M Sarfarazi, et al.
Page
of 123
Search research articles
Search
Showing results (541-550 of 1,225) with videos related to
Sort By:
Page
of 123
Nature
|
November 4, 1982
Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy
J M Murray, K E Davies, P S Harper, et al.
Clinical Genetics
|
April 1, 1981
Huntington's Chorea in South Wales. A genetic and epidemiological study
D A Walker, P S Harper, C E Wells, et al.
American Journal of Medical Genetics
|
August 1, 1992
Five years experience of predictive testing for myotonic dystrophy using linked DNA markers
W Reardon, J L Floyd, J Myring, et al.
Neuromuscular Disorders : NMD
|
January 1, 1992
Molecular analysis for the myotonic dystrophy mutation in neuromuscular disorders
J C MacMillan, J Myring, H G Harley, et al.
American Journal of Dentistry
|
January 5, 2002
Caries inhibition efficacy of an antiplaque/antigingivitis dentifrice
D Yu, S K Pearson, W H Bowen, et al.
Basic Research in Cardiology
|
September 1, 1993
Inhibition of Na+/H+ exchange preserves viability, restores mechanical function, and prevents the pH paradox in reperfusion injury to rat neonatal myocytes
I S Harper, J M Bond, E Chacon, et al.
Molecular Pharmacology
|
July 1, 1999
The staurosporine-like compound L-753,000 (NB-506) potentiates the neurotrophic effects of neurotrophin-3 by acting selectively at the TrkA receptor
S Pollack, L Young, J Bilsland, et al.
Basic Research in Cardiology
|
January 1, 1987
Ultrastructural observations on the effects of different substrates on ischaemic contracture in global subtotal ischaemia in the rat heart
E van der Merwe, I S Harper, P Owen, et al.
Radiology
|
November 1, 1985
MR imaging of calcified intracranial lesions
B A Holland, W Kucharczyk, M Brant-Zawadzki, et al.
Lancet (London, England)
|
November 24, 1990
DNA marker applicable to presymptomatic and prenatal diagnosis of facioscapulohumeral disease
M Upadhyaya, P W Lunt, M Sarfarazi, et al.
Page
of 123