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European Journal of Applied Physiology
|
April 1, 2004
The upper limit of physiological cardiac hypertrophy in elite male and female athletes: the British experience
G P Whyte, K George, S Sharma, et al.
Genomics
|
November 10, 2004
X-linked hypoparathyroidism region on Xq27 is evolutionarily conserved with regions on 3q26 and 13q34 and contains a novel P-type ATPase
M Andrew Nesbit, Michael R Bowl, Brian Harding, et al.
Zoonoses and Public Health
|
November 27, 2007
Surveillance of dairy production holdings supplying raw milk to the farmhouse cheese sector for Escherichia coli O157, O26 and O111
M Murphy, J F Buckley, P Whyte, et al.
The Veterinary Record
|
April 23, 2016
Microbiological contamination of colostrum on Irish dairy farms
C G McAloon, M L Doherty, J Donlon, et al.
JBMR Plus
|
April 17, 2023
LRP6 High Bone Mass Characterized in Two Generations Harboring a Unique Mutation of Low-Density Lipoprotein Receptor-Related Protein 6
Michael P Whyte, Steven Mumm, Jonathan C Baker, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
November 4, 2014
Lenz-Majewski hyperostotic dwarfism with hyperphosphoserinuria from a novel mutation in PTDSS1 encoding phosphatidylserine synthase 1
Michael P Whyte, Amanda Blythe, William H McAlister, et al.
Medicine and Science in Sports and Exercise
|
January 19, 2008
Determinants of 800-m and 1500-m running performance using allometric models
Stephen A Ingham, Gregory P Whyte, Charles Pedlar, et al.
Clinical Endocrinology
|
December 1, 1996
Calcium-sensing receptor mutations in familial hypocalciuric hypercalcaemia with recurrent pancreatitis
S H Pearce, C Wooding, M Davies, et al.
Biochemical and Biophysical Research Communications
|
February 24, 1997
Expression and cloning of the human X-linked hypophosphatemia gene cDNA
M Grieff, S Mumm, P Waeltz, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
March 14, 2007
Juvenile Paget's disease: the second reported, oldest patient is homozygous for the TNFRSF11B "Balkan" mutation (966_969delTGACinsCTT), which elevates circulating immunoreactive osteoprotegerin levels
Michael P Whyte, Panagiotis N Singhellakis, Michael B Petersen, et al.
Page
of 52
Search research articles
Search
Showing results (301-310 of 515) with videos related to
Sort By:
Page
of 52
European Journal of Applied Physiology
|
April 1, 2004
The upper limit of physiological cardiac hypertrophy in elite male and female athletes: the British experience
G P Whyte, K George, S Sharma, et al.
Genomics
|
November 10, 2004
X-linked hypoparathyroidism region on Xq27 is evolutionarily conserved with regions on 3q26 and 13q34 and contains a novel P-type ATPase
M Andrew Nesbit, Michael R Bowl, Brian Harding, et al.
Zoonoses and Public Health
|
November 27, 2007
Surveillance of dairy production holdings supplying raw milk to the farmhouse cheese sector for Escherichia coli O157, O26 and O111
M Murphy, J F Buckley, P Whyte, et al.
The Veterinary Record
|
April 23, 2016
Microbiological contamination of colostrum on Irish dairy farms
C G McAloon, M L Doherty, J Donlon, et al.
JBMR Plus
|
April 17, 2023
LRP6 High Bone Mass Characterized in Two Generations Harboring a Unique Mutation of Low-Density Lipoprotein Receptor-Related Protein 6
Michael P Whyte, Steven Mumm, Jonathan C Baker, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
November 4, 2014
Lenz-Majewski hyperostotic dwarfism with hyperphosphoserinuria from a novel mutation in PTDSS1 encoding phosphatidylserine synthase 1
Michael P Whyte, Amanda Blythe, William H McAlister, et al.
Medicine and Science in Sports and Exercise
|
January 19, 2008
Determinants of 800-m and 1500-m running performance using allometric models
Stephen A Ingham, Gregory P Whyte, Charles Pedlar, et al.
Clinical Endocrinology
|
December 1, 1996
Calcium-sensing receptor mutations in familial hypocalciuric hypercalcaemia with recurrent pancreatitis
S H Pearce, C Wooding, M Davies, et al.
Biochemical and Biophysical Research Communications
|
February 24, 1997
Expression and cloning of the human X-linked hypophosphatemia gene cDNA
M Grieff, S Mumm, P Waeltz, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
March 14, 2007
Juvenile Paget's disease: the second reported, oldest patient is homozygous for the TNFRSF11B "Balkan" mutation (966_969delTGACinsCTT), which elevates circulating immunoreactive osteoprotegerin levels
Michael P Whyte, Panagiotis N Singhellakis, Michael B Petersen, et al.
Page
of 52