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Diabetes Therapy : Research, Treatment and Education of Diabetes and Related Disorders
|
September 30, 2023
Is the Current Cut Point for Glycated Haemoglobin (HbA1c) Correct for Diagnosing Diabetes Mellitus in Premenopausal Women? Evidence to Inform Discussion
David Holland, Anthony A Fryer, Mike Stedman, et al.
Neuromuscular Disorders : NMD
|
December 10, 1997
Confirmation of linkage of oculopharyngeal muscular dystrophy to chromosome 14q11.2-q13 in American families suggests the existence of a second causal mutation
J M Stajich, J M Gilchrist, F Lennon, et al.
F1000Research
|
July 17, 2023
Researchers on research integrity: a survey of European and American researchers
Nick Allum, Abigail Reid, Miriam Bidoglia, et al.
Annals of Neurology
|
October 23, 1997
Apolipoprotein E epsilon2 does not increase risk of early-onset sporadic Alzheimer's disease
W K Scott, A M Saunders, P C Gaskell, et al.
American Journal of Human Genetics
|
June 1, 1991
Linkage studies in familial Alzheimer disease: evidence for chromosome 19 linkage
M A Pericak-Vance, J L Bebout, P C Gaskell, et al.
Neuromuscular Disorders : NMD
|
September 1, 1994
Development of a microsatellite genetic map spanning 5q31-q33 and subsequent placement of the LGMD1A locus between D5S178 and IL9
L H Yamaoka, C A Westbrook, M C Speer, et al.
Pharmacology
|
December 18, 2008
Preclinical toxicokinetic evaluation of phortress [2-(4-amino-3-methylphenyl)-5-fluorobenzothiazole lysylamide dihydrochloride] in two rodent species
T D Bradshaw, J E Wren, M Bruce, et al.
Experimental Neurology
|
December 1, 1988
Genetic linkage studies in Alzheimer's disease families
M A Pericak-Vance, L H Yamaoka, C S Haynes, et al.
Applied and Environmental Microbiology
|
August 12, 2018
Multi-omic Analyses of Extensively Decayed Pinus contorta Reveal Expression of a Diverse Array of Lignocellulose-Degrading Enzymes
Chiaki Hori, Jill Gaskell, Dan Cullen, et al.
American Journal of Human Genetics
|
October 2, 2002
A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10)
Evan Reid, Mark Kloos, Allison Ashley-Koch, et al.
Page
of 95
Search research articles
Search
Showing results (781-790 of 941) with videos related to
Sort By:
Page
of 95
Diabetes Therapy : Research, Treatment and Education of Diabetes and Related Disorders
|
September 30, 2023
Is the Current Cut Point for Glycated Haemoglobin (HbA1c) Correct for Diagnosing Diabetes Mellitus in Premenopausal Women? Evidence to Inform Discussion
David Holland, Anthony A Fryer, Mike Stedman, et al.
Neuromuscular Disorders : NMD
|
December 10, 1997
Confirmation of linkage of oculopharyngeal muscular dystrophy to chromosome 14q11.2-q13 in American families suggests the existence of a second causal mutation
J M Stajich, J M Gilchrist, F Lennon, et al.
F1000Research
|
July 17, 2023
Researchers on research integrity: a survey of European and American researchers
Nick Allum, Abigail Reid, Miriam Bidoglia, et al.
Annals of Neurology
|
October 23, 1997
Apolipoprotein E epsilon2 does not increase risk of early-onset sporadic Alzheimer's disease
W K Scott, A M Saunders, P C Gaskell, et al.
American Journal of Human Genetics
|
June 1, 1991
Linkage studies in familial Alzheimer disease: evidence for chromosome 19 linkage
M A Pericak-Vance, J L Bebout, P C Gaskell, et al.
Neuromuscular Disorders : NMD
|
September 1, 1994
Development of a microsatellite genetic map spanning 5q31-q33 and subsequent placement of the LGMD1A locus between D5S178 and IL9
L H Yamaoka, C A Westbrook, M C Speer, et al.
Pharmacology
|
December 18, 2008
Preclinical toxicokinetic evaluation of phortress [2-(4-amino-3-methylphenyl)-5-fluorobenzothiazole lysylamide dihydrochloride] in two rodent species
T D Bradshaw, J E Wren, M Bruce, et al.
Experimental Neurology
|
December 1, 1988
Genetic linkage studies in Alzheimer's disease families
M A Pericak-Vance, L H Yamaoka, C S Haynes, et al.
Applied and Environmental Microbiology
|
August 12, 2018
Multi-omic Analyses of Extensively Decayed Pinus contorta Reveal Expression of a Diverse Array of Lignocellulose-Degrading Enzymes
Chiaki Hori, Jill Gaskell, Dan Cullen, et al.
American Journal of Human Genetics
|
October 2, 2002
A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10)
Evan Reid, Mark Kloos, Allison Ashley-Koch, et al.
Page
of 95