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Annals of the New York Academy of Sciences
|
January 1, 1984
Red cells genetically deficient in carbonic anhydrase II have elevated levels of a carbonic anhydrase indistinguishable from muscle CA III
N D Carter, R Heath, R J Welty, et al.
American Journal of Medical Genetics
|
January 1, 1985
Fetal plasma carbonic anhydrase III in prenatal diagnosis of Duchenne muscular dystrophy
R Heath, N D Carter, S Jeffery, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
August 1, 1978
Plasma vitamin D-binding globulin in vitamin D deficiency, pregnancy and chronic liver disease
J M Barragry, D Corless, J Auton, et al.
Endocrinology
|
November 20, 2001
Leptin requirement for conception, implantation, and gestation in the mouse
N M Malik, N D Carter, J F Murray, et al.
Diabetologia
|
October 4, 2006
Phosphatidylinositol 3-kinase p85alpha regulatory subunit gene PIK3R1 haplotype is associated with body fat and serum leptin in a female twin population
Y Jamshidi, H Snieder, X Wang, et al.
American Journal of Medical Genetics
|
November 14, 2000
Three novel mutations of the proto-oncogene KIT cause human piebaldism
P Syrris, N M Malik, V A Murday, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
August 11, 2001
Circulating cardiac troponin-T in patients before and after renal transplantation
S Fredericks, R Chang, H Gregson, et al.
The American Journal of Physiology
|
December 1, 1996
Carbonic anhydrase and cardiac pH regulation
J I Vandenberg, N D Carter, H W Bethell, et al.
Investigative Ophthalmology & Visual Science
|
August 1, 1994
Membrane-bound carbonic anhydrase in human retinal pigment epithelium
T J Wolfensberger, I Mahieu, J Jarvis-Evans, et al.
Annals of Human Genetics
|
July 1, 1992
Nucleotide sequence and chromosomal assignment of a cDNA encoding the large isoform of human glutamate decarboxylase
C D Kelly, Y Edwards, A P Johnstone, et al.
Page
of 14
Search research articles
Search
Showing results (111-120 of 140) with videos related to
Sort By:
Page
of 14
Annals of the New York Academy of Sciences
|
January 1, 1984
Red cells genetically deficient in carbonic anhydrase II have elevated levels of a carbonic anhydrase indistinguishable from muscle CA III
N D Carter, R Heath, R J Welty, et al.
American Journal of Medical Genetics
|
January 1, 1985
Fetal plasma carbonic anhydrase III in prenatal diagnosis of Duchenne muscular dystrophy
R Heath, N D Carter, S Jeffery, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
August 1, 1978
Plasma vitamin D-binding globulin in vitamin D deficiency, pregnancy and chronic liver disease
J M Barragry, D Corless, J Auton, et al.
Endocrinology
|
November 20, 2001
Leptin requirement for conception, implantation, and gestation in the mouse
N M Malik, N D Carter, J F Murray, et al.
Diabetologia
|
October 4, 2006
Phosphatidylinositol 3-kinase p85alpha regulatory subunit gene PIK3R1 haplotype is associated with body fat and serum leptin in a female twin population
Y Jamshidi, H Snieder, X Wang, et al.
American Journal of Medical Genetics
|
November 14, 2000
Three novel mutations of the proto-oncogene KIT cause human piebaldism
P Syrris, N M Malik, V A Murday, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
August 11, 2001
Circulating cardiac troponin-T in patients before and after renal transplantation
S Fredericks, R Chang, H Gregson, et al.
The American Journal of Physiology
|
December 1, 1996
Carbonic anhydrase and cardiac pH regulation
J I Vandenberg, N D Carter, H W Bethell, et al.
Investigative Ophthalmology & Visual Science
|
August 1, 1994
Membrane-bound carbonic anhydrase in human retinal pigment epithelium
T J Wolfensberger, I Mahieu, J Jarvis-Evans, et al.
Annals of Human Genetics
|
July 1, 1992
Nucleotide sequence and chromosomal assignment of a cDNA encoding the large isoform of human glutamate decarboxylase
C D Kelly, Y Edwards, A P Johnstone, et al.
Page
of 14