Search research articles
Contact Us
Filters
Showing results (11-20 of 51) with videos related to
Page
of 6
Sort By:
Journal of Neuroscience Research
|
June 1, 1989
Oligodendrocytes express a normal phenotype in carbonic anhydrase II-deficient mice
M S Ghandour, R P Skoff, P J Venta, et al.
FEBS Letters
|
June 5, 1989
Carbonic anhydrase II is induced in HL-60 cells by 1,25-dihydroxyvitamin D3: a model for osteoclast gene regulation
L Hillstrom Shapiro, P J Venta, Y S Yu, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 1, 1992
Molecular basis of human carbonic anhydrase II deficiency
D E Roth, P J Venta, R E Tashian, et al.
Gene
|
September 15, 1993
Characterization of the genes encoding carbonic anhydrase I of chimpanzee and gorilla: comparative analysis of 5' flanking erythroid-specific promoter sequences
B R Epperly, N C Bergenham, P J Venta, et al.
Gene
|
April 30, 1993
The deduced amino acid sequence of human carbonic anhydrase-related protein (CARP) is 98% identical to the mouse homologue
L A Skaggs, N C Bergenhem, P J Venta, et al.
Biochemical Genetics
|
August 1, 1996
Gene-specific universal mammalian sequence-tagged sites: application to the canine genome
P J Venta, J A Brouillette, V Yuzbasiyan-Gurkan, et al.
The Veterinary Clinics of North America. Small Animal Practice
|
March 1, 1996
Viral infections of the feline urinary tract
J M Kruger, C A Osborne, P J Venta, et al.
Biochimica Et Biophysica Acta
|
December 18, 1985
Comparison of the 5' regions of human and mouse carbonic anhydrase II genes and identification of possible regulatory elements
P J Venta, J C Montgomery, D Hewett-Emmett, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 1, 1983
Polymorphic gene for human carbonic anhydrase II: a molecular disease marker located on chromosome 8
P J Venta, T B Shows, P J Curtis, et al.
Journal of Veterinary Internal Medicine
|
January 18, 2014
Selective intestinal cobalamin malabsorption with proteinuria (Imerslund-Gräsbeck syndrome) in juvenile Beagles
J C Fyfe, S L Hemker, P J Venta, et al.
Page
of 6
Search research articles
Search
Showing results (11-20 of 51) with videos related to
Sort By:
Page
of 6
Journal of Neuroscience Research
|
June 1, 1989
Oligodendrocytes express a normal phenotype in carbonic anhydrase II-deficient mice
M S Ghandour, R P Skoff, P J Venta, et al.
FEBS Letters
|
June 5, 1989
Carbonic anhydrase II is induced in HL-60 cells by 1,25-dihydroxyvitamin D3: a model for osteoclast gene regulation
L Hillstrom Shapiro, P J Venta, Y S Yu, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 1, 1992
Molecular basis of human carbonic anhydrase II deficiency
D E Roth, P J Venta, R E Tashian, et al.
Gene
|
September 15, 1993
Characterization of the genes encoding carbonic anhydrase I of chimpanzee and gorilla: comparative analysis of 5' flanking erythroid-specific promoter sequences
B R Epperly, N C Bergenham, P J Venta, et al.
Gene
|
April 30, 1993
The deduced amino acid sequence of human carbonic anhydrase-related protein (CARP) is 98% identical to the mouse homologue
L A Skaggs, N C Bergenhem, P J Venta, et al.
Biochemical Genetics
|
August 1, 1996
Gene-specific universal mammalian sequence-tagged sites: application to the canine genome
P J Venta, J A Brouillette, V Yuzbasiyan-Gurkan, et al.
The Veterinary Clinics of North America. Small Animal Practice
|
March 1, 1996
Viral infections of the feline urinary tract
J M Kruger, C A Osborne, P J Venta, et al.
Biochimica Et Biophysica Acta
|
December 18, 1985
Comparison of the 5' regions of human and mouse carbonic anhydrase II genes and identification of possible regulatory elements
P J Venta, J C Montgomery, D Hewett-Emmett, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 1, 1983
Polymorphic gene for human carbonic anhydrase II: a molecular disease marker located on chromosome 8
P J Venta, T B Shows, P J Curtis, et al.
Journal of Veterinary Internal Medicine
|
January 18, 2014
Selective intestinal cobalamin malabsorption with proteinuria (Imerslund-Gräsbeck syndrome) in juvenile Beagles
J C Fyfe, S L Hemker, P J Venta, et al.
Page
of 6