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P J Venta

Showing results (31-40 of 51) with videos related to

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Gene|November 1, 1983
The nucleotide sequence and derived amino acid sequence of cDNA coding for mouse carbonic anhydrase IIP J Curtis, E Withers, D Demuth, et al.
American Journal of Human Genetics|November 1, 1991
Carbonic anhydrase II deficiency syndrome in a Belgian family is caused by a point mutation at an invariant histidine residue (107 His----Tyr): complete structure of the normal human CA II geneP J Venta, R J Welty, T M Johnson, et al.
Cytogenetic and Genome Research|February 19, 2004
Comparative mapping of genes flanking the human chromosome 12 evolutionary breakpoint in the pigC R Farber, N E Raney, V D Rilington, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 15, 1992
Mutation creates an open reading frame within the 5' untranslated region of macaque erythrocyte carbonic anhydrase (CA) I mRNA that suppresses CA I expression and supports the scanning model for translationN C Bergenhem, P J Venta, P J Hopkins, et al.
Life Sciences|July 23, 1998
Promoter activity of carbonic anhydrase II regulatory regions in cultured renal proximal tubular cellsL W Lai, R P Erickson, P J Venta, et al.
Nature|July 15, 1982
Phylogenetic origins and adaptive evolution of avian and mammalian haemoglobin genesJ Czelusniak, M Goodman, D Hewett-Emmett, et al.
Veterinary Pathology|May 11, 2004
A von Willebrand's factor genomic nucleotide variant and polymerase chain reaction diagnostic test associated with inheritable type-2 von Willebrand's disease in a line of german shorthaired pointer dogsJ W Kramer, P J Venta, S R Klein, et al.
Rapid Communications in Mass Spectrometry : RCM|January 1, 1995
Rapid screening of genetic polymorphisms using buccal cell DNA with detection by matrix-assisted laser desorption/ionization mass spectrometryY H Liu, J Bai, Y Zhu, et al.
American Journal of Human Genetics|April 1, 1994
Carbonic anhydrase II deficiency: single-base deletion in exon 7 is the predominant mutation in Caribbean Hispanic patientsP Y Hu, A R Ernst, W S Sly, et al.
Equine Veterinary Journal|March 24, 2009
Expression of toll-like receptor 2 mRNA in bronchial epithelial cells is not induced in RAO-affected horsesA Berndt, F J Derksen, P J Venta, et al.
Pageof 6

Showing results (31-40 of 51) with videos related to

Sort By:
Pageof 6
Gene|November 1, 1983
The nucleotide sequence and derived amino acid sequence of cDNA coding for mouse carbonic anhydrase IIP J Curtis, E Withers, D Demuth, et al.
American Journal of Human Genetics|November 1, 1991
Carbonic anhydrase II deficiency syndrome in a Belgian family is caused by a point mutation at an invariant histidine residue (107 His----Tyr): complete structure of the normal human CA II geneP J Venta, R J Welty, T M Johnson, et al.
Cytogenetic and Genome Research|February 19, 2004
Comparative mapping of genes flanking the human chromosome 12 evolutionary breakpoint in the pigC R Farber, N E Raney, V D Rilington, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 15, 1992
Mutation creates an open reading frame within the 5' untranslated region of macaque erythrocyte carbonic anhydrase (CA) I mRNA that suppresses CA I expression and supports the scanning model for translationN C Bergenhem, P J Venta, P J Hopkins, et al.
Life Sciences|July 23, 1998
Promoter activity of carbonic anhydrase II regulatory regions in cultured renal proximal tubular cellsL W Lai, R P Erickson, P J Venta, et al.
Nature|July 15, 1982
Phylogenetic origins and adaptive evolution of avian and mammalian haemoglobin genesJ Czelusniak, M Goodman, D Hewett-Emmett, et al.
Veterinary Pathology|May 11, 2004
A von Willebrand's factor genomic nucleotide variant and polymerase chain reaction diagnostic test associated with inheritable type-2 von Willebrand's disease in a line of german shorthaired pointer dogsJ W Kramer, P J Venta, S R Klein, et al.
Rapid Communications in Mass Spectrometry : RCM|January 1, 1995
Rapid screening of genetic polymorphisms using buccal cell DNA with detection by matrix-assisted laser desorption/ionization mass spectrometryY H Liu, J Bai, Y Zhu, et al.
American Journal of Human Genetics|April 1, 1994
Carbonic anhydrase II deficiency: single-base deletion in exon 7 is the predominant mutation in Caribbean Hispanic patientsP Y Hu, A R Ernst, W S Sly, et al.
Equine Veterinary Journal|March 24, 2009
Expression of toll-like receptor 2 mRNA in bronchial epithelial cells is not induced in RAO-affected horsesA Berndt, F J Derksen, P J Venta, et al.
Pageof 6