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L M King

Showing results (61-70 of 75) with videos related to

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Toxicologic Pathology|April 20, 1999
Coronary arteriopathy in monkeys following administration of CI-1020, an endothelin A receptor antagonistM A Albassam, A L Metz, N J Gragtmans, et al.
Annals of the New York Academy of Sciences|June 8, 1996
Mutations in the cartilage oligomeric matrix protein (COMP) gene in pseudoachondroplasia and multiple epiphyseal dysplasiaD H Cohn, M D Briggs, L M King, et al.
British Poultry Science|September 11, 2003
Field testing the influence of sperm competition based on sperm mobility in breeder turkey tomsA M Donoghue, J D Kirby, D P Froman, et al.
Toxicologic Pathology|May 1, 1996
Hepatotumorigenicity and peroxisome proliferation induced by the hypolipidemic CI-924 in a two-year study in male and female B6C3F1 miceR M Walker, Z W Wojcinski, A H Hofstra, et al.
Protein Expression and Purification|October 26, 2000
High-level periplasmic expression in Escherichia coli using a eukaryotic signal peptide: importance of codon usage at the 5' end of the coding sequenceD P Humphreys, M Sehdev, A P Chapman, et al.
Protein Engineering|April 25, 2000
Improved efficiency of site-specific copper(II) ion-catalysed protein cleavage effected by mutagenesis of cleavage siteD P Humphreys, L M King, S M West, et al.
Clinical Genetics|December 25, 2004
Fine mapping of the X-linked split-hand/split-foot malformation (SHFM2) locus to a 5.1-Mb region on Xq26.3 and analysis of candidate genesM Faiyaz-Ul-Haque, S H E Zaidi, L M King, et al.
Journal of Medical Genetics|April 4, 2000
Report of five novel and one recurrent COL2A1 mutations with analysis of genotype-phenotype correlation in patients with a lethal type II collagen disorderG R Mortier, M Weis, L Nuytinck, et al.
Nature Genetics|July 1, 1995
Pseudoachondroplasia and multiple epiphyseal dysplasia due to mutations in the cartilage oligomeric matrix protein geneM D Briggs, S M Hoffman, L M King, et al.
Magma (New York, N.Y.)|February 24, 2001
Muscular dystrophy: from gene to patientJ C Hopkins, B L Bia, J G Crilley, et al.
Pageof 8

Showing results (61-70 of 75) with videos related to

Sort By:
Pageof 8
Toxicologic Pathology|April 20, 1999
Coronary arteriopathy in monkeys following administration of CI-1020, an endothelin A receptor antagonistM A Albassam, A L Metz, N J Gragtmans, et al.
Annals of the New York Academy of Sciences|June 8, 1996
Mutations in the cartilage oligomeric matrix protein (COMP) gene in pseudoachondroplasia and multiple epiphyseal dysplasiaD H Cohn, M D Briggs, L M King, et al.
British Poultry Science|September 11, 2003
Field testing the influence of sperm competition based on sperm mobility in breeder turkey tomsA M Donoghue, J D Kirby, D P Froman, et al.
Toxicologic Pathology|May 1, 1996
Hepatotumorigenicity and peroxisome proliferation induced by the hypolipidemic CI-924 in a two-year study in male and female B6C3F1 miceR M Walker, Z W Wojcinski, A H Hofstra, et al.
Protein Expression and Purification|October 26, 2000
High-level periplasmic expression in Escherichia coli using a eukaryotic signal peptide: importance of codon usage at the 5' end of the coding sequenceD P Humphreys, M Sehdev, A P Chapman, et al.
Protein Engineering|April 25, 2000
Improved efficiency of site-specific copper(II) ion-catalysed protein cleavage effected by mutagenesis of cleavage siteD P Humphreys, L M King, S M West, et al.
Clinical Genetics|December 25, 2004
Fine mapping of the X-linked split-hand/split-foot malformation (SHFM2) locus to a 5.1-Mb region on Xq26.3 and analysis of candidate genesM Faiyaz-Ul-Haque, S H E Zaidi, L M King, et al.
Journal of Medical Genetics|April 4, 2000
Report of five novel and one recurrent COL2A1 mutations with analysis of genotype-phenotype correlation in patients with a lethal type II collagen disorderG R Mortier, M Weis, L Nuytinck, et al.
Nature Genetics|July 1, 1995
Pseudoachondroplasia and multiple epiphyseal dysplasia due to mutations in the cartilage oligomeric matrix protein geneM D Briggs, S M Hoffman, L M King, et al.
Magma (New York, N.Y.)|February 24, 2001
Muscular dystrophy: from gene to patientJ C Hopkins, B L Bia, J G Crilley, et al.
Pageof 8