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S E Lloyd

Showing results (11-20 of 18) with videos related to

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Kidney International|November 5, 1997
Mutations of CLCN5 in Japanese children with idiopathic low molecular weight proteinuria, hypercalciuria and nephrocalcinosisN Akuta, S E Lloyd, T Igarashi, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 17, 2001
Identification of multiple quantitative trait loci linked to prion disease incubation period in miceS E Lloyd, O N Onwuazor, J A Beck, et al.
The Journal of Biological Chemistry|June 20, 1997
Y13C Azotobacter vinelandii ferredoxin I. A designed [Fe-S] ligand motif contains a cysteine persulfideM A Kemper, C D Stout, S J Lloyd, et al.
Human Genetics|June 1, 1996
Genetic mapping studies of 40 loci and 23 cosmids in chromosome 11p13-11q13, and exclusion of mu-calpain as the multiple endocrine neoplasia type 1 geneJ T Pang, S E Lloyd, C Wooding, et al.
Human Molecular Genetics|August 1, 1997
Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disordersS E Lloyd, W Gunther, S H Pearce, et al.
Kidney International|January 5, 2000
Isolated hypercalciuria with mutation in CLCN5: relevance to idiopathic hypercalciuriaS J Scheinman, J P Cox, S E Lloyd, et al.
Nature|February 1, 1996
A common molecular basis for three inherited kidney stone diseasesS E Lloyd, S H Pearce, S E Fisher, et al.
American Journal of Human Genetics|April 16, 1998
Characterization of mutations in patients with multiple endocrine neoplasia type 1J H Bassett, S A Forbes, A A Pannett, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Kidney International|November 5, 1997
Mutations of CLCN5 in Japanese children with idiopathic low molecular weight proteinuria, hypercalciuria and nephrocalcinosisN Akuta, S E Lloyd, T Igarashi, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 17, 2001
Identification of multiple quantitative trait loci linked to prion disease incubation period in miceS E Lloyd, O N Onwuazor, J A Beck, et al.
The Journal of Biological Chemistry|June 20, 1997
Y13C Azotobacter vinelandii ferredoxin I. A designed [Fe-S] ligand motif contains a cysteine persulfideM A Kemper, C D Stout, S J Lloyd, et al.
Human Genetics|June 1, 1996
Genetic mapping studies of 40 loci and 23 cosmids in chromosome 11p13-11q13, and exclusion of mu-calpain as the multiple endocrine neoplasia type 1 geneJ T Pang, S E Lloyd, C Wooding, et al.
Human Molecular Genetics|August 1, 1997
Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disordersS E Lloyd, W Gunther, S H Pearce, et al.
Kidney International|January 5, 2000
Isolated hypercalciuria with mutation in CLCN5: relevance to idiopathic hypercalciuriaS J Scheinman, J P Cox, S E Lloyd, et al.
Nature|February 1, 1996
A common molecular basis for three inherited kidney stone diseasesS E Lloyd, S H Pearce, S E Fisher, et al.
American Journal of Human Genetics|April 16, 1998
Characterization of mutations in patients with multiple endocrine neoplasia type 1J H Bassett, S A Forbes, A A Pannett, et al.
Pageof 2