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J E Metherall

Showing results (11-20 of 16) with videos related to

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The EMBO Journal|October 1, 1986
Beta zero thalassemia caused by a base substitution that creates an alternative splice acceptor site in an intronJ E Metherall, F S Collins, J Pan, et al.
The Journal of Biological Chemistry|May 15, 1991
Genetic distinction between sterol-mediated transcriptional and posttranscriptional control of 3-hydroxy-3-methylglutaryl-coenzyme A reductaseP A Dawson, J E Metherall, N D Ridgway, et al.
The Journal of Biological Chemistry|July 5, 1991
A 25-hydroxycholesterol-resistant cell line deficient in acyl-CoA: cholesterol acyltransferaseJ E Metherall, N D Ridgway, P A Dawson, et al.
Nature|January 24, 1985
A point mutation in the A gamma-globin gene promoter in Greek hereditary persistence of fetal haemoglobinF S Collins, J E Metherall, M Yamakawa, et al.
Molecular and Cellular Biology|August 1, 1987
Expression of the affected A gamma globin gene associated with Greek nondeletion hereditary persistence of fetal hemoglobinC J Stoeckert, J E Metherall, M Yamakawa, et al.
American Journal of Medical Genetics|December 10, 1999
Hemizygosity for the COP9 signalosome subunit gene, SGN3, in the Smith-Magenis syndromeS H Elsea, K Mykytyn, K Ferrell, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
The EMBO Journal|October 1, 1986
Beta zero thalassemia caused by a base substitution that creates an alternative splice acceptor site in an intronJ E Metherall, F S Collins, J Pan, et al.
The Journal of Biological Chemistry|May 15, 1991
Genetic distinction between sterol-mediated transcriptional and posttranscriptional control of 3-hydroxy-3-methylglutaryl-coenzyme A reductaseP A Dawson, J E Metherall, N D Ridgway, et al.
The Journal of Biological Chemistry|July 5, 1991
A 25-hydroxycholesterol-resistant cell line deficient in acyl-CoA: cholesterol acyltransferaseJ E Metherall, N D Ridgway, P A Dawson, et al.
Nature|January 24, 1985
A point mutation in the A gamma-globin gene promoter in Greek hereditary persistence of fetal haemoglobinF S Collins, J E Metherall, M Yamakawa, et al.
Molecular and Cellular Biology|August 1, 1987
Expression of the affected A gamma globin gene associated with Greek nondeletion hereditary persistence of fetal hemoglobinC J Stoeckert, J E Metherall, M Yamakawa, et al.
American Journal of Medical Genetics|December 10, 1999
Hemizygosity for the COP9 signalosome subunit gene, SGN3, in the Smith-Magenis syndromeS H Elsea, K Mykytyn, K Ferrell, et al.
Pageof 2