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L Mandel

Showing results (221-230 of 451) with videos related to

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Annals of Botany|October 26, 2005
Genecology of Douglas fir in western Oregon and WashingtonJ Bradley St Clair, Nancy L Mandel, Kenneth W Vance-Borland
Biochemical and Biophysical Research Communications|March 27, 1970
Calf thymus RNA polymerases exhibit template specificityM Gniazdowski, J L Mandel, F Gissinger, et al.
American Journal of Medical Genetics|April 1, 1992
On some technical aspects of direct DNA diagnosis of the fragile X syndromeF Rousseau, D Heitz, V Biancalana, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1985
The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequencyI Oberlé, D Drayna, G Camerino, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1990
Additional polymorphisms at marker loci D9S5 and D9S15 generate extended haplotypes in linkage disequilibrium with Friedreich ataxiaR Fujita, A Hanauer, G Sirugo, et al.
Biochemical and Biophysical Research Communications|January 6, 1970
Alpha-amanitin: a specific inhibitor of one of two DNA-pendent RNA polymerase activities from calf thymusC Kedinger, M Gniazdowski, J L Mandel, et al.
Human Mutation|September 30, 1999
Identification of novel mutations in the MTM1 gene causing severe and mild forms of X-linked myotubular myopathyA Buj-Bello, V Biancalana, C Moutou, et al.
Genomics|November 23, 2000
Characterization of the adrenoleukodystrophy-related (ALDR, ABCD2) gene promoter: inductibility by retinoic acid and forskolinA Pujol, N Troffer-Charlier, E Metzger, et al.
Nature Genetics|August 1, 1993
The FMR-1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutationD Devys, Y Lutz, N Rouyer, et al.
Cytogenetics and Cell Genetics|January 1, 1985
Report of the Committee on Human Gene Mapping by Recombinant DNA TechniquesH F Willard, M H Skolnick, P L Pearson, et al.
Pageof 46

Showing results (221-230 of 451) with videos related to

Sort By:
Pageof 46
Annals of Botany|October 26, 2005
Genecology of Douglas fir in western Oregon and WashingtonJ Bradley St Clair, Nancy L Mandel, Kenneth W Vance-Borland
Biochemical and Biophysical Research Communications|March 27, 1970
Calf thymus RNA polymerases exhibit template specificityM Gniazdowski, J L Mandel, F Gissinger, et al.
American Journal of Medical Genetics|April 1, 1992
On some technical aspects of direct DNA diagnosis of the fragile X syndromeF Rousseau, D Heitz, V Biancalana, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1985
The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequencyI Oberlé, D Drayna, G Camerino, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1990
Additional polymorphisms at marker loci D9S5 and D9S15 generate extended haplotypes in linkage disequilibrium with Friedreich ataxiaR Fujita, A Hanauer, G Sirugo, et al.
Biochemical and Biophysical Research Communications|January 6, 1970
Alpha-amanitin: a specific inhibitor of one of two DNA-pendent RNA polymerase activities from calf thymusC Kedinger, M Gniazdowski, J L Mandel, et al.
Human Mutation|September 30, 1999
Identification of novel mutations in the MTM1 gene causing severe and mild forms of X-linked myotubular myopathyA Buj-Bello, V Biancalana, C Moutou, et al.
Genomics|November 23, 2000
Characterization of the adrenoleukodystrophy-related (ALDR, ABCD2) gene promoter: inductibility by retinoic acid and forskolinA Pujol, N Troffer-Charlier, E Metzger, et al.
Nature Genetics|August 1, 1993
The FMR-1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutationD Devys, Y Lutz, N Rouyer, et al.
Cytogenetics and Cell Genetics|January 1, 1985
Report of the Committee on Human Gene Mapping by Recombinant DNA TechniquesH F Willard, M H Skolnick, P L Pearson, et al.
Pageof 46