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T Raz

Showing results (31-40 of 37) with videos related to

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International Journal of Cancer|November 15, 1990
Evidence for the role of 34-kDa galactoside-binding lectin in transformation and metastasisA Raz, D G Zhu, V Hogan, et al.
Human Genetics|December 18, 1998
Refined mapping of the gene for thiamine-responsive megaloblastic anemia syndrome and evidence for genetic homogeneityT Raz, T Barrett, R Szargel, et al.
American Journal of Medical Genetics|January 8, 1999
Atrichia with papular lesions maps to 8p in the region containing the human hairless geneE Sprecher, R Bergman, R Szargel, et al.
American Journal of Human Genetics|December 18, 1997
Localization of the gene for thiamine-responsive megaloblastic anemia syndrome, on the long arm of chromosome 1, by homozygosity mappingE J Neufeld, H Mandel, T Raz, et al.
Nature Genetics|July 3, 1999
Mutations in SLC19A2 cause thiamine-responsive megaloblastic anaemia associated with diabetes mellitus and deafnessV Labay, T Raz, D Baron, et al.
Oncogene|August 9, 2007
Quantitative monitoring by polymerase colony assay of known mutations resistant to ABL kinase inhibitorsV Nardi, T Raz, X Cao, et al.
Human Mutation|June 30, 2000
The spectrum of mutations, including four novel ones, in the thiamine-responsive megaloblastic anemia gene SLC19A2 of eight familiesT Raz, V Labay, D Baron, et al.
Pageof 4

Showing results (31-40 of 37) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 37 results.
International Journal of Cancer|November 15, 1990
Evidence for the role of 34-kDa galactoside-binding lectin in transformation and metastasisA Raz, D G Zhu, V Hogan, et al.
Human Genetics|December 18, 1998
Refined mapping of the gene for thiamine-responsive megaloblastic anemia syndrome and evidence for genetic homogeneityT Raz, T Barrett, R Szargel, et al.
American Journal of Medical Genetics|January 8, 1999
Atrichia with papular lesions maps to 8p in the region containing the human hairless geneE Sprecher, R Bergman, R Szargel, et al.
American Journal of Human Genetics|December 18, 1997
Localization of the gene for thiamine-responsive megaloblastic anemia syndrome, on the long arm of chromosome 1, by homozygosity mappingE J Neufeld, H Mandel, T Raz, et al.
Nature Genetics|July 3, 1999
Mutations in SLC19A2 cause thiamine-responsive megaloblastic anaemia associated with diabetes mellitus and deafnessV Labay, T Raz, D Baron, et al.
Oncogene|August 9, 2007
Quantitative monitoring by polymerase colony assay of known mutations resistant to ABL kinase inhibitorsV Nardi, T Raz, X Cao, et al.
Human Mutation|June 30, 2000
The spectrum of mutations, including four novel ones, in the thiamine-responsive megaloblastic anemia gene SLC19A2 of eight familiesT Raz, V Labay, D Baron, et al.
Pageof 4