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Gideon Bach

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

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Traffic (Copenhagen, Denmark)|January 25, 2012
Role of protein kinase d in Golgi exit and lysosomal targeting of the transmembrane protein, Mcoln1David L Marks, Eileen L Holicky, Christine L Wheatley, et al.
Immunogenetics|July 13, 2014
Age-dependent HLA profiles of the Israeli population: impact on hematopoietic cell donor recruitment and availabilityMoshe Israeli, Machteld Oudshoorn, Geert W Haasnoot, et al.
Molecular Genetics and Metabolism|March 19, 2005
A mutation in the saposin A coding region of the prosaposin gene in an infant presenting as Krabbe disease: first report of saposin A deficiency in humansRonen Spiegel, Gideon Bach, Vivi Sury, et al.
American Journal of Medical Genetics. Part A|August 19, 2004
Mutation frequencies for glycogen storage disease Ia in the Ashkenazi Jewish populationJosef Ekstein, Berish Y Rubin, Sylvia L Anderson, et al.
Molecular Genetics and Metabolism|April 25, 2006
When Mucolipidosis III meets Mucolipidosis II: GNPTA gene mutations in 24 patientsRuth Bargal, Marsha Zeigler, Bassam Abu-Libdeh, et al.
Experimental Dermatology|March 31, 2021
Molecular epidemiology of non-syndromic autosomal recessive congenital ichthyosis in a Middle-Eastern populationJanan Mohamad, Liat Samuelov, Natalia Malchin, 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.
Traffic (Copenhagen, Denmark)|January 25, 2012
Role of protein kinase d in Golgi exit and lysosomal targeting of the transmembrane protein, Mcoln1David L Marks, Eileen L Holicky, Christine L Wheatley, et al.
Immunogenetics|July 13, 2014
Age-dependent HLA profiles of the Israeli population: impact on hematopoietic cell donor recruitment and availabilityMoshe Israeli, Machteld Oudshoorn, Geert W Haasnoot, et al.
Molecular Genetics and Metabolism|March 19, 2005
A mutation in the saposin A coding region of the prosaposin gene in an infant presenting as Krabbe disease: first report of saposin A deficiency in humansRonen Spiegel, Gideon Bach, Vivi Sury, et al.
American Journal of Medical Genetics. Part A|August 19, 2004
Mutation frequencies for glycogen storage disease Ia in the Ashkenazi Jewish populationJosef Ekstein, Berish Y Rubin, Sylvia L Anderson, et al.
Molecular Genetics and Metabolism|April 25, 2006
When Mucolipidosis III meets Mucolipidosis II: GNPTA gene mutations in 24 patientsRuth Bargal, Marsha Zeigler, Bassam Abu-Libdeh, et al.
Experimental Dermatology|March 31, 2021
Molecular epidemiology of non-syndromic autosomal recessive congenital ichthyosis in a Middle-Eastern populationJanan Mohamad, Liat Samuelov, Natalia Malchin, et al.
Pageof 2