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G Weber

Showing results (881-890 of 1,377) with videos related to

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Genomics|August 1, 1993
Assignment of the human FAU gene to a subregion of chromosome 11q13K Kas, E Schoenmakers, W van de Ven, et al.
Advances in Enzyme Regulation|January 1, 1993
Regulation of deoxycytidine kinase activity and inhibition by DFDCG Weber, R L Singhal, M Abonyi, et al.
Journal De Radiologie|August 9, 2011
[Periprocedural management of hemostasis risk in interventional radiology]J Potet, G Weber-Donat, A Thome, et al.
Cytogenetic and Genome Research|March 22, 2012
Familial translocation t(6;20)(p21;p13) resulting in partial trisomy 6p and partial monosomy 20p: report of a new case and review of the literatureA L Berner, S Bağci, E Wohlleber, et al.
International Journal of Cancer|April 17, 2001
Analysis of human meningiomas for aberrations of the MADH2, MADH4, APM-1 and DCC tumor suppressor genes on the long arm of chromosome 18R Büschges, J Boström, M Wolter, et al.
The Journal of Biological Chemistry|April 25, 1984
Modulation of IMP dehydrogenase activity and guanylate metabolism by tiazofurin (2-beta-D-ribofuranosylthiazole-4-carboxamide)M S Lui, M A Faderan, J J Liepnieks, et al.
Dalton Transactions (Cambridge, England : 2003)|November 4, 2017
A robust viologen and Mn-based porous coordination polymer with two types of Lewis acid sites providing high affinity for H<sub>2</sub>O, CO<sub>2</sub> and NH<sub>3</sub>A Leblanc, N Mercier, M Allain, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Assignment of the mouse homologue of a human MEN1 candidate gene, phospholipase C-beta 3 (Plcb3), to chromosome region 19B by FISHA E Gobl, B P Chowdhary, W Shu, et al.
Burns : Journal of the International Society for Burn Injuries|December 7, 2010
Effect of N-acetylcysteine treatment on the expression of leukocyte surface markers after burn injuryC Csontos, B Rezman, V Foldi, et al.
The Journal of Clinical Endocrinology and Metabolism|November 30, 2000
Mutational analysis of GNAS1 in patients with pseudohypoparathyroidism: identification of two novel mutationsG Mantovani, R Romoli, G Weber, et al.
Pageof 138

Showing results (881-890 of 1,377) with videos related to

Sort By:
Pageof 138
Genomics|August 1, 1993
Assignment of the human FAU gene to a subregion of chromosome 11q13K Kas, E Schoenmakers, W van de Ven, et al.
Advances in Enzyme Regulation|January 1, 1993
Regulation of deoxycytidine kinase activity and inhibition by DFDCG Weber, R L Singhal, M Abonyi, et al.
Journal De Radiologie|August 9, 2011
[Periprocedural management of hemostasis risk in interventional radiology]J Potet, G Weber-Donat, A Thome, et al.
Cytogenetic and Genome Research|March 22, 2012
Familial translocation t(6;20)(p21;p13) resulting in partial trisomy 6p and partial monosomy 20p: report of a new case and review of the literatureA L Berner, S Bağci, E Wohlleber, et al.
International Journal of Cancer|April 17, 2001
Analysis of human meningiomas for aberrations of the MADH2, MADH4, APM-1 and DCC tumor suppressor genes on the long arm of chromosome 18R Büschges, J Boström, M Wolter, et al.
The Journal of Biological Chemistry|April 25, 1984
Modulation of IMP dehydrogenase activity and guanylate metabolism by tiazofurin (2-beta-D-ribofuranosylthiazole-4-carboxamide)M S Lui, M A Faderan, J J Liepnieks, et al.
Dalton Transactions (Cambridge, England : 2003)|November 4, 2017
A robust viologen and Mn-based porous coordination polymer with two types of Lewis acid sites providing high affinity for H<sub>2</sub>O, CO<sub>2</sub> and NH<sub>3</sub>A Leblanc, N Mercier, M Allain, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Assignment of the mouse homologue of a human MEN1 candidate gene, phospholipase C-beta 3 (Plcb3), to chromosome region 19B by FISHA E Gobl, B P Chowdhary, W Shu, et al.
Burns : Journal of the International Society for Burn Injuries|December 7, 2010
Effect of N-acetylcysteine treatment on the expression of leukocyte surface markers after burn injuryC Csontos, B Rezman, V Foldi, et al.
The Journal of Clinical Endocrinology and Metabolism|November 30, 2000
Mutational analysis of GNAS1 in patients with pseudohypoparathyroidism: identification of two novel mutationsG Mantovani, R Romoli, G Weber, et al.
Pageof 138