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M Vance

Showing results (121-130 of 466) with videos related to

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Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association|January 8, 2019
The relationship between zinc intake and cadmium burden is influenced by smoking statusKijoon Kim, Melissa M Melough, Terrence M Vance, et al.
Poultry Science|September 24, 2008
Effects of prelay 6/85-strain Mycoplasma gallisepticum inoculation alone or in conjunction with the inoculation of F-strain Mycoplasma gallisepticum during lay on the blood characteristics of commercial egg-laying hensE D Peebles, K A Viscione, S L Branton, et al.
Journal of Neurology|December 2, 2009
Copy number variations are a rare cause of non-CMT1A Charcot-Marie-Tooth diseaseJia Huang, Xingyao Wu, Gladys Montenegro, et al.
Human Mutation|May 2, 2000
Identification of seven novel SNPS (five nucleotide and two amino acid substitutions) in the connexin31 (GJB3) geneN López-Bigas, R Rabionet, E Martínez, et al.
Human Mutation|April 26, 2013
High-resolution survey in familial Parkinson disease genes reveals multiple independent copy number variation events in PARK2Liyong Wang, Karen Nuytemans, Guney Bademci, et al.
Stem Cell Research|June 7, 2022
Generation of two iPSC lines (UMi038-A & UMi039-A) from siblings bearing an Alzheimer's disease-associated variant in SORL1Brooke A DeRosa, Shaina A Simon, Christina A Velez, et al.
Gene Expression|July 28, 2009
Gene expression pattern and downregulation of DNA methyltransferase 1 using siRNA in porcine somatic cellsAngelica M Giraldo, Todd D Vaught, Limin Fu, et al.
Journal of Microbiology and Biotechnology|October 27, 2016
Validation of Analytical Methods for Plasma Total Antioxidant Capacity by Comparing with Urinary 8-Isoprostane LevelSang Gil Lee, Taoran Wang, Terrence M Vance, et al.
Clinical Genetics|August 1, 1981
Carrier detection in Sanfilippo syndrome type B: report of six familiesJ M Vance, P M Conneally, R S Wappner, et al.
Advances in Experimental Medicine and Biology|March 26, 2014
Mutation K42E in dehydrodolichol diphosphate synthase (DHDDS) causes recessive retinitis pigmentosaByron L Lam, Stephan L Züchner, Julia Dallman, et al.
Pageof 47

Showing results (121-130 of 466) with videos related to

Sort By:
Pageof 47
Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association|January 8, 2019
The relationship between zinc intake and cadmium burden is influenced by smoking statusKijoon Kim, Melissa M Melough, Terrence M Vance, et al.
Poultry Science|September 24, 2008
Effects of prelay 6/85-strain Mycoplasma gallisepticum inoculation alone or in conjunction with the inoculation of F-strain Mycoplasma gallisepticum during lay on the blood characteristics of commercial egg-laying hensE D Peebles, K A Viscione, S L Branton, et al.
Journal of Neurology|December 2, 2009
Copy number variations are a rare cause of non-CMT1A Charcot-Marie-Tooth diseaseJia Huang, Xingyao Wu, Gladys Montenegro, et al.
Human Mutation|May 2, 2000
Identification of seven novel SNPS (five nucleotide and two amino acid substitutions) in the connexin31 (GJB3) geneN López-Bigas, R Rabionet, E Martínez, et al.
Human Mutation|April 26, 2013
High-resolution survey in familial Parkinson disease genes reveals multiple independent copy number variation events in PARK2Liyong Wang, Karen Nuytemans, Guney Bademci, et al.
Stem Cell Research|June 7, 2022
Generation of two iPSC lines (UMi038-A & UMi039-A) from siblings bearing an Alzheimer's disease-associated variant in SORL1Brooke A DeRosa, Shaina A Simon, Christina A Velez, et al.
Gene Expression|July 28, 2009
Gene expression pattern and downregulation of DNA methyltransferase 1 using siRNA in porcine somatic cellsAngelica M Giraldo, Todd D Vaught, Limin Fu, et al.
Journal of Microbiology and Biotechnology|October 27, 2016
Validation of Analytical Methods for Plasma Total Antioxidant Capacity by Comparing with Urinary 8-Isoprostane LevelSang Gil Lee, Taoran Wang, Terrence M Vance, et al.
Clinical Genetics|August 1, 1981
Carrier detection in Sanfilippo syndrome type B: report of six familiesJ M Vance, P M Conneally, R S Wappner, et al.
Advances in Experimental Medicine and Biology|March 26, 2014
Mutation K42E in dehydrodolichol diphosphate synthase (DHDDS) causes recessive retinitis pigmentosaByron L Lam, Stephan L Züchner, Julia Dallman, et al.
Pageof 47