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A Reis

Showing results (681-690 of 1,144) with videos related to

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Molecular Syndromology|July 24, 2012
In-Frame Deletion and Missense Mutations of the C-Terminal Helicase Domain of SMARCA2 in Three Patients with Nicolaides-Baraitser SyndromeD Wolff, S Endele, S Azzarello-Burri, et al.
Human Genetics|January 24, 1998
Localisation of a gene for Papillon-Lefèvre syndrome to chromosome 11q14-q21 by homozygosity mappingM W Laass, H C Hennies, S Preis, et al.
American Journal of Human Genetics|August 1, 1997
Localization of the gene causing keratolytic winter erythema to chromosome 8p22-p23, and evidence for a founder effect in South African Afrikaans-speakersM Starfield, H C Hennies, M Jung, et al.
Asian-Australasian Journal of Animal Sciences|June 25, 2015
Lipid Sources with Different Fatty Acid Profile Alters the Fatty Acid Profile and Quality of Beef from Confined Nellore SteersGiovani Fiorentini, Josiane F Lage, Isabela P C Carvalho, et al.
The Analyst|November 1, 1987
Photoacoustic spectroscopy for depth-profile analysis and herbicide monitoring in leavesJ W Nery, O Pessoa Júnior, H Vargas, et al.
International Wound Journal|December 15, 2017
Effect of 670 nm laser photobiomodulation on vascular density and fibroplasia in late stages of tissue repairTila Fortuna, Ana Cristina Gonzalez, Maíra F Sá, et al.
Operative Dentistry|January 1, 2020
Clinical Effects of Desensitizing Prefilled Disposable Trays in In-office Bleaching: A Randomized Single-blind Clinical TrialL M Martins, L A Lima E Souza, E Sutil, et al.
European Journal of Human Genetics : EJHG|November 28, 2000
Clinical ascertainment of Nijmegen breakage syndrome (NBS) and prevalence of the major mutation, 657del5, in three Slav populationsR Varon, E Seemanova, K Chrzanowska, et al.
The British Journal of Nutrition|May 12, 2001
Magnesium deficiency improves glucose homeostasis in the rat: studies in vivo and in isolated islets in vitroM A Reis, M Q Latorraca, E M Carneiro, et al.
Nature Genetics|June 1, 1994
The origin of the major cystic fibrosis mutation (delta F508) in European populationsN Morral, J Bertranpetit, X Estivill, et al.
Pageof 115

Showing results (681-690 of 1,144) with videos related to

Sort By:
Pageof 115
Molecular Syndromology|July 24, 2012
In-Frame Deletion and Missense Mutations of the C-Terminal Helicase Domain of SMARCA2 in Three Patients with Nicolaides-Baraitser SyndromeD Wolff, S Endele, S Azzarello-Burri, et al.
Human Genetics|January 24, 1998
Localisation of a gene for Papillon-Lefèvre syndrome to chromosome 11q14-q21 by homozygosity mappingM W Laass, H C Hennies, S Preis, et al.
American Journal of Human Genetics|August 1, 1997
Localization of the gene causing keratolytic winter erythema to chromosome 8p22-p23, and evidence for a founder effect in South African Afrikaans-speakersM Starfield, H C Hennies, M Jung, et al.
Asian-Australasian Journal of Animal Sciences|June 25, 2015
Lipid Sources with Different Fatty Acid Profile Alters the Fatty Acid Profile and Quality of Beef from Confined Nellore SteersGiovani Fiorentini, Josiane F Lage, Isabela P C Carvalho, et al.
The Analyst|November 1, 1987
Photoacoustic spectroscopy for depth-profile analysis and herbicide monitoring in leavesJ W Nery, O Pessoa Júnior, H Vargas, et al.
International Wound Journal|December 15, 2017
Effect of 670 nm laser photobiomodulation on vascular density and fibroplasia in late stages of tissue repairTila Fortuna, Ana Cristina Gonzalez, Maíra F Sá, et al.
Operative Dentistry|January 1, 2020
Clinical Effects of Desensitizing Prefilled Disposable Trays in In-office Bleaching: A Randomized Single-blind Clinical TrialL M Martins, L A Lima E Souza, E Sutil, et al.
European Journal of Human Genetics : EJHG|November 28, 2000
Clinical ascertainment of Nijmegen breakage syndrome (NBS) and prevalence of the major mutation, 657del5, in three Slav populationsR Varon, E Seemanova, K Chrzanowska, et al.
The British Journal of Nutrition|May 12, 2001
Magnesium deficiency improves glucose homeostasis in the rat: studies in vivo and in isolated islets in vitroM A Reis, M Q Latorraca, E M Carneiro, et al.
Nature Genetics|June 1, 1994
The origin of the major cystic fibrosis mutation (delta F508) in European populationsN Morral, J Bertranpetit, X Estivill, et al.
Pageof 115