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Ursula Matte

Showing results (81-90 of 158) with videos related to

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Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|February 7, 2012
Analysis of cDNA molecules is not suitable for the molecular diagnosis of Mucopolysaccharidosis type IAndresa Cardoso Grandini Almeida, Gabriela Pasqualim, Fabiana Q Mayer, et al.
Journal of Assisted Reproduction and Genetics|May 4, 2015
LH (Trp8Arg/Ile15Thr), LHR (insLQ) and FSHR (Asn680Ser) polymorphisms genotypic prevalence in women with endometriosis and infertilityCarla Regina Schmitz, Carlos Augusto Bastos de Souza, Vanessa Krebs Genro, et al.
Molecular Genetics and Metabolism Reports|November 30, 2016
A <i>de novo</i> or germline mutation in a family with Mucolipidosis III gamma: Implications for molecular diagnosis and genetic counselingRenata Voltolini Velho, Taciane Alegra, Fernanda Sperb, et al.
Journal of Human Genetics|March 4, 2016
Enigmatic in vivo GlcNAc-1-phosphotransferase (GNPTG) transcript correction to wild type in two mucolipidosis III gamma siblings homozygous for nonsense mutationsRenata Voltolini Velho, Nataniel Floriano Ludwig, Taciane Alegra, et al.
European Journal of Cardio-Thoracic Surgery : Official Journal of the European Association for Cardio-Thoracic Surgery|February 26, 2008
Vascular endothelial growth factor gene therapy induces early re-establishment of canine bronchial circulationMaurício G Saueressig, Amarilio Macedo Neto, Elaine A F Fortis, et al.
International Journal of Experimental Pathology|June 22, 2013
Characterization of joint disease in mucopolysaccharidosis type I micePatricia G de Oliveira, Guilherme Baldo, Fabiana Q Mayer, et al.
Genetics and Molecular Biology|December 4, 2018
Lack of association between genetic polymorphisms in IGF1 and IGFBP3 with twin births in a Brazilian population (Cândido Godói, Rio Grande do Sul)Mariana de Oliveira-Klein, Augusto César Cardoso-Dos-Santos, Alice Tagliani-Ribeiro, et al.
Life Sciences|January 26, 2018
Cathepsin B inhibition attenuates cardiovascular pathology in mucopolysaccharidosis I miceEsteban Alberto Gonzalez, Giselle Renata Martins, Angela Maria Vicente Tavares, et al.
Biotechnology Letters|January 19, 2018
A simple protocol for transfecting human mesenchymal stem cellsTalita Giacomet de Carvalho, Felipe Matheus Pellenz, Alvaro Laureano, et al.
Advanced Drug Delivery Reviews|November 10, 2022
Gene editing strategies to treat lysosomal disorders: The example of mucopolysaccharidosesFlávia Nathiely Silveira Fachel, Lariane Frâncio, Édina Poletto, et al.
Pageof 16

Showing results (81-90 of 158) with videos related to

Sort By:
Pageof 16
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|February 7, 2012
Analysis of cDNA molecules is not suitable for the molecular diagnosis of Mucopolysaccharidosis type IAndresa Cardoso Grandini Almeida, Gabriela Pasqualim, Fabiana Q Mayer, et al.
Journal of Assisted Reproduction and Genetics|May 4, 2015
LH (Trp8Arg/Ile15Thr), LHR (insLQ) and FSHR (Asn680Ser) polymorphisms genotypic prevalence in women with endometriosis and infertilityCarla Regina Schmitz, Carlos Augusto Bastos de Souza, Vanessa Krebs Genro, et al.
Molecular Genetics and Metabolism Reports|November 30, 2016
A <i>de novo</i> or germline mutation in a family with Mucolipidosis III gamma: Implications for molecular diagnosis and genetic counselingRenata Voltolini Velho, Taciane Alegra, Fernanda Sperb, et al.
Journal of Human Genetics|March 4, 2016
Enigmatic in vivo GlcNAc-1-phosphotransferase (GNPTG) transcript correction to wild type in two mucolipidosis III gamma siblings homozygous for nonsense mutationsRenata Voltolini Velho, Nataniel Floriano Ludwig, Taciane Alegra, et al.
European Journal of Cardio-Thoracic Surgery : Official Journal of the European Association for Cardio-Thoracic Surgery|February 26, 2008
Vascular endothelial growth factor gene therapy induces early re-establishment of canine bronchial circulationMaurício G Saueressig, Amarilio Macedo Neto, Elaine A F Fortis, et al.
International Journal of Experimental Pathology|June 22, 2013
Characterization of joint disease in mucopolysaccharidosis type I micePatricia G de Oliveira, Guilherme Baldo, Fabiana Q Mayer, et al.
Genetics and Molecular Biology|December 4, 2018
Lack of association between genetic polymorphisms in IGF1 and IGFBP3 with twin births in a Brazilian population (Cândido Godói, Rio Grande do Sul)Mariana de Oliveira-Klein, Augusto César Cardoso-Dos-Santos, Alice Tagliani-Ribeiro, et al.
Life Sciences|January 26, 2018
Cathepsin B inhibition attenuates cardiovascular pathology in mucopolysaccharidosis I miceEsteban Alberto Gonzalez, Giselle Renata Martins, Angela Maria Vicente Tavares, et al.
Biotechnology Letters|January 19, 2018
A simple protocol for transfecting human mesenchymal stem cellsTalita Giacomet de Carvalho, Felipe Matheus Pellenz, Alvaro Laureano, et al.
Advanced Drug Delivery Reviews|November 10, 2022
Gene editing strategies to treat lysosomal disorders: The example of mucopolysaccharidosesFlávia Nathiely Silveira Fachel, Lariane Frâncio, Édina Poletto, et al.
Pageof 16