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Neuro-Oncology
|
December 21, 2013
A deletion causing NF2 exon 9 skipping is associated with familial autosomal dominant intramedullary ependymoma
Ilyess Zemmoura, Patrick Vourc'h, Agathe Paubel, et al.
Biological Psychiatry
|
June 24, 2009
Autism and nonsyndromic mental retardation associated with a de novo mutation in the NLGN4X gene promoter causing an increased expression level
Hussein Daoud, Frédérique Bonnet-Brilhault, Sylviane Védrine, et al.
JAMA
|
April 22, 1992
Longitudinal evaluation of prostate-specific antigen levels in men with and without prostate disease
H B Carter, J D Pearson, E J Metter, et al.
Analytical Biochemistry
|
January 16, 1999
Cell ashing for trace element analysis: A new approach based on ultraviolet/ozone
G De Stasio, B Gilbert, L Perfetti, et al.
Cells
|
January 1, 2020
TDP-43-Mediated Toxicity in HEK293T Cells: A Fast and Reproducible Protocol To Be Employed in the Search of New Therapeutic Options against Amyotrophic Lateral Sclerosis
Débora Lanznaster, Jérôme Bourgeais, Clement Bruno, et al.
Journal of Proteome Research
|
November 6, 2015
Metabolomics Study of Urine in Autism Spectrum Disorders Using a Multiplatform Analytical Methodology
Binta Diémé, Sylvie Mavel, Hélène Blasco, et al.
Journal of Pharmaceutical and Biomedical Analysis
|
May 23, 2017
Workflow methodology for rat brain metabolome exploration using NMR, LC-MS and GC-MS analytical platforms
Binta Diémé, Antoine Lefèvre, Lydie Nadal-Desbarats, et al.
International Journal of Molecular Sciences
|
March 6, 2021
Dysregulations of Expression of Genes of the Ubiquitin/SUMO Pathways in an In Vitro Model of Amyotrophic Lateral Sclerosis Combining Oxidative Stress and SOD1 Gene Mutation
Audrey Dangoumau, Sylviane Marouillat, Roxane Coelho, et al.
Neurobiology of Aging
|
August 20, 2013
Novel SOD1 mutation p.V31A identified with a slowly progressive form of amyotrophic lateral sclerosis
Audrey Dangoumau, Annie Verschueren, Ellen Hammouche, et al.
Antimicrobial Agents and Chemotherapy
|
October 17, 2018
Mutations in the MAB_2299c TetR Regulator Confer Cross-Resistance to Clofazimine and Bedaquiline in <i>Mycobacterium abscessus</i>
Matthias Richard, Ana Victoria Gutiérrez, Albertus Viljoen, et al.
Page
of 39
Search research articles
Search
Showing results (231-240 of 382) with videos related to
Sort By:
Page
of 39
Neuro-Oncology
|
December 21, 2013
A deletion causing NF2 exon 9 skipping is associated with familial autosomal dominant intramedullary ependymoma
Ilyess Zemmoura, Patrick Vourc'h, Agathe Paubel, et al.
Biological Psychiatry
|
June 24, 2009
Autism and nonsyndromic mental retardation associated with a de novo mutation in the NLGN4X gene promoter causing an increased expression level
Hussein Daoud, Frédérique Bonnet-Brilhault, Sylviane Védrine, et al.
JAMA
|
April 22, 1992
Longitudinal evaluation of prostate-specific antigen levels in men with and without prostate disease
H B Carter, J D Pearson, E J Metter, et al.
Analytical Biochemistry
|
January 16, 1999
Cell ashing for trace element analysis: A new approach based on ultraviolet/ozone
G De Stasio, B Gilbert, L Perfetti, et al.
Cells
|
January 1, 2020
TDP-43-Mediated Toxicity in HEK293T Cells: A Fast and Reproducible Protocol To Be Employed in the Search of New Therapeutic Options against Amyotrophic Lateral Sclerosis
Débora Lanznaster, Jérôme Bourgeais, Clement Bruno, et al.
Journal of Proteome Research
|
November 6, 2015
Metabolomics Study of Urine in Autism Spectrum Disorders Using a Multiplatform Analytical Methodology
Binta Diémé, Sylvie Mavel, Hélène Blasco, et al.
Journal of Pharmaceutical and Biomedical Analysis
|
May 23, 2017
Workflow methodology for rat brain metabolome exploration using NMR, LC-MS and GC-MS analytical platforms
Binta Diémé, Antoine Lefèvre, Lydie Nadal-Desbarats, et al.
International Journal of Molecular Sciences
|
March 6, 2021
Dysregulations of Expression of Genes of the Ubiquitin/SUMO Pathways in an In Vitro Model of Amyotrophic Lateral Sclerosis Combining Oxidative Stress and SOD1 Gene Mutation
Audrey Dangoumau, Sylviane Marouillat, Roxane Coelho, et al.
Neurobiology of Aging
|
August 20, 2013
Novel SOD1 mutation p.V31A identified with a slowly progressive form of amyotrophic lateral sclerosis
Audrey Dangoumau, Annie Verschueren, Ellen Hammouche, et al.
Antimicrobial Agents and Chemotherapy
|
October 17, 2018
Mutations in the MAB_2299c TetR Regulator Confer Cross-Resistance to Clofazimine and Bedaquiline in <i>Mycobacterium abscessus</i>
Matthias Richard, Ana Victoria Gutiérrez, Albertus Viljoen, et al.
Page
of 39