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Cellular and Molecular Life Sciences : CMLS
|
July 22, 2022
Liver-specific deletion of miR-181ab1 reduces liver tumour progression via upregulation of CBX7
Jinbiao Chen, Yang Zhao, Fan Zhang, et al.
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases
|
June 4, 2019
Association of a single nucleotide polymorphism in the ubxn6 gene with long-term non-progression phenotype in HIV-positive individuals
F Díez-Fuertes, H E De La Torre-Tarazona, E Calonge, et al.
European Journal of Neurology
|
February 14, 2018
Novel mutations in DNAJB6 cause LGMD1D and distal myopathy in French families
P H Jonson, J Palmio, M Johari, et al.
Annals of Neurology
|
September 17, 2013
Phylogenetic and epidemiologic evidence of multiyear incubation in human rabies
Torrey A Boland, Declan McGuone, Jenelle Jindal, et al.
Molecular Psychiatry
|
July 22, 2015
De novo deleterious genetic variations target a biological network centered on Aβ peptide in early-onset Alzheimer disease
A Rovelet-Lecrux, C Charbonnier, D Wallon, et al.
BMC Health Services Research
|
April 21, 2023
Cost of exome analysis in patients with intellectual disability: a micro-costing study in a French setting
A L Soilly, C Robert-Viard, C Besse, et al.
Human Genetics
|
January 16, 2016
A genome-wide association study of pulmonary tuberculosis in Morocco
A V Grant, A Sabri, A Abid, et al.
Molecular Psychiatry
|
August 26, 2015
SORL1 rare variants: a major risk factor for familial early-onset Alzheimer's disease
G Nicolas, C Charbonnier, D Wallon, et al.
Molecular Psychiatry
|
May 12, 2016
CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders
O Mercati, G Huguet, A Danckaert, et al.
Molecular Psychiatry
|
December 14, 2016
17q21.31 duplication causes prominent tau-related dementia with increased MAPT expression
K Le Guennec, O Quenez, G Nicolas, et al.
Page
of 21
Search research articles
Search
Showing results (191-200 of 203) with videos related to
Sort By:
Page
of 21
Cellular and Molecular Life Sciences : CMLS
|
July 22, 2022
Liver-specific deletion of miR-181ab1 reduces liver tumour progression via upregulation of CBX7
Jinbiao Chen, Yang Zhao, Fan Zhang, et al.
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases
|
June 4, 2019
Association of a single nucleotide polymorphism in the ubxn6 gene with long-term non-progression phenotype in HIV-positive individuals
F Díez-Fuertes, H E De La Torre-Tarazona, E Calonge, et al.
European Journal of Neurology
|
February 14, 2018
Novel mutations in DNAJB6 cause LGMD1D and distal myopathy in French families
P H Jonson, J Palmio, M Johari, et al.
Annals of Neurology
|
September 17, 2013
Phylogenetic and epidemiologic evidence of multiyear incubation in human rabies
Torrey A Boland, Declan McGuone, Jenelle Jindal, et al.
Molecular Psychiatry
|
July 22, 2015
De novo deleterious genetic variations target a biological network centered on Aβ peptide in early-onset Alzheimer disease
A Rovelet-Lecrux, C Charbonnier, D Wallon, et al.
BMC Health Services Research
|
April 21, 2023
Cost of exome analysis in patients with intellectual disability: a micro-costing study in a French setting
A L Soilly, C Robert-Viard, C Besse, et al.
Human Genetics
|
January 16, 2016
A genome-wide association study of pulmonary tuberculosis in Morocco
A V Grant, A Sabri, A Abid, et al.
Molecular Psychiatry
|
August 26, 2015
SORL1 rare variants: a major risk factor for familial early-onset Alzheimer's disease
G Nicolas, C Charbonnier, D Wallon, et al.
Molecular Psychiatry
|
May 12, 2016
CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders
O Mercati, G Huguet, A Danckaert, et al.
Molecular Psychiatry
|
December 14, 2016
17q21.31 duplication causes prominent tau-related dementia with increased MAPT expression
K Le Guennec, O Quenez, G Nicolas, et al.
Page
of 21