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Molecular Neurobiology
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January 29, 2022
Huntington Disease Gene Expression Signatures in Blood Compared to Brain of YAC128 Mice as Candidates for Monitoring of Pathology
Elsa C Kuijper, Lodewijk J A Toonen, Maurice Overzier, et al.
American Journal of Physiology. Renal Physiology
|
February 3, 2017
Meta-analysis of polycystic kidney disease expression profiles defines strong involvement of injury repair processes
Tareq B Malas, Chiara Formica, Wouter N Leonhard, et al.
BMJ Open
|
July 12, 2023
Process evaluation in practice based research networks: a study protocol for a mixed-methods implementation study
Linda Sanftenberg, Tobias Dreischulte, Annette Härdtlein, et al.
BMC Bioinformatics
|
October 3, 2009
Structuring and extracting knowledge for the support of hypothesis generation in molecular biology
Marco Roos, M Scott Marshall, Andrew P Gibson, et al.
BMC Primary Care
|
October 11, 2023
"The measures taken by the government overburdened the daily practice" - insights of the PRICOV-19 study on German general practitioners in times of COVID-19
Stefanie Stark, Emmily Schaubroeck, Marie Kluge, et al.
Journal of Biomedical Semantics
|
October 15, 2015
Nanopublications for exposing experimental data in the life-sciences: a Huntington's Disease case study
Eleni Mina, Mark Thompson, Rajaram Kaliyaperumal, et al.
Studies in Health Technology and Informatics
|
August 28, 2018
OSSE Goes FAIR - Implementation of the FAIR Data Principles for an Open-Source Registry for Rare Diseases
Jannik Schaaf, Dennis Kadioglu, Jens Goebel, et al.
Nucleic Acids Research
|
May 27, 2010
myExperiment: a repository and social network for the sharing of bioinformatics workflows
Carole A Goble, Jiten Bhagat, Sergejs Aleksejevs, et al.
Orphanet Journal of Rare Diseases
|
January 15, 2025
Multi-omics analysis in inclusion body myositis identifies mir-16 responsible for HLA overexpression
Daphne Wijnbergen, Mridul Johari, Ozan Ozisik, et al.
Orphanet Journal of Rare Diseases
|
August 2, 2016
Common disease signatures from gene expression analysis in Huntington's disease human blood and brain
Eleni Mina, Willeke van Roon-Mom, Kristina Hettne, et al.
Page
of 11
Search research articles
Search
Showing results (61-70 of 109) with videos related to
Sort By:
Page
of 11
Molecular Neurobiology
|
January 29, 2022
Huntington Disease Gene Expression Signatures in Blood Compared to Brain of YAC128 Mice as Candidates for Monitoring of Pathology
Elsa C Kuijper, Lodewijk J A Toonen, Maurice Overzier, et al.
American Journal of Physiology. Renal Physiology
|
February 3, 2017
Meta-analysis of polycystic kidney disease expression profiles defines strong involvement of injury repair processes
Tareq B Malas, Chiara Formica, Wouter N Leonhard, et al.
BMJ Open
|
July 12, 2023
Process evaluation in practice based research networks: a study protocol for a mixed-methods implementation study
Linda Sanftenberg, Tobias Dreischulte, Annette Härdtlein, et al.
BMC Bioinformatics
|
October 3, 2009
Structuring and extracting knowledge for the support of hypothesis generation in molecular biology
Marco Roos, M Scott Marshall, Andrew P Gibson, et al.
BMC Primary Care
|
October 11, 2023
"The measures taken by the government overburdened the daily practice" - insights of the PRICOV-19 study on German general practitioners in times of COVID-19
Stefanie Stark, Emmily Schaubroeck, Marie Kluge, et al.
Journal of Biomedical Semantics
|
October 15, 2015
Nanopublications for exposing experimental data in the life-sciences: a Huntington's Disease case study
Eleni Mina, Mark Thompson, Rajaram Kaliyaperumal, et al.
Studies in Health Technology and Informatics
|
August 28, 2018
OSSE Goes FAIR - Implementation of the FAIR Data Principles for an Open-Source Registry for Rare Diseases
Jannik Schaaf, Dennis Kadioglu, Jens Goebel, et al.
Nucleic Acids Research
|
May 27, 2010
myExperiment: a repository and social network for the sharing of bioinformatics workflows
Carole A Goble, Jiten Bhagat, Sergejs Aleksejevs, et al.
Orphanet Journal of Rare Diseases
|
January 15, 2025
Multi-omics analysis in inclusion body myositis identifies mir-16 responsible for HLA overexpression
Daphne Wijnbergen, Mridul Johari, Ozan Ozisik, et al.
Orphanet Journal of Rare Diseases
|
August 2, 2016
Common disease signatures from gene expression analysis in Huntington's disease human blood and brain
Eleni Mina, Willeke van Roon-Mom, Kristina Hettne, et al.
Page
of 11