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European Journal of Medical Genetics
|
March 30, 2022
Cutis marmorata telangiectatica congenita being caused by postzygotic GNA11 mutations
Claudia Schuart, Andrea Bassi, Friedrich Kapp, et al.
Acta Dermato-Venereologica
|
August 16, 2021
Vitamin D Status in Distinct Types of Ichthyosis: Importance of Genetic Type and Severity of Scaling
Mi-Ran Kim, Vinzenz Oji, Frederic Valentin, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 22, 2016
Novel compound heterozygous synaptojanin-1 mutation causes l-dopa-responsive dystonia-parkinsonism syndrome
Marc-Alexander Rauschendorf, Meike Jost, Friedrich Stock, et al.
The Journal of Investigative Dermatology
|
March 9, 2007
Confirmation of psoriasis susceptibility loci on chromosome 6p21 and 20p13 in French families
Fabienne Lesueur, Caroline Lefèvre, Cristina Has, et al.
Plos Biology
|
November 20, 2004
DNA methylation profiling of the human major histocompatibility complex: a pilot study for the human epigenome project
Vardhman K Rakyan, Thomas Hildmann, Karen L Novik, et al.
American Journal of Human Genetics
|
September 28, 2011
Mutations in CSTA, encoding Cystatin A, underlie exfoliative ichthyosis and reveal a role for this protease inhibitor in cell-cell adhesion
Diana C Blaydon, Daniela Nitoiu, Katja-Martina Eckl, et al.
Journal of the American Academy of Dermatology
|
December 6, 2020
Molecular characterization and natural history of linear porokeratosis: A case series
Mina Saleva-Stateva, Maria Hess, Kristin Technau-Hafsi, et al.
Nature Neuroscience
|
February 24, 2025
Astrocyte heterogeneity reveals region-specific astrogenesis in the white matter
Riccardo Bocchi, Manja Thorwirth, Tatiana Simon-Ebert, et al.
International Journal of Molecular Sciences
|
January 23, 2024
CRISPR-Cas12a for Highly Efficient and Marker-Free Targeted Integration in Human Pluripotent Stem Cells
Ruba Hammad, Jamal Alzubi, Manuel Rhiel, et al.
Frontiers in Immunology
|
January 11, 2021
Modeling MyD88 Deficiency <i>In Vitro</i> Provides New Insights in Its Function
Nils Craig-Mueller, Ruba Hammad, Roland Elling, et al.
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Search research articles
Search
Showing results (141-150 of 174) with videos related to
Sort By:
Page
of 18
European Journal of Medical Genetics
|
March 30, 2022
Cutis marmorata telangiectatica congenita being caused by postzygotic GNA11 mutations
Claudia Schuart, Andrea Bassi, Friedrich Kapp, et al.
Acta Dermato-Venereologica
|
August 16, 2021
Vitamin D Status in Distinct Types of Ichthyosis: Importance of Genetic Type and Severity of Scaling
Mi-Ran Kim, Vinzenz Oji, Frederic Valentin, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
November 22, 2016
Novel compound heterozygous synaptojanin-1 mutation causes l-dopa-responsive dystonia-parkinsonism syndrome
Marc-Alexander Rauschendorf, Meike Jost, Friedrich Stock, et al.
The Journal of Investigative Dermatology
|
March 9, 2007
Confirmation of psoriasis susceptibility loci on chromosome 6p21 and 20p13 in French families
Fabienne Lesueur, Caroline Lefèvre, Cristina Has, et al.
Plos Biology
|
November 20, 2004
DNA methylation profiling of the human major histocompatibility complex: a pilot study for the human epigenome project
Vardhman K Rakyan, Thomas Hildmann, Karen L Novik, et al.
American Journal of Human Genetics
|
September 28, 2011
Mutations in CSTA, encoding Cystatin A, underlie exfoliative ichthyosis and reveal a role for this protease inhibitor in cell-cell adhesion
Diana C Blaydon, Daniela Nitoiu, Katja-Martina Eckl, et al.
Journal of the American Academy of Dermatology
|
December 6, 2020
Molecular characterization and natural history of linear porokeratosis: A case series
Mina Saleva-Stateva, Maria Hess, Kristin Technau-Hafsi, et al.
Nature Neuroscience
|
February 24, 2025
Astrocyte heterogeneity reveals region-specific astrogenesis in the white matter
Riccardo Bocchi, Manja Thorwirth, Tatiana Simon-Ebert, et al.
International Journal of Molecular Sciences
|
January 23, 2024
CRISPR-Cas12a for Highly Efficient and Marker-Free Targeted Integration in Human Pluripotent Stem Cells
Ruba Hammad, Jamal Alzubi, Manuel Rhiel, et al.
Frontiers in Immunology
|
January 11, 2021
Modeling MyD88 Deficiency <i>In Vitro</i> Provides New Insights in Its Function
Nils Craig-Mueller, Ruba Hammad, Roland Elling, et al.
Page
of 18