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Cells
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November 27, 2021
Experimental Epileptogenesis in a Cell Culture Model of Primary Neurons from Rat Brain: A Temporal Multi-Scale Study
Janos Jablonski, Lucas Hoffmann, Ingmar Blümcke, et al.
Clinical Genetics
|
April 11, 2024
Severe manifestation of Rauch-Azzarello syndrome associated with biallelic deletion of CTNND2
Melissa Pauly, Mandy Krumbiegel, Sandra Trumpp, et al.
HGG Advances
|
March 21, 2025
Proteasomal activation ameliorates neuronal phenotypes linked to FBXO11-deficiency
Anne Gregor, Laila Distel, Arif B Ekici, et al.
European Journal of Medical Genetics
|
March 27, 2022
SRD5A3-CDG: Twins with an intragenic tandem duplication
Melissa Rieger, Matthias Türk, Cornelia Kraus, et al.
BMC Medical Genomics
|
November 29, 2017
High resolution chromosomal microarray analysis in paediatric obsessive-compulsive disorder
Edna Grünblatt, Beatrice Oneda, Arif B Ekici, et al.
BMC Cancer
|
May 12, 2019
Dissecting TSC2-mutated renal and hepatic angiomyolipomas in an individual with ARID1B-associated intellectual disability
Bernt Popp, Abbas Agaimy, Cornelia Kraus, et al.
American Journal of Human Genetics
|
September 5, 2015
Chromatin-Remodeling-Factor ARID1B Represses Wnt/β-Catenin Signaling
Georgia Vasileiou, Arif B Ekici, Steffen Uebe, et al.
The Plant Journal : for Cell and Molecular Biology
|
October 16, 2016
Choline transporter-like1 (CHER1) is crucial for plasmodesmata maturation in Arabidopsis thaliana
Max E Kraner, Katrin Link, Michael Melzer, et al.
American Journal of Medical Genetics. Part A
|
December 15, 2018
A biallelic truncating AEBP1 variant causes connective tissue disorder in two siblings
Moritz Hebebrand, Georgia Vasileiou, Mandy Krumbiegel, et al.
Human Mutation
|
September 17, 2014
Altered GPM6A/M6 dosage impairs cognition and causes phenotypes responsive to cholesterol in human and Drosophila
Anne Gregor, Jamie M Kramer, Monique van der Voet, et al.
Page
of 9
Search research articles
Search
Showing results (11-20 of 88) with videos related to
Sort By:
Page
of 9
Cells
|
November 27, 2021
Experimental Epileptogenesis in a Cell Culture Model of Primary Neurons from Rat Brain: A Temporal Multi-Scale Study
Janos Jablonski, Lucas Hoffmann, Ingmar Blümcke, et al.
Clinical Genetics
|
April 11, 2024
Severe manifestation of Rauch-Azzarello syndrome associated with biallelic deletion of CTNND2
Melissa Pauly, Mandy Krumbiegel, Sandra Trumpp, et al.
HGG Advances
|
March 21, 2025
Proteasomal activation ameliorates neuronal phenotypes linked to FBXO11-deficiency
Anne Gregor, Laila Distel, Arif B Ekici, et al.
European Journal of Medical Genetics
|
March 27, 2022
SRD5A3-CDG: Twins with an intragenic tandem duplication
Melissa Rieger, Matthias Türk, Cornelia Kraus, et al.
BMC Medical Genomics
|
November 29, 2017
High resolution chromosomal microarray analysis in paediatric obsessive-compulsive disorder
Edna Grünblatt, Beatrice Oneda, Arif B Ekici, et al.
BMC Cancer
|
May 12, 2019
Dissecting TSC2-mutated renal and hepatic angiomyolipomas in an individual with ARID1B-associated intellectual disability
Bernt Popp, Abbas Agaimy, Cornelia Kraus, et al.
American Journal of Human Genetics
|
September 5, 2015
Chromatin-Remodeling-Factor ARID1B Represses Wnt/β-Catenin Signaling
Georgia Vasileiou, Arif B Ekici, Steffen Uebe, et al.
The Plant Journal : for Cell and Molecular Biology
|
October 16, 2016
Choline transporter-like1 (CHER1) is crucial for plasmodesmata maturation in Arabidopsis thaliana
Max E Kraner, Katrin Link, Michael Melzer, et al.
American Journal of Medical Genetics. Part A
|
December 15, 2018
A biallelic truncating AEBP1 variant causes connective tissue disorder in two siblings
Moritz Hebebrand, Georgia Vasileiou, Mandy Krumbiegel, et al.
Human Mutation
|
September 17, 2014
Altered GPM6A/M6 dosage impairs cognition and causes phenotypes responsive to cholesterol in human and Drosophila
Anne Gregor, Jamie M Kramer, Monique van der Voet, et al.
Page
of 9