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Nature Communications
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December 5, 2024
X-linked deletion of Crossfirre, Firre, and Dxz4 in vivo uncovers diverse phenotypes and combinatorial effects on autosomes
Tim P Hasenbein, Sarah Hoelzl, Zachary D Smith, et al.
Molecular Metabolism
|
October 21, 2022
Validation of Mct8/Oatp1c1 dKO mice as a model organism for the Allan-Herndon-Dudley Syndrome
Gandhari Maity-Kumar, Lisa Ständer, Meri DeAngelis, et al.
The Journal of Biological Chemistry
|
April 27, 2013
High mobility group N proteins modulate the fidelity of the cellular transcriptional profile in a tissue- and variant-specific manner
Jamie E Kugler, Marion Horsch, Di Huang, et al.
Journal of Inherited Metabolic Disease
|
May 22, 2019
Low catalytic activity is insufficient to induce disease pathology in triosephosphate isomerase deficiency
Joanna Segal, Michael Mülleder, Antje Krüger, et al.
International Journal of Cancer
|
October 29, 2014
MiR-34a deficiency accelerates medulloblastoma formation in vivo
Theresa Thor, Annette Künkele, Kristian W Pajtler, et al.
Neuroscience Applied
|
July 14, 2025
Co-expression of prepulse inhibition and Schizophrenia genes in the mouse and human brain
Lillian Garrett, Dietrich Trümbach, Donghyung Lee, et al.
Science Advances
|
May 24, 2024
A brain-enriched circular RNA controls excitatory neurotransmission and restricts sensitivity to aversive stimuli
Sebastian A Giusti, Natalia S Pino, Camila Pannunzio, et al.
Genome Research
|
March 20, 2014
Restless legs syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon
Derek Spieler, Maria Kaffe, Franziska Knauf, et al.
Genes & Development
|
March 29, 2020
The rRNA m<sup>6</sup>A methyltransferase METTL5 is involved in pluripotency and developmental programs
Valentina V Ignatova, Paul Stolz, Steffen Kaiser, et al.
Plos One
|
August 12, 2014
Pleiotropic functions for transcription factor zscan10
Petra Kraus, Sivakamasundari V, Hong Bing Yu, et al.
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of 8
Search research articles
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Showing results (51-60 of 75) with videos related to
Sort By:
Page
of 8
Nature Communications
|
December 5, 2024
X-linked deletion of Crossfirre, Firre, and Dxz4 in vivo uncovers diverse phenotypes and combinatorial effects on autosomes
Tim P Hasenbein, Sarah Hoelzl, Zachary D Smith, et al.
Molecular Metabolism
|
October 21, 2022
Validation of Mct8/Oatp1c1 dKO mice as a model organism for the Allan-Herndon-Dudley Syndrome
Gandhari Maity-Kumar, Lisa Ständer, Meri DeAngelis, et al.
The Journal of Biological Chemistry
|
April 27, 2013
High mobility group N proteins modulate the fidelity of the cellular transcriptional profile in a tissue- and variant-specific manner
Jamie E Kugler, Marion Horsch, Di Huang, et al.
Journal of Inherited Metabolic Disease
|
May 22, 2019
Low catalytic activity is insufficient to induce disease pathology in triosephosphate isomerase deficiency
Joanna Segal, Michael Mülleder, Antje Krüger, et al.
International Journal of Cancer
|
October 29, 2014
MiR-34a deficiency accelerates medulloblastoma formation in vivo
Theresa Thor, Annette Künkele, Kristian W Pajtler, et al.
Neuroscience Applied
|
July 14, 2025
Co-expression of prepulse inhibition and Schizophrenia genes in the mouse and human brain
Lillian Garrett, Dietrich Trümbach, Donghyung Lee, et al.
Science Advances
|
May 24, 2024
A brain-enriched circular RNA controls excitatory neurotransmission and restricts sensitivity to aversive stimuli
Sebastian A Giusti, Natalia S Pino, Camila Pannunzio, et al.
Genome Research
|
March 20, 2014
Restless legs syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon
Derek Spieler, Maria Kaffe, Franziska Knauf, et al.
Genes & Development
|
March 29, 2020
The rRNA m<sup>6</sup>A methyltransferase METTL5 is involved in pluripotency and developmental programs
Valentina V Ignatova, Paul Stolz, Steffen Kaiser, et al.
Plos One
|
August 12, 2014
Pleiotropic functions for transcription factor zscan10
Petra Kraus, Sivakamasundari V, Hong Bing Yu, et al.
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of 8