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Annals of the New York Academy of Sciences
|
August 3, 2021
Harnessing rare variants in neuropsychiatric and neurodevelopment disorders-a Keystone Symposia report
Jennifer Cable, Ryan H Purcell, Elise Robinson, et al.
Biorxiv : the Preprint Server for Biology
|
June 19, 2026
A Retinoic Acid Autoregulatory Loop Governing Prefrontal-Motor Arealization
Lin Yang, Mikihito Shibata, Saejeong Park, et al.
Journal of Clinical Pharmacology
|
September 15, 2022
Prenatal Somatic Cell Gene Therapies: Charting a Path Toward Clinical Applications (Proceedings of the CERSI-FDA Meeting)
Akos Herzeg, Graça Almeida-Porada, R Alta Charo, et al.
Communications Biology
|
November 12, 2023
A Cre-dependent massively parallel reporter assay allows for cell-type specific assessment of the functional effects of non-coding elements in vivo
Tomas Lagunas, Stephen P Plassmeyer, Anthony D Fischer, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
February 8, 2024
Prenatal delivery of a therapeutic antisense oligonucleotide achieves broad biodistribution in the brain and ameliorates Angelman syndrome phenotype in mice
Maria T Clarke, Laura Remesal, Lea Lentz, et al.
Biorxiv : the Preprint Server for Biology
|
May 7, 2024
Massively parallel reporter assays and mouse transgenic assays provide complementary information about neuronal enhancer activity
Michael Kosicki, Dianne Laboy Cintrón, Nicholas F Page, et al.
Genome Medicine
|
September 4, 2025
Publisher Correction: Evaluation of familial phenotype deviation to measure the impact of de novo mutations in autism
Soo-Whee Kim, Hyeji Lee, Da Yea Song, et al.
Nature Communications
|
March 11, 2015
The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment
Justin Cotney, Rebecca A Muhle, Stephan J Sanders, et al.
Nature Genetics
|
February 14, 2017
Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples
Jack A Kosmicki, Kaitlin E Samocha, Daniel P Howrigan, et al.
Biorxiv : the Preprint Server for Biology
|
January 23, 2026
Modulating splicing in 5' untranslated regions to treat rare haploinsufficient disease
Eloise S Beer Wells, Laura De Conti, Hyung Chul Kim, et al.
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of 16
Search research articles
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Showing results (61-70 of 154) with videos related to
Sort By:
Page
of 16
Annals of the New York Academy of Sciences
|
August 3, 2021
Harnessing rare variants in neuropsychiatric and neurodevelopment disorders-a Keystone Symposia report
Jennifer Cable, Ryan H Purcell, Elise Robinson, et al.
Biorxiv : the Preprint Server for Biology
|
June 19, 2026
A Retinoic Acid Autoregulatory Loop Governing Prefrontal-Motor Arealization
Lin Yang, Mikihito Shibata, Saejeong Park, et al.
Journal of Clinical Pharmacology
|
September 15, 2022
Prenatal Somatic Cell Gene Therapies: Charting a Path Toward Clinical Applications (Proceedings of the CERSI-FDA Meeting)
Akos Herzeg, Graça Almeida-Porada, R Alta Charo, et al.
Communications Biology
|
November 12, 2023
A Cre-dependent massively parallel reporter assay allows for cell-type specific assessment of the functional effects of non-coding elements in vivo
Tomas Lagunas, Stephen P Plassmeyer, Anthony D Fischer, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
February 8, 2024
Prenatal delivery of a therapeutic antisense oligonucleotide achieves broad biodistribution in the brain and ameliorates Angelman syndrome phenotype in mice
Maria T Clarke, Laura Remesal, Lea Lentz, et al.
Biorxiv : the Preprint Server for Biology
|
May 7, 2024
Massively parallel reporter assays and mouse transgenic assays provide complementary information about neuronal enhancer activity
Michael Kosicki, Dianne Laboy Cintrón, Nicholas F Page, et al.
Genome Medicine
|
September 4, 2025
Publisher Correction: Evaluation of familial phenotype deviation to measure the impact of de novo mutations in autism
Soo-Whee Kim, Hyeji Lee, Da Yea Song, et al.
Nature Communications
|
March 11, 2015
The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment
Justin Cotney, Rebecca A Muhle, Stephan J Sanders, et al.
Nature Genetics
|
February 14, 2017
Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples
Jack A Kosmicki, Kaitlin E Samocha, Daniel P Howrigan, et al.
Biorxiv : the Preprint Server for Biology
|
January 23, 2026
Modulating splicing in 5' untranslated regions to treat rare haploinsufficient disease
Eloise S Beer Wells, Laura De Conti, Hyung Chul Kim, et al.
Page
of 16