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American Journal of Human Genetics
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December 30, 2019
Loss-of-Function Variants in PPP1R12A: From Isolated Sex Reversal to Holoprosencephaly Spectrum and Urogenital Malformations
Joel J Hughes, Ebba Alkhunaizi, Paul Kruszka, et al.
Nature Structural & Molecular Biology
|
September 28, 2023
Live-cell three-dimensional single-molecule tracking reveals modulation of enhancer dynamics by NuRD
S Basu, O Shukron, D Hall, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 18, 2020
Defining the clinical phenotype of Saul-Wilson syndrome
Carlos R Ferreira, Wadih M Zein, Laryssa A Huryn, et al.
Nature Structural & Molecular Biology
|
December 15, 2023
Publisher Correction: Live-cell three-dimensional single-molecule tracking reveals modulation of enhancer dynamics by NuRD
S Basu, O Shukron, D Hall, et al.
Biorxiv : the Preprint Server for Biology
|
July 10, 2023
Tessellation of artificial touch via microstimulation of human somatosensory cortex
Charles M Greenspon, Natalya D Shelchkova, Giacomo Valle, et al.
Stem Cell Reports
|
November 5, 2021
A library of induced pluripotent stem cells from clinically well-characterized, diverse healthy human individuals
Christoph Schaniel, Priyanka Dhanan, Bin Hu, et al.
Nature Biomedical Engineering
|
December 6, 2024
Evoking stable and precise tactile sensations via multi-electrode intracortical microstimulation of the somatosensory cortex
Charles M Greenspon, Giacomo Valle, Natalya D Shelchkova, et al.
Brain : a Journal of Neurology
|
July 24, 2019
Cohesin complex-associated holoprosencephaly
Paul Kruszka, Seth I Berger, Valentina Casa, et al.
Biorxiv : the Preprint Server for Biology
|
June 4, 2026
Building an Interoperable Rare Disease Multi-omic Resource: The GREGoR Data Model and Dataset
Benjamin D Heavner, Marsha M Wheeler, Jesse D Bengtsson, et al.
American Journal of Human Genetics
|
January 20, 2022
Rare germline heterozygous missense variants in BRCA1-associated protein 1, BAP1, cause a syndromic neurodevelopmental disorder
Sébastien Küry, Frédéric Ebstein, Alice Mollé, et al.
Page
of 41
Search research articles
Search
Showing results (391-400 of 406) with videos related to
Sort By:
Page
of 41
American Journal of Human Genetics
|
December 30, 2019
Loss-of-Function Variants in PPP1R12A: From Isolated Sex Reversal to Holoprosencephaly Spectrum and Urogenital Malformations
Joel J Hughes, Ebba Alkhunaizi, Paul Kruszka, et al.
Nature Structural & Molecular Biology
|
September 28, 2023
Live-cell three-dimensional single-molecule tracking reveals modulation of enhancer dynamics by NuRD
S Basu, O Shukron, D Hall, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 18, 2020
Defining the clinical phenotype of Saul-Wilson syndrome
Carlos R Ferreira, Wadih M Zein, Laryssa A Huryn, et al.
Nature Structural & Molecular Biology
|
December 15, 2023
Publisher Correction: Live-cell three-dimensional single-molecule tracking reveals modulation of enhancer dynamics by NuRD
S Basu, O Shukron, D Hall, et al.
Biorxiv : the Preprint Server for Biology
|
July 10, 2023
Tessellation of artificial touch via microstimulation of human somatosensory cortex
Charles M Greenspon, Natalya D Shelchkova, Giacomo Valle, et al.
Stem Cell Reports
|
November 5, 2021
A library of induced pluripotent stem cells from clinically well-characterized, diverse healthy human individuals
Christoph Schaniel, Priyanka Dhanan, Bin Hu, et al.
Nature Biomedical Engineering
|
December 6, 2024
Evoking stable and precise tactile sensations via multi-electrode intracortical microstimulation of the somatosensory cortex
Charles M Greenspon, Giacomo Valle, Natalya D Shelchkova, et al.
Brain : a Journal of Neurology
|
July 24, 2019
Cohesin complex-associated holoprosencephaly
Paul Kruszka, Seth I Berger, Valentina Casa, et al.
Biorxiv : the Preprint Server for Biology
|
June 4, 2026
Building an Interoperable Rare Disease Multi-omic Resource: The GREGoR Data Model and Dataset
Benjamin D Heavner, Marsha M Wheeler, Jesse D Bengtsson, et al.
American Journal of Human Genetics
|
January 20, 2022
Rare germline heterozygous missense variants in BRCA1-associated protein 1, BAP1, cause a syndromic neurodevelopmental disorder
Sébastien Küry, Frédéric Ebstein, Alice Mollé, et al.
Page
of 41