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European Journal of Human Genetics : EJHG
|
May 15, 2025
Recessive variants in WSB2 encoding a substrate receptor of E3 ubiquitin ligase underlie a neurodevelopmental syndrome
Shiyu Luo, Valérie Gailus-Durner, Bobbi McGivern, et al.
Cell Stem Cell
|
May 7, 2016
Age-Related Accumulation of Somatic Mitochondrial DNA Mutations in Adult-Derived Human iPSCs
Eunju Kang, Xinjian Wang, Rebecca Tippner-Hedges, et al.
Plos Genetics
|
July 7, 2021
A homozygous stop-gain variant in ARHGAP42 is associated with childhood interstitial lung disease, systemic hypertension, and immunological findings
Qifei Li, Michal Dibus, Alicia Casey, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)
|
October 24, 2023
Stable Decoding from a Speech BCI Enables Control for an Individual with ALS without Recalibration for 3 Months
Shiyu Luo, Miguel Angrick, Christopher Coogan, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao
|
May 19, 2021
Exome sequencing reveals genetic architecture in patients with isolated or syndromic short stature
Xin Fan, Sen Zhao, Chenxi Yu, et al.
Nature
|
March 1, 2019
Author Correction: Mitochondrial replacement in human oocytes carrying pathogenic mitochondrial DNA mutations
Eunju Kang, Jun Wu, Nuria Marti Gutierrez, et al.
Nature
|
December 6, 2016
Mitochondrial replacement in human oocytes carrying pathogenic mitochondrial DNA mutations
Eunju Kang, Jun Wu, Nuria Marti Gutierrez, et al.
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of 11
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Showing results (101-110 of 107) with videos related to
Sort By:
Page
of 11
You have reached the last page of results.
This site can display upto 107 results.
European Journal of Human Genetics : EJHG
|
May 15, 2025
Recessive variants in WSB2 encoding a substrate receptor of E3 ubiquitin ligase underlie a neurodevelopmental syndrome
Shiyu Luo, Valérie Gailus-Durner, Bobbi McGivern, et al.
Cell Stem Cell
|
May 7, 2016
Age-Related Accumulation of Somatic Mitochondrial DNA Mutations in Adult-Derived Human iPSCs
Eunju Kang, Xinjian Wang, Rebecca Tippner-Hedges, et al.
Plos Genetics
|
July 7, 2021
A homozygous stop-gain variant in ARHGAP42 is associated with childhood interstitial lung disease, systemic hypertension, and immunological findings
Qifei Li, Michal Dibus, Alicia Casey, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)
|
October 24, 2023
Stable Decoding from a Speech BCI Enables Control for an Individual with ALS without Recalibration for 3 Months
Shiyu Luo, Miguel Angrick, Christopher Coogan, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao
|
May 19, 2021
Exome sequencing reveals genetic architecture in patients with isolated or syndromic short stature
Xin Fan, Sen Zhao, Chenxi Yu, et al.
Nature
|
March 1, 2019
Author Correction: Mitochondrial replacement in human oocytes carrying pathogenic mitochondrial DNA mutations
Eunju Kang, Jun Wu, Nuria Marti Gutierrez, et al.
Nature
|
December 6, 2016
Mitochondrial replacement in human oocytes carrying pathogenic mitochondrial DNA mutations
Eunju Kang, Jun Wu, Nuria Marti Gutierrez, et al.
Page
of 11