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Human genomics

Showing results (941-950 of 1,110) with videos related to

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Human Genomics|December 16, 2014
Molecular signatures that correlate with induction of lens regeneration in newts: lessons from proteomic analysisKonstantinos Sousounis, Rital Bhavsar, Mario Looso, et al.
Human Genomics|September 10, 2020
Delineation of molecular findings by whole-exome sequencing for suspected cases of paediatric-onset mitochondrial diseases in the Southern Chinese populationMandy H Y Tsang, Anna K Y Kwong, Kate L S Chan, et al.
Human Genomics|September 12, 2020
Analysis of ACE2 genetic variants in 131 Italian SARS-CoV-2-positive patientsAntonio Novelli, Michela Biancolella, Paola Borgiani, et al.
Human Genomics|February 20, 2020
TRPM3_miR-204: a complex locus for eye development and diseaseAlan Shiels
Human Genomics|March 8, 2020
Hyperinsulinism associated with GLUD1 mutation: allosteric regulation and functional characterization of p.G446V glutamate dehydrogenaseKarolina Luczkowska, Caroline Stekelenburg, Frédérique Sloan-Béna, et al.
Human Genomics|February 1, 2018
Meeting report of the 2017 KidGen Renal Genetics SymposiumKushani Jayasinghe, Cathy Quinlan, Zornitza Stark, et al.
Human Genomics|February 4, 2018
The genetic structure of the Belgian populationJimmy Van den Eynden, Tine Descamps, Els Delporte, et al.
Human Genomics|May 18, 2022
Evaluating standards for 'serious' disease for preimplantation genetic testing: a multi-case study on regulatory frameworks in Japan, the UK, and Western AustraliaKate Nakasato, Beverley Anne Yamamoto, Kazuto Kato
Human Genomics|May 18, 2022
Genomic supremacy: the harm of conflating genetic ancestry and raceJessica P Cerdeña, Vanessa Grubbs, Amy L Non
Human Genomics|July 20, 2021
ACER3-related leukoencephalopathy: expanding the clinical and imaging findings spectrum due to novel variantsAli Zare Dehnavi, Erfan Heidari, Maryam Rasulinezhad, et al.
Pageof 111

Showing results (941-950 of 1,110) with videos related to

Sort By:
Pageof 111
Human Genomics|December 16, 2014
Molecular signatures that correlate with induction of lens regeneration in newts: lessons from proteomic analysisKonstantinos Sousounis, Rital Bhavsar, Mario Looso, et al.
Human Genomics|September 10, 2020
Delineation of molecular findings by whole-exome sequencing for suspected cases of paediatric-onset mitochondrial diseases in the Southern Chinese populationMandy H Y Tsang, Anna K Y Kwong, Kate L S Chan, et al.
Human Genomics|September 12, 2020
Analysis of ACE2 genetic variants in 131 Italian SARS-CoV-2-positive patientsAntonio Novelli, Michela Biancolella, Paola Borgiani, et al.
Human Genomics|February 20, 2020
TRPM3_miR-204: a complex locus for eye development and diseaseAlan Shiels
Human Genomics|March 8, 2020
Hyperinsulinism associated with GLUD1 mutation: allosteric regulation and functional characterization of p.G446V glutamate dehydrogenaseKarolina Luczkowska, Caroline Stekelenburg, Frédérique Sloan-Béna, et al.
Human Genomics|February 1, 2018
Meeting report of the 2017 KidGen Renal Genetics SymposiumKushani Jayasinghe, Cathy Quinlan, Zornitza Stark, et al.
Human Genomics|February 4, 2018
The genetic structure of the Belgian populationJimmy Van den Eynden, Tine Descamps, Els Delporte, et al.
Human Genomics|May 18, 2022
Evaluating standards for 'serious' disease for preimplantation genetic testing: a multi-case study on regulatory frameworks in Japan, the UK, and Western AustraliaKate Nakasato, Beverley Anne Yamamoto, Kazuto Kato
Human Genomics|May 18, 2022
Genomic supremacy: the harm of conflating genetic ancestry and raceJessica P Cerdeña, Vanessa Grubbs, Amy L Non
Human Genomics|July 20, 2021
ACER3-related leukoencephalopathy: expanding the clinical and imaging findings spectrum due to novel variantsAli Zare Dehnavi, Erfan Heidari, Maryam Rasulinezhad, et al.
Pageof 111