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Showing results (181-190 of 193) with videos related to

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Molecular Ecology|September 23, 2021
The relevance of pedigrees in the conservation genomics eraStephanie J Galla, Liz Brown, Yvette Couch-Lewis Ngāi Tahu Te Hapū O Ngāti Wheke Ngāti Waewae, et al.
Neuron|July 19, 2025
The polypharmacology of psychedelics reveals multiple targets for potential therapeuticsManish K Jain, Ryan H Gumpper, Samuel T Slocum, et al.
Annual Review of Economics|March 14, 2013
The Promises and Pitfalls of Genoeconomics*Daniel J Benjamin, David Cesarini, Christopher F Chabris, et al.
Nature Genetics|August 16, 2011
Exome sequencing identifies ACSF3 as a cause of combined malonic and methylmalonic aciduriaJennifer L Sloan, Jennifer J Johnston, Irini Manoli, et al.
Nature Metabolism|June 13, 2024
Characterization of genetic variants of GIPR reveals a contribution of β-arrestin to metabolic phenotypesHüsün S Kizilkaya, Kimmie V Sørensen, Jakob S Madsen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 30, 2017
FOXG1 syndrome: genotype-phenotype association in 83 patients with FOXG1 variantsDiana Mitter, Milka Pringsheim, Marc Kaulisch, et al.
International Journal of Agricultural Sustainability|January 15, 2019
Looking back and moving forward: 50 years of soil and soil fertility management research in sub-Saharan AfricaB Vanlauwe, A H AbdelGadir, J Adewopo, et al.
HGG Advances|January 20, 2022
Novel pathogenic variants and quantitative phenotypic analyses of Robinow syndrome: WNT signaling perturbation and phenotypic variabilityChaofan Zhang, Angad Jolly, Brian J Shayota, et al.
Journal of Inherited Metabolic Disease|July 19, 2020
Predominant and novel de novo variants in 29 individuals with ALG13 deficiency: Clinical description, biomarker status, biochemical analysis, and treatment suggestionsBobby G Ng, Erik A Eklund, Sergey A Shiryaev, et al.
American Journal of Human Genetics|May 30, 2024
MSL2 variants lead to a neurodevelopmental syndrome with lack of coordination, epilepsy, specific dysmorphisms, and a distinct episignatureRemzi Karayol, Maria Carla Borroto, Sadegheh Haghshenas, et al.
Pageof 20

Showing results (181-190 of 193) with videos related to

Sort By:
Pageof 20
Molecular Ecology|September 23, 2021
The relevance of pedigrees in the conservation genomics eraStephanie J Galla, Liz Brown, Yvette Couch-Lewis Ngāi Tahu Te Hapū O Ngāti Wheke Ngāti Waewae, et al.
Neuron|July 19, 2025
The polypharmacology of psychedelics reveals multiple targets for potential therapeuticsManish K Jain, Ryan H Gumpper, Samuel T Slocum, et al.
Annual Review of Economics|March 14, 2013
The Promises and Pitfalls of Genoeconomics*Daniel J Benjamin, David Cesarini, Christopher F Chabris, et al.
Nature Genetics|August 16, 2011
Exome sequencing identifies ACSF3 as a cause of combined malonic and methylmalonic aciduriaJennifer L Sloan, Jennifer J Johnston, Irini Manoli, et al.
Nature Metabolism|June 13, 2024
Characterization of genetic variants of GIPR reveals a contribution of β-arrestin to metabolic phenotypesHüsün S Kizilkaya, Kimmie V Sørensen, Jakob S Madsen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 30, 2017
FOXG1 syndrome: genotype-phenotype association in 83 patients with FOXG1 variantsDiana Mitter, Milka Pringsheim, Marc Kaulisch, et al.
International Journal of Agricultural Sustainability|January 15, 2019
Looking back and moving forward: 50 years of soil and soil fertility management research in sub-Saharan AfricaB Vanlauwe, A H AbdelGadir, J Adewopo, et al.
HGG Advances|January 20, 2022
Novel pathogenic variants and quantitative phenotypic analyses of Robinow syndrome: WNT signaling perturbation and phenotypic variabilityChaofan Zhang, Angad Jolly, Brian J Shayota, et al.
Journal of Inherited Metabolic Disease|July 19, 2020
Predominant and novel de novo variants in 29 individuals with ALG13 deficiency: Clinical description, biomarker status, biochemical analysis, and treatment suggestionsBobby G Ng, Erik A Eklund, Sergey A Shiryaev, et al.
American Journal of Human Genetics|May 30, 2024
MSL2 variants lead to a neurodevelopmental syndrome with lack of coordination, epilepsy, specific dysmorphisms, and a distinct episignatureRemzi Karayol, Maria Carla Borroto, Sadegheh Haghshenas, et al.
Pageof 20