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American Journal of Human Genetics
|
October 6, 2018
A Recurrent De Novo Heterozygous COG4 Substitution Leads to Saul-Wilson Syndrome, Disrupted Vesicular Trafficking, and Altered Proteoglycan Glycosylation
Carlos R Ferreira, Zhi-Jie Xia, Aurélie Clément, et al.
Nature
|
November 26, 2025
Healthy forests safeguard traditional wild meat food systems in Amazonia
André Pinassi Antunes, Pedro de Araujo Lima Constantino, Julia E Fa, et al.
The Science of the Total Environment
|
August 3, 2023
Global taxonomic, functional, and phylogenetic diversity of bees in apple orchards
N Leclercq, L Marshall, T Weekers, et al.
The Science of the Total Environment
|
December 23, 2021
Toxicity of spike fragments SARS-CoV-2 S protein for zebrafish: A tool to study its hazardous for human health?
Bianca H Ventura Fernandes, Natália Martins Feitosa, Ana Paula Barbosa, et al.
Clinics (Sao Paulo, Brazil)
|
December 1, 2021
Persistent symptoms and decreased health-related quality of life after symptomatic pediatric COVID-19: A prospective study in a Latin American tertiary hospital
Thais T Fink, Heloisa H S Marques, Bruno Gualano, et al.
Molecular Genetics and Metabolism Reports
|
August 14, 2018
Early feeding practices in infants with phenylketonuria across Europe
A Pinto, S Adams, K Ahring, et al.
Molecular Genetics and Metabolism Reports
|
February 2, 2019
Weaning practices in phenylketonuria vary between health professionals in Europe
A Pinto, S Adams, K Ahring, et al.
American Journal of Human Genetics
|
September 12, 2007
Clinical and molecular phenotype of Aicardi-Goutieres syndrome
Gillian Rice, Teresa Patrick, Rekha Parmar, et al.
Fungal Diversity
|
February 28, 2023
Fungal diversity notes 1512-1610: taxonomic and phylogenetic contributions on genera and species of fungal taxa
Ruvishika S Jayawardena, Kevin D Hyde, Song Wang, et al.
American Journal of Medical Genetics. Part A
|
January 22, 2015
Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1
Yanick J Crow, Diana S Chase, Johanna Lowenstein Schmidt, et al.
Page
of 95
Search research articles
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Showing results (931-940 of 941) with videos related to
Sort By:
Page
of 95
American Journal of Human Genetics
|
October 6, 2018
A Recurrent De Novo Heterozygous COG4 Substitution Leads to Saul-Wilson Syndrome, Disrupted Vesicular Trafficking, and Altered Proteoglycan Glycosylation
Carlos R Ferreira, Zhi-Jie Xia, Aurélie Clément, et al.
Nature
|
November 26, 2025
Healthy forests safeguard traditional wild meat food systems in Amazonia
André Pinassi Antunes, Pedro de Araujo Lima Constantino, Julia E Fa, et al.
The Science of the Total Environment
|
August 3, 2023
Global taxonomic, functional, and phylogenetic diversity of bees in apple orchards
N Leclercq, L Marshall, T Weekers, et al.
The Science of the Total Environment
|
December 23, 2021
Toxicity of spike fragments SARS-CoV-2 S protein for zebrafish: A tool to study its hazardous for human health?
Bianca H Ventura Fernandes, Natália Martins Feitosa, Ana Paula Barbosa, et al.
Clinics (Sao Paulo, Brazil)
|
December 1, 2021
Persistent symptoms and decreased health-related quality of life after symptomatic pediatric COVID-19: A prospective study in a Latin American tertiary hospital
Thais T Fink, Heloisa H S Marques, Bruno Gualano, et al.
Molecular Genetics and Metabolism Reports
|
August 14, 2018
Early feeding practices in infants with phenylketonuria across Europe
A Pinto, S Adams, K Ahring, et al.
Molecular Genetics and Metabolism Reports
|
February 2, 2019
Weaning practices in phenylketonuria vary between health professionals in Europe
A Pinto, S Adams, K Ahring, et al.
American Journal of Human Genetics
|
September 12, 2007
Clinical and molecular phenotype of Aicardi-Goutieres syndrome
Gillian Rice, Teresa Patrick, Rekha Parmar, et al.
Fungal Diversity
|
February 28, 2023
Fungal diversity notes 1512-1610: taxonomic and phylogenetic contributions on genera and species of fungal taxa
Ruvishika S Jayawardena, Kevin D Hyde, Song Wang, et al.
American Journal of Medical Genetics. Part A
|
January 22, 2015
Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1
Yanick J Crow, Diana S Chase, Johanna Lowenstein Schmidt, et al.
Page
of 95