Search research articles
Contact Us
Filters
Showing results (11-20 of 57) with videos related to
Page
of 6
Sort By:
Journal of Proteomics
|
September 7, 2012
Serum levels of the hepcidin-20 isoform in a large general population: the Val Borbera study
Natascia Campostrini, Michela Traglia, Nicola Martinelli, et al.
European Journal of Human Genetics : EJHG
|
May 5, 2018
Whole-genome sequencing reveals new insights into age-related hearing loss: cumulative effects, pleiotropy and the role of selection
Dragana Vuckovic, Massimo Mezzavilla, Massimiliano Cocca, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 2, 2016
MCM8 and MCM9 Nucleotide Variants in Women With Primary Ovarian Insufficiency
Swapna Desai, Michelle Wood-Trageser, Jelena Matic, et al.
Genes
|
November 27, 2021
Poking COVID-19: Insights on Genomic Constraints among Immune-Related Genes between Qatari and Italian Populations
Hamdi Mbarek, Massimiliano Cocca, Yasser Al-Sarraj, et al.
Journal of Experimental & Clinical Cancer Research : CR
|
May 16, 2025
HBV-driven host chromatin accessibility changes affect liver metabolic pathways, iron homeostasis and promote a preneoplastic phenotype
Vincenzo Alfano, Giuseppe Rubens Pascucci, Giacomo Corleone, et al.
Liver International : Official Journal of the International Association for the Study of the Liver
|
January 22, 2025
Simultaneous Activation of Beta-Oxidation and De Novo Lipogenesis in MASLD-HCC: A New Paradigm
Fatima Dahboul, Jihan Sun, Benjamin Buchard, et al.
European Journal of Human Genetics : EJHG
|
December 1, 2019
A bird's-eye view of Italian genomic variation through whole-genome sequencing
Massimiliano Cocca, Caterina Barbieri, Maria Pina Concas, et al.
Human Molecular Genetics
|
June 1, 2021
Variants in USP48 encoding ubiquitin hydrolase are associated with autosomal dominant non-syndromic hereditary hearing loss
Sissy Bassani, Edward van Beelen, Mireille Rossel, et al.
Plos Genetics
|
April 19, 2014
A general approach for haplotype phasing across the full spectrum of relatedness
Jared O'Connell, Deepti Gurdasani, Olivier Delaneau, et al.
Journal of the American Society of Nephrology : JASN
|
March 1, 2014
Common variants in UMOD associate with urinary uromodulin levels: a meta-analysis
Matthias Olden, Tanguy Corre, Caroline Hayward, et al.
Page
of 6
Search research articles
Search
Showing results (11-20 of 57) with videos related to
Sort By:
Page
of 6
Journal of Proteomics
|
September 7, 2012
Serum levels of the hepcidin-20 isoform in a large general population: the Val Borbera study
Natascia Campostrini, Michela Traglia, Nicola Martinelli, et al.
European Journal of Human Genetics : EJHG
|
May 5, 2018
Whole-genome sequencing reveals new insights into age-related hearing loss: cumulative effects, pleiotropy and the role of selection
Dragana Vuckovic, Massimo Mezzavilla, Massimiliano Cocca, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 2, 2016
MCM8 and MCM9 Nucleotide Variants in Women With Primary Ovarian Insufficiency
Swapna Desai, Michelle Wood-Trageser, Jelena Matic, et al.
Genes
|
November 27, 2021
Poking COVID-19: Insights on Genomic Constraints among Immune-Related Genes between Qatari and Italian Populations
Hamdi Mbarek, Massimiliano Cocca, Yasser Al-Sarraj, et al.
Journal of Experimental & Clinical Cancer Research : CR
|
May 16, 2025
HBV-driven host chromatin accessibility changes affect liver metabolic pathways, iron homeostasis and promote a preneoplastic phenotype
Vincenzo Alfano, Giuseppe Rubens Pascucci, Giacomo Corleone, et al.
Liver International : Official Journal of the International Association for the Study of the Liver
|
January 22, 2025
Simultaneous Activation of Beta-Oxidation and De Novo Lipogenesis in MASLD-HCC: A New Paradigm
Fatima Dahboul, Jihan Sun, Benjamin Buchard, et al.
European Journal of Human Genetics : EJHG
|
December 1, 2019
A bird's-eye view of Italian genomic variation through whole-genome sequencing
Massimiliano Cocca, Caterina Barbieri, Maria Pina Concas, et al.
Human Molecular Genetics
|
June 1, 2021
Variants in USP48 encoding ubiquitin hydrolase are associated with autosomal dominant non-syndromic hereditary hearing loss
Sissy Bassani, Edward van Beelen, Mireille Rossel, et al.
Plos Genetics
|
April 19, 2014
A general approach for haplotype phasing across the full spectrum of relatedness
Jared O'Connell, Deepti Gurdasani, Olivier Delaneau, et al.
Journal of the American Society of Nephrology : JASN
|
March 1, 2014
Common variants in UMOD associate with urinary uromodulin levels: a meta-analysis
Matthias Olden, Tanguy Corre, Caroline Hayward, et al.
Page
of 6