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Plos One
|
September 30, 2016
Lack of Postprandial Peak in Brain-Derived Neurotrophic Factor in Adults with Prader-Willi Syndrome
Marta Bueno, Susanna Esteba-Castillo, Ramon Novell, et al.
Plos One
|
April 12, 2013
Common genetic variants of surfactant protein-D (SP-D) are associated with type 2 diabetes
Neus Pueyo, Francisco J Ortega, Josep M Mercader, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 4, 2017
Dysregulation of Placental miRNA in Maternal Obesity Is Associated With Pre- and Postnatal Growth
Gemma Carreras-Badosa, Alexandra Bonmatí, Francisco-Jose Ortega, et al.
Cancer Treatment and Research Communications
|
September 13, 2018
Genomic profiling in advanced stage non-small-cell lung cancer patients with platinum-based chemotherapy identifies germline variants with prognostic value in SMYD2
Iván Galván-Femenía, Marta Guindo, Xavier Duran, et al.
Cell Genomics
|
August 31, 2024
ONCOLINER: A new solution for monitoring, improving, and harmonizing somatic variant calling across genomic oncology centers
Rodrigo Martín, Nicolás Gaitán, Frédéric Jarlier, et al.
Journal of Medical Genetics
|
September 1, 2018
Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort
Iván Galván-Femenía, Mireia Obón-Santacana, David Piñeyro, et al.
The Journal of Clinical Endocrinology and Metabolism
|
September 26, 2015
Altered Circulating miRNA Expression Profile in Pregestational and Gestational Obesity
Gemma Carreras-Badosa, Alexandra Bonmatí, Francisco-Jose Ortega, et al.
Plos Genetics
|
December 14, 2012
Identification of novel type 2 diabetes candidate genes involved in the crosstalk between the mitochondrial and the insulin signaling systems
Josep M Mercader, Montserrat Puiggros, Ayellet V Segrè, et al.
European Journal of Human Genetics : EJHG
|
May 22, 2024
Germline NPAT inactivating variants as cause of hereditary colorectal cancer
Mariona Terradas, Stephanie A Schubert, Julen Viana-Errasti, et al.
Cell Genomics
|
October 23, 2023
Mutational topography reflects clinical neuroblastoma heterogeneity
Elias Rodriguez-Fos, Mercè Planas-Fèlix, Martin Burkert, et al.
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of 11
Search research articles
Search
Showing results (51-60 of 105) with videos related to
Sort By:
Page
of 11
Plos One
|
September 30, 2016
Lack of Postprandial Peak in Brain-Derived Neurotrophic Factor in Adults with Prader-Willi Syndrome
Marta Bueno, Susanna Esteba-Castillo, Ramon Novell, et al.
Plos One
|
April 12, 2013
Common genetic variants of surfactant protein-D (SP-D) are associated with type 2 diabetes
Neus Pueyo, Francisco J Ortega, Josep M Mercader, et al.
The Journal of Clinical Endocrinology and Metabolism
|
April 4, 2017
Dysregulation of Placental miRNA in Maternal Obesity Is Associated With Pre- and Postnatal Growth
Gemma Carreras-Badosa, Alexandra Bonmatí, Francisco-Jose Ortega, et al.
Cancer Treatment and Research Communications
|
September 13, 2018
Genomic profiling in advanced stage non-small-cell lung cancer patients with platinum-based chemotherapy identifies germline variants with prognostic value in SMYD2
Iván Galván-Femenía, Marta Guindo, Xavier Duran, et al.
Cell Genomics
|
August 31, 2024
ONCOLINER: A new solution for monitoring, improving, and harmonizing somatic variant calling across genomic oncology centers
Rodrigo Martín, Nicolás Gaitán, Frédéric Jarlier, et al.
Journal of Medical Genetics
|
September 1, 2018
Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort
Iván Galván-Femenía, Mireia Obón-Santacana, David Piñeyro, et al.
The Journal of Clinical Endocrinology and Metabolism
|
September 26, 2015
Altered Circulating miRNA Expression Profile in Pregestational and Gestational Obesity
Gemma Carreras-Badosa, Alexandra Bonmatí, Francisco-Jose Ortega, et al.
Plos Genetics
|
December 14, 2012
Identification of novel type 2 diabetes candidate genes involved in the crosstalk between the mitochondrial and the insulin signaling systems
Josep M Mercader, Montserrat Puiggros, Ayellet V Segrè, et al.
European Journal of Human Genetics : EJHG
|
May 22, 2024
Germline NPAT inactivating variants as cause of hereditary colorectal cancer
Mariona Terradas, Stephanie A Schubert, Julen Viana-Errasti, et al.
Cell Genomics
|
October 23, 2023
Mutational topography reflects clinical neuroblastoma heterogeneity
Elias Rodriguez-Fos, Mercè Planas-Fèlix, Martin Burkert, et al.
Page
of 11