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Methods (San Diego, Calif.)
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June 30, 2020
Universal Southern blot protocol with cold or radioactive probes for the validation of alleles obtained by homologous recombination
Gemma F Codner, Valerie Erbs, Jorik Loeffler, et al.
Gene
|
April 2, 2013
ErbB3 silencing reduces osteosarcoma cell proliferation and tumor growth in vivo
Nicolas Jullien, François-Xavier Dieudonné, Nadia Habel, et al.
Nature Communications
|
May 14, 2025
Concurrent superimposed ice formation and meltwater runoff on Greenland's ice slabs
Andrew Tedstone, Horst Machguth, Nicole Clerx, et al.
Stem Cell Research
|
October 23, 2015
Autologous bone marrow stromal cells are promising candidates for cell therapy approaches to treat bone degeneration in sickle cell disease
Angélique Lebouvier, Alexandre Poignard, Laura Coquelin-Salsac, et al.
Scientific Data
|
March 13, 2026
CODE beyond FAIR: a roadmap for reusable research software
Roberto Di Cosmo, Sabrina Granger, Konrad Hinsen, et al.
European Journal of Human Genetics : EJHG
|
September 29, 2018
Heterozygous LHX3 mutations may lead to a mild phenotype of combined pituitary hormone deficiency
Nicolas Jullien, Pauline Romanet, Mélanie Philippon, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
June 12, 2021
MT5-MMP controls APP and β-CTF/C99 metabolism through proteolytic-dependent and -independent mechanisms relevant for Alzheimer's disease
Laura García-González, Jean-Michel Paumier, Laurence Louis, et al.
Hormone Research in Paediatrics
|
September 13, 2017
Pilot Neonatal Screening Program for Central Congenital Hypothyroidism: Evidence of Significant Detection
Débora Braslavsky, Maria Virginia Méndez, Laura Prieto, et al.
Journal of Neuroendocrinology
|
June 16, 2023
Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reports
Thi Thom Mac, Frederic Castinetti, Céline Bar, et al.
Plos One
|
May 9, 2015
Identifying the Deleterious Effect of Rare LHX4 Allelic Variants, a Challenging Issue
Claire Rochette, Nicolas Jullien, Alexandru Saveanu, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 36) with videos related to
Sort By:
Page
of 4
Methods (San Diego, Calif.)
|
June 30, 2020
Universal Southern blot protocol with cold or radioactive probes for the validation of alleles obtained by homologous recombination
Gemma F Codner, Valerie Erbs, Jorik Loeffler, et al.
Gene
|
April 2, 2013
ErbB3 silencing reduces osteosarcoma cell proliferation and tumor growth in vivo
Nicolas Jullien, François-Xavier Dieudonné, Nadia Habel, et al.
Nature Communications
|
May 14, 2025
Concurrent superimposed ice formation and meltwater runoff on Greenland's ice slabs
Andrew Tedstone, Horst Machguth, Nicole Clerx, et al.
Stem Cell Research
|
October 23, 2015
Autologous bone marrow stromal cells are promising candidates for cell therapy approaches to treat bone degeneration in sickle cell disease
Angélique Lebouvier, Alexandre Poignard, Laura Coquelin-Salsac, et al.
Scientific Data
|
March 13, 2026
CODE beyond FAIR: a roadmap for reusable research software
Roberto Di Cosmo, Sabrina Granger, Konrad Hinsen, et al.
European Journal of Human Genetics : EJHG
|
September 29, 2018
Heterozygous LHX3 mutations may lead to a mild phenotype of combined pituitary hormone deficiency
Nicolas Jullien, Pauline Romanet, Mélanie Philippon, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
June 12, 2021
MT5-MMP controls APP and β-CTF/C99 metabolism through proteolytic-dependent and -independent mechanisms relevant for Alzheimer's disease
Laura García-González, Jean-Michel Paumier, Laurence Louis, et al.
Hormone Research in Paediatrics
|
September 13, 2017
Pilot Neonatal Screening Program for Central Congenital Hypothyroidism: Evidence of Significant Detection
Débora Braslavsky, Maria Virginia Méndez, Laura Prieto, et al.
Journal of Neuroendocrinology
|
June 16, 2023
Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reports
Thi Thom Mac, Frederic Castinetti, Céline Bar, et al.
Plos One
|
May 9, 2015
Identifying the Deleterious Effect of Rare LHX4 Allelic Variants, a Challenging Issue
Claire Rochette, Nicolas Jullien, Alexandru Saveanu, et al.
Page
of 4