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Proceedings of the National Academy of Sciences of the United States of America
|
September 7, 2019
PHF2 histone demethylase prevents DNA damage and genome instability by controlling cell cycle progression of neural progenitors
Stella Pappa, Natalia Padilla, Simona Iacobucci, et al.
EMBO Reports
|
June 18, 2024
PHF2-mediated H3K9me balance orchestrates heterochromatin stability and neural progenitor proliferation
Samuel Aguirre, Stella Pappa, Núria Serna-Pujol, et al.
Molecular Genetics & Genomic Medicine
|
June 2, 2015
Functional consequences of transferrin receptor-2 mutations causing hereditary hemochromatosis type 3
Ricky Joshi, Maya Shvartsman, Erica Morán, et al.
Journal of Clinical Immunology
|
March 31, 2016
Novel Mutations Causing C5 Deficiency in Three North-African Families
Roger Colobran, Clara Franco-Jarava, Andrea Martín-Nalda, et al.
Journal of Biomolecular Structure & Dynamics
|
December 21, 2005
Data mining of molecular dynamics trajectories of nucleic acids
Agnes Noy, Tim Meyer, Manuel Rueda, et al.
International Journal of Hematology
|
December 23, 2019
Molecular analysis of the novel L243R mutation in STXBP2 reveals impairment of degranulation activity
Laura Viñas-Giménez, Laura Donadeu, Laia Alsina, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease
|
September 11, 2016
Identification and characterization of the novel point mutation m.3634A>G in the mitochondrial MT-ND1 gene associated with LHON syndrome
Lidia Carreño-Gago, Josep Gamez, Yolanda Cámara, et al.
Nucleic Acids Research
|
February 14, 2018
Lineage specific transcription factors and epigenetic regulators mediate TGFβ-dependent enhancer activation
Raquel Fueyo, Simona Iacobucci, Stella Pappa, et al.
Journal of Clinical Immunology
|
September 25, 2017
Early Versus Late Diagnosis of Complement Factor I Deficiency: Clinical Consequences Illustrated in Two Families with Novel Homozygous CFI Mutations
Clara Franco-Jarava, Elena Álvarez de la Campa, Xavier Solanich, et al.
Nucleic Acids Research
|
January 20, 2017
The histone demethylase PHF8 is a molecular safeguard of the IFNγ response
Elena Asensio-Juan, Raquel Fueyo, Stella Pappa, et al.
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Search research articles
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Showing results (51-60 of 77) with videos related to
Sort By:
Page
of 8
Proceedings of the National Academy of Sciences of the United States of America
|
September 7, 2019
PHF2 histone demethylase prevents DNA damage and genome instability by controlling cell cycle progression of neural progenitors
Stella Pappa, Natalia Padilla, Simona Iacobucci, et al.
EMBO Reports
|
June 18, 2024
PHF2-mediated H3K9me balance orchestrates heterochromatin stability and neural progenitor proliferation
Samuel Aguirre, Stella Pappa, Núria Serna-Pujol, et al.
Molecular Genetics & Genomic Medicine
|
June 2, 2015
Functional consequences of transferrin receptor-2 mutations causing hereditary hemochromatosis type 3
Ricky Joshi, Maya Shvartsman, Erica Morán, et al.
Journal of Clinical Immunology
|
March 31, 2016
Novel Mutations Causing C5 Deficiency in Three North-African Families
Roger Colobran, Clara Franco-Jarava, Andrea Martín-Nalda, et al.
Journal of Biomolecular Structure & Dynamics
|
December 21, 2005
Data mining of molecular dynamics trajectories of nucleic acids
Agnes Noy, Tim Meyer, Manuel Rueda, et al.
International Journal of Hematology
|
December 23, 2019
Molecular analysis of the novel L243R mutation in STXBP2 reveals impairment of degranulation activity
Laura Viñas-Giménez, Laura Donadeu, Laia Alsina, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease
|
September 11, 2016
Identification and characterization of the novel point mutation m.3634A>G in the mitochondrial MT-ND1 gene associated with LHON syndrome
Lidia Carreño-Gago, Josep Gamez, Yolanda Cámara, et al.
Nucleic Acids Research
|
February 14, 2018
Lineage specific transcription factors and epigenetic regulators mediate TGFβ-dependent enhancer activation
Raquel Fueyo, Simona Iacobucci, Stella Pappa, et al.
Journal of Clinical Immunology
|
September 25, 2017
Early Versus Late Diagnosis of Complement Factor I Deficiency: Clinical Consequences Illustrated in Two Families with Novel Homozygous CFI Mutations
Clara Franco-Jarava, Elena Álvarez de la Campa, Xavier Solanich, et al.
Nucleic Acids Research
|
January 20, 2017
The histone demethylase PHF8 is a molecular safeguard of the IFNγ response
Elena Asensio-Juan, Raquel Fueyo, Stella Pappa, et al.
Page
of 8