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P Monteiro

Showing results (611-620 of 624) with videos related to

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Angewandte Chemie (International Ed. in English)|October 6, 2018
Discovery of an MLLT1/3 YEATS Domain Chemical ProbeMoses Moustakim, Thomas Christott, Octovia P Monteiro, et al.
Molecular Syndromology|December 7, 2016
Identifying CNVs in 15q11q13 and 16p11.2 of Patients with Seizures Increases the Rates of Detecting Pathogenic ChangesGabrielle S Vianna, Mariana L Freitas, Valdirene T de Oliveira, et al.
Angewandte Chemie (International Ed. in English)|December 15, 2016
Discovery of a PCAF Bromodomain Chemical ProbeMoses Moustakim, Peter G K Clark, Laura Trulli, et al.
Cardiovascular Research|April 4, 2025
Loss of conserved long non-coding RNA MIR503HG leads to altered NOTCH pathway signalling and left ventricular non-compaction cardiomyopathyJoão P Monteiro, Diptarka Saha, Ana-Mishel Spiroski, et al.
Cardiovascular Research|September 16, 2021
Single-cell RNA sequencing profiling of mouse endothelial cells in response to pulmonary arterial hypertensionJulie Rodor, Shiau Haln Chen, Jessica P Scanlon, et al.
Magnetic Resonance in Medicine|March 19, 2024
Reproducibility of arterial spin labeling cerebral blood flow image processing: A report of the ISMRM open science initiative for perfusion imaging (OSIPI) and the ASL MRI challengeAndre M Paschoal, Joseph G Woods, Joana Pinto, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 9, 2021
Biallelic UBE4A loss-of-function variants cause intellectual disability and global developmental delayUirá Souto Melo, Devon Bonner, Kevin C Kent Lloyd, et al.
Circulation Research|March 11, 2021
MIR503HG Loss Promotes Endothelial-to-Mesenchymal Transition in Vascular DiseaseJoão P Monteiro, Julie Rodor, Axelle Caudrillier, et al.
HGG Advances|March 30, 2024
Menke-Hennekam syndrome; delineation of domain-specific subtypes with distinct clinical and DNA methylation profilesSadegheh Haghshenas, Hidde J Bout, Josephine M Schijns, et al.
Journal of Investigational Allergology & Clinical Immunology|July 12, 2014
Severe combined immunodeficiency in Brazil: management, prognosis, and BCG-associated complicationsJ T L Mazzucchelli, C Bonfim, G G Castro, et al.
Pageof 63

Showing results (611-620 of 624) with videos related to

Sort By:
Pageof 63
Angewandte Chemie (International Ed. in English)|October 6, 2018
Discovery of an MLLT1/3 YEATS Domain Chemical ProbeMoses Moustakim, Thomas Christott, Octovia P Monteiro, et al.
Molecular Syndromology|December 7, 2016
Identifying CNVs in 15q11q13 and 16p11.2 of Patients with Seizures Increases the Rates of Detecting Pathogenic ChangesGabrielle S Vianna, Mariana L Freitas, Valdirene T de Oliveira, et al.
Angewandte Chemie (International Ed. in English)|December 15, 2016
Discovery of a PCAF Bromodomain Chemical ProbeMoses Moustakim, Peter G K Clark, Laura Trulli, et al.
Cardiovascular Research|April 4, 2025
Loss of conserved long non-coding RNA MIR503HG leads to altered NOTCH pathway signalling and left ventricular non-compaction cardiomyopathyJoão P Monteiro, Diptarka Saha, Ana-Mishel Spiroski, et al.
Cardiovascular Research|September 16, 2021
Single-cell RNA sequencing profiling of mouse endothelial cells in response to pulmonary arterial hypertensionJulie Rodor, Shiau Haln Chen, Jessica P Scanlon, et al.
Magnetic Resonance in Medicine|March 19, 2024
Reproducibility of arterial spin labeling cerebral blood flow image processing: A report of the ISMRM open science initiative for perfusion imaging (OSIPI) and the ASL MRI challengeAndre M Paschoal, Joseph G Woods, Joana Pinto, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 9, 2021
Biallelic UBE4A loss-of-function variants cause intellectual disability and global developmental delayUirá Souto Melo, Devon Bonner, Kevin C Kent Lloyd, et al.
Circulation Research|March 11, 2021
MIR503HG Loss Promotes Endothelial-to-Mesenchymal Transition in Vascular DiseaseJoão P Monteiro, Julie Rodor, Axelle Caudrillier, et al.
HGG Advances|March 30, 2024
Menke-Hennekam syndrome; delineation of domain-specific subtypes with distinct clinical and DNA methylation profilesSadegheh Haghshenas, Hidde J Bout, Josephine M Schijns, et al.
Journal of Investigational Allergology & Clinical Immunology|July 12, 2014
Severe combined immunodeficiency in Brazil: management, prognosis, and BCG-associated complicationsJ T L Mazzucchelli, C Bonfim, G G Castro, et al.
Pageof 63