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Frontiers in Medicine
|
January 10, 2022
Longitudinal Analysis of Antibody Responses to the mRNA BNT162b2 Vaccine in Patients Undergoing Maintenance Hemodialysis: A 6-Month Follow-Up
André Weigert, Marie-Louise Bergman, Lígia A Gonçalves, et al.
Ecology and Evolution
|
February 6, 2025
A Seascape Genomics Perspective on Restrictive Genetic Connectivity Overcoming Signals of Local Adaptations in the Green Abalone (<i>Haliotis fulgens</i>) of the California Current System
Jorge Alberto Mares-Mayagoitia, Paulina Mejía-Ruíz, Fabiola Lafarga-De la Cruz, et al.
Current Pharmaceutical Biotechnology
|
December 20, 2021
Synthesis, Characterization, Antiproliferative Activity of Galloyl Derivatives and Investigation of Cytotoxic Properties in HepG2/C3A Cells
Rafael Claudino Dos Santos, Raquel Oliveira Nascimento de Freitas, Mary Ann Foglio, et al.
Current Pharmaceutical Biotechnology
|
September 6, 2024
<i>Guettarda viburnoides</i> Cham. & Schltdl.: Neuroprotective Activities in Mice, Molecular Docking and Microchemical and Morphoanatomical Characteristics of Leaves and Stems
Pedro Cruz de Oliveira Junior, Eliana Janet Sanjinez-Argandona, Janaine Alberto Marangoni Faoro, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 6, 2012
Specific inactivation of two immunomodulatory SIGLEC genes during human evolution
Xiaoxia Wang, Nivedita Mitra, Ismael Secundino, et al.
Plos One
|
June 12, 2013
Sequencing of candidate chromosome instability genes in endometrial cancers reveals somatic mutations in ESCO1, CHTF18, and MRE11A
Jessica C Price, Lana M Pollock, Meghan L Rudd, et al.
BMC Genomics
|
June 26, 2010
Light whole genome sequence for SNP discovery across domestic cat breeds
James C Mullikin, Nancy F Hansen, Lei Shen, et al.
Neuromuscular Disorders : NMD
|
March 5, 2013
Novel SNP array analysis and exome sequencing detect a homozygous exon 7 deletion of MEGF10 causing early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD)
Tyler Mark Pierson, Thomas Markello, John Accardi, et al.
American Journal of Human Genetics
|
October 6, 2010
Compound heterozygosity for loss-of-function lysyl-tRNA synthetase mutations in a patient with peripheral neuropathy
Heather M McLaughlin, Reiko Sakaguchi, Cuiping Liu, et al.
Nature Genetics
|
July 19, 2011
NBEAL2 is mutated in gray platelet syndrome and is required for biogenesis of platelet α-granules
Meral Gunay-Aygun, Tzipora C Falik-Zaccai, Thierry Vilboux, et al.
Page
of 13
Search research articles
Search
Showing results (111-120 of 126) with videos related to
Sort By:
Page
of 13
Frontiers in Medicine
|
January 10, 2022
Longitudinal Analysis of Antibody Responses to the mRNA BNT162b2 Vaccine in Patients Undergoing Maintenance Hemodialysis: A 6-Month Follow-Up
André Weigert, Marie-Louise Bergman, Lígia A Gonçalves, et al.
Ecology and Evolution
|
February 6, 2025
A Seascape Genomics Perspective on Restrictive Genetic Connectivity Overcoming Signals of Local Adaptations in the Green Abalone (<i>Haliotis fulgens</i>) of the California Current System
Jorge Alberto Mares-Mayagoitia, Paulina Mejía-Ruíz, Fabiola Lafarga-De la Cruz, et al.
Current Pharmaceutical Biotechnology
|
December 20, 2021
Synthesis, Characterization, Antiproliferative Activity of Galloyl Derivatives and Investigation of Cytotoxic Properties in HepG2/C3A Cells
Rafael Claudino Dos Santos, Raquel Oliveira Nascimento de Freitas, Mary Ann Foglio, et al.
Current Pharmaceutical Biotechnology
|
September 6, 2024
<i>Guettarda viburnoides</i> Cham. & Schltdl.: Neuroprotective Activities in Mice, Molecular Docking and Microchemical and Morphoanatomical Characteristics of Leaves and Stems
Pedro Cruz de Oliveira Junior, Eliana Janet Sanjinez-Argandona, Janaine Alberto Marangoni Faoro, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 6, 2012
Specific inactivation of two immunomodulatory SIGLEC genes during human evolution
Xiaoxia Wang, Nivedita Mitra, Ismael Secundino, et al.
Plos One
|
June 12, 2013
Sequencing of candidate chromosome instability genes in endometrial cancers reveals somatic mutations in ESCO1, CHTF18, and MRE11A
Jessica C Price, Lana M Pollock, Meghan L Rudd, et al.
BMC Genomics
|
June 26, 2010
Light whole genome sequence for SNP discovery across domestic cat breeds
James C Mullikin, Nancy F Hansen, Lei Shen, et al.
Neuromuscular Disorders : NMD
|
March 5, 2013
Novel SNP array analysis and exome sequencing detect a homozygous exon 7 deletion of MEGF10 causing early onset myopathy, areflexia, respiratory distress and dysphagia (EMARDD)
Tyler Mark Pierson, Thomas Markello, John Accardi, et al.
American Journal of Human Genetics
|
October 6, 2010
Compound heterozygosity for loss-of-function lysyl-tRNA synthetase mutations in a patient with peripheral neuropathy
Heather M McLaughlin, Reiko Sakaguchi, Cuiping Liu, et al.
Nature Genetics
|
July 19, 2011
NBEAL2 is mutated in gray platelet syndrome and is required for biogenesis of platelet α-granules
Meral Gunay-Aygun, Tzipora C Falik-Zaccai, Thierry Vilboux, et al.
Page
of 13