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Scientific Reports
|
July 18, 2018
Structural cortical network reorganization associated with early conversion to multiple sclerosis
C Tur, A Eshaghi, D R Altmann, et al.
American Journal of Medical Genetics. Part A
|
November 19, 2013
Phenotypic and molecular characterization of 19q12q13.1 deletions: a report of five patients
Shimul Chowdhury, Anne M Bandholz, Sandhya Parkash, et al.
Cell Genomics
|
June 24, 2026
The Single-Cell Pediatric Cancer Atlas: Data portal and open-source tools for single-cell transcriptomics of pediatric tumors
Allegra G Hawkins, Joshua A Shapiro, Stephanie J Spielman, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
April 1, 2021
Plasma tumor gene conversions after one cycle abiraterone acetate for metastatic castration-resistant prostate cancer: a biomarker analysis of a multicenter international trial
A Jayaram, A Wingate, D Wetterskog, et al.
Journal of Molecular and Cellular Cardiology
|
January 25, 2012
Transgenic swine: expression of human CD39 protects against myocardial injury
Debra G Wheeler, Matthew E Joseph, Shouvik D Mahamud, et al.
Cold Spring Harbor Molecular Case Studies
|
May 6, 2016
De novo POGZ mutations are associated with neurodevelopmental disorders and microcephaly
Yizhou Ye, Megan T Cho, Kyle Retterer, et al.
Journal of Molecular and Cellular Cardiology
|
September 24, 2011
Transgenic over expression of ectonucleotide triphosphate diphosphohydrolase-1 protects against murine myocardial ischemic injury
Ming Cai, Zachary M Huttinger, Heng He, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
April 19, 2018
Mutations That Alter the Carboxy-Terminal-Propeptide Cleavage Site of the Chains of Type I Procollagen Are Associated With a Unique Osteogenesis Imperfecta Phenotype
Tim Cundy, Michael Dray, John Delahunt, et al.
Neural Plasticity
|
September 25, 2018
Cortical AAV-CNTF Gene Therapy Combined with Intraspinal Mesenchymal Precursor Cell Transplantation Promotes Functional and Morphological Outcomes after Spinal Cord Injury in Adult Rats
Stuart I Hodgetts, Jun Han Yoon, Alysia Fogliani, et al.
Annals of Clinical and Translational Neurology
|
May 15, 2024
Emerging variants, unique phenotypes, and transcriptomic signatures: an integrated study of COASY-associated diseases
Chiara Cavestro, Francesca Morra, Andrea Legati, et al.
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of 39
Search research articles
Search
Showing results (341-350 of 383) with videos related to
Sort By:
Page
of 39
Scientific Reports
|
July 18, 2018
Structural cortical network reorganization associated with early conversion to multiple sclerosis
C Tur, A Eshaghi, D R Altmann, et al.
American Journal of Medical Genetics. Part A
|
November 19, 2013
Phenotypic and molecular characterization of 19q12q13.1 deletions: a report of five patients
Shimul Chowdhury, Anne M Bandholz, Sandhya Parkash, et al.
Cell Genomics
|
June 24, 2026
The Single-Cell Pediatric Cancer Atlas: Data portal and open-source tools for single-cell transcriptomics of pediatric tumors
Allegra G Hawkins, Joshua A Shapiro, Stephanie J Spielman, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology
|
April 1, 2021
Plasma tumor gene conversions after one cycle abiraterone acetate for metastatic castration-resistant prostate cancer: a biomarker analysis of a multicenter international trial
A Jayaram, A Wingate, D Wetterskog, et al.
Journal of Molecular and Cellular Cardiology
|
January 25, 2012
Transgenic swine: expression of human CD39 protects against myocardial injury
Debra G Wheeler, Matthew E Joseph, Shouvik D Mahamud, et al.
Cold Spring Harbor Molecular Case Studies
|
May 6, 2016
De novo POGZ mutations are associated with neurodevelopmental disorders and microcephaly
Yizhou Ye, Megan T Cho, Kyle Retterer, et al.
Journal of Molecular and Cellular Cardiology
|
September 24, 2011
Transgenic over expression of ectonucleotide triphosphate diphosphohydrolase-1 protects against murine myocardial ischemic injury
Ming Cai, Zachary M Huttinger, Heng He, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
April 19, 2018
Mutations That Alter the Carboxy-Terminal-Propeptide Cleavage Site of the Chains of Type I Procollagen Are Associated With a Unique Osteogenesis Imperfecta Phenotype
Tim Cundy, Michael Dray, John Delahunt, et al.
Neural Plasticity
|
September 25, 2018
Cortical AAV-CNTF Gene Therapy Combined with Intraspinal Mesenchymal Precursor Cell Transplantation Promotes Functional and Morphological Outcomes after Spinal Cord Injury in Adult Rats
Stuart I Hodgetts, Jun Han Yoon, Alysia Fogliani, et al.
Annals of Clinical and Translational Neurology
|
May 15, 2024
Emerging variants, unique phenotypes, and transcriptomic signatures: an integrated study of COASY-associated diseases
Chiara Cavestro, Francesca Morra, Andrea Legati, et al.
Page
of 39