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Bioconjugate Chemistry
|
April 14, 2022
Design, Synthesis, and Preliminary Evaluation of [<sup>68</sup>Ga]Ga-NOTA-Insulin as a PET Probe in an Alzheimer's Disease Mouse Model
Jillissa C Taubel, Nicholas R Nelson, Aditya Bansal, et al.
Molecular Genetics and Metabolism
|
May 24, 2018
Deoxysphingolipid precursors indicate abnormal sphingolipid metabolism in individuals with primary and secondary disturbances of serine availability
C R Ferreira, S M I Goorden, A Soldatos, et al.
Nature Communications
|
March 15, 2026
Modifying muscle metabolic dysregulation in inclusion body myositis with pioglitazone: a single-arm trial
Brittany L Adler, Michael R Bene, Cissy Zhang, 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.
American Journal of Otolaryngology
|
March 5, 2021
Aerosol and droplet generation from orbital repair: Surgical risk in the pandemic era
Michael J Ye, Raghav B Vadhul, Dhruv Sharma, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
August 19, 2025
<sup>18</sup>F-FDG PET in detection of primary age-related tauopathy (PART) - Is there a role? Insights from an imaging-pathology correlation study
Anna Lavrova, Nha Trang Thu Pham, Cynthia J Vernon, et al.
Facial Plastic Surgery & Aesthetic Medicine
|
December 29, 2021
Aerosol and Droplet Generation from Open Rhinoplasty: Surgical Risk in the Pandemic Era
Michael J Ye, Vincent J Campiti, Megan Falls, et al.
American Journal of Medical Genetics. Part A
|
November 30, 2019
Phenotypic expansion of POGZ-related intellectual disability syndrome (White-Sutton syndrome)
Nurit Assia Batzir, Jennifer E Posey, Xiaofei Song, et al.
Journal of Medical Genetics
|
September 4, 2017
Missense variants in the chromatin remodeler <i>CHD1</i> are associated with neurodevelopmental disability
Genay O Pilarowski, Hilary J Vernon, Carolyn D Applegate, et al.
Orphanet Journal of Rare Diseases
|
March 10, 2026
Characterizing the frequency of clinical events and assessing biomarkers in propionic acidemia: a natural history study
Bernd C Schwahn, Gerard T Berry, Hilary J Vernon, et al.
Page
of 28
Search research articles
Search
Showing results (261-270 of 279) with videos related to
Sort By:
Page
of 28
Bioconjugate Chemistry
|
April 14, 2022
Design, Synthesis, and Preliminary Evaluation of [<sup>68</sup>Ga]Ga-NOTA-Insulin as a PET Probe in an Alzheimer's Disease Mouse Model
Jillissa C Taubel, Nicholas R Nelson, Aditya Bansal, et al.
Molecular Genetics and Metabolism
|
May 24, 2018
Deoxysphingolipid precursors indicate abnormal sphingolipid metabolism in individuals with primary and secondary disturbances of serine availability
C R Ferreira, S M I Goorden, A Soldatos, et al.
Nature Communications
|
March 15, 2026
Modifying muscle metabolic dysregulation in inclusion body myositis with pioglitazone: a single-arm trial
Brittany L Adler, Michael R Bene, Cissy Zhang, 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.
American Journal of Otolaryngology
|
March 5, 2021
Aerosol and droplet generation from orbital repair: Surgical risk in the pandemic era
Michael J Ye, Raghav B Vadhul, Dhruv Sharma, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
August 19, 2025
<sup>18</sup>F-FDG PET in detection of primary age-related tauopathy (PART) - Is there a role? Insights from an imaging-pathology correlation study
Anna Lavrova, Nha Trang Thu Pham, Cynthia J Vernon, et al.
Facial Plastic Surgery & Aesthetic Medicine
|
December 29, 2021
Aerosol and Droplet Generation from Open Rhinoplasty: Surgical Risk in the Pandemic Era
Michael J Ye, Vincent J Campiti, Megan Falls, et al.
American Journal of Medical Genetics. Part A
|
November 30, 2019
Phenotypic expansion of POGZ-related intellectual disability syndrome (White-Sutton syndrome)
Nurit Assia Batzir, Jennifer E Posey, Xiaofei Song, et al.
Journal of Medical Genetics
|
September 4, 2017
Missense variants in the chromatin remodeler <i>CHD1</i> are associated with neurodevelopmental disability
Genay O Pilarowski, Hilary J Vernon, Carolyn D Applegate, et al.
Orphanet Journal of Rare Diseases
|
March 10, 2026
Characterizing the frequency of clinical events and assessing biomarkers in propionic acidemia: a natural history study
Bernd C Schwahn, Gerard T Berry, Hilary J Vernon, et al.
Page
of 28