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American Journal of Medical Genetics. Part A
|
February 5, 2016
ADAT3-related intellectual disability: Further delineation of the phenotype
Ayman W El-Hattab, Mohammed A Saleh, Amal Hashem, et al.
American Journal of Human Genetics
|
May 6, 2017
GZF1 Mutations Expand the Genetic Heterogeneity of Larsen Syndrome
Nisha Patel, Hanan E Shamseldin, Nadia Sakati, et al.
Nature
|
July 10, 2024
Dissociable hindbrain GLP1R circuits for satiety and aversion
Kuei-Pin Huang, Alisha A Acosta, Misgana Y Ghidewon, et al.
Cell Reports
|
October 27, 2016
Loss of MACF1 Abolishes Ciliogenesis and Disrupts Apicobasal Polarity Establishment in the Retina
Helen L May-Simera, Jessica D Gumerson, Chun Gao, et al.
Blood Advances
|
November 8, 2023
Transient responses and significant toxicities of anti-CD30 CAR T cells for CD30+ lymphomas: results of a phase 1 trial
Jennifer N Brudno, Danielle A Natrakul, Jeremiah Karrs, et al.
Medical Dosimetry : Official Journal of the American Association of Medical Dosimetrists
|
November 19, 2013
Bilateral implant reconstruction does not affect the quality of postmastectomy radiation therapy
Alice Y Ho, Nisha Patel, Nisha Ohri, et al.
Biorxiv : the Preprint Server for Biology
|
April 16, 2025
Molecular basis for multidrug efflux by an anaerobic RND transporter
Ryan Lawrence, Mohd Athar, Muhammad R Uddin, et al.
Antioxidants (Basel, Switzerland)
|
October 26, 2024
PET Imaging with [<sup>18</sup>F]ROStrace Detects Oxidative Stress and Predicts Parkinson's Disease Progression in Mice
Yi Zhu, Neha Kohli, Anthony Young, et al.
Nature Communications
|
December 3, 2025
Molecular basis for multidrug efflux by an anaerobic-associated RND transporter
Ryan Lawrence, Mohd Athar, Muhammad R Uddin, et al.
Genome Biology
|
July 30, 2017
A novel mechanism for variable phenotypic expressivity in Mendelian diseases uncovered by an AU-rich element (ARE)-creating mutation
Nisha Patel, Arif O Khan, Maher Al-Saif, et al.
Page
of 20
Search research articles
Search
Showing results (151-160 of 200) with videos related to
Sort By:
Page
of 20
American Journal of Medical Genetics. Part A
|
February 5, 2016
ADAT3-related intellectual disability: Further delineation of the phenotype
Ayman W El-Hattab, Mohammed A Saleh, Amal Hashem, et al.
American Journal of Human Genetics
|
May 6, 2017
GZF1 Mutations Expand the Genetic Heterogeneity of Larsen Syndrome
Nisha Patel, Hanan E Shamseldin, Nadia Sakati, et al.
Nature
|
July 10, 2024
Dissociable hindbrain GLP1R circuits for satiety and aversion
Kuei-Pin Huang, Alisha A Acosta, Misgana Y Ghidewon, et al.
Cell Reports
|
October 27, 2016
Loss of MACF1 Abolishes Ciliogenesis and Disrupts Apicobasal Polarity Establishment in the Retina
Helen L May-Simera, Jessica D Gumerson, Chun Gao, et al.
Blood Advances
|
November 8, 2023
Transient responses and significant toxicities of anti-CD30 CAR T cells for CD30+ lymphomas: results of a phase 1 trial
Jennifer N Brudno, Danielle A Natrakul, Jeremiah Karrs, et al.
Medical Dosimetry : Official Journal of the American Association of Medical Dosimetrists
|
November 19, 2013
Bilateral implant reconstruction does not affect the quality of postmastectomy radiation therapy
Alice Y Ho, Nisha Patel, Nisha Ohri, et al.
Biorxiv : the Preprint Server for Biology
|
April 16, 2025
Molecular basis for multidrug efflux by an anaerobic RND transporter
Ryan Lawrence, Mohd Athar, Muhammad R Uddin, et al.
Antioxidants (Basel, Switzerland)
|
October 26, 2024
PET Imaging with [<sup>18</sup>F]ROStrace Detects Oxidative Stress and Predicts Parkinson's Disease Progression in Mice
Yi Zhu, Neha Kohli, Anthony Young, et al.
Nature Communications
|
December 3, 2025
Molecular basis for multidrug efflux by an anaerobic-associated RND transporter
Ryan Lawrence, Mohd Athar, Muhammad R Uddin, et al.
Genome Biology
|
July 30, 2017
A novel mechanism for variable phenotypic expressivity in Mendelian diseases uncovered by an AU-rich element (ARE)-creating mutation
Nisha Patel, Arif O Khan, Maher Al-Saif, et al.
Page
of 20