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Neuro-Oncology
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October 31, 2019
Metabolic reprogramming associated with aggressiveness occurs in the G-CIMP-high molecular subtypes of IDH1mut lower grade gliomas
Victor Ruiz-Rodado, Tathiane M Malta, Tomohiro Seki, et al.
Molecular Genetics and Metabolism
|
January 29, 2023
Glb1 knockout mouse model shares natural history with type II GM1 gangliosidosis patients
Elena-Raluca Nicoli, Mylene Huebecker, Sangwoo T Han, et al.
JNCI Cancer Spectrum
|
January 17, 2025
Head and neck paraganglioma in Pacak-Zhuang syndrome
Jared S Rosenblum, Yasemin Cole, Danielle Dang, et al.
JCI Insight
|
January 26, 2021
Developmental vascular malformations in EPAS1 gain-of-function syndrome
Jared S Rosenblum, Herui Wang, Pauline M Dmitriev, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 11, 2026
Clinical, <i>in vitro,</i> and <i>in vivo</i> evidence of <i>WAPL</i> as a novel cohesinopathy gene and phenotypic driver of 10q22.3q23.2 genomic disorder
Philip M Boone, Serkan Erdin, Abucar Mohamed, et al.
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of 6
Search research articles
Search
Showing results (51-60 of 55) with videos related to
Sort By:
Page
of 6
You have reached the last page of results.
This site can display upto 55 results.
Neuro-Oncology
|
October 31, 2019
Metabolic reprogramming associated with aggressiveness occurs in the G-CIMP-high molecular subtypes of IDH1mut lower grade gliomas
Victor Ruiz-Rodado, Tathiane M Malta, Tomohiro Seki, et al.
Molecular Genetics and Metabolism
|
January 29, 2023
Glb1 knockout mouse model shares natural history with type II GM1 gangliosidosis patients
Elena-Raluca Nicoli, Mylene Huebecker, Sangwoo T Han, et al.
JNCI Cancer Spectrum
|
January 17, 2025
Head and neck paraganglioma in Pacak-Zhuang syndrome
Jared S Rosenblum, Yasemin Cole, Danielle Dang, et al.
JCI Insight
|
January 26, 2021
Developmental vascular malformations in EPAS1 gain-of-function syndrome
Jared S Rosenblum, Herui Wang, Pauline M Dmitriev, et al.
Medrxiv : the Preprint Server for Health Sciences
|
March 11, 2026
Clinical, <i>in vitro,</i> and <i>in vivo</i> evidence of <i>WAPL</i> as a novel cohesinopathy gene and phenotypic driver of 10q22.3q23.2 genomic disorder
Philip M Boone, Serkan Erdin, Abucar Mohamed, et al.
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of 6