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Alex Parker

Showing results (101-110 of 109) with videos related to

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American Journal of Human Genetics|May 7, 2016
Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic ParaplegiaZiv Gan-Or, Naima Bouslam, Nazha Birouk, et al.
Cell|February 8, 2023
PIKFYVE inhibition mitigates disease in models of diverse forms of ALSShu-Ting Hung, Gabriel R Linares, Wen-Hsuan Chang, et al.
Nature Medicine|February 14, 2012
Identification of new ALK and RET gene fusions from colorectal and lung cancer biopsiesDoron Lipson, Marzia Capelletti, Roman Yelensky, et al.
Journal of Experimental Neurology|September 22, 2025
Protein Assembly Modulation: A New Approach to Amyotrophic Lateral Sclerosis (ALS) TherapeuticsShao Feng Yu, Kumar Paulvannan, Dennis Solas, et al.
Nature Biotechnology|October 22, 2013
Development and validation of a clinical cancer genomic profiling test based on massively parallel DNA sequencingGarrett M Frampton, Alex Fichtenholtz, Geoff A Otto, et al.
Nature Metabolism|April 14, 2026
Neuronal lipid droplets play a conserved and sex-biased role in maintaining whole-body energy homeostasisRomane Manceau, Celena M Cherian, Danie Majeur, et al.
Science (New York, N.Y.)|April 30, 2020
Feasibility of blood testing combined with PET-CT to screen for cancer and guide interventionAnne Marie Lennon, Adam H Buchanan, Isaac Kinde, et al.
Brain : a Journal of Neurology|September 8, 2022
ATP6V0C variants impair V-ATPase function causing a neurodevelopmental disorder often associated with epilepsyKari A Mattison, Gilles Tossing, Fred Mulroe, et al.
American Journal of Human Genetics|December 25, 2024
Heterozygous UBR5 variants result in a neurodevelopmental syndrome with developmental delay, autism, and intellectual disabilityPascale Sabeh, Samantha A Dumas, Claudia Maios, et al.
Pageof 11

Showing results (101-110 of 109) with videos related to

Sort By:
Pageof 11
You have reached the last page of results.This site can display upto 109 results.
American Journal of Human Genetics|May 7, 2016
Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic ParaplegiaZiv Gan-Or, Naima Bouslam, Nazha Birouk, et al.
Cell|February 8, 2023
PIKFYVE inhibition mitigates disease in models of diverse forms of ALSShu-Ting Hung, Gabriel R Linares, Wen-Hsuan Chang, et al.
Nature Medicine|February 14, 2012
Identification of new ALK and RET gene fusions from colorectal and lung cancer biopsiesDoron Lipson, Marzia Capelletti, Roman Yelensky, et al.
Journal of Experimental Neurology|September 22, 2025
Protein Assembly Modulation: A New Approach to Amyotrophic Lateral Sclerosis (ALS) TherapeuticsShao Feng Yu, Kumar Paulvannan, Dennis Solas, et al.
Nature Biotechnology|October 22, 2013
Development and validation of a clinical cancer genomic profiling test based on massively parallel DNA sequencingGarrett M Frampton, Alex Fichtenholtz, Geoff A Otto, et al.
Nature Metabolism|April 14, 2026
Neuronal lipid droplets play a conserved and sex-biased role in maintaining whole-body energy homeostasisRomane Manceau, Celena M Cherian, Danie Majeur, et al.
Science (New York, N.Y.)|April 30, 2020
Feasibility of blood testing combined with PET-CT to screen for cancer and guide interventionAnne Marie Lennon, Adam H Buchanan, Isaac Kinde, et al.
Brain : a Journal of Neurology|September 8, 2022
ATP6V0C variants impair V-ATPase function causing a neurodevelopmental disorder often associated with epilepsyKari A Mattison, Gilles Tossing, Fred Mulroe, et al.
American Journal of Human Genetics|December 25, 2024
Heterozygous UBR5 variants result in a neurodevelopmental syndrome with developmental delay, autism, and intellectual disabilityPascale Sabeh, Samantha A Dumas, Claudia Maios, et al.
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