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Megan Li

Showing results (11-20 of 20) with videos related to

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Biorxiv : the Preprint Server for Biology|July 9, 2024
Modulation of ribosomal subunit associations by eIF6 is critical for mitotic exit and cancer progressionPoonam Roshan, Aparna Biswas, Stella Anagnos, et al.
ACS Pharmacology & Translational Science|January 15, 2026
Measurement of Endogenous Fatty Acid Esters of Hydroxy Fatty Acid (FAHFA) and Alkyl-diacylglycerol (TG(O)) from Human Breast MilkMegan Li Xian Lee, Kim Ngan T Nguyen, Wei Wei Pang, et al.
Nucleic Acids Research|December 27, 2024
Sequestration of ribosomal subunits as inactive 80S by targeting eIF6 limits mitotic exit and cancer progressionPoonam Roshan, Aparna Biswas, Sinthyia Ahmed, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 5, 2024
De novo FRMD5 Missense Variants in Patients with Childhood-Onset Ataxia, Prominent Nystagmus, and SeizuresIgnacio J Keller Sarmiento, Bernabe I Bustos, Joanna Blackburn, et al.
American Journal of Human Genetics|October 7, 2022
De novo variants in FRMD5 are associated with developmental delay, intellectual disability, ataxia, and abnormalities of eye movementShenzhao Lu, Mengqi Ma, Xiao Mao, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|June 7, 2018
Identification of a Genomic Region between <i>SLC29A1</i> and <i>HSP90AB1</i> Associated with Risk of Bevacizumab-Induced Hypertension: CALGB 80405 (Alliance)Megan Li, Flora Mulkey, Chen Jiang, et al.
HGG Advances|August 25, 2024
LARP1 haploinsufficiency is associated with an autosomal dominant neurodevelopmental disorderJames Chettle, Raymond J Louie, Olivia Larner, et al.
Human Genetics|March 25, 2024
Heterozygous loss-of-function variants in DOCK4 cause neurodevelopmental delay and microcephalyCharlotte Herbst, Viktoria Bothe, Meret Wegler, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 18, 2022
Biallelic PRMT7 pathogenic variants are associated with a recognizable syndromic neurodevelopmental disorder with short stature, obesity, and craniofacial and digital abnormalitiesElisa Cali, Mohnish Suri, Marcello Scala, et al.
The Journal of Clinical Investigation|November 14, 2023
Spliceosome malfunction causes neurodevelopmental disorders with overlapping featuresDong Li, Qin Wang, Allan Bayat, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Biorxiv : the Preprint Server for Biology|July 9, 2024
Modulation of ribosomal subunit associations by eIF6 is critical for mitotic exit and cancer progressionPoonam Roshan, Aparna Biswas, Stella Anagnos, et al.
ACS Pharmacology & Translational Science|January 15, 2026
Measurement of Endogenous Fatty Acid Esters of Hydroxy Fatty Acid (FAHFA) and Alkyl-diacylglycerol (TG(O)) from Human Breast MilkMegan Li Xian Lee, Kim Ngan T Nguyen, Wei Wei Pang, et al.
Nucleic Acids Research|December 27, 2024
Sequestration of ribosomal subunits as inactive 80S by targeting eIF6 limits mitotic exit and cancer progressionPoonam Roshan, Aparna Biswas, Sinthyia Ahmed, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 5, 2024
De novo FRMD5 Missense Variants in Patients with Childhood-Onset Ataxia, Prominent Nystagmus, and SeizuresIgnacio J Keller Sarmiento, Bernabe I Bustos, Joanna Blackburn, et al.
American Journal of Human Genetics|October 7, 2022
De novo variants in FRMD5 are associated with developmental delay, intellectual disability, ataxia, and abnormalities of eye movementShenzhao Lu, Mengqi Ma, Xiao Mao, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|June 7, 2018
Identification of a Genomic Region between <i>SLC29A1</i> and <i>HSP90AB1</i> Associated with Risk of Bevacizumab-Induced Hypertension: CALGB 80405 (Alliance)Megan Li, Flora Mulkey, Chen Jiang, et al.
HGG Advances|August 25, 2024
LARP1 haploinsufficiency is associated with an autosomal dominant neurodevelopmental disorderJames Chettle, Raymond J Louie, Olivia Larner, et al.
Human Genetics|March 25, 2024
Heterozygous loss-of-function variants in DOCK4 cause neurodevelopmental delay and microcephalyCharlotte Herbst, Viktoria Bothe, Meret Wegler, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 18, 2022
Biallelic PRMT7 pathogenic variants are associated with a recognizable syndromic neurodevelopmental disorder with short stature, obesity, and craniofacial and digital abnormalitiesElisa Cali, Mohnish Suri, Marcello Scala, et al.
The Journal of Clinical Investigation|November 14, 2023
Spliceosome malfunction causes neurodevelopmental disorders with overlapping featuresDong Li, Qin Wang, Allan Bayat, et al.
Pageof 2