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Emily G Allen

Showing results (31-40 of 59) with videos related to

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Human Molecular Genetics|August 10, 2022
Cell type-specific DNA methylome signatures reveal epigenetic mechanisms for neuronal diversity and neurodevelopmental disorderYulin Jin, Kenong Su, Ha Eun Kong, et al.
Neurobiology of Disease|June 10, 2019
Amyotrophic Lateral Sclerosis-associated GGGGCC repeat expansion promotes Tau phosphorylation and toxicityHua He, Wen Huang, Ruoxi Wang, et al.
Human Molecular Genetics|July 4, 2021
Stress modulates Ahi1-dependent nuclear localization of ten-eleven translocation protein 2Qian Zhang, Qicheng Hu, Junjie Wang, et al.
Frontiers in Genetics|August 21, 2018
FXPOI: Pattern of AGG Interruptions Does not Show an Association With Age at Amenorrhea Among Women With a PremutationEmily G Allen, Anne Glicksman, Nicole Tortora, et al.
Reproductive Biology and Endocrinology : RB&E|June 21, 2024
FMR1 allelic complexity in premutation carriers provides no evidence for a correlation with age at amenorrheaBárbara Rodrigues, Vanessa Sousa, Carolyn M Yrigollen, et al.
Molecular Genetics & Genomic Medicine|April 14, 2020
Development of Chinese genetic reference panel for Fragile X Syndrome and its application to the screen of 10,000 Chinese pregnant women and women planning pregnancyFei Gao, Wen Huang, Yanjun You, et al.
Neurobiology of Disease|July 13, 2020
Neddylation activity modulates the neurodegeneration associated with fragile X associated tremor/ataxia syndrome (FXTAS) through regulating SimaYunting Lin, Jin Xue, Jing Deng, et al.
Genome Biology|January 6, 2021
N6-methyladenosine dynamics in neurodevelopment and aging, and its potential role in Alzheimer's diseaseAndrew M Shafik, Feiran Zhang, Zhenxing Guo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 21, 2011
Predictors and risk model development for menopausal age in fragile X premutation carriersMarian A Spath, Ton B Feuth, Arie P T Smits, et al.
Nature Communications|January 8, 2026
Integrative transcriptome-wide association analyses reveal PRKCG-linked GABAergic dysfunction in Fragile X-associated tremor/ataxia syndromeYulin Jin, Yiqu Cao, Wenjing Ma, et al.
Pageof 6

Showing results (31-40 of 59) with videos related to

Sort By:
Pageof 6
Human Molecular Genetics|August 10, 2022
Cell type-specific DNA methylome signatures reveal epigenetic mechanisms for neuronal diversity and neurodevelopmental disorderYulin Jin, Kenong Su, Ha Eun Kong, et al.
Neurobiology of Disease|June 10, 2019
Amyotrophic Lateral Sclerosis-associated GGGGCC repeat expansion promotes Tau phosphorylation and toxicityHua He, Wen Huang, Ruoxi Wang, et al.
Human Molecular Genetics|July 4, 2021
Stress modulates Ahi1-dependent nuclear localization of ten-eleven translocation protein 2Qian Zhang, Qicheng Hu, Junjie Wang, et al.
Frontiers in Genetics|August 21, 2018
FXPOI: Pattern of AGG Interruptions Does not Show an Association With Age at Amenorrhea Among Women With a PremutationEmily G Allen, Anne Glicksman, Nicole Tortora, et al.
Reproductive Biology and Endocrinology : RB&E|June 21, 2024
FMR1 allelic complexity in premutation carriers provides no evidence for a correlation with age at amenorrheaBárbara Rodrigues, Vanessa Sousa, Carolyn M Yrigollen, et al.
Molecular Genetics & Genomic Medicine|April 14, 2020
Development of Chinese genetic reference panel for Fragile X Syndrome and its application to the screen of 10,000 Chinese pregnant women and women planning pregnancyFei Gao, Wen Huang, Yanjun You, et al.
Neurobiology of Disease|July 13, 2020
Neddylation activity modulates the neurodegeneration associated with fragile X associated tremor/ataxia syndrome (FXTAS) through regulating SimaYunting Lin, Jin Xue, Jing Deng, et al.
Genome Biology|January 6, 2021
N6-methyladenosine dynamics in neurodevelopment and aging, and its potential role in Alzheimer's diseaseAndrew M Shafik, Feiran Zhang, Zhenxing Guo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 21, 2011
Predictors and risk model development for menopausal age in fragile X premutation carriersMarian A Spath, Ton B Feuth, Arie P T Smits, et al.
Nature Communications|January 8, 2026
Integrative transcriptome-wide association analyses reveal PRKCG-linked GABAergic dysfunction in Fragile X-associated tremor/ataxia syndromeYulin Jin, Yiqu Cao, Wenjing Ma, et al.
Pageof 6