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Yue Si

Showing results (171-180 of 194) with videos related to

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Journal of Neuroinflammation|October 30, 2025
Diabetes exacerbates myasthenia gravis by enhancing pathological thymic output via the GPR183-7α,25-OHC axisJing Dong, Xin Shi, Xu-Dong Gu, et al.
Blood|July 8, 2010
Genetic disruption of both Fancc and Fancg in mice recapitulates the hematopoietic manifestations of Fanconi anemiaAnna C Pulliam-Leath, Samantha L Ciccone, Grzegorz Nalepa, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 28, 2020
Heterozygous variants that disturb the transcriptional repressor activity of FOXP4 cause a developmental disorder with speech/language delays and multiple congenital abnormalitiesLot Snijders Blok, Arianna Vino, Joery den Hoed, et al.
American Journal of Medical Genetics. Part A|April 18, 2015
Further supporting evidence for the SATB2-associated syndrome found through whole exome sequencingYuri A Zarate, Hazel Perry, Tawfeg Ben-Omran, et al.
European Journal of Human Genetics : EJHG|August 10, 2019
Phenotype and mutation expansion of the PTPN23 associated disorder characterized by neurodevelopmental delay and structural brain abnormalitiesRenee Bend, Lior Cohen, Melissa T Carter, et al.
HGG Advances|January 20, 2022
Variants in <i>LSM7</i> impair LSM complexes assembly, neurodevelopment in zebrafish and may be associated with an ultra-rare neurological diseaseAlexa Derksen, Hung-Yu Shih, Diane Forget, et al.
Environmental Science & Technology|March 2, 2022
Observational Insights into Isoprene Secondary Organic Aerosol Formation through the Epoxide Pathway at Three Urban Sites from Northern to Southern ChinaYu-Qing Zhang, Xiang Ding, Quan-Fu He, et al.
European Journal of Medical Genetics|September 18, 2020
A novel pathogenic variant in DYNC1H1 causes various upper and lower motor neuron anomaliesLouis M Viollet, Kathryn J Swoboda, Rong Mao, et al.
Chinese Medical Sciences Journal = Chung-Kuo I Hsueh K'O Hsueh Tsa Chih|May 21, 2025
Development and Initial Validation of the Multi-dimensional Attention Rating Scale in Highly Educated AdultsXin-Yang Zhang, Karen Spruyt, Jia-Yue Si, et al.
Clinical Genetics|November 1, 2020
Expanding the molecular spectrum and the neurological phenotype related to CAMTA1 variantsEva Z Jacobs, Kathleen Brown, Melissa C Byler, et al.
Pageof 20

Showing results (171-180 of 194) with videos related to

Sort By:
Pageof 20
Journal of Neuroinflammation|October 30, 2025
Diabetes exacerbates myasthenia gravis by enhancing pathological thymic output via the GPR183-7α,25-OHC axisJing Dong, Xin Shi, Xu-Dong Gu, et al.
Blood|July 8, 2010
Genetic disruption of both Fancc and Fancg in mice recapitulates the hematopoietic manifestations of Fanconi anemiaAnna C Pulliam-Leath, Samantha L Ciccone, Grzegorz Nalepa, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 28, 2020
Heterozygous variants that disturb the transcriptional repressor activity of FOXP4 cause a developmental disorder with speech/language delays and multiple congenital abnormalitiesLot Snijders Blok, Arianna Vino, Joery den Hoed, et al.
American Journal of Medical Genetics. Part A|April 18, 2015
Further supporting evidence for the SATB2-associated syndrome found through whole exome sequencingYuri A Zarate, Hazel Perry, Tawfeg Ben-Omran, et al.
European Journal of Human Genetics : EJHG|August 10, 2019
Phenotype and mutation expansion of the PTPN23 associated disorder characterized by neurodevelopmental delay and structural brain abnormalitiesRenee Bend, Lior Cohen, Melissa T Carter, et al.
HGG Advances|January 20, 2022
Variants in <i>LSM7</i> impair LSM complexes assembly, neurodevelopment in zebrafish and may be associated with an ultra-rare neurological diseaseAlexa Derksen, Hung-Yu Shih, Diane Forget, et al.
Environmental Science & Technology|March 2, 2022
Observational Insights into Isoprene Secondary Organic Aerosol Formation through the Epoxide Pathway at Three Urban Sites from Northern to Southern ChinaYu-Qing Zhang, Xiang Ding, Quan-Fu He, et al.
European Journal of Medical Genetics|September 18, 2020
A novel pathogenic variant in DYNC1H1 causes various upper and lower motor neuron anomaliesLouis M Viollet, Kathryn J Swoboda, Rong Mao, et al.
Chinese Medical Sciences Journal = Chung-Kuo I Hsueh K'O Hsueh Tsa Chih|May 21, 2025
Development and Initial Validation of the Multi-dimensional Attention Rating Scale in Highly Educated AdultsXin-Yang Zhang, Karen Spruyt, Jia-Yue Si, et al.
Clinical Genetics|November 1, 2020
Expanding the molecular spectrum and the neurological phenotype related to CAMTA1 variantsEva Z Jacobs, Kathleen Brown, Melissa C Byler, et al.
Pageof 20