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Showing results (231-240 of 252) with videos related to

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Oncogene|January 20, 2009
Regulation of non-AU-rich element containing c-fms proto-oncogene expression by HuR in breast cancerH-H Woo, Y Zhou, X Yi, et al.
Pediatric Research|January 13, 2023
Child and family factors associated with positive outcomes among youth born extremely pretermCrisma Emmanuel, Joe X Yi, Robert M Joseph, et al.
Oncogene|May 24, 2017
UTX promotes hormonally responsive breast carcinogenesis through feed-forward transcription regulation with estrogen receptorG Xie, X Liu, Y Zhang, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|September 28, 2021
Prevalence and risk factors for cognitive impairment in patients with psoriasisY Kuang, Y Luo, X Yi, et al.
Brain Research|May 16, 2020
Activation of p38MAPK in spinal microglia contributes to autologous nucleus pulposus-induced mechanical hyperalgesia in a modified rat model of lumbar disk herniationY-M Wang, F-J Gao, Sh-Q Lin, et al.
Optics Express|July 14, 2016
Sensitive determinations of Cu, Pb, Cd, and Cr elements in aqueous solutions using chemical replacement combined with surface-enhanced laser-induced breakdown spectroscopyX Y Yang, Z Q Hao, C M Li, et al.
The Journal of Pediatrics|June 28, 2025
Count of Neonatal Morbidities Predicts Outcomes at Age 10 and 15 Years in Infants Born Extremely PretermRuben Vaidya, Joe X Yi, T Michael O'Shea, et al.
Pediatrics|October 6, 2022
Long-Term Outcome of Necrotizing Enterocolitis and Spontaneous Intestinal PerforationRuben Vaidya, Joe X Yi, T Michael O'Shea, et al.
Zhonghua Yi Xue Za Zhi|September 29, 2025
[A multicenter study on the effect of continued antiplatelet therapy on postprocedural bleeding after transrectal ultrasound-guided prostate biopsy]B A Hong, Y X Bo, K X Ren, et al.
Genetics and Molecular Research : GMR|November 25, 2015
Mutation analysis of four Chinese families with pure hereditary spastic paraplegia: pseudo- X-linked dominant inheritance and male lethality due to a novel ATL1 mutationN Zhao, Y Sui, X F Li, et al.
Pageof 26

Showing results (231-240 of 252) with videos related to

Sort By:
Pageof 26
Oncogene|January 20, 2009
Regulation of non-AU-rich element containing c-fms proto-oncogene expression by HuR in breast cancerH-H Woo, Y Zhou, X Yi, et al.
Pediatric Research|January 13, 2023
Child and family factors associated with positive outcomes among youth born extremely pretermCrisma Emmanuel, Joe X Yi, Robert M Joseph, et al.
Oncogene|May 24, 2017
UTX promotes hormonally responsive breast carcinogenesis through feed-forward transcription regulation with estrogen receptorG Xie, X Liu, Y Zhang, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|September 28, 2021
Prevalence and risk factors for cognitive impairment in patients with psoriasisY Kuang, Y Luo, X Yi, et al.
Brain Research|May 16, 2020
Activation of p38MAPK in spinal microglia contributes to autologous nucleus pulposus-induced mechanical hyperalgesia in a modified rat model of lumbar disk herniationY-M Wang, F-J Gao, Sh-Q Lin, et al.
Optics Express|July 14, 2016
Sensitive determinations of Cu, Pb, Cd, and Cr elements in aqueous solutions using chemical replacement combined with surface-enhanced laser-induced breakdown spectroscopyX Y Yang, Z Q Hao, C M Li, et al.
The Journal of Pediatrics|June 28, 2025
Count of Neonatal Morbidities Predicts Outcomes at Age 10 and 15 Years in Infants Born Extremely PretermRuben Vaidya, Joe X Yi, T Michael O'Shea, et al.
Pediatrics|October 6, 2022
Long-Term Outcome of Necrotizing Enterocolitis and Spontaneous Intestinal PerforationRuben Vaidya, Joe X Yi, T Michael O'Shea, et al.
Zhonghua Yi Xue Za Zhi|September 29, 2025
[A multicenter study on the effect of continued antiplatelet therapy on postprocedural bleeding after transrectal ultrasound-guided prostate biopsy]B A Hong, Y X Bo, K X Ren, et al.
Genetics and Molecular Research : GMR|November 25, 2015
Mutation analysis of four Chinese families with pure hereditary spastic paraplegia: pseudo- X-linked dominant inheritance and male lethality due to a novel ATL1 mutationN Zhao, Y Sui, X F Li, et al.
Pageof 26