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Jinglan Zhang

Showing results (61-70 of 94) with videos related to

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Human Molecular Genetics|August 12, 2025
Loss of function variants in TMPRSS7 linked to a neurodevelopmental disorder disrupt synaptic functionWeiliang Lu, Shuyuan Li, Songchang Chen, et al.
Zhonghua Nei Ke Za Zhi|December 18, 2015
[The application of peripartum use of pulmonary artery catheter in pregnant patients with pulmonary hypertension]Tengke Wang, Jiakai Lu, Yao Chen, et al.
Molecular Psychiatry|July 14, 2023
BACE1 in PV interneuron tunes hippocampal CA1 local circuits and resets priming of fear memory extinctionXuansheng Xiao, Xiaotong Wang, Ke Zhu, et al.
Orphanet Journal of Rare Diseases|June 13, 2026
Diagnosis of de novo fetal aceruloplasminemia via whole exome sequencing and fetal umbilical blood ceruloplasmin measurementPengzhen Jin, Guangmei Dai, Jiawei Hong, et al.
Peerj. Computer Science|November 1, 2021
Deepening into the suitability of using pre-trained models of ImageNet against a lightweight convolutional neural network in medical imaging: an experimental studyLaith Alzubaidi, Ye Duan, Ayad Al-Dujaili, et al.
Cancers|April 3, 2021
Novel Transfer Learning Approach for Medical Imaging with Limited Labeled DataLaith Alzubaidi, Muthana Al-Amidie, Ahmed Al-Asadi, et al.
Journal of Big Data|April 5, 2021
Review of deep learning: concepts, CNN architectures, challenges, applications, future directionsLaith Alzubaidi, Jinglan Zhang, Amjad J Humaidi, et al.
The Journal of Biological Chemistry|May 27, 2010
Genome-wide reinforcement of cohesin binding at pre-existing cohesin sites in response to ionizing radiation in human cellsBeom-Jun Kim, Yehua Li, Jinglan Zhang, et al.
Human Molecular Genetics|January 8, 2019
Homozygous hydroxymethylbilane synthase knock-in mice provide pathogenic insights into the severe neurological impairments present in human homozygous dominant acute intermittent porphyriaMakiko Yasuda, Lin Gan, Brenden Chen, et al.
Frontiers in Genetics|October 20, 2022
<i>HTRA1</i> rs11528744, <i>BCRA1</i> rs9928736, and <i>B</i>3<i>GLCT</i> rs4381465 are associated with age-related macular degeneration in a Chinese populationGuo Huang, Huan Li, Shuang Lai, et al.
Pageof 10

Showing results (61-70 of 94) with videos related to

Sort By:
Pageof 10
Human Molecular Genetics|August 12, 2025
Loss of function variants in TMPRSS7 linked to a neurodevelopmental disorder disrupt synaptic functionWeiliang Lu, Shuyuan Li, Songchang Chen, et al.
Zhonghua Nei Ke Za Zhi|December 18, 2015
[The application of peripartum use of pulmonary artery catheter in pregnant patients with pulmonary hypertension]Tengke Wang, Jiakai Lu, Yao Chen, et al.
Molecular Psychiatry|July 14, 2023
BACE1 in PV interneuron tunes hippocampal CA1 local circuits and resets priming of fear memory extinctionXuansheng Xiao, Xiaotong Wang, Ke Zhu, et al.
Orphanet Journal of Rare Diseases|June 13, 2026
Diagnosis of de novo fetal aceruloplasminemia via whole exome sequencing and fetal umbilical blood ceruloplasmin measurementPengzhen Jin, Guangmei Dai, Jiawei Hong, et al.
Peerj. Computer Science|November 1, 2021
Deepening into the suitability of using pre-trained models of ImageNet against a lightweight convolutional neural network in medical imaging: an experimental studyLaith Alzubaidi, Ye Duan, Ayad Al-Dujaili, et al.
Cancers|April 3, 2021
Novel Transfer Learning Approach for Medical Imaging with Limited Labeled DataLaith Alzubaidi, Muthana Al-Amidie, Ahmed Al-Asadi, et al.
Journal of Big Data|April 5, 2021
Review of deep learning: concepts, CNN architectures, challenges, applications, future directionsLaith Alzubaidi, Jinglan Zhang, Amjad J Humaidi, et al.
The Journal of Biological Chemistry|May 27, 2010
Genome-wide reinforcement of cohesin binding at pre-existing cohesin sites in response to ionizing radiation in human cellsBeom-Jun Kim, Yehua Li, Jinglan Zhang, et al.
Human Molecular Genetics|January 8, 2019
Homozygous hydroxymethylbilane synthase knock-in mice provide pathogenic insights into the severe neurological impairments present in human homozygous dominant acute intermittent porphyriaMakiko Yasuda, Lin Gan, Brenden Chen, et al.
Frontiers in Genetics|October 20, 2022
<i>HTRA1</i> rs11528744, <i>BCRA1</i> rs9928736, and <i>B</i>3<i>GLCT</i> rs4381465 are associated with age-related macular degeneration in a Chinese populationGuo Huang, Huan Li, Shuang Lai, et al.
Pageof 10