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Qian Pan

Showing results (131-140 of 282) with videos related to

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Cell Reports|December 11, 2024
Mapping functional elements of the DNA damage response through base editor screensQian Pan, Zhixuan Zhang, Yangfang Xiong, et al.
Zhong Nan Da Xue Xue Bao. Yi Xue Ban = Journal of Central South University. Medical Sciences|March 28, 2006
[Biotoxicology and biodynamics of silica nanoparticle]Zhi-gang Xue, Shai-hong Zhu, Qian Pan, et al.
Journal of Human Genetics|April 20, 2007
Molecular analysis of hearing loss associated with enlarged vestibular aqueduct in the mainland Chinese: a unique SLC26A4 mutation spectrumHao Hu, Lingqian Wu, Yong Feng, et al.
Neural Regeneration Research|September 11, 2014
A novel transgenic mouse model of Chinese Charcot-Marie-Tooth disease type 2LRuxu Zhang, Fufeng Zhang, Xiaobo Li, et al.
BMC Medical Genetics|November 9, 2016
Three novel mutations of STK11 gene in Chinese patients with Peutz-Jeghers syndromeHu Tan, Libin Mei, Yanru Huang, et al.
Zhong Nan Da Xue Xue Bao. Yi Xue Ban = Journal of Central South University. Medical Sciences|July 12, 2011
Spinocerebellar ataxias in mainland China: an updated genetic analysis among a large cohort of familial and sporadic casesJunling Wang, Lu Shen, Lifang Lei, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|October 9, 2008
[Studies on the CTA/CTG trinucleotide repeats of ATXN8OS gene in Chinese Hans]Junling Wang, Shen Zhang, Qian Xu, et al.
Medicine|September 21, 2017
Health-related quality-of-life assessment in surgical patients with papillary thyroid carcinoma: A single-center analysis from Mainland ChinaJuxiang Gou, Wenjie Cheng, Jianyong Lei, et al.
Clinical Dysmorphology|August 26, 2010
Report of two FOP cases with 617G>A mutation in the ACVR1 gene from Chinese populationHui Guo, Dan Peng, Min Xu, et al.
Molecular Vision|May 27, 2004
A novel PRPF31 splice-site mutation in a Chinese family with autosomal dominant retinitis pigmentosaKun Xia, Duo Zheng, Qian Pan, et al.
Pageof 29

Showing results (131-140 of 282) with videos related to

Sort By:
Pageof 29
Cell Reports|December 11, 2024
Mapping functional elements of the DNA damage response through base editor screensQian Pan, Zhixuan Zhang, Yangfang Xiong, et al.
Zhong Nan Da Xue Xue Bao. Yi Xue Ban = Journal of Central South University. Medical Sciences|March 28, 2006
[Biotoxicology and biodynamics of silica nanoparticle]Zhi-gang Xue, Shai-hong Zhu, Qian Pan, et al.
Journal of Human Genetics|April 20, 2007
Molecular analysis of hearing loss associated with enlarged vestibular aqueduct in the mainland Chinese: a unique SLC26A4 mutation spectrumHao Hu, Lingqian Wu, Yong Feng, et al.
Neural Regeneration Research|September 11, 2014
A novel transgenic mouse model of Chinese Charcot-Marie-Tooth disease type 2LRuxu Zhang, Fufeng Zhang, Xiaobo Li, et al.
BMC Medical Genetics|November 9, 2016
Three novel mutations of STK11 gene in Chinese patients with Peutz-Jeghers syndromeHu Tan, Libin Mei, Yanru Huang, et al.
Zhong Nan Da Xue Xue Bao. Yi Xue Ban = Journal of Central South University. Medical Sciences|July 12, 2011
Spinocerebellar ataxias in mainland China: an updated genetic analysis among a large cohort of familial and sporadic casesJunling Wang, Lu Shen, Lifang Lei, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|October 9, 2008
[Studies on the CTA/CTG trinucleotide repeats of ATXN8OS gene in Chinese Hans]Junling Wang, Shen Zhang, Qian Xu, et al.
Medicine|September 21, 2017
Health-related quality-of-life assessment in surgical patients with papillary thyroid carcinoma: A single-center analysis from Mainland ChinaJuxiang Gou, Wenjie Cheng, Jianyong Lei, et al.
Clinical Dysmorphology|August 26, 2010
Report of two FOP cases with 617G>A mutation in the ACVR1 gene from Chinese populationHui Guo, Dan Peng, Min Xu, et al.
Molecular Vision|May 27, 2004
A novel PRPF31 splice-site mutation in a Chinese family with autosomal dominant retinitis pigmentosaKun Xia, Duo Zheng, Qian Pan, et al.
Pageof 29