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Plos One
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February 8, 2014
Quantitative methylation level of the EPHX1 promoter in peripheral blood DNA is associated with polycystic ovary syndrome
Qing Sang, Xin Li, Haojue Wang, et al.
Peptides
|
May 31, 2011
Virucidal activity of a scorpion venom peptide variant mucroporin-M1 against measles, SARS-CoV and influenza H5N1 viruses
Qiaoli Li, Zhenhuan Zhao, Dihan Zhou, et al.
Journal of Assisted Reproduction and Genetics
|
February 21, 2021
A novel splicing variant in DNAH8 causes asthenozoospermia
Zhou Zhou, Xiaoyan Mao, Biaobang Chen, et al.
Plos One
|
February 6, 2013
Identification and functional study of a new missense mutation in the motor head domain of myosin VIIA in a family with autosomal dominant hearing impairment (DFNA11)
Qing Sang, Xukun Yan, Huan Wang, et al.
Journal of Assisted Reproduction and Genetics
|
November 22, 2025
Novel missense variants in COX15 cause oocyte degeneration and female infertility
Ran Yu, Xuelin Zhang, Qian Dou, et al.
Plos Genetics
|
April 28, 2022
ENPP1 variants in patients with GACI and PXE expand the clinical and genetic heterogeneity of heritable disorders of ectopic calcification
Douglas Ralph, Yvonne Nitschke, Michael A Levine, et al.
The Journal of Investigative Dermatology
|
September 7, 2013
Mutations in the ABCC6 gene as a cause of generalized arterial calcification of infancy: genotypic overlap with pseudoxanthoma elasticum
Qiaoli Li, Jill L Brodsky, Laura K Conlin, et al.
The British Journal of Psychiatry : the Journal of Mental Science
|
July 25, 2015
Loci with genome-wide associations with schizophrenia in the Han Chinese population
Zhiqiang Li, Yuqian Xiang, Jianhua Chen, et al.
The International Journal of Neuropsychopharmacology
|
December 19, 2014
Prenatal nutritional deficiency reprogrammed postnatal gene expression in mammal brains: implications for schizophrenia
Jiawei Xu, Guang He, Jingde Zhu, et al.
International Journal of Cancer
|
September 15, 2020
Unraveling most abundant mutational signatures in head and neck cancer
Michaela Plath, Johanna Gass, Mario Hlevnjak, et al.
Page
of 21
Search research articles
Search
Showing results (151-160 of 208) with videos related to
Sort By:
Page
of 21
Plos One
|
February 8, 2014
Quantitative methylation level of the EPHX1 promoter in peripheral blood DNA is associated with polycystic ovary syndrome
Qing Sang, Xin Li, Haojue Wang, et al.
Peptides
|
May 31, 2011
Virucidal activity of a scorpion venom peptide variant mucroporin-M1 against measles, SARS-CoV and influenza H5N1 viruses
Qiaoli Li, Zhenhuan Zhao, Dihan Zhou, et al.
Journal of Assisted Reproduction and Genetics
|
February 21, 2021
A novel splicing variant in DNAH8 causes asthenozoospermia
Zhou Zhou, Xiaoyan Mao, Biaobang Chen, et al.
Plos One
|
February 6, 2013
Identification and functional study of a new missense mutation in the motor head domain of myosin VIIA in a family with autosomal dominant hearing impairment (DFNA11)
Qing Sang, Xukun Yan, Huan Wang, et al.
Journal of Assisted Reproduction and Genetics
|
November 22, 2025
Novel missense variants in COX15 cause oocyte degeneration and female infertility
Ran Yu, Xuelin Zhang, Qian Dou, et al.
Plos Genetics
|
April 28, 2022
ENPP1 variants in patients with GACI and PXE expand the clinical and genetic heterogeneity of heritable disorders of ectopic calcification
Douglas Ralph, Yvonne Nitschke, Michael A Levine, et al.
The Journal of Investigative Dermatology
|
September 7, 2013
Mutations in the ABCC6 gene as a cause of generalized arterial calcification of infancy: genotypic overlap with pseudoxanthoma elasticum
Qiaoli Li, Jill L Brodsky, Laura K Conlin, et al.
The British Journal of Psychiatry : the Journal of Mental Science
|
July 25, 2015
Loci with genome-wide associations with schizophrenia in the Han Chinese population
Zhiqiang Li, Yuqian Xiang, Jianhua Chen, et al.
The International Journal of Neuropsychopharmacology
|
December 19, 2014
Prenatal nutritional deficiency reprogrammed postnatal gene expression in mammal brains: implications for schizophrenia
Jiawei Xu, Guang He, Jingde Zhu, et al.
International Journal of Cancer
|
September 15, 2020
Unraveling most abundant mutational signatures in head and neck cancer
Michaela Plath, Johanna Gass, Mario Hlevnjak, et al.
Page
of 21