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Mitochondrion
|
October 13, 2009
Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation
Jianxin Lu, Yaping Qian, Zhiyuan Li, et al.
Environmental Research
|
September 17, 2022
Cow bone-derived biochar enhances microbial biomass and alters bacterial community composition and diversity in a smelter contaminated soil
Muhammad Azeem, Parimala Gnana Soundari Arockiam Jeyasundar, Amjad Ali, et al.
Global Change Biology
|
November 22, 2019
Growing-season temperature and precipitation are independent drivers of global variation in xylem hydraulic conductivity
Pengcheng He, Sean M Gleason, Ian J Wright, et al.
Nature Communications
|
July 23, 2021
A machine learning approach to brain epigenetic analysis reveals kinases associated with Alzheimer's disease
Yanting Huang, Xiaobo Sun, Huige Jiang, et al.
Nature Communications
|
March 23, 2025
Brain 5-hydroxymethylcytosine alterations are associated with Alzheimer's disease neuropathology
Jinying Zhao, Tongjun Gu, Cheng Gao, et al.
Biochemical and Biophysical Research Communications
|
December 27, 2005
Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA mutation in 16 Chinese families: implication for early detection and prevention of deafness
Pu Dai, Xin Liu, Dongyi Han, et al.
Nature Neuroscience
|
August 1, 2017
Zika virus directly infects peripheral neurons and induces cell death
Yohan Oh, Feiran Zhang, Yaqing Wang, et al.
American Journal of Human Genetics
|
July 11, 2006
Mutation in TRMU related to transfer RNA modification modulates the phenotypic expression of the deafness-associated mitochondrial 12S ribosomal RNA mutations
Min-Xin Guan, Qingfeng Yan, Xiaoming Li, et al.
Mitochondrion
|
January 27, 2010
Mitochondrial 12S rRNA variants in 1642 Han Chinese pediatric subjects with aminoglycoside-induced and nonsyndromic hearing loss
Jianxin Lu, Zhiyuan Li, Yi Zhu, et al.
Plos Genetics
|
March 26, 2015
Mutations of human NARS2, encoding the mitochondrial asparaginyl-tRNA synthetase, cause nonsyndromic deafness and Leigh syndrome
Mariella Simon, Elodie M Richard, Xinjian Wang, et al.
Page
of 36
Search research articles
Search
Showing results (351-360 of 360) with videos related to
Sort By:
Page
of 36
You have reached the last page of results.
This site can display upto 360 results.
Mitochondrion
|
October 13, 2009
Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation
Jianxin Lu, Yaping Qian, Zhiyuan Li, et al.
Environmental Research
|
September 17, 2022
Cow bone-derived biochar enhances microbial biomass and alters bacterial community composition and diversity in a smelter contaminated soil
Muhammad Azeem, Parimala Gnana Soundari Arockiam Jeyasundar, Amjad Ali, et al.
Global Change Biology
|
November 22, 2019
Growing-season temperature and precipitation are independent drivers of global variation in xylem hydraulic conductivity
Pengcheng He, Sean M Gleason, Ian J Wright, et al.
Nature Communications
|
July 23, 2021
A machine learning approach to brain epigenetic analysis reveals kinases associated with Alzheimer's disease
Yanting Huang, Xiaobo Sun, Huige Jiang, et al.
Nature Communications
|
March 23, 2025
Brain 5-hydroxymethylcytosine alterations are associated with Alzheimer's disease neuropathology
Jinying Zhao, Tongjun Gu, Cheng Gao, et al.
Biochemical and Biophysical Research Communications
|
December 27, 2005
Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA mutation in 16 Chinese families: implication for early detection and prevention of deafness
Pu Dai, Xin Liu, Dongyi Han, et al.
Nature Neuroscience
|
August 1, 2017
Zika virus directly infects peripheral neurons and induces cell death
Yohan Oh, Feiran Zhang, Yaqing Wang, et al.
American Journal of Human Genetics
|
July 11, 2006
Mutation in TRMU related to transfer RNA modification modulates the phenotypic expression of the deafness-associated mitochondrial 12S ribosomal RNA mutations
Min-Xin Guan, Qingfeng Yan, Xiaoming Li, et al.
Mitochondrion
|
January 27, 2010
Mitochondrial 12S rRNA variants in 1642 Han Chinese pediatric subjects with aminoglycoside-induced and nonsyndromic hearing loss
Jianxin Lu, Zhiyuan Li, Yi Zhu, et al.
Plos Genetics
|
March 26, 2015
Mutations of human NARS2, encoding the mitochondrial asparaginyl-tRNA synthetase, cause nonsyndromic deafness and Leigh syndrome
Mariella Simon, Elodie M Richard, Xinjian Wang, et al.
Page
of 36