Search research articles
Contact Us
Filters
Showing results (381-390 of 449) with videos related to
Page
of 45
Sort By:
Journal of the Neurological Sciences
|
October 7, 2008
Novel mutations of the SPG11 gene in hereditary spastic paraplegia with thin corpus callosum
Shu-sheng Liao, Lu Shen, Juan Du, et al.
Clinical Genetics
|
August 10, 2019
MAGEL2-related disorders: A study and case series
Jameson Patak, James Gilfert, Melissa Byler, et al.
American Journal of Human Genetics
|
August 21, 2018
De Novo Mutations of CCNK Cause a Syndromic Neurodevelopmental Disorder with Distinctive Facial Dysmorphism
Yanjie Fan, Wu Yin, Bing Hu, et al.
Autophagy
|
June 17, 2020
NRBF2 is a RAB7 effector required for autophagosome maturation and mediates the association of APP-CTFs with active form of RAB7 for degradation
Cui-Zan Cai, Chuanbin Yang, Xu-Xu Zhuang, et al.
Journal of Medical Genetics
|
August 13, 2015
WAC loss-of-function mutations cause a recognisable syndrome characterised by dysmorphic features, developmental delay and hypotonia and recapitulate 10p11.23 microdeletion syndrome
Cori DeSanto, Kristin D'Aco, Gabriel C Araujo, et al.
Neurobiology of Aging
|
June 4, 2013
Using next-generation sequencing as a genetic diagnostic tool in rare autosomal recessive neurologic Mendelian disorders
Zhao Chen, Jun-Ling Wang, Bei-Sha Tang, et al.
Scientific Reports
|
December 21, 2017
PiT2 regulates neuronal outgrowth through interaction with microtubule-associated protein 1B
Xi-Xiang Ma, Xiangyang Li, Ping Yi, et al.
NPJ Digital Medicine
|
February 24, 2026
Distinction between primary and metastatic mucinous ovarian carcinoma from histopathology images using deep learning
Ming-Yi Zhang, Bin Liu, Zhao-Juan Qin, et al.
Plant Biotechnology Journal
|
March 3, 2025
An efficient target-mutant screening platform of model variety Ci846 facilitates genetic studies of Setaria
Hui Zhang, Hongkai Liang, Hui Zhi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 23, 2018
Proline-rich transmembrane protein 2-negative paroxysmal kinesigenic dyskinesia: Clinical and genetic analyses of 163 patients
Wo-Tu Tian, Xiao-Jun Huang, Xiao Mao, et al.
Page
of 45
Search research articles
Search
Showing results (381-390 of 449) with videos related to
Sort By:
Page
of 45
Journal of the Neurological Sciences
|
October 7, 2008
Novel mutations of the SPG11 gene in hereditary spastic paraplegia with thin corpus callosum
Shu-sheng Liao, Lu Shen, Juan Du, et al.
Clinical Genetics
|
August 10, 2019
MAGEL2-related disorders: A study and case series
Jameson Patak, James Gilfert, Melissa Byler, et al.
American Journal of Human Genetics
|
August 21, 2018
De Novo Mutations of CCNK Cause a Syndromic Neurodevelopmental Disorder with Distinctive Facial Dysmorphism
Yanjie Fan, Wu Yin, Bing Hu, et al.
Autophagy
|
June 17, 2020
NRBF2 is a RAB7 effector required for autophagosome maturation and mediates the association of APP-CTFs with active form of RAB7 for degradation
Cui-Zan Cai, Chuanbin Yang, Xu-Xu Zhuang, et al.
Journal of Medical Genetics
|
August 13, 2015
WAC loss-of-function mutations cause a recognisable syndrome characterised by dysmorphic features, developmental delay and hypotonia and recapitulate 10p11.23 microdeletion syndrome
Cori DeSanto, Kristin D'Aco, Gabriel C Araujo, et al.
Neurobiology of Aging
|
June 4, 2013
Using next-generation sequencing as a genetic diagnostic tool in rare autosomal recessive neurologic Mendelian disorders
Zhao Chen, Jun-Ling Wang, Bei-Sha Tang, et al.
Scientific Reports
|
December 21, 2017
PiT2 regulates neuronal outgrowth through interaction with microtubule-associated protein 1B
Xi-Xiang Ma, Xiangyang Li, Ping Yi, et al.
NPJ Digital Medicine
|
February 24, 2026
Distinction between primary and metastatic mucinous ovarian carcinoma from histopathology images using deep learning
Ming-Yi Zhang, Bin Liu, Zhao-Juan Qin, et al.
Plant Biotechnology Journal
|
March 3, 2025
An efficient target-mutant screening platform of model variety Ci846 facilitates genetic studies of Setaria
Hui Zhang, Hongkai Liang, Hui Zhi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
January 23, 2018
Proline-rich transmembrane protein 2-negative paroxysmal kinesigenic dyskinesia: Clinical and genetic analyses of 163 patients
Wo-Tu Tian, Xiao-Jun Huang, Xiao Mao, et al.
Page
of 45