E-LIB Suche - Ergebnisse für: Vemula, Satya

1

Consequences of Cre‐mediated deletion of Ciz1 exon 5 in mic:

Xiao, Jianfeng ; Khan, Mohammad Moshahid ; Vemula, Satya..
FEBS Letters. 592 (2018) 18 - p. 3101-3110 , 2018

Link: https://doi.org/10.1002/..

2

Rodent Models of Autosomal Dominant Parkinson Disease:

, In: Movement Disorders,

Xiao, Jianfeng ; Vemula, Satya ; Yue, Zhenyu - p. 307-328 , 2015

Link: https://doi.org/10.1016/..

3

Contributors:

, In: Movement Disorders,

Ajjuri, Rami R. ; Ali, Yousuf ; Arena, Giuseppe... - p. xix-xxiii , 2015

Link: https://doi.org/10.1016/..

4

Genetic Screening Study in 1005 Subjects with Isolated Cerv..:

LeDoux, Mark ; Vemula, Satya ; Xiao, Jianfeng
Neurology. 84 (2015) 14_supplement - p. , 2015

Link: https://doi.org/10.1212/..

5

GNALMutations Cause Adult-Onset Primary Dystonia (P02.076):

Vemula, Satya ; Puschmann, Andreas ; Xiao, Jianfeng...
Neurology. 80 (2013) 7_supplement - p. , 2013

Link: https://doi.org/10.1212/..

6

Hardware implementation of WPT Charging System for EV Vehic..:

Devi P, Srividya ; Vemula, Satya Narayana ; Pohanekar, Om...
E3S Web of Conferences. 552 (2024) - p. 01148 , 2024

Link: https://doi.org/10.1051/..

7

Whole‐exome sequencing for variant discovery in blepharospa..:

Tian, Jun ; Vemula, Satya R. ; Xiao, Jianfeng...
Molecular Genetics & Genomic Medicine. 6 (2018) 4 - p. 601-626 , 2018

Link: https://doi.org/10.1002/..

8

Role of major and brain-specific Sgce isoforms in the patho..:

Xiao, Jianfeng ; Vemula, Satya R. ; Xue, Yi...
Neurobiology of Disease. 98 (2017) - p. 52-65 , 2017

Link: https://doi.org/10.1016/..

9

Motor phenotypes and molecular networks associated with ger..:

Xiao, Jianfeng ; Vemula, Satya R. ; Xue, Yi...
Experimental Neurology. 283 (2016) - p. 110-120 , 2016

Link: https://doi.org/10.1016/..

10

Blepharospasm in a multiplex African-American pedigree:

Xiao, Jianfeng ; Thompson, Misty M. ; Vemula, Satya R..
Journal of the Neurological Sciences. 362 (2016) - p. 299-303 , 2016

Link: https://doi.org/10.1016/..

11

Recent Advances in the Genetics of Dystonia:

Xiao, Jianfeng ; Vemula, Satya R. ; LeDoux, Mark S.
Current Neurology and Neuroscience Reports. 14 (2014) 8 - p. , 2014

Link: https://doi.org/10.1007/..

12

A rare sequence variant in intron 1 of THAP1 is associated ..:

Vemula, Satya R. ; Xiao, Jianfeng ; Zhao, Yu...
Molecular Genetics & Genomic Medicine. 2 (2014) 3 - p. 261-272 , 2014

Link: https://doi.org/10.1002/..

13

Pathogenic variants inTUBB4Aare not found in primary dyston..:

Vemula, Satya R. ; Xiao, Jianfeng ; Bastian, Robert W....
Neurology. 82 (2014) 14 - p. 1227-1230 , 2014

Link: https://doi.org/10.1212/..

14

Role of Gα(olf) in familial and sporadic adult-onset primar..:

Vemula, Satya R. ; Puschmann, Andreas ; Xiao, Jianfeng...
Human Molecular Genetics. 22 (2013) 12 - p. 2510-2519 , 2013

Link: https://doi.org/10.1093/..

15

Dystonia, facial dysmorphism, intellectual disability and b..:

Moscovich, Mariana ; LeDoux, Mark S ; Xiao, Jianfeng...
BMC Medical Genetics. 14 (2013) 1 - p. , 2013

Link: https://doi.org/10.1186/..