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Author Details
Full Name
Shoko Watanabe
Affiliation
The Jikei University School of Medicine
ORCID
Career Start Year
2010
Papers
11
H Index
6
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
33721335
Novel gross deletion mutation c.-105_4042+498del in the TNXB gene in a Japanese woman with classical-like Ehlers-Danlos syndrome: A case of uneventful pregnancy and delivery.
J Dermatol
2021
30842224
Genetic landscape of Rett syndrome-like phenotypes revealed by whole exome sequencing.
J Med Genet
2019
30538238
Author Correction: Transcription start site profiling of 15 anatomical regions of the Macaca mulatta central nervous system.
Sci Data
2018
29858092
Supplemental Treatment for Huntington's Disease with miR-132 that Is Deficient in Huntington's Disease Brain.
Mol Ther Nucleic Acids
2018
28850106
FANTOM5 CAGE profiles of human and mouse samples.
Sci Data
2017
29087374
Transcription start site profiling of 15 anatomical regions of the Macaca mulatta central nervous system.
Sci Data
2017
29182598
Monitoring transcription initiation activities in rat and dog.
Sci Data
2017
27896316
Compound heterozygous intermediate MJD alleles cause cerebellar ataxia with sensory neuropathy.
Neurol Genet
2016
25965551
Normalization of Overexpressed α-Synuclein Causing Parkinson's Disease By a Moderate Gene Silencing With RNA Interference.
Mol Ther Nucleic Acids
2015
24670764
A promoter-level mammalian expression atlas.
Nature
2014
21098280
Tailor-made RNAi knockdown against triplet repeat disease-causing alleles.
Proc Natl Acad Sci U S A
2010
1 - 11 of 11
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