Chie Ishigami

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Publication record
15 papers · 679 citations · H-index 10

PAPERS

Mizuo–Nakamura phenomenon in X-linked retinoschisis
20221 citationsauthor #3
Retinitis Pigmentosa with EYS Mutations Is the Most Prevalent Inherited Retinal Dystrophy in Japanese Populations
201573 citationsauthor #4
Constructive rescue of TFIIH instability by an alternative isoform of XPD derived from a mutated XPD allele in mild but not severe XP-D/CS
201519 citationsauthor #3
The first USH2A mutation analysis of Japanese autosomal recessive retinitis pigmentosa patients: a totally different mutation profile with the lack of frequent mutations found in Caucasian patients
201422 citationsauthor #4
Mutation Analysis of the USH2A Gene in Japanese Patients with Autosomal Recessive Retinitis Pigmentosa
20140 citationsauthor #3
A point mutation in Semaphorin 4A associates with defective endosomal sorting and causes retinal degeneration
201325 citationsauthor #4
Mutations in UVSSA cause UV-sensitive syndrome and destabilize ERCC6 in transcription-coupled DNA repair
2012190 citationsauthor #4
An Adenine Insertion between Nucleotide Positions 4957 and 4958 in the EYS Gene Is a Possible Major Cause of arRP in the Japanese Population
20120 citationsauthor #2
Two Novel Mutations in the EYS Gene Are Possible Major Causes of Autosomal Recessive Retinitis Pigmentosa in the Japanese Population
201297 citationsauthor #2
Oguchi disease masked by retinitis pigmentosa
201116 citationsauthor #3
[A case of Oguchi disease with disappearance of golden tapetal-like fundus reflex after vitreous resection].
20114 citationsauthor #5
Use of Lectins to Enrich Mouse ES-Derived Retinal Progenitor Cells for the Purpose of Transplantation Therapy
201018 citationsauthor #5
Efficient Generation of Photoreceptors From Mouse Es Cells by Negative Selection Using Lectins to Enrich Retinal Progenitor Cells
20080 citationsauthor #4
Allelic copy number variation in FSCN2 detected using allele-specific genotyping and multiplex real-time PCRs.
200811 citationsauthor #4
XPG stabilizes TFIIH, allowing transactivation of nuclear receptors: implications for Cockayne syndrome in XP-G/CS patients.
2007203 citationsauthor #6

TIMELINE

2007 203 citations

2008 11 citations

2010 18 citations

2011 20 citations

2012 287 citations

2013 25 citations

2014 22 citations

2015 92 citations

2022 1 citations

Chie Ishigami

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