Shinsei Minoshima

发表

The KMDB/MutationView: a mutation database for human disease genes

Shinsei Minoshima, Susumu Mitsuyama, Masafumi Ohtsubo, 2001, Nucleic Acids Res..

GeneView: multi-language human gene mapping library with a graphical user interface

Mitsuru Ishizuka, Hiroshi Dohi, Shinsei Minoshima, 1993, Comput. Appl. Biosci..

Keio Mutation Database (KMDB) for human disease gene mutations

Shinsei Minoshima, Susumu Mitsuyama, Takashi Kawamura, 2000, Nucleic Acids Res..

Keio Mutation Database for eye disease genes (KMeyeDB)

Shinsei Minoshima, Susumu Mitsuyama, Takashi Kawamura, 1999, Nucleic Acids Res..

The H-Invitational Database (H-InvDB), a comprehensive annotation resource for human genes and transcripts

Teruyoshi Hishiki, Katsuhiko Murakami, Yoshihiro Kawahara, 2007, Nucleic Acids Res..

KMDB/Mutation View: An Integrated Knowledge Base for Mutations and Polymorphisms in Human Disease Genes

Shinsei Minoshima, Susumu Mitsuyama, Masafumi Ohtsubo, 2001 .

KMeyeDB: Keio Mutation Database for Eye Disease Genes Constructed on a Graphical Distributed Database System Mutation View

Shinsei Minoshima, Susumu Mitsuyama, Takashi Kawamura, 1998 .

KMDB: Keio Mutation Database for Human Disease Gene

Shinsei Minoshima, Susumu Mitsuyama, Takashi Kawamura, 1999 .

Locus-in: a new database system with graphical front end to integrate mapping data

Shinsei Minoshima, Nobuyoshi Shimizu, 1993 .

Construction of Human Gene Mapping Library System on X-window

Mitsuru Ishizuka, Hiroshi Dohi, Shinsei Minoshima, 1991 .

A New Version of the KMDB/Mutation View

Shinsei Minoshima, Susumu Mitsuyama, Masafumi Ohtsubo, 2000 .

Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase

Shinsei Minoshima, Nobutaka Hattori, Yoshikuni Mizuno, 2000, Nature Genetics.

KMeyeDB: a graphical database of mutations in genes that cause eye diseases

Shinsei Minoshima, Susumu Mitsuyama, Masafumi Ohtsubo, 2010, Human mutation.

Erratum: The DNA sequence of human chromosome 21: The chromosome 21 mapping and sequencing consortium (Nature (2000) 405 (311-319))

Shinsei Minoshima, Susumu Mitsuyama, Yoshiyuki Sakaki, 2000 .

A cluster of 21 keratin-associated protein genes within introns of another gene on human chromosome 21q22.3.

Shinsei Minoshima, Kazunori Shibuya, Shuichi Asakawa, 2004, Genomics.

Positional cloning of the APECED gene

Shinsei Minoshima, Stylianos E. Antonarakis, Hamish S. Scott, 1997, Nature Genetics.

Identification of eight members of the Argonaute family in the human genome.

Shinsei Minoshima, S. Minoshima, A. Shiohama, 2003, Genomics.

Two Novel Mutations in the EYS Gene Are Possible Major Causes of Autosomal Recessive Retinitis Pigmentosa in the Japanese Population

Shinsei Minoshima, Miho Sato, Tadashi Yokoi, 2012, PloS one.

Insertion of β-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafness

Shinsei Minoshima, Stylianos E. Antonarakis, Kazunori Shibuya, 2001, Nature Genetics.

Mutation View: A Distributed Database for Human Disease Gene Mutations

Shinsei Minoshima, Susumu Mitsuyama, Saho Ohno, 1997 .

Elevated Transcription Factor Specificity Protein 1 in Autistic Brains Alters the Expression of Autism Candidate Genes

Shinsei Minoshima, Masafumi Ohtsubo, Hideo Matsuzaki, 2012, Biological Psychiatry.