S. Asakawa

发表

Melanie E. Goward, Antony V. Cox, R. Durbin, 1999, Nature.

Isolation of cDNA for a novel human protein KNP-I that is homologous to the E. coli SCRP-27A protein from the autoimmune polyglandular disease type I (APECED) region of chromosome 21q22.3.

N. Shimizu, K. Kawasaki, S. Minoshima, 1996, Biochemical and biophysical research communications.

Parkin Mutations (Park 2)

S. Minoshima, N. Shimizu, N. Hattori, 2003 .

COH1 analysis and linkage study in two Japanese families with Cohen syndrome

N. Shimizu, S. Asakawa, Y. Tabara, 2005, Clinical genetics.

Genomic organization of the OS-9 gene amplified in human sarcomas.

N. Shimizu, S. Asakawa, M. Yamada, 1997, Journal of biochemistry.

Mapping of the human HPC-1/syntaxin 1A gene (STX1A) to chromosome 7 band q11.2.

K. Mikoshiba, S. Asakawa, K. Akagawa, 1997, Genomics.

Point mutations (Thr240Arg and Gln311Stop) [correction of Thr240Arg and Ala311Stop] in the Parkin gene.

A. Brookes, S. Minoshima, N. Shimizu, 1998, Biochemical and biophysical research communications.

Organization of the gene for gelatin-binding protein (GBP28).

N. Shimizu, S. Minoshima, S. Asakawa, 1999, Gene.

Positional cloning of the autosomal recessive juvenile parkinsonism (AR-JP) gene and its diversity in deletion mutations.

S. Minoshima, N. Shimizu, N. Hattori, 1999, Parkinsonism & related disorders.

Chromosomal mapping of a family of human glutamine synthetase genes: functional gene (GLUL) on 1q25, pseudogene (GLULP) on 9p13, and three related genes (GLULL1, GLULL2, GLULL3) on 5q33, 11p15, and 11q24.

N. Shimizu, S. Minoshima, S. Asakawa, 1996, Genomics.

The gene for death agonist BID maps to the region of human 22q11.2 duplicated in cat eye syndrome chromosomes and to mouse chromosome 6.

B. Birren, N. Shimizu, S. Minoshima, 1998, Genomics.

Evolutionary dynamics of the human immunoglobulin kappa locus and the germline repertoire of the Vkappa genes.

N. Shimizu, K. Kawasaki, S. Minoshima, 2001, European journal of immunology.

A 2-Mb sequence-ready contig map and a novel immunoglobulin superfamily gene IGSF4 in the LOH region of chromosome 11q23.2.

M. Hattori, A. Tanigami, Y. Sakaki, 1999, Genomics.

Human biotin-containing subunit of 3-methylcrotonyl-CoA carboxylase gene (MCCA): cDNA sequence, genomic organization, localization to chromosomal band 3q27, and expression.

N. Shimizu, K. Ihara, S. Asakawa, 2001, Genomics.

Molecular cloning of a novel putative Ca2+ channel protein (TRPC7) highly expressed in brain.

N. Shimizu, K. Kawasaki, S. Minoshima, 1998, Genomics.

The DNA sequence of human chromosome 21

M. Hattori, T. Takagi, Y. Sakaki, 2000, Nature.

A 3-Mb sequence-ready contig map encompassing the multiple disease gene cluster on chromosome 11q13.1-q13.3.

N. Shimizu, F. Hosoda, S. Asakawa, 1997, DNA research : an international journal for rapid publication of reports on genes and genomes.

A 1.5-Mb contig within the cat eye syndrome critical region at human chromosome 22q11.2.

B. Roe, N. Shimizu, S. Minoshima, 1999, Genomics.

Genomic organization, chromosomal localization, and the complete 22 kb DNA sequence of the human GCMa/GCM1, a placenta-specific transcription factor gene.

N. Shimizu, S. Asakawa, G. Tamiya, 2000, Biochemical and biophysical research communications.

Cloning of the cDNA for a new member of the immunoglobulin superfamily (ISLR) containing leucine-rich repeat (LRR).

S Minoshima, Y Mashima, N. Shimizu, 1997, Genomics.

High-fidelity digital hybridization screening.

N. Shimizu, S. Asakawa, 1998, Genomics.

Human BAC library: construction and rapid screening.

N. Shimizu, K. Kawasaki, S. Minoshima, 1997, Gene.

The organization of the human immunoglobulin lambda gene locus.

P. D. de Jong, N. Shimizu, K. Kawasaki, 1995, Genome research.

Wpkci, encoding an altered form of PKCI, is conserved widely on the avian W chromosome and expressed in early female embryos: implication of its role in female sex determination.

N. Shimizu, T. Hori, S. Asakawa, 2000, Molecular biology of the cell.

The medaka genome: why we need multiple fish models in vertebrate functional genomics.

N. Shimizu, T. Todo, T. Sasaki, 2006, Genome dynamics.

Isolation and characterization of a human chromosome 21q22.3 gene (WDR4) and its mouse homologue that code for a WD-repeat protein.

S Minoshima, S. Antonarakis, N. Shimizu, 2000, Genomics.

Detailed deletion mapping of chromosome band 14q32 in human neuroblastoma defines a 1.1-Mb region of common allelic loss

N. Shimizu, S. Asakawa, Y. Kaneko, 2000, British Journal of Cancer.

Genomic organization and complete nucleotide sequence of the TMEM1 gene on human chromosome 21q22.3.

N. Shimizu, K. Kawasaki, S. Minoshima, 1997, Biochemical and biophysical research communications.

Localization of 16 exons to a 450-kb region involved in the autoimmune polyglandular disease type I (APECED) on human chromosome 21q22.3.

N. Shimizu, K. Kawasaki, S. Minoshima, 1997, DNA research : an international journal for rapid publication of reports on genes and genomes.

Isolation of two novel genes, DSCR5 and DSCR6, from Down syndrome critical region on human chromosome 21q22.2.

N. Shimizu, K. Kawasaki, S. Minoshima, 2000, Biochemical and biophysical research communications.

Progress in the clinical and molecular genetics of familial parkinsonism

S. Minoshima, N. Shimizu, N. Hattori, 2000, Neurogenetics.

A novel myosin-like protein (myocilin) expressed in the connecting cilium of the photoreceptor: molecular cloning, tissue expression, and chromosomal mapping.

S Minoshima, Y Mashima, N. Shimizu, 1997, Genomics.

Isolation and characterization of the plasma hyaluronan-binding protein (PHBP) gene (HABP2).

N. Shimizu, S. Minoshima, S. Asakawa, 1997, Journal of biochemistry.

The genomic structure and promoter region of the human parkin gene.

A. Mungall, S. Beck, N. Shimizu, 2001, Biochemical and biophysical research communications.

Human retina-specific amine oxidase (RAO): cDNA cloning, tissue expression, and chromosomal mapping.

Y Mashima, N. Shimizu, S. Asakawa, 1997, Genomics.

Cloning and characterization of a putative human glycerol 3-phosphate permease gene (SLC37A1 or G3PP) on 21q22.3: mutation analysis in two candidate phenotypes, DFNB10 and a glycerol kinase deficiency.

S. Antonarakis, N. Shimizu, K. Kawasaki, 2000, Genomics.

Refined localization of autosomal recessive nonsyndromic deafness DFNB10 locus using 34 novel microsatellite markers, genomic structure, and exclusion of six known genes in the region.

S. Antonarakis, N. Shimizu, K. Kawasaki, 2000, Genomics.

Efficient selection of genomic clones from a female chicken bacterial artificial chromosome library by four-dimensional polymerase chain reactions.

N. Shimizu, T. Hori, S. Asakawa, 2002, Poultry science.

Familial Parkinson's disease. Alpha-synuclein and parkin.

S. Minoshima, N. Shimizu, N. Hattori, 2001, Advances in neurology.

Genomic organization of the human myocilin gene (MYOC) responsible for primary open angle glaucoma (GLC1A).

S Minoshima, Y Mashima, N. Shimizu, 1998, Biochemical and biophysical research communications.

Characterization and chromosomal mapping of a novel human gene, ANKHZN.

N. Shimizu, S. Minoshima, S. Asakawa, 2000, Gene.

Structure and chromosome mapping of the human SIX4 and murine Six4 genes

N. Shimizu, S. Minoshima, M. Kajitani, 1999, Cytogenetic and Genome Research.

Genomic organization and complete nucleotide sequence of the human PWP2 gene on chromosome 21.

N. Shimizu, K. Kawasaki, S. Minoshima, 1997, Genomics.