A. Kuwano

发表

Human ubiquitin‐protein ligase Nedd4: expression, subcellular localization and selective interaction with ubiquitin‐conjugating enzymes

M. Nakao, H. Saya, H. Koga, 1998, Genes to cells : devoted to molecular & cellular mechanisms.

Microdeletions of chromosome 17p13 as a cause of isolated lissencephaly.

D. Ledbetter, W. Dobyns, A. Kuwano, 1992, American journal of human genetics.

Detection of deletions and cryptic translocations in Miller-Dieker syndrome by in situ hybridization.

D. Ledbetter, B. Emanuel, W. Dobyns, 1991, American journal of human genetics.

Midkine gene (MDK), a gene for prenatal differentiation and neuroregulation, maps to band 11p11.2 by fluorescence in situ hybridization.

A. Kuwano, T. Muramatsu, T. Kaname, 1993, Genomics.

Evidence that poor metabolizers of (S)-mephenytoin could be identified by haplotypes of CYP2C19 in Japanese.

A. Kuwano, I. Kondo, F. Takakubo, 1996, Pharmacogenetics.

Mapping basigin (BSG), a member of the immunoglobulin superfamily, to 19p13.3.

A. Kuwano, T. Muramatsu, T. Kaname, 1993, Cytogenetics and cell genetics.

Dinucleotide repeat polymorphism at the GABAA receptor β3 (GABRB3) locus in the Angelman/Prader— Willi region (AS/PWS) of chromosome 15

D. Ledbetter, A. C. Chinault, A. Kuwano, 1992 .

Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11–13) by YAC cloning and FISH analysis

D. Ledbetter, A. C. Chinault, N. Niikawa, 1992 .

Dinucleotide repeat polymorphism at the D15S11 locus in the Angelman/Prader-Willi region (AS/PWS) of chromosome 15.

D. Ledbetter, A. C. Chinault, A. Kuwano, 1992, Human molecular genetics.

Isolation, Characterization, and Chromosomal Mapping of the Human Insulin Promoter Factor 1 (IPF-1) Gene

M. Permutt, A. Kuwano, H. Donis-Keller, 1996, Diabetes.

Benign adult familial myoclonus epilepsy (BAFME): an autosomal dominant form not linked to the dentatorubral pallidoluysian atrophy (DRPLA) gene.

A. Kuwano, I. Kondo, M. Uchino, 1996, Journal of medical genetics.

N‐myc oncogene and stage iv‐s neuroblastoma preliminary observations on ten cases

T. Sasazuki, A. Nakagawara, A. Kuwano, 1990, Cancer.

Mapping of the human gene for inducible heme oxygenase to chromosome 22q12.

S. Shibahara, A. Kuwano, H. Nakai, 1994, The Tohoku journal of experimental medicine.

Molecular cloning and gene mapping of human basic and acidic calponins.

K. Kohara, A. Kuwano, K. Hiwada, 1995, Biochemical and biophysical research communications.

Translocation t(X;21)(q13.3; p11.1) in a girl with Menkes disease.

N. Niikawa, A. Kuwano, K. Yamada, 1998, American journal of medical genetics.

Efficacy of feed additive sulfamonomethoxine and ormetoprim against chicken infectious coryza : a case study

A. Kuwano, Masahiro Kato, K. Nakamura, 1991 .

Production of biologically active recombinant bovine interferon-gamma by two different baculovirus gene expression systems using insect cells and silkworm larvae.

T. Yada, A. Kuwano, Y. Mori, 2001, Cytokine.

Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-13) by YAC cloning and FISH analysis.

N. Niikawa, A. Chinault, S. Saitoh, 1992, Human molecular genetics.

A human pancreatic islet inwardly rectifying potassium channel: cDNA cloning, determination of the genomic structure and genetic variations in Japanese NIDDM patients

M. Permutt, A. Kuwano, H. Katagiri, 1996, Diabetologia.

Isochromosome 15q of maternal origin in two Prader-Willi syndrome patients previously diagnosed erroneously as cytogenetic deletions.

D. Ledbetter, N. Niikawa, S. Saitoh, 1994, American journal of medical genetics.

Fibroblast-specific common fragile sites induced by aphidicolin

A. Kuwano, T. Kajii, I. Murano, 1989, Human Genetics.

Gene dosage is a mechanism for Charcot-Marie-Tooth disease type 1A

D. Ledbetter, J. Lupski, P. Patel, 1992, Nature Genetics.

Mosaicism for del(17)(p11.2p11.2) underlying the Smith-Magenis syndrome.

P. Patel, A. Baldini, F. Zara, 1996, American journal of medical genetics.

Congenital heart defects in Sotos sequence.

J. Opitz, A. Kuwano, H. Kurashige, 1987, American journal of medical genetics.

Replication patterns of the fragile X in heterozygous carriers: analysis by a BrdUrd antibody method.

T. Arinami, A. Kuwano, H. Ohashi, 1990, American journal of human genetics.

Cloning and characterization of NE-dlg: a novel human homolog of the Drosophila discs large (dlg) tumor suppressor protein interacts with the APC protein

K. Makino, M. Nakao, H. Saya, 1997, Oncogene.

Possible mapping of the gene for transient myeloproliferative syndrome at 21q11.2

Y. Fukushima, N. Niikawa, Y. Kaneko, 1991, Human Genetics.

Dentatorubral-pallidoluysian atrophy (DRPLA): clinical, genetic, and neuroradiologic studies in a family

A. Kuwano, I. Kondo, M. Uchino, 1995, Journal of the Neurological Sciences.

Association analysis of a polymorphism of the monoamine oxidase B gene with Parkinson's disease in a Japanese population.

A. Kuwano, Y. Mizuno, N. Murayama, 1995, American journal of medical genetics.

Precise chromosomal locations of the genes for dentatorubral-pallidoluysian atrophy (DRPLA), von Willebrand factor (F8vWF) and parathyroid hormone-like hormone (PTHLH) in human chromosome 12p by deletion mapping

Y. Fukushima, A. Kuwano, H. Ohashi, 2004, Human Genetics.

High-resolution banding in chromosomes of B lymphoblastoid cells and cultured skin fibroblasts.

A. Kuwano, T. Kajii, 1991, Cytogenetics and cell genetics.

Inverted insertion (9)(q34.3q22.3q21.2) and its recombination product: Duplication 9q21.2q22.3

S. Matsuura, A. Kuwano, T. Kajii, 1987, Japanese Journal of Human Genetics.

Cell type-dependent difference in the distribution and frequency of aphidicolin-induced fragile sites: T and B lymphocytes and bone marrow cells

A. Kuwano, T. Kajii, I. Murano, 1989, Human Genetics.

Telomere association of human chromosomes induced by aphidicolin.

S. Matsuura, A. Kuwano, T. Kajii, 1992, Mutation research.

Serological diagnosis of equine influenza using the hemagglutinin protein produced in a baculovirus expression system.

A. Kuwano, T. Kanaya, H. Imagawa, 2001, Journal of virological methods.

Hemizygosity at the elastin locus and clinical features of Williams syndrome

A. Kuwano, K. Kuwajima, Y. Morimoto, 1994 .

Common fragile sites induced by folate deprivation, BrdU and aphidicolin: Their frequency and distribution in Japanese individuals

A. Kuwano, T. Kajii, I. Murano, 1988, The Japanese Journal of Human Genetics.

Cell type-dependent difference in the distribution and frequency of excess thymidine-induced common fragile sites: T lymphocytes and skin fibroblasts

A. Kuwano, T. Kajii, I. Murano, 1990, Human Genetics.

Comparison of the inhibitory effect of sulfamonomethoxine and other sulfonamides on capsule formation of Bordetella bronchiseptica.

A. Kuwano, T. Ito, H. Tachi, 1992, Journal of Veterinary Medical Science.

Synergistic effect of aphidicolin and ethanol on the induction of common fragile sites

A. Kuwano, T. Kajii, 1987, Human Genetics.