H. Sasaki

发表

Genomic organization of the human-amyloid beta-protein precursor gene.

Y. Sakaki, K. Doh-ura, H. Furuya, 1990, Gene.

A Quantitative Polymerase Chain Reaction Study

Y. Itoyama, J. Kira, Y. Koyanagi, 2004 .

Unusually high conservation of untranslated sequences in cDNAs for Trimeresurus flavoviridis phospholipase A2 isozymes.

M. Hattori, Y. Sakaki, N. Oda, 1992, Proceedings of the National Academy of Sciences of the United States of America.

Structure and expression of the alternatively-spliced forms of mRNA for the mouse homolog of Alzheimer's disease amyloid beta protein precursor.

Y. Sakaki, I. Goto, H. Sasaki, 1989, Biochemical and biophysical research communications.

Mechanism of chromosomal integration of transgenes in microinjected mouse eggs: sequence analysis of genome-transgene and transgene-transgene junctions at two loci.

Y. Sakaki, T. Hamada, H. Sasaki, 1993, Gene.

Production of recombinant human transthyretin with biological activities toward the understanding of the molecular basis of familial amyloidotic polyneuropathy (FAP).

Y. Sakaki, M. Saraiva, H. Furuya, 1991, Biochemistry.

Tetramer formation of a variant type human transthyretin (prealbumin) produced by Escherichia coli expression system.

Y. Sakaki, S. Costa, M. Saraiva, 1989, Biochemical and biophysical research communications.

Pro----leu change at position 102 of prion protein is the most common but not the sole mutation related to Gerstmann-Sträussler syndrome.

Y. Sakaki, K. Doh-ura, T. Kitamoto, 1989, Biochemical and biophysical research communications.

Biochemical and genetic characterization of type I familial amyloidotic polyneuropathy

M. Nakazato, K. Kangawa, H. Matsuo, 1987, Annals of neurology.

Inherited type of allelic methylation variations in a mouse chromosome region where an integrated transgene shows methylation imprinting.

Y. Sakaki, T. Hamada, T. Ueda, 1991, Development.

Molecular analysis of a variant type of familial amyloidotic polyneuropathy showing cerebellar ataxia and pyramidal tract signs.

Y. Sakaki, N. Yanagisawa, M. Nakazato, 1987, The Journal of clinical investigation.

“Sporadic” prealbumin-related amyloid polyneuropathy: report of two cases

Y. Sakaki, J. Satoh, M. Nakazato, 2004, Journal of Neurology.

Sequence-based structural features between Kvlqt1 and Tapa1 on mouse chromosome 7F4/F5 corresponding to the Beckwith-Wiedemann syndrome region on human 11p15.5: long-stretches of unusually well conserved intronic sequences of kvlqt1 between mouse and human.

M. Hattori, Y. Sakaki, H. Watanabe, 2000, DNA research : an international journal for rapid publication of reports on genes and genomes.

Structure and Expression of mRNA for the Mouse Homolog of Alzheimer Amyloid Beta Protein Precursor

H. Furuya, I. Goto, Yoshiyuki Sasaki, 1990 .

PRESYMPTOMATIC DIAGNOSIS OF HETEROZYGOSITY FOR FAMILIAL AMYLOIDOTIC POLYNEUROPATHY BY RECOMBINANT DNA TECHNIQUES

Y. Sakaki, Y. Kuroiwa, K. Sahashi, 1985, The Lancet.

Molecular Cloning and Structural Analysis of the Human Amyloid ß Protein Precursor Gene

Y. Sakaki, H. Furuya, S. Yoshikai, 1990 .

Amyloid beta-protein gene duplication is not common in Alzheimer's disease: analysis by polymorphic restriction fragments.

Y. Sakaki, G. Glenner, C. Wong, 1988, Biochemical and biophysical research communications.

Structure of the mutant prealbumin gene responsible for familial amyloidotic polyneuropathy.

Y. Sakaki, H. Furuya, T. Harada, 1986, Molecular biology & medicine.

Diagnosis of Familial Amyloid Polyneuropathy by Recombinant DNA Techniques in Relation with Clinical Features

Y. Sakaki, S. Katayama, H. Furuya, 1988 .

Isolation and sequencing of a cDNA clone encoding 96 kDa sialoglycoprotein in rat liver lysosomal membranes.

Y. Sakaki, K. Kato, Y. Tanaka, 1989, Biochemical and biophysical research communications.

Haplotype analysis of familial amyloidotic polyneuropathy

Y. Sakaki, M. Saraiva, H. Furuya, 1989, Human Genetics.

Diagnosis of familial amyloidotic polyneuropathy by recombinant DNA techniques.

Y Sakaki, Y Kuroiwa, Y. Sakaki, 1984, Biochemical and biophysical research communications.

Positive and negative regulatory elements for the expression of the Alzheimer's disease amyloid precursor-encoding gene in mouse.

M. Hattori, Y. Sakaki, S. Yoshikai, 1992, Gene.

Generation of transgenic mice producing a human transthyretin variant: a possible mouse model for familial amyloidotic polyneuropathy.

Y. Sakaki, M. Nakazato, H. Matsuo, 1986, Biochemical and biophysical research communications.

Type I familial amyloid polyneuropathy. A pathological study of the peripheral nervous system.

Y. Sakaki, G. Sobue, A. Takahashi, 1990, Brain : a journal of neurology.

Clinical features and diagnosis by recombinant DNA techniques of familial amyloid polyneuropathy in Japan.

Y. Sakaki, F. Ishizaki, S. Katayama, 1989, Research communications in chemical pathology and pharmacology.

Complementary DNA for the mouse homolog of the human amyloid beta protein precursor.

Y. Sakaki, T. Miyata, H. Furuya, 1987, Biochemical and biophysical research communications.

Creutzfeldt‐Jakob disease patients with congophilic kuru plaques have the missense variant prion protein common to Gerstmann‐Sträussler syndrome

K. Doh-ura, T. Kitamoto, J. Tateishi, 1990, Annals of neurology.

Isolation and sequencing of a cDNA clone encoding 107 kDa sialoglycoprotein in rat liver lysosomal membranes

Y. Sakaki, H. Sasaki, M. Himeno, 1989, FEBS letters.

Expression of Alzheimer amyloid beta-protein precursor gene in neuronal cells.

Y. Sakaki, H. Sasaki, I. Goto, 1991, Gerontology.

[Familial amyloid polyneuropathy (FAP), in an inborn habitat of Hiroshima Prefecture, Japan].

Y. Sakaki, T. Harada, K. Nitta, 1986, Rinshō shinkeigaku Clinical neurology.

Structure of the chromosomal gene for human serum prealbumin.

Y. Sakaki, N. Yoshioka, H. Sasaki, 1985, Gene.

Genetic analysis of familial amyloidotic polyneuropathy, an autosomal dominant disease.

Y. Sakaki, H. Furuya, H. Sasaki, 1989, Clinica chimica acta; international journal of clinical chemistry.

DNA Polymorphisms Analysis in Families with Familial Amyloidotic Polyneuropathy (FAP) from Different Ethnic Origins

Y. Sakaki, M. Saraiva, M. R. Almeida, 1988 .

Genetic and clinical studies of Japanese patients with familial amyloid polyneuropathy.

Y. Sakaki, S. Katayama, H. Furuya, 1989, European neurology.

Cloning and sequence analysis of cDNA for Trimeresurus flavoviridis phospholipase A2, and consequent revision of the amino acid sequence.

Y. Sakaki, N. Oda, M. Ohno, 1990, Journal of biochemistry.

Human transthyretin (prealbumin) gene and molecular genetics of familial amyloidotic polyneuropathy.

Y. Sakaki, H. Furuya, H. Sasaki, 1989, Molecular biology & medicine.

A Recombinants System for Production of Variant Type Human Transthyretin(TTR)

M. Saraiva, H. Furuya, I. Goto, 1991 .

A Quantitative Polymerase Chain Reaction Study

Y. Itoyama, J. Kira, Y. Koyanagi, 2004 .

Haplotype analysis of familial amyloidotic polyneuropathy. Evidence for multiple origins of the Val----Met mutation most common to the disease.

Y. Sakaki, M. Saraiva, H. Furuya, 1989, Human genetics.