A. Iwaki

发表

Sense and antisense modification of glial alpha B-crystallin production results in alterations of stress fiber formation and thermoresistance

T. Iwaki, J. Goldman, J. Tateishi, 1994, The Journal of cell biology.

αB-Crystallin in C6 glioma cells supports their survival in elevated extracellular K+: the implication of a protective role of αB-crystallin accumulation in reactive glia

T. Iwaki, Y. Fukumaki, J. Tateishi, 1995, Brain Research.

Multiple mRNAs of rat brain alpha-crystallin B chain result from alternative transcriptional initiation.

T. Iwaki, R. Liem, J. Goldman, 1990, The Journal of biological chemistry.

AlphaB-crystallin protects glial cells from hypertonic stress.

T. Iwaki, J. Goldman, K. Kegel, 1996, The American journal of physiology.

Amphiphysin I but not dynamin I nor synaptojanin mRNA expression increased after repeated methamphetamine administration in the rat cerebrum and cerebellum

Y. Fukumaki, H. Ozawa, A. Iwaki, 2013, Journal of Neural Transmission.

Identification and Characterization of the Gene Encoding a New Member of the α-Crystallin/Small hsp Family, Closely Linked to the αB-Crystallin Gene in a Head-to-Head Manner

T. Iwaki, Y. Fukumaki, A. Iwaki, 1997 .

An autopsied case of sporadic adult‐onset amyotrophic lateral sclerosis with FUS‐positive basophilic inclusions

Satoshi O. Suzuki, T. Iwaki, H. Honda, 2011, Neuropathology : official journal of the Japanese Society of Neuropathology.

Rosenthal fibers share epitopes with alpha B-crystallin, glial fibrillary acidic protein, and ubiquitin, but not with vimentin. Immunoelectron microscopy with colloidal gold.

T. Iwaki, J. Goldman, J. Tateishi, 1991, The American journal of pathology.

The contactin 4 gene locus at 3p26 is a candidate gene of SCA16

J. Kira, T. Taniwaki, H. Shibata, 2006, Neurology.

Alpha B-crystallin in C6 glioma cells supports their survival in elevated extracellular K+: the implication of a protective role of alpha B-crystallin accumulation in reactive glia.

Y. Fukumaki, J. Tateishi, A. Iwaki, 1995, Brain research.

Alpha B-crystallin and 27-kd heat shock protein are regulated by stress conditions in the central nervous system and accumulate in Rosenthal fibers.

Y. Sakaki, T. Iwaki, J. Goldman, 1993, The American journal of pathology.

Accumulation of αB-crystallin in brains of patients with Alexander's disease is not due to an abnormality of the 5′-flanking and coding sequence of the genomic DNA

Y. Sakaki, T. Iwaki, J. Goldman, 1992, Neuroscience Letters.

Accumulation of alpha B-crystallin in central nervous system glia and neurons in pathologic conditions.

T. Wisniewski, T. Iwaki, J. Goldman, 1992, The American journal of pathology.

Multiple system degeneration with basophilic inclusions in Japanese ALS patients with FUS mutation

T. Iwaki, J. Kira, N. Nukina, 2010, Acta Neuropathologica.

FALS with FUS mutation in Japan, with early onset, rapid progress and basophilic inclusion

Y. Itoyama, H. Konno, N. Suzuki, 2010, Journal of Human Genetics.

FALS with FUS mutation in Japan, with early onset, rapid progress and basophilic inclusion

Y. Itoyama, H. Konno, N. Suzuki, 2010, Journal of Human Genetics.

Opposite Effects of Cyclic AMP and Cell Density on Expression of αB-Crystallin and Glial Fibrillary Acidic Protein in C-6 Glioma Cells

Y. Sakaki, T. Iwaki, R. Liem, 1991 .

αB-crystallin in oxidative muscle fibers and its accumulation in ragged-red fibers: a comparative immunohistochemical and histochemical study in human skeletal muscle

T. Iwaki, J. Goldman, A. Iwaki, 1993, Acta Neuropathologica.

Hereditary motor and sensory neuropathy with proximal dominancy in the lower extremities, urinary disturbance, and paroxysmal dry cough

T. Taniwaki, H. Aizawa, Y. Fukumaki, 2008, Journal of the Neurological Sciences.

Expression of αB-crystallin in the developing rat kidney

T. Iwaki, R. Liem, J. Goldman, 1991 .

Autopsy case of autosomal recessive hereditary spastic paraplegia with reference to the muscular pathology

T. Iwaki, A. Iwaki, Y. Tsuruta, 2001, Neuropathology : official journal of the Japanese Society of Neuropathology.

Cloning and characterization of the 5'-flanking region of the human dopamine D4 receptor gene.

Y. Fukumaki, S. Kamakura, M. Matsumoto, 1997, Biochemical and biophysical research communications.

Epidemiological, clinical, and genetic landscapes of hypomyelinating leukodystrophies

Leo Gotoh, H. Osaka, Toshiyuki Yamamoto, 2014, Journal of Neurology.

Heterozygous deletion of ITPR1, but not SUMF1, in spinocerebellar ataxia type 16

H Furuya, Wei Li, J. Kira, 2007, Journal of Medical Genetics.

A novel expression system for artificial miRNAs containing no endogenous miRNA precursor sequences

Y. Fukumaki, Atsushi Shibata, A. Iwaki, 2007, Journal of RNAi and gene silencing : an international journal of RNA and gene targeting research.

Comprehensive behavioral study of mGluR3 knockout mice: implication in schizophrenia related endophenotypes

I. Ito, T. Miyakawa, Y. Fukumaki, 2014, Molecular Brain.

Comprehensive behavioural study of GluR4 knockout mice: implication in cognitive function

H. Sugiyama, I. Ito, T. Tsuzuki, 2010, Genes, brain, and behavior.

Clinical and genetic characterization of a 2-year-old boy with complete PLP1 deletion

A. Hiwatashi, T. Hara, K. Takeshita, 2012, Brain and Development.

Preferential expression of αB‐crystallin in astrocytic elements of neuroectodermal tumors

J. Goldman, M. Miyazono, A. Iwaki, 1991 .

Comprehensive behavioral study of mGluR3 knockout mice: implication in schizophrenia related endophenotypes

I. Ito, T. Miyakawa, Y. Fukumaki, 2014, Molecular Brain.

The magnetic resonance imaging spectrum of Pelizaeus–Merzbacher disease: A multicenter study of 19 patients

K. Yokochi, H. Matsuda, J. Takanashi, 2016, Brain and Development.

An autopsy case of adult-onset hereditary spastic paraplegia type 2 with a novel mutation in exon 7 of the proteolipid protein 1 gene

Satoshi O. Suzuki, T. Iwaki, K. Arakawa, 2011, Acta Neuropathologica.

A novel PLP mutation in a Japanese patient with mild Pelizaeus-Merzbacher disease

K. Yokochi, T. Kibe, A. Iwaki, 2009, Brain and Development.

Heat shock factor 2 is involved in the upregulation of alphaB-crystallin by high extracellular potassium.

C. Sadamitsu, Y. Fukumaki, A. Iwaki, 2001, Journal of biochemistry.

Partial SPAST and DPY30 deletions in a Japanese spastic paraplegia type 4 family

T. Taniwaki, H. Aizawa, Y. Fukumaki, 2011, neurogenetics.

Preferential expression of alpha B-crystallin in astrocytic elements of neuroectodermal tumors.

J. Goldman, M. Miyazono, A. Iwaki, 1991, Cancer.

Two autopsy cases with Pelizaeus-Merzbacher disease phenotype of adult onset, without mutation of proteolipid protein gene

T. Iwaki, A. Sasaki, Y. Nakazato, 2000, Acta Neuropathologica.

Association of HSPB2, a member of the small heat shock protein family, with mitochondria.

T. Iwaki, H. Nakagawa, Y. Fukumaki, 2001, Experimental cell research.

Identification and characterization of the gene encoding a new member of the alpha-crystallin/small hsp family, closely linked to the alphaB-crystallin gene in a head-to-head manner.

T. Iwaki, Y. Fukumaki, A. Iwaki, 1997, Genomics.

A missense mutation in the proteolipid protein gene responsible for Pelizaeus-Merzbacher disease in a Japanese family.

J. Tateishi, A. Iwaki, I. Iwaki, 1993, Human molecular genetics.

Case report A novel PLP mutation in a Japanese patient with mild Pelizaeus-Merzbacher disease

K. Yokochi, T. Kibe, A. Iwaki, 2009 .

A novel insertional mutation at exon VII of the myelin proteolipid protein gene in Pelizaeus-Merzbacher disease.

Y. Kuroki, K. Kurosawa, K. Imaizumi, 1993, Human molecular genetics.

Expression of alpha B-crystallin in the developing rat kidney.

T. Iwaki, R. Liem, J. Goldman, 1991, Kidney international.

Distal Sox binding elements of the alphaB-crystallin gene show lens enhancer activity in transgenic mouse embryos.

T. Iwaki, Y. Fukumaki, N. Tsujimoto, 2004, Journal of biochemistry.

Epitope mapping and characterization of monoclonal antibodies to human protein C.

T. Matsuishi, A. Iwaki, S. Tanaka, 1993, Biochimica et biophysica acta.