H. Wada

发表

Multiple functional involvement of Thymosin beta-4 in tooth germ development

H. Yamaza, K. Nagata, K. Nonaka, 2013, Histochemistry and Cell Biology.

Oxidative stress caused by a low concentration of hydrogen peroxide induces senescence-like changes in mouse gingival fibroblasts

K. Nagata, Yukiko F. Ookuma, T. Kiyoshima, 2012, International journal of molecular medicine.

Enhanced Nogo-P3 amplitudes of mothers compared with non-mother women during an emotional Go/Nogo task

Sung-Phil Kim, S. Higuchi, Y. Motomura, 2018, Journal of Physiological Anthropology.

Estimation of prognosis of tongue cancer using tumor depth and margin shape obtained from ultrasonography

K. Yoshiura, H. Wada, Sitti Fadhillah Oemar Mattalitti, 2016, Oral Radiology.

Nonsense mutation of the alpha-actinin-3 gene is not associated with dystrophinopathy.

Y. Takeshima, M. Matsuo, H. Wada, 2000, American journal of medical genetics.

Alteration of p16 and p15 genes in human uterine tumours

K. Wakasa, M. Inoue, T. Enomoto, 1999, British Journal of Cancer.

Type II/III Runx2/Cbfa1 is required for tooth germ development.

K. Koyano, K. Matsuo, K. Nonaka, 2006, Bone.

Facioscapulohumeral muscular dystrophy (FSHD) region gene 1 (FRG1) expression and possible function in mouse tooth germ development

K. Nagata, T. Kiyoshima, H. Wada, 2016, Journal of Molecular Histology.

Thymosin beta 4 is associated with RUNX2 expression through the Smad and Akt signaling pathways in mouse dental epithelial cells

K. Koyano, K. Nagata, T. Kiyoshima, 2015, International journal of molecular medicine.

Protogenin, a new member of the immunoglobulin superfamily, is implicated in the development of the mouse lower first molar

H. Yamaza, Keiko Takahashi, K. Nagata, 2010, BMC Developmental Biology.

Possible functional involvement of thymosin beta 4 in developing tooth germ of mouse lower first molar

H. Yamaza, K. Matsuo, T. Kiyoshima, 2005, Histochemistry and Cell Biology.

STAT3 signal transduction through interleukin-22 in oral squamous cell carcinoma

K. Nagata, Seiji Nakamura, S. Ozeki, 2012, International journal of oncology.

Molecular evidence that most but not all carcinosarcomas of the uterus are combination tumors.

K. Shroyer, K. Wakasa, T. Hongyo, 1997, Cancer research.

Glucose, free fatty acid and ketone body metabolism in duchenne muscular dystrophy

H. Nishio, M. Matsuo, H. Wada, 1990, Brain and Development.

Mutational analysis of the PTEN gene in endometrial carcinoma and hyperplasia.

T Nakamura, T. Enomoto, Takafumi Nakamura, 2001, American journal of clinical pathology.

Induction of dental epithelial cell differentiation marker gene expression in non-odontogenic human keratinocytes by transfection with thymosin beta 4.

K. Nagata, Yukiko F. Ookuma, T. Kiyoshima, 2014, Stem cell research.

Detection of differentially expressed genes in the early developmental stage of the mouse mandible.

H. Yamaza, K. Matsuo, N. Shigemura, 2001, The International journal of developmental biology.

Mutations in the STK11 Gene Characterize Minimal Deviation Adenocarcinoma of the Uterine Cervix

T. Enomoto, I. Konishi, T. Toki, 2003, Laboratory Investigation.

Intraperitoneal administration of phosphorothioate antisense oligodeoxynucleotide against splicing enhancer sequence induced exon skipping in dystrophin mRNA expressed in mdx skeletal muscle

Y. Takeshima, M. Matsuo, M. Yagi, 2005, Brain and Development.

Itm2a Expression in the Developing Mouse First Lower Molar, and the Subcellular Localization of Itm2a in Mouse Dental Epithelial Cells

K. Nagata, T. Kiyoshima, H. Wada, 2014, PloS one.

Local application of statin promotes bone repair through the suppression of osteoclasts and the enhancement of osteoblasts at bone-healing sites in rats.

K. Koyano, Y. Ayukawa, Y. Ogino, 2009, Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics.

Analysis of dystrophin mRNA from skeletal muscle but not from lymphocytes led to identification of a novel nonsense mutation in a carrier of Duchenne muscular dystrophy

Y. Takeshima, M. Matsuo, M. Yagi, 2003, Journal of Neurology.

FHIT alterations in cancerous and non‐cancerous cervical epithelium

T. Enomoto, Takafumi Nakamura, Yoh Watanabe, 2000, International journal of cancer.

Aberrant FHIT transcripts in squamous cell carcinoma of the uterine cervix

T. Enomoto, Takafumi Nakamura, K. Noda, 1998, International journal of cancer.

Expression of Set-α during Morphogenesis of Mouse Lower First Molar

A. Akamine, H. Yamaza, K. Matsuo, 2001, The Histochemical Journal.

Decreased expression of full‐length mRNA for cBCD541 does not correlate with spinal muscular atrophy phenotype severity

Y. Takeshima, H. Nishio, M. Matsuo, 1997, Neurology.

K-ras mutations appear in the premalignant phase of both microsatellite stable and unstable endometrial carcinogenesis.

T. Enomoto, G. Mutter, W. Faquin, 1999, Molecular pathology : MP.

Carcinosarcoma of the breast: molecular-biological study for analysis of histogenesis.

K. Shroyer, T. Enomoto, H. Wada, 1998, Human pathology.

Somatic mosaicism of a CDKL5 mutation identified by next-generation sequencing

T. Nakagawa, K. Nozu, K. Iijima, 2015, Brain and Development.

Application of clonal analysis. Differential diagnosis for synchronous primary ovarian and endometrial cancers and metastatic cancer.

K. Shroyer, M. Inoue, T. Enomoto, 1996, American journal of clinical pathology.

Molecular genetics of spinal muscular atrophy: contribution of the NAIP gene to clinical severity.

T. Akutsu, Y. Takeshima, H. Nishio, 2002, The Kobe journal of medical sciences.

Hybrid survival motor neuron genes in Japanese patients with spinal muscular atrophy

Y. Takeshima, H. Nishio, M. Matsuo, 1999, Acta Neurologica Scandinavica.

High incidence of a survival motor neuron gene/cBCD541 gene ratio of 2 in Japanese parents of spinal muscular atrophy patients: a characteristic background of spinal muscular atrophy in Japan?

Y. Takeshima, H. Nishio, M. Matsuo, 1999, Journal of Neurology.

Intravenous Infusion of an Antisense Oligonucleotide Results in Exon Skipping in Muscle Dystrophin mRNA of Duchenne Muscular Dystrophy

Y. Takeshima, M. Matsuo, T. Sakaeda, 2006, Pediatric Research.

A G-to-A transition at the fifth position of intron-32 of the dystrophin gene inactivates a splice-donor site both in vivo and in vitro.

Y. Takeshima, M. Matsuo, M. Yagi, 2005, Molecular genetics and metabolism.

Vascular involvement in benign infantile mitochondrial myopathy caused by reversible cytochrome c oxidase deficiency

C. Ohbayashi, H. Nishio, M. Matsuo, 1996, Brain and Development.

Heterogous Dystrophin mRNA Produced by a Novel Splice Acceptor Site Mutation in Intermediate Dystrophinopathy

Y. Takeshima, M. Matsuo, M. Yagi, 2003, Pediatric Research.

Complete skipping of exon 66 due to novel mutations of the dystrophin gene was identified in two Japanese families of Duchenne muscular dystrophy with severe mental retardation

Y. Takeshima, M. Matsuo, A. Surono, 2000, Brain and Development.

Oligonucleotides against a splicing enhancer sequence led to dystrophin production in muscle cells from a Duchenne muscular dystrophy patient

Y. Takeshima, M. Matsuo, M. Yagi, 2001, Brain and Development.

In Situ Expression of Heat Shock Proteins, Hsc73, Hsj2 and Hsp86 in the Developing Tooth Germ of Mouse Lower First Molar

K. Koyano, H. Yamaza, K. Matsuo, 2002, The Histochemical Journal.

Chemoresistance to Concanamycin A1 in Human Oral Squamous Cell Carcinoma Is Attenuated by an HDAC Inhibitor Partly via Suppression of Bcl-2 Expression

K. Nagata, T. Kiyoshima, H. Wada, 2013, PloS one.

Multiple functional involvement of Thymosin beta-4 in tooth germ development

H. Yamaza, K. Nagata, K. Nonaka, 2013, Histochemistry and Cell Biology.

Severe neonatal nemaline myopathy with delayed maturation of muscle

H. Nishio, M. Matsuo, M. Kugo, 1996, Brain and Development.

Alteration of p16 and p15 genes in common epithelial ovarian tumors

T. Enomoto, G. Buzard, T. Haba, 1997, International journal of cancer.

Localization of Activated Caspase-3-positive and Apoptotic Cells in the Developing Tooth Germ of the Mouse Lower First Molar

A. Akamine, H. Yamaza, K. Matsuo, 2004, The Histochemical Journal.

A Novel Point Mutation (G' to T) in a 5' Splice Donor Site of Intron 13 of the Dystrophin Gene Results in Exon Skipping and Is Responsible for Becker Muscular Dystrophy

Y. Takeshima, H. Nishio, H. Wada, 2007 .

A case of liver cirrhosis associated with multiple necrotic nodules in the liver after the hepatic hydrothorax

T. Kiyoshima, H. Wada, H. Fujiwara, 2013 .

Immunohistochemical localization of telomerase hTERT protein and analysis of clonality in multifocal vulvar intraepithelial neoplasia.

K. Shroyer, T. Enomoto, H. Kurachi, 2000, American journal of clinical pathology.

The TRPV4-AKT axis promotes oral squamous cell carcinoma cell proliferation via CaMKII activation

S. Ozeki, M. Kido, T. Kiyoshima, 2019, Laboratory Investigation.

GLI-mediated Keratin 17 expression promotes tumor cell growth through the anti-apoptotic function in oral squamous cell carcinomas

K. Nagata, Seiji Nakamura, T. Kiyoshima, 2017, Journal of Cancer Research and Clinical Oncology.

Chimeric RNA/ethylene-bridged nucleic acids promote dystrophin expression in myocytes of duchenne muscular dystrophy by inducing skipping of the nonsense mutation-encoding exon.

Y. Takeshima, M. Matsuo, M. Yagi, 2004, Human gene therapy.

Two alternative exons can result from activation of the cryptic splice acceptor site deep within intron 2 of the dystrophin gene in a patient with as yet asymptomatic dystrophinopathy

Y. Takeshima, M. Matsuo, M. Yagi, 2003, Human Genetics.

Correlation between SMN2 copy number and clinical phenotype of spinal muscular atrophy: three SMN2 copies fail to rescue some patients from the disease severity

R. Sutomo, T. Akutsu, Y. Takeshima, 2002, Journal of Neurology.

In situ expression of 15 kDa interferon alpha responsive gene in the developing tooth germ of the mouse lower first molar

K. Nagata, Yukiko F. Ookuma, T. Kiyoshima, 2010, Journal of Molecular Histology.

A novel point mutation (G-1 to T) in a 5' splice donor site of intron 13 of the dystrophin gene results in exon skipping and is responsible for Becker muscular dystrophy.

Y. Takeshima, H. Nishio, M. Matsuo, 1994, American journal of human genetics.

Cardiac involvement in a family with Becker muscular dystrophy.

H. Nishio, M. Matsuo, Y. Yokota, 1995, Internal medicine.

C-Terminal Truncated Dystrophin Identified in Skeletal Muscle of an Asymptomatic Boy with a Novel Nonsense Mutation of the Dystrophin Gene

Y. Takeshima, M. Matsuo, M. Yagi, 2004, Pediatric Research.

Amino‐terminal deletion of 53% of dystrophin results in an intermediate Duchenne‐Becker muscular dystrophy phenotype

Y. Takeshima, H. Nishio, M. Matsuo, 1994, Neurology.

In situ expression of the mitochondrial ATPase6 gene in the developing tooth germ of the mouse lower first molar

K. Nagata, Yukiko F. Ookuma, T. Kiyoshima, 2011, Journal of Molecular Histology.

Clonal analysis of high‐grade squamous intra‐epithelial lesions of the uterine cervix

K. Shroyer, T. Enomoto, H. Kurachi, 1997, International journal of cancer.

Two patients with PNKP mutations presenting with microcephaly, seizure, and oculomotor apraxia

H. Kurahashi, H. Nishio, N. Okamoto, 2018, Clinical genetics.

Accelerated dentinogenesis by inhibiting the mitochondrial fission factor, dynamin related protein 1.

H. Yamaza, K. Nonaka, H. Kato, 2018, Biochemical and biophysical research communications.

The Semaphorin 3A-AKT axis-mediated cell proliferation in salivary gland morphogenesis and adenoid cystic carcinoma pathogenesis.

T. Kiyoshima, H. Wada, K. Kurppa, 2022, Pathology, research and practice.

Enhanced Nogo-P3 amplitudes of mothers compared with non-mother women during an emotional Go/Nogo task

Sung-Phil Kim, S. Higuchi, Y. Motomura, 2018, Journal of Physiological Anthropology.

Estimation of prognosis of tongue cancer using tumor depth and margin shape obtained from ultrasonography

K. Yoshiura, H. Wada, Sitti Fadhillah Oemar Mattalitti, 2017, Oral Radiology.

The expression and function of thymosin beta 10 in tooth germ development.

K. Nagata, T. Kiyoshima, H. Wada, 2013, The International journal of developmental biology.

Facioscapulohumeral muscular dystrophy (FSHD) region gene 1 (FRG1) expression and possible function in mouse tooth germ development

K. Nagata, T. Kiyoshima, H. Wada, 2016, Journal of Molecular Histology.

The von-Hippel-Lindau (VHL) tumor suppressor gene is not mutated in sporadic ovarian carcinomas.

T. Enomoto, M. Yao, K. Yoshino, 1996, Oncology reports.

Preventive effects of dexamethasone on hypoxic-ischemic brain damage in the neonatal rat

H. Wada, S. Takada, H. Itoh, 1995, Brain and Development.

K-ras mutations appear in the premalignant phase of both microsatellite stable and unstable endometrial carcinogenesis.

T. Enomoto, G. Mutter, W. Faquin, 1999, Molecular pathology : MP.