A. Watanabe

发表

Association of HLA-A*31: 01 Screening With the Incidence of Carbamazepine-Induced Cutaneous Adverse Reactions in a Japanese Population

Y. Shimo, T. Kinoshita, T. Mushiroda, 2018, JAMA neurology.

Biological effects of cellular stretch on human dermal fibroblasts.

R. Ogawa, A. Watanabe, S. Akaishi, 2013, Journal of plastic, reconstructive & aesthetic surgery : JPRAS.

Chondrogenic and osteogenic differentiation of adipose-derived stem cells isolated from GFP transgenic mice.

M. Migita, T. Shimada, R. Ogawa, 2004, Journal of Nippon Medical School = Nippon Ika Daigaku zasshi.

Successful gene therapy in utero for lethal murine hypophosphatasia.

J. Millán, M. Migita, T. Shimada, 2012, Human gene therapy.

Spectrum of mutations and genotype–phenotype analysis in Noonan syndrome patients with RIT1 mutations

O. Migita, P. Lapunzina, T. Ogata, 2016, Human Genetics.

BRAF, KIT and NRAS mutations and expression of c‐KIT, phosphorylated extracellular signal‐regulated kinase and phosphorylated AKT in Japanese melanoma patients

T. Takizawa, S. Kawana, A. Watanabe, 2015, The Journal of dermatology.

Overview of BioBank Japan follow-up data in 32 diseases

Yusuke Nakamura, Hiromu Kutsumi, Yoshio Miki, 2017, Journal of epidemiology.

The Establishment of an Ethics Consultation System in Clinical Genetics: Trial at the Nippon Medical School Main Hospital

A. Watanabe, T. Shimada, 2007 .

Vascular type of Ehlers-Danlos syndrome.

T. Shimada, A. Watanabe, 2008, Journal of Nippon Medical School = Nippon Ika Daigaku zasshi.

IL-6 Polymorphism and Susceptibility to Keloid Formation in a Japanese Population.

M. Ghazizadeh, A. Watanabe, Mamiko Tosa, 2016, The Journal of investigative dermatology.

Prevalence of c.1559delT in ALPL, a common mutation resulting in the perinatal (lethal) form of hypophosphatasia in Japanese and effects of the mutation on heterozygous carriers

S. Ikegawa, T. Shimada, A. Watanabe, 2011, Journal of Human Genetics.

Polymorphism in Organic Anion-Transporting Polypeptide Gene Related to Methotrexate Response in Rheumatoid Arthritis Treatment.

T. Majima, S. Takai, Hiroshi Nakamura, 2019, Journal of Nippon Medical School = Nippon Ika Daigaku zasshi.

Spontaneous Colon Perforations Associated with a Vascular Type of Ehlers-Danlos Syndrome

T. Shimada, A. Watanabe, H. Okubo, 2014, Case Reports in Gastroenterology.

Ehlers‐Danlos syndrome, vascular type: A novel missense mutation in the COL3A1 gene

Y. Kuroki, W. Fujimoto, K. Kadota, 2012, Congenital anomalies.

A novel point mutation in type III collagen gene resulting in exon 24 skipping in a case of vascular type Ehlers-Danlos syndrome

T. Shimada, A. Watanabe, F. Sato, 2008, Archives of Dermatological Research.

Ehlers-Danlos syndrome type IV with few extrathoracic findings: a newly recognized point mutation in the COL3A1 gene

Y. Kawabata, H. Kimura, T. Kuriyama, 2002, European Respiratory Journal.

Identification of the protein components of mismatch binding complexes in human cells using a gel‐shift assay

T. Shimada, A. Watanabe, M. Ikejima, 1999, FEBS letters.

Improvement of bone disease with increased dose of glucocerebrosidase in a Gaucher disease patient who had a bone lesion presenting during low‐dose enzyme replacement therapy

M. Migita, T. Ueda, Y. Fukunaga, 1996, Acta paediatrica Japonica : Overseas edition.

Progression of bone disease without deterioration of hematological parameters in a child with Gaucher disease during low-dose glucocerebrosidase therapy.

M. Migita, T. Ueda, A. Watanabe, 1994, Nihon Ika Daigaku zasshi.

Novel missense and frameshift mutations in the tissue-nonspecific alkaline phosphatase gene in a Japanese patient with hypophosphatasia.

T. Shimada, A. Watanabe, H. Orimo, 1994, Human molecular genetics.

Identification of a novel frameshift mutation (383insT) in the RUNX2 (PEBP2 α/CBFA1/AML3) gene in a Japanese patient with cleidocranial dysplasia

T. Shimada, Hisashi Watanabe, S. Oida, 2001, Journal of Bone and Mineral Metabolism.

Presymptomatic genetic analysis during pregnancy for vascular type Ehlers–Danlos syndrome

T. Shimada, A. Watanabe, M. Iwashita, 2014, International medical case reports journal.

Ehlers–Danlos type IV in pregnancy with a history of myocardial infarction

Mitsuaki Suzuki, T. Mitsuhashi, S. Matsubara, 2009, The journal of obstetrics and gynaecology research.

Genetic aspects of the vascular type of Ehlers-Danlos syndrome (vEDS, EDSIV) in Japan.

Y. Fukushima, T. Shimada, M. Fujimoto, 2007, Circulation journal : official journal of the Japanese Circulation Society.

Identical germline mutations in the TMEM127 gene in two unrelated Japanese patients with bilateral pheochromocytoma

H. Shimano, Tsuyoshi Watanabe, Yuria Saito, 2012, Clinical endocrinology.

Transient cardiomyopathy in a patient with congenital contractural arachnodactyly (Beals syndrome).

J. Hayakawa, M. Migita, T. Shimada, 2006, Journal of Nippon Medical School = Nippon Ika Daigaku zasshi.

A new type of familial macrothrombocytopenia with increased platelet calpain activity

Hidenori Suzuki, M. Migita, T. Saido, 1994 .

Glucocerebrosidase level in the cerebrospinal fluid during enzyme replacement therapy – unsuccessful treatment of the neurological abnormality in type 2 Gaucher disease

M. Migita, T. Shimada, Y. Fukunaga, 2003, European Journal of Pediatrics.

Prevention of Lethal Murine Hypophosphatasia by Neonatal Ex Vivo Gene Therapy Using Lentivirally Transduced Bone Marrow Cells.

J. Millán, N. Miyake, T. Shimada, 2015, Human gene therapy.

FIRST‐TRIMESTER PRENATAL MOLECULAR DIAGNOSIS OF INFANTILE HYPOPHOSPHATASIA IN A JAPANESE FAMILY

T. Shimada, A. Watanabe, T. Araki, 1996, Prenatal diagnosis.

Prenatal genetic diagnosis of severe perinatal (lethal) hypophosphatasia.

T. Shimada, T. Takeshita, A. Watanabe, 2007, Journal of Nippon Medical School = Nippon Ika Daigaku zasshi.

Prenatal Diagnosis of Severe Perinatal (Lethal) Hypophosphatasia

T. Shimada, T. Takeshita, A. Watanabe, 2012 .

2 Prenatal Diagnosis of Severe Perinatal ( Lethal ) Hypophosphatasia

T. Shimada, T. Takeshita, A. Watanabe, 2012 .

Loss of expression of the human MSH3 gene in hematological malignancies.

T. Shimada, A. Watanabe, H. Orimo, 1995, Biochemical and biophysical research communications.

Interaction effect between handedness and CNTNAP2 polymorphism (rs7794745 genotype) on voice-specific frontotemporal activity in healthy individuals: an fMRI study

Yoshiro Okubo, Masato Matsuura, Michihiko Koeda, 2015, Front. Behav. Neurosci..

Osteogenic and chondrogenic differentiation by adipose-derived stem cells harvested from GFP transgenic mice.

M. Migita, T. Shimada, R. Ogawa, 2004, Biochemical and biophysical research communications.

Conservative management of hyperreactio luteinalis: a case report.

T. Takeshita, A. Watanabe, T. Abe, 2011, Journal of Nippon Medical School = Nippon Ika Daigaku zasshi.

Spectrum of mutations and genotype–phenotype analysis in Noonan syndrome patients with RIT1 mutations

O. Migita, P. Lapunzina, T. Ogata, 2016, Human Genetics.

Treatment of hypophosphatasia by muscle-directed expression of bone-targeted alkaline phosphatase via self-complementary AAV8 vector

J. Millán, N. Miyake, T. Shimada, 2016, Molecular therapy. Methods & clinical development.

A novel mutation screening system for Ehlers-Danlos Syndrome, vascular type by high-resolution melting curve analysis in combination with small amplicon genotyping using genomic DNA.

T. Shimada, A. Watanabe, B. T. Naing, 2011, Biochemical and biophysical research communications.

Ehlers–Danlos syndrome type IV with a unique point mutation in COL3A1 and familial phenotype of myocardial infarction without organic coronary stenosis

Y. Katayama, K. Tamura, T. Takano, 2001, Journal of internal medicine.

Effectiveness of Measuring Genetic Polymorphisms in Metabolizing Enzymes of Tacrolimus within One Medical Facility.

S. Tsuruoka, A. Watanabe, T. Kaneko, 2017, Journal of Nippon Medical School = Nippon Ika Daigaku zasshi.

Global diffuse distribution in the brain and efficient gene delivery to the dorsal root ganglia by intrathecal injection of adeno‐associated viral vector serotype 1

N. Miyake, T. Shimada, A. Teramoto, 2009, The journal of gene medicine.

Adipogenic differentiation by adipose-derived stem cells harvested from GFP transgenic mice-including relationship of sex differences.

M. Migita, T. Shimada, R. Ogawa, 2004, Biochemical and biophysical research communications.

Systems-Based Approach to Drug Response

T. Shimada, A. Watanabe, B. T. Naing, 2013, Current Genetic Medicine Reports.

Genomic organization and expression of the human MSH3 gene.

T. Shimada, N. Suzuki, A. Watanabe, 1996, Genomics.

Associations between keloid severity and single-nucleotide polymorphisms: importance of rs8032158 as a biomarker of keloid severity.

M. Sasaki, T. Shimada, R. Ogawa, 2014, The Journal of investigative dermatology.

Bone-Targeted Alkaline Phosphatase Treatment of Mandibular Bone and Teeth in Lethal Hypophosphatasia via an scAAV8 Vector

Toru Sato, T. Muramatsu, A. Watanabe, 2018, Molecular therapy. Methods & clinical development.

Perinatal hypophosphatasia caused by uniparental isodisomy.

T. Shimada, A. Watanabe, H. Orimo, 2014, Bone.

Mutations in p53 cDNA sequence introduced by retroviral vector.

T. Shimada, K. Miyake, A. Watanabe, 2006, Biochemical and biophysical research communications.

Targeted gene delivery to selected liver segments via isolated hepatic perfusion.

T. Shimada, S. Hisayasu, A. Watanabe, 2010, The Journal of surgical research.

Lentivirus-mediated expression of angiostatin efficiently inhibits neovascularization in a murine proliferative retinopathy model

M. Ishizaki, T. Shimada, K. Miyake, 2003, Gene Therapy.

High-Level Expression of Alkaline Phosphatase by Adeno-Associated Virus Vector Ameliorates Pathological Bone Structure in a Hypophosphatasia Mouse Model

A. Yamaguchi, S. Abe, A. Watanabe, 2020, Calcified Tissue International.

Case Report: A Case of Moyamoya Syndrome Associated With Multiple Endocrine Neoplasia Type 2A

T. Igarashi, T. Shimada, Y. Murai, 2021, Frontiers in Endocrinology.