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Leukocytapheresis for treatment of IBD.
Published in:
2003
By:
- Kohgo Y;
- Ashida T;
- Maemoto A;
- Ayabe T
Publication type:
Journal Article
46, XY gonadal dysgenesis: new SRY point mutation in two siblings with paternal germ line mosaicism.
Published in:
Clinical Genetics, 2012, v. 82, n. 6, p. 505, doi. 10.1111/j.1399-0004.2011.01832.x
By:
- Stoppa-Vaucher, S;
- Ayabe, T;
- Paquette, J;
- Patey, N;
- Francoeur, D;
- Vuissoz, J-M;
- Deladoëy, J;
- Samuels, ME;
- Ogata, T;
- Deal, CL
Publication type:
Article
Clinical characteristics of symptomatic narcolepsy or hypersomnia: an analysis of 182 consecutive cases with neurological disorders associated with hypersomnolence.
Published in:
Sleep & Biological Rhythms, 2019, v. 17, n. 1, p. 123, doi. 10.1007/s41105-018-0186-2
By:
- Ono, H.;
- Imanishi, A.;
- Sagawa, Y.;
- Tsutsui, K.;
- Ohmori, Y.;
- Takeshima, M.;
- Kanbayashi, T.;
- Shimizu, T.;
- Ayabe, T.;
- Nishino, S.
Publication type:
Article
Low prevalence of maternal microchimerism in peripheral blood of Japanese children with type 1 diabetes.
Published in:
Diabetic Medicine, 2020, v. 37, n. 12, p. 2131, doi. 10.1111/dme.14221
By:
- Ushijima, K.;
- Okuno, M.;
- Ayabe, T.;
- Kikuchi, N.;
- Kawamura, T.;
- Urakami, T.;
- Yokota, I.;
- Amemiya, S.;
- Uchiyama, T.;
- Kikuchi, T.;
- Ogata, T.;
- Sugihara, S.;
- Fukami, M.
Publication type:
Article
Protein-altering variants of PTPN2 in childhood-onset Type 1A diabetes.
Published in:
Diabetic Medicine, 2018, v. 35, n. 3, p. 376, doi. 10.1111/dme.13566
By:
- Okuno, M.;
- Ayabe, T.;
- Yokota, I.;
- Musha, I.;
- Shiga, K.;
- Kikuchi, T.;
- Kikuchi, N.;
- Ohtake, A.;
- Nakamura, A.;
- Nakabayashi, K.;
- Okamura, K.;
- Momozawa, Y.;
- Kubo, M.;
- Suzuki, J.;
- Urakami, T.;
- Kawamura, T.;
- Amemiya, S.;
- Ogata, T.;
- Sugihara, S.;
- Fukami, M.
Publication type:
Article
FUT2 non-secretor status is associated with Type 1 diabetes susceptibility in Japanese children.
Published in:
Diabetic Medicine, 2017, v. 34, n. 4, p. 586, doi. 10.1111/dme.13288
By:
- Ihara, K.;
- Fukano, C.;
- Ayabe, T.;
- Fukami, M.;
- Ogata, T.;
- Kawamura, T.;
- Urakami, T.;
- Kikuchi, N.;
- Yokota, I.;
- Takemoto, K.;
- Mukai, T.;
- Nishii, A.;
- Kikuchi, T.;
- Mori, T.;
- Shimura, N.;
- Sasaki, G.;
- Kizu, R.;
- Takubo, N.;
- Soneda, S.;
- Fujisawa, T.
Publication type:
Article
Variants associated with autoimmune Type 1 diabetes in Japanese children: implications for age-specific effects of cis-regulatory haplotypes at 17q12-q21.
Published in:
Diabetic Medicine, 2016, v. 33, n. 12, p. 1717, doi. 10.1111/dme.13175
By:
- Ayabe, T.;
- Fukami, M.;
- Ogata, T.;
- Kawamura, T.;
- Urakami, T.;
- Kikuchi, N.;
- Yokota, I.;
- Ihara, K.;
- Takemoto, K.;
- Mukai, T.;
- Nishii, A.;
- Kikuchi, T.;
- Mori, T.;
- Shimura, N.;
- Sasaki, G.;
- Kizu, R.;
- Takubo, N.;
- Soneda, S.;
- Fujisawa, T.;
- Takaya, R.
Publication type:
Article
Association of Primary Ovarian Insufficiency with a Specific Human Leukocyte Antigen Haplotype (A*24:02-C*03:03-B*35:01) in Japanese Women.
Published in:
Sexual Development, 2011, v. 5, n. 5, p. 235, doi. 10.1159/000330122
By:
- Ayabe, T.;
- Ishizuka, B.;
- Maruyama, T.;
- Fukami, M.;
- Yoshida, R.;
- Uchida, H.;
- Yoshimura, Y.;
- Nagai, T.;
- Ogata, T.
Publication type:
Article
Anti-IL-la autoantibodies in patients with rheumatic diseases and in healthy subjects.
Published in:
Clinical & Experimental Immunology, 1991, v. 85, n. 3, p. 407
By:
- Suzuki, H.;
- Ayabe, T.;
- Kamimura, J.;
- Kashiwagi, H.
Publication type:
Article
Hexokinase activity in mouse embryos developed in vivo and in vitro.
Published in:
1994
By:
- Ayabe, T.;
- Tsutsumi, O.;
- Taketani, Y.
Publication type:
journal article
Retrograde tube drainage for esophageal anastomotic leaks and perforation.
Published in:
Diseases of the Esophagus, 2007, v. 20, n. 3, p. 247, doi. 10.1111/j.1442-2050.2007.00680.x
By:
- Tomita, M.;
- Matsuzaki, Y.;
- Shimizu, T.;
- Hara, M.;
- Ayabe, T.;
- Onitsuka, T.
Publication type:
Article
Having small‐for‐gestational‐age infants was associated with maternal allergic features in the JECS birth cohort.
Published in:
Allergy, 2018, v. 73, n. 9, p. 1908, doi. 10.1111/all.13490
By:
- Saito, M.;
- Yamamoto‐Hanada, K.;
- Pak, K.;
- Ayabe, T.;
- Mezawa, H.;
- Ishitsuka, K.;
- Konishi, M.;
- Yang, L.;
- Matsumoto, K.;
- Saito, H.;
- Ohya, Y.;
- The Japan Environment and Children's Study (JECS) Group
Publication type:
Article
Decreased secretion of Paneth cell α-defensins in graft-versus-host disease.
Published in:
Transplant Infectious Disease, 2015, v. 17, n. 5, p. 702, doi. 10.1111/tid.12423
By:
- Eriguchi, Y.;
- Nakamura, K.;
- Hashimoto, D.;
- Shimoda, S.;
- Shimono, N.;
- Akashi, K.;
- Ayabe, T.;
- Teshima, T.
Publication type:
Article
Expression of nm23-H1 gene product in esophageal squamous cell carcinoma and its association with vessel invasion and survival.
Published in:
2001
By:
- Tomita, Masaki;
- Ayabe, Takanori;
- Matsuzaki, Yasunori;
- Edagawa, Masao;
- Maeda, Masayuki;
- Shimizu, Tetsuya;
- Hara, Masaki;
- Onitsuka, Toshio;
- Tomita, M;
- Ayabe, T;
- Matsuzaki, Y;
- Edagawa, M;
- Maeda, M;
- Shimizu, T;
- Hara, M;
- Onitsuka, T
Publication type:
journal article

Found: 14

Leukocytapheresis for treatment of IBD.

46, XY gonadal dysgenesis: new SRY point mutation in two siblings with paternal germ line mosaicism.

Clinical characteristics of symptomatic narcolepsy or hypersomnia: an analysis of 182 consecutive cases with neurological disorders associated with hypersomnolence.

Low prevalence of maternal microchimerism in peripheral blood of Japanese children with type 1 diabetes.

Protein-altering variants of PTPN2 in childhood-onset Type 1A diabetes.

FUT2 non-secretor status is associated with Type 1 diabetes susceptibility in Japanese children.

Variants associated with autoimmune Type 1 diabetes in Japanese children: implications for age-specific effects of cis-regulatory haplotypes at 17q12-q21.

Association of Primary Ovarian Insufficiency with a Specific Human Leukocyte Antigen Haplotype (A24:02-C03:03-B*35:01) in Japanese Women.

Anti-IL-la autoantibodies in patients with rheumatic diseases and in healthy subjects.

Hexokinase activity in mouse embryos developed in vivo and in vitro.

Retrograde tube drainage for esophageal anastomotic leaks and perforation.

Having small‐for‐gestational‐age infants was associated with maternal allergic features in the JECS birth cohort.

Decreased secretion of Paneth cell α-defensins in graft-versus-host disease.

Expression of nm23-H1 gene product in esophageal squamous cell carcinoma and its association with vessel invasion and survival.