Search Results - "Takeichi, T"

Roles of aberrant hemichannel activities due to mutant connexin26 in the pathogenesis of KID syndrome by Taki, T., Takeichi, T., Sugiura, K., Akiyama, M.

“…Germline missense mutations in GJB2 encoding connexin (Cx) 26 have been found in keratitis, ichthyosis and deafness (KID) syndrome. We explored the effects of…”
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Studies on thermal and mechanical properties of polyimide–clay nanocomposites by Agag, T, Koga, T, Takeichi, T

“…Nanocomposites from polyimide and clay were prepared aiming at finding a promising method for enhancing particularly the tensile modulus of polyimide films…”
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Epithelioid cell granuloma formation in CARD14‐associated papulosquamous eruptions by Takeichi, T., Ikeda, K., Muro, Y., Ogi, T., Morizane, S., Akiyama, M.

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Influence of SEBS-g-MA on morphology, mechanical, and thermal properties of PA6/PP/organoclay nanocomposites by Kusmono, Mohd Ishak, Z.A., Chow, W.S., Takeichi, T., Rochmadi

“…Polyamide 6/polypropylene (PA6/PP = 70/30 parts) blends containing 4 phr (parts per hundred resin) of organically modified clay (organoclay) toughened with…”
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A novel NCSTN missense mutation in the signal peptide domain causes hidradenitis suppurativa, which has features characteristic of an autoinflammatory keratinization disease by Takeichi, T., Matsumoto, T., Nomura, T., Takeda, M., Niwa, H., Kono, M., Shimizu, H., Ogi, T., Akiyama, M.

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Intravenous allogeneic multilineage‐differentiating stress‐enduring cells in adults with dystrophic epidermolysis bullosa: a phase 1/2 open‐label study by Fujita, Y., Nohara, T., Takashima, S., Natsuga, K., Adachi, M., Yoshida, K., Shinkuma, S., Takeichi, T., Nakamura, H., Wada, O., Akiyama, M., Ishiko, A., Shimizu, H.

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A patient with CARD14‐associated papulosquamous eruptions showing atopic dermatitis‐like features by Takeichi, T., Terawaki, S., Kubota, Y., Ito, Y., Tanahashi, K., Muro, Y., Akiyama, M.

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Novel Benzoxazine Monomers Containing p-Phenyl Propargyl Ether:  Polymerization of Monomers and Properties of Polybenzoxazines by Agag, Tarek, Takeichi, Tsutomu

“…Novel benzoxazine monomers containing arylpropargyl ether were prepared, and highly thermally stable polybenzoxazines were obtained by the thermal cure of the…”
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Autosomal dominant familial generalized pustular psoriasis caused by a CARD14 mutation by Takeichi, T., Kobayashi, A., Ogawa, E., Okuno, Y., Kataoka, S., Kono, M., Sugiura, K., Okuyama, R., Akiyama, M.

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A juvenile male case of dermatofibrosarcoma protuberans on the breast by Murase, Y., Takeichi, T., Matsumoto, T., Sakakibara, A., Akiyama, M.

“…Click here for the corresponding questions to this CME article…”
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Cutaneous extramedullary hematopoiesis in a patient with secondary myelofibrosis due to MPL gene mutation by Murase, Y., Takeichi, T., Tanahashi, K., Marumo, Y., Suzuki, Y., Nakamura, S., Akiyama, M.

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A novel IL36RN/IL1F5 homozygous nonsense mutation, p.Arg10X, in a Japanese patient with adult-onset generalized pustular psoriasis by Sugiura, K., Takeichi, T., Kono, M., Ogawa, Y., Shimoyama, Y., Muro, Y., Akiyama, M.

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Polybenzoxazine–montmorillonite hybrid nanocomposites: synthesis and characterization by Agag, T, Takeichi, T

“…Polybenzoxazine–clay hybrid nanocomposites were prepared from a polybenzoxazine precursor ( B-a) and organically modified-montmorillonite ( OMMT) as a type of…”
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Unique reticular hyperkeratotic eruptions seen in a patient with Darier's disease and attention deficit hyperactivity disorder by Yoshikawa, T., Takeichi, T., Suga, Y., Kitajima, Y., Akiyama, M.

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Two cases of generalized pustular psoriasis complicated by IgG4‐related disease by Miyazawa, H., Fujita, Y., Iwata, H., Ishikawa, Y., Nishio, S., Ishijima, K., Shinmei, Y., Takeichi, T., Goto, K., Oi, R., Akiyama, M., Shimizu, H.

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A patient with bullous pemphigoid with mucosal involvement serologically positive for anti‐BP230 autoantibodies only by Taki, T., Takeichi, T., Kono, M., Sugiura, K., Sugimura, Y., Ishii, N., Hashimoto, T., Akiyama, M.

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Whole-exome sequencing improves mutation detection in a diagnostic epidermolysis bullosa laboratory by Takeichi, T., Liu, L., Fong, K., Ozoemena, L., McMillan, J.R., Salam, A., Campbell, P., Akiyama, M., Mellerio, J.E., McLean, W.H.I., Simpson, M.A., McGrath, J.A.

“…Summary Background Subtypes of inherited epidermolysis bullosa (EB) vary significantly in their clinical presentation and prognosis. Establishing an accurate…”
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Mild Hailey–Hailey disease cases with aberrant splicing variants of ATP2C1 successfully controlled with excimer light by Kono, M., Niizawa, M., Takeichi, T., Muro, Y., Akiyama, M.

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Autosomal dominant progressive hyperpigmentation and lentigines in a Japanese pedigree due to a missense mutation near the C‐terminus of KIT by Takeichi, T., Sugiura, K., Tanahashi, K., Noda, K., Kono, M., Akiyama, M.

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Granulocyte and monocyte apheresis can control juvenile generalized pustular psoriasis with mutation of IL36RN by Koike, Y., Okubo, M., Kiyohara, T., Fukuchi, R., Sato, Y., Kuwatsuka, S., Takeichi, T., Akiyama, M., Sugiura, K., Utani, A.

“…Summary Patients with deficiency of interleukin‐36 receptor antagonist (DITRA), due to mutation of IL36RN, exhibit psoriatic phenotypes, typically generalized…”
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