Yamamoto M - Search Results

1

Knocking-in the R142C mutation in transglutaminase 1 disrupts the stratum corneum barrier and postnatal survival of mice.

Nakagawa N, Yamamoto M, Imai Y, Sakaguchi Y, Takizawa T, Ohta N, Yagi N, Hatta I, Hitomi K, Takizawa T, Takeda J, Tsuda T, Matsuki M, Yamanishi K. Nakagawa N, et al. Among authors: yamamoto m. J Dermatol Sci. 2012 Mar;65(3):196-206. doi: 10.1016/j.jdermsci.2011.12.011. Epub 2011 Dec 24. J Dermatol Sci. 2012. PMID: 22258055

2

Lamellar ichthyosis with pseudoexon activation in the transglutaminase 1 gene.

Suga Y, Tsuda T, Nagai M, Sakaguchi Y, Jitsukawa O, Yamamoto M, Hitomi K, Yamanishi K. Suga Y, et al. Among authors: yamamoto m. J Dermatol. 2015 Jun;42(6):642-5. doi: 10.1111/1346-8138.12846. Epub 2015 Mar 21. J Dermatol. 2015. PMID: 25808943

3

Serum cytokines correlated with the disease severity of generalized pustular psoriasis.

Yamamoto M, Imai Y, Sakaguchi Y, Haneda T, Yamanishi K. Yamamoto M, et al. Dis Markers. 2013;34(3):153-61. doi: 10.3233/DMA-120958. Dis Markers. 2013. PMID: 23334651 Free PMC article.

4

A Case of Old Age-Onset Generalized Pustular Psoriasis with a Deficiency of IL-36RN (DITRA) Treated by Granulocyte and Monocyte Apheresis.

Tominaga C, Yamamoto M, Imai Y, Yamanishi K. Tominaga C, et al. Among authors: yamamoto m. Case Rep Dermatol. 2015 Feb 21;7(1):29-35. doi: 10.1159/000380876. eCollection 2015 Jan-Apr. Case Rep Dermatol. 2015. PMID: 25848350 Free PMC article.

5

Mild case of congenital ichthyosiform erythroderma with periodic exacerbation: Novel mutations in ABCA12 and upregulation of calprotectin in the epidermis.

Wada Y, Kusakabe M, Nagai M, Yamamoto M, Imai Y, Ide YH, Hirota S, Yamanishi K. Wada Y, et al. Among authors: yamamoto m. J Dermatol. 2017 Nov;44(11):e282-e283. doi: 10.1111/1346-8138.13976. Epub 2017 Aug 3. J Dermatol. 2017. PMID: 28771802 No abstract available.

6

ABCA12-deficient Congenital Ichthyosiform Erythroderma in a Boy with an Intellectual Developmental Delay.

Inoue Y, Yamamoto M, Sakaguchi Y, Jitsukawa O, Hayano K, Yamane M, Sakamoto M, Yamanishi K. Inoue Y, et al. Among authors: yamamoto m. Acta Derm Venereol. 2015 Jul;95(6):747-9. doi: 10.2340/00015555-2062. Acta Derm Venereol. 2015. PMID: 25655901 Free article. No abstract available.

7

Lichen planus-like dermatosis distributed along the lines of Blaschko.

Yamamoto M, Imai Y, Nakagawa N, Yamanishi K. Yamamoto M, et al. J Dermatol. 2011 Feb;38(2):190-1. doi: 10.1111/j.1346-8138.2010.00975.x. Epub 2010 Sep 28. J Dermatol. 2011. PMID: 21269318 No abstract available.

8

Case of epidermolytic ichthyosis (bullous congenial ichthyosiform erythroderma) with a novel L157P mutation in KRT10 complicated by hypercalcemia.

Yamamoto M, Tsuda T, Otaki Y, Nakanishi T, Yamanishi K. Yamamoto M, et al. J Dermatol. 2012 Aug;39(8):716-8. doi: 10.1111/j.1346-8138.2011.01410.x. Epub 2011 Oct 31. J Dermatol. 2012. PMID: 22035476 No abstract available.

9

Cutaneous malignant fibrous histiocytoma (undifferentiated pleomorphic sarcoma) arising in a chronic scalp ulcer of a patient with non-bullous congenital ichthyosiform erythroderma.

Fujimoto T, Tsuda T, Yamamoto M, Tarutani M, Natsuaki M, Minami S, Ito T, Kozuka T, Yamanishi K. Fujimoto T, et al. Among authors: yamamoto m. J Eur Acad Dermatol Venereol. 2009 Feb;23(2):202-3. doi: 10.1111/j.1468-3083.2008.02780.x. Epub 2008 Apr 23. J Eur Acad Dermatol Venereol. 2009. PMID: 18435726 No abstract available.

10

Returning genetic risk information for hereditary cancers to participants in a population-based cohort study in Japan.

Ohneda K, Suzuki Y, Hamanaka Y, Tadaka S, Shimada M, Hasegawa-Minato J, Takahashi M, Fuse N, Nagami F, Kawame H, Kobayashi T, Yamaguchi-Kabata Y, Kinoshita K, Nakamura T, Ogishima S, Kumada K, Kudo H, Kuriyama SI, Izumi Y, Shimizu R, Tochigi M, Motonari T, Tokunaga H, Kikuchi A, Masamune A, Aoki Y, Ishioka C, Ishida T, Yamamoto M. Ohneda K, et al. Among authors: yamamoto m. J Hum Genet. 2025 Jan 17. doi: 10.1038/s10038-024-01314-w. Online ahead of print. J Hum Genet. 2025. PMID: 39825003

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