鈴木 民夫 すずき たみお 先生

来歴等

論文

(代表論文20編)
1. Zhang Q, Li W, Novak EK, Karim A, Mishra V, Kingsmore S, Roe B, Suzuki T and Swank RT: The gene for the muted(mu) mouse, a model for Hermansky-Pudlak syndrome, defines a novel protein which regulates vesicle trafficking. Hum Mol Genet 11 : 697-706 (2002) IF: 5.340
2. Suzuki T, Li W, Zhang Q, Karim A, Novak EK, Sviderskaya EV, Hill SP, Bennett DC, Levin AV, Nieuwenhuis HK, Fong CT, Castellan C, Miterski B, Swank RT and Spritz RA: Hermansky-Pudlak syndrome is caused by mutations in HPS4, the human homolog of the mouse light ear gene. Nature Genetics 30 : 321-324 (2002) IF: 31.616
3. Suzuki T*, Oiso N*, Gautam R*, Novak EK, Panthier JJ, Suprabha PG, Vida T, Swank RT, and Spritz RA : The mouse organellar biogenesis mutant buff results from a mutation in Vps33a, a homologue of yeast vps33 and Drosophila carnation. Proc Natl Acad Sci USA 100 : 1146-1150 (2003) IF: 9.423
4. Suzuki T, Miyamura Y, Matsunaga J, Shimizu H, Kawachi Y, Ohyama N, Ishikawa O, Ishikawa T, Terao H, and Tomita Y: Six Novel P Gene Mutations and OCA2 Frequency in Japanese Albino Patients. J Invest Dermatol 120: 781-783 (2003) IF: 6.287
5. Miyamura Y*, Suzuki T*, Kono M, Inagaki K, Ito S, Suzuki N, and Tomita Y : Mutations of the RNA-specific adenosine deaminase gene (DSRAD) are involved in Dyschromatosis Symmetrica Hereditaria. Am J Hum Genet 73: 693-699 (2003) *These authors contributed equally to the paper. IF: 9.025
6. Inagaki K*, Suzuki T*, Shimizu H, Ishii N, Umezawa Y, Tada J, Kikuchi N, Takata M, Takamori K, Kishibe M, Tanaka M, Miyamura Y, Ito S, and Tomita Y : Oculocutaneous albinism type 4 is one of the most common types of albinism in Japan. Am J Hum Genet 74: 466-471 (2004)
*These authors contributed equally to the paper. IF: 9.025
7. Suzuki N, Suzuki T, Inagaki K, Ito S, Kono M, Fukai K, Takama H, Sato K, Ishikawa O, Abe M, Shimizu H, Kawai M, Horikawa T, Yoshida K, Matsumoto K, Terui T, Tsujioka K, and Tomita Y: Mutation Analysis of the ADAR1 gene in Dyschromatosis Symmetrica Hereditaria and Genetic Differentiation from both Dyschromatosis Universalis Hereditaria and Acropigmentatio Reticularis. J Invest Dermatol 124: 1186-1192 (2005) IF: 6.287
8. Miyamura Y, Verma IC, Saxena R, Hoshi M, Murase A, Nakamura E, Kono M, Suzuki T, Yasue S, Shibata S, Sakakibara A, and Tomita Y: Five novel mutations in tyrosinase gene of Japanese and Indian patients with oculocutaneous albinism type I (OCAI). J Invest Dermatol 125: 397-398 (2005) IF: 6.287
9. Ito S*, Suzuki T*, Inagaki K, Suzuki N, Takamori K, Yamada T, Nakazawa M, Hatano M, Takiwaki H, Spritz RA, and Tomita Y: High Frequency of Hermansky-Pudlak Syndrome Type 1 (HPS1) Among Japanese Albinism Patients and Functional Analysis of HPS1 Mutant Protein. J Invest Dermatol 125: 715-720 (2005) *These authors contributed equally to the paper. IF: 6.287
10. Inagaki K, Suzuki T, Ito S, Suzuki N, Adachi K, Okuyama T, Nakata Y, Shimizu H, Matsuura H, Oono T, Iwamatsu H, Kono M, and Tomita Y: Oculocutaneous albinism type 4: six novel mutations in the membrane-associated transporter protein gene (SLC45A2) and their phenotype. Pigment Cell Res 19:451-453 (2006) IF: 5.17
11. Suzuki N, Suzuki T, Inagaki K, Ito S, Kono M, Horikawa T, Fujiwara S, Ishiko A, Matsunaga K, Aoyama Y, Tosaki-Ichikawa H, and Tomita Y: Ten Novel Mutations of the ADAR1 Gene in Japanese Patients with Dyschromatosis Symmetrica Hereditaria. J Invest Dermatol 127: 309-311 (2007) IF: 6.287
12. Konno T, Abe Y, Kawaguchi M, Kondo T, Tomita Y, and Suzuki T: Functional analysis of OCA4 mutant sequences using under white mouse melanocytes. Pigment Cell Melanoma Res 22:235-237 (2009) IF: 5.17
13. Yamada M, Hayashi M, Sakai K, Hozumi Y, Abe Y, Kawaguchi M, Ihn H, and Suzuki T: Oculocutaneous Albinism Type 3: a Japanese Girl With Novel Mutations in TYRP1 gene. J Dermatol Sci 64:217-222 (2011) IF: 3.733
14. Kawaguchi M, Valencia JC, Namiki T, Suzuki T, and Hearing VJ: Diacylglycerol kinase regulates tyrosinase expression and function in human melanocytes. J Invest Dermatol 132: 2791-2799 (2012) 　IF: 6.287
15. Rice GI, Kasher PR, Forte GMA, Mannion NM, Greenwood SM, Szynkiewicz M, Dickerson JE, Bhaskar SS, Zampini M, Briggs TA, Jenkinson EM, Bacino CA, Battini R, Bertini E, Brogan PA, Brueton LA, Carpanelli M, Laet CD, Lonlay PD, Toro MD, Desguerre I, Fazzi E, Garcia-Cazorla A, Heiberg A, Kawaguchi M, Kumar R, Lin JS, Lourenco CM, Male AM, Marques JW, Mignot C, Olivieri I, Orcesi S, Prabhakar P, Rasmussen M, Robinson RA, Rozenberg F, Schmidt JL, Steindl K, Tan TY, van der Merwe WG, Vanderver A, Vassallo G, Wakeling EL, Wassmer E, Whittaker E, Livingston JH, Lebon P, Suzuki T, McLaughlin PJ, Keegan LP, O’Connell MA, Lovell SC and Crow YJ: Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signature. Nat Genet 44:1243-1248 (2012) IF: 31.616
16. Abe Y, Tamiya G, Nakamura T, Hozumi Y, and Suzuki T: Association of melanogenesis genes with skin color variation among Japanese females. J Dermatol Sci 69:167-172 (2013) IF: 3.733
17. Kono M, Sugiura K, Suganuma M, Hayashi M, Takama H, Suzuki T, Matsunaga K, Tomita Y, and Akiyama M: Whole-exome sequencing identifies ADAM10 mutations as a cause of reticulate acropigmentation of Kitamura, a clinical entity distinct from Dowling-Degos disease. Hum Mol Genet 22: 3524-33 (2013) IF: 5.340
18. Shimanuki M, Abe Y, Tamiya G, Ueki M, Hozumi Y, and Suzuki T: Positive selection with diversity in oculocutaneous albinisms type 2 gene (OCA2) among Japanese. Pigment Cell Melanoma Res 28:233-235 (2015) IF: 5.17
19. Abe Y, Okamura K, Kawaguchi M, Hozumi Y, Aoki H, Kunisada T, Ito S, Wakamatsu K, Matsunaga K, and Suzuki T: Rhododenol-induced leukoderma in a mouse model mimicking Japanese skin. J Dermatol Sci. 81(1):35-43 (2016) IF: 3.733
20. Okamura K, Abe Y, Araki Y, Hozumi Y, Kawaguchi M, and Suzuki T: Behavior of melanocytes and keratinocytes in reticulate acropigmentation of Kitamura. Pigment Cell Melanoma Res. 29(2):243-246 (2016) IF: 5.17

著書

1. Tomita Y, Kono M, and Suzuki T, Dyschromatosis Symmetrica Hereditaria. Asian Skin and Skin Diseases. Edited by HC Eun, SC Kim, and WS Lee. Medrang Inc., Seoul, 2011, pp.161-165
2. Suzuki T, and Tomita Y. Oculocutaneous albinism in Asians. Asian Skin and Skin Diseases. Edited by HC Eun, SC Kim, and WS Lee. Medrang Inc., Seoul, 2011, pp.175-180
3. 南山堂医学大辞典20版、（分担執筆）眼皮膚白皮症p.477, 色素異常症p985, 尋常性白斑p.1235, チロシナーゼ反応p.1645, まだら症p.2345、鈴木民夫、南山堂、2015
4. 伊藤祥輔ら監修、色素細胞第2版－基礎から臨床へ－、P207－222、第16章遺伝子異常から解明される先天性異常症：大磯直毅、鈴木民夫、深井和吉。慶應義塾大学出版会、2015
5. 永井良三総監修、皮膚科研修ノート　P555-557、先天性色素異常症：鈴木民夫、阿部優子。診断と治療社、2016
6. 福井次矢ら編、今日の治療指針2017私はこう治療している、P1226、尋常性白斑：鈴木民夫。医学書院、2017
7. 渡辺晋一ら編、皮膚疾患最新の治療2017‐2018、P241-242、母斑細胞母斑：鈴木民夫。南江堂、2017

その他

• 【受賞】平成15年度日本皮膚科学会基礎医学研究費

• 【受賞】日本研究皮膚科学会Fellowship SHISEIDO Award 2003

• 【受賞】第５回ガルデルマ賞(平成16年度)　

• 【受賞】平成16年度日本リデイアオリリー協会研究助成金

• 【受賞】平成17年日本皮膚科学会　皆見省吾記念賞

• 【受賞】コスメトロジー研究振興財団　平成17年度研究助成