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Main 10 Publications of Faculty Staff: Associate Professor Satoru Shinkuma

1. Saito N, Qiao H, Yanagi T, Shinkuma S, Nishimura K, Suto A, Fujita Y, Suzuki S, Nomura T, Nakamura H, Nagao K, Obuse C, Shimizu H, Abe R:
An annexin A1-FPR1 interaction contributes to necroptosis of keratinocytes in severe cutaneous adverse drug reactions.
Sci Transl Med. 16: 245ra95, 2014.


2. Shinkuma S, Sawamura D, Fujita Y, Kawasaki H, Nakamura H, Inoie M, Nishie W, Shimizu H:
Long-term follow-up of cultured epidermal autograft in a recessive dystrophic epidermolysis bullosa patient.
Acta Derm Venereol. 94: 98-99, 2014.


3. Shinkuma S, Nishie W, Jacyk WK, Natsuga K, Ujiie H, Nakamura H, Akiyama M, Shimizu H:
A novel keratin 5 mutation in an African family with epidermolysis bullosa simplex indicates importance of the amino acid located at the boundary site between the H1 and coil 1A domains.
Acta Derm Venereol. 93: 585-587, 2013.


4. Shinkuma S, Inoue A, Aoki J, Nishie W, Natsuga K, Ujiie H, Nomura T, Abe R, Akiyama M, Shimizu H:
The β9 loop domain of PA-PLA1α plays a crucial role in autosomal recessive woolly hair/hypotrichosis.
J Invest Dermatol, 132: 2093-2095, 2012.


5. Hayashi I, Shinkuma S, Shimizu S, Natsuga K, Ujiie H, Yasui C, Tsuchiya K, Nishie W, Shimizu H:
Mucous membrane pemphigoid with generalized blisters: IgA and IgG autoantibodies target both laminin-332 and type XVII collagen.
Br J Dermatol, 166: 1116-1120, 2012.


6. Natsuga K, Shinkuma S, Kanda M, Suzuki Y, Chosa N, Narita Y, Setoyama M, Nishie W, Akiyama M, Shimizu H:
Possible modifier effects of keratin 17 gene mutation on keratitis-ichthyosis-deafness syndrome.
Br J Dermatol. 166: 903-905, 2012.


7. Shinkuma S, McMillan JR, Shimizu H:
Ultrastructure and molecular pathogenesis of epidermolysis bullosa.
Clin Dermatol. 29: 412-419, 2011.


8. Shinkuma S, Natsuga K, Nishie W, Shimizu H:
Epidermolysis bullosa in Japan.
Dermatol Clin 28:431-432, 2010.


9. Shinkuma S, Akiyama M, Inoue A, Aoki J, Natsuga K, Nomura T, Arita K, Abe R, Ito K, Nakamura H, Ujiie H, Shibaki A, Suga H, Tsunemi Y, Nishie W, Shimizu H:
Prevalent LIPH founder mutations lead to loss of P2Y5 activation ability of PA-PLA1alpha in autosomal recessive hypotrichosis.
Hum Mutat 31: 602-610, 2010.


10. Shinkuma S, Nishie W, Shibaki A, Sawamura D, Kei I, Tsuji-Abe Y, Natsuga K, Chan PT, Amagai M, Shimizu H:
Cutaneous pemphigus vulgaris with skin features similar to the classic mucocutaneous type: a case report and review of the literature.
Clin Exp Dermatol 33: 724-728, 2008.

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Hiroshi Shimizu
(Professor & Chairman)
Wataru Nishie
(Senior associate professor)
Yasuyuki Fujita
(Associate professor)
Hideyuki Ujiie
(Associate professor)
Toshifumi Nomura
(Associate professor)
Ken Natsuga
(Associate professor)
Hiroo Hata
(Associate professor)
Hiroaki Iwata
(Associate professor)
Satoru Shinkuma
(Assistant professor)
Teruki Yanagi
(Assistant professor)
Publications of Faculty Staff
Hiroshi Shimizu
(Professor & Chairman)
Wataru Nishie
(Senior associate professor)
Yasuyuki Fujita
(Associate professor)
Hideyuki Ujiie
(Associate professor)
Toshifumi Nomura
(Associate professor)
Ken Natsuga
(Associate professor)
Hiroo Hata
(Associate professor)
Hiroaki Iwata
(Associate professor)
Satoru Shinkuma
(Assistant professor)
Teruki Yanagi
(Assistant professor)

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