Report for Shinkuma S

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References (4)

Title : Prevalent founder mutation c.736T>A of LIPH in autosomal recessive woolly hair of Japanese leads to variable severity of hypotrichosis in adulthood - Tanahashi_2013_J.Eur.Acad.Dermatol.Venereol_27_1182
Author(s) : Tanahashi K , Sugiura K , Takeichi T , Takama H , Shinkuma S , Shimizu H , Akiyama M
Ref : J Eur Acad Dermatol Venereol , 27 :1182 , 2013
Abstract : Tanahashi_2013_J.Eur.Acad.Dermatol.Venereol_27_1182
ESTHER : Tanahashi_2013_J.Eur.Acad.Dermatol.Venereol_27_1182
PubMedSearch : Tanahashi_2013_J.Eur.Acad.Dermatol.Venereol_27_1182
PubMedID: 22449147
Gene_locus related to this paper: human-LIPH

Title : The beta9 loop domain of PA-PLA1alpha has a crucial role in autosomal recessive woolly hair\/hypotrichosis -
Author(s) : Shinkuma S , Inoue A , Aoki J , Nishie W , Natsuga K , Ujiie H , Nomura T , Abe R , Akiyama M , Shimizu H
Ref : Journal of Investigative Dermatology , 132 :2093 , 2012
PubMedID: 22475755
Gene_locus related to this paper: human-LIPH

Title : Hair shaft abnormalities in localized autosomal recessive hypotrichosis 2 and a review of other non-syndromic human alopecias -
Author(s) : Suga H , Tsunemi Y , Sugaya M , Shinkuma S , Akiyama M , Shimizu H , Sato S
Ref : Acta Derm Venereol , 91 :486 , 2011
PubMedID: 21537821

Title : Prevalent LIPH founder mutations lead to loss of P2Y5 activation ability of PA-PLA1alpha in autosomal recessive hypotrichosis - Shinkuma_2010_Hum.Mutat_31_602
Author(s) : 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
Ref : Hum Mutat , 31 :602 , 2010
Abstract : Shinkuma_2010_Hum.Mutat_31_602
ESTHER : Shinkuma_2010_Hum.Mutat_31_602
PubMedSearch : Shinkuma_2010_Hum.Mutat_31_602
PubMedID: 20213768
Gene_locus related to this paper: human-LIPH