Report for Miyake N

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References (4)

Title : Deficiency of TMEM53 causes a previously unknown sclerosing bone disorder by dysregulation of BMP-SMAD signaling - Guo_2021_Nat.Commun_12_2046
Author(s) : Guo L , Iida A , Bhavani GS , Gowrishankar K , Wang Z , Xue JY , Wang J , Miyake N , Matsumoto N , Hasegawa T , Iizuka Y , Matsuda M , Nakashima T , Takechi M , Iseki S , Yambe S , Nishimura G , Koseki H , Shukunami C , Girisha KM , Ikegawa S
Ref : Nat Commun , 12 :2046 , 2021
Abstract : Guo_2021_Nat.Commun_12_2046
ESTHER : Guo_2021_Nat.Commun_12_2046
PubMedSearch : Guo_2021_Nat.Commun_12_2046
PubMedID: 33824347
Gene_locus related to this paper: human-TMEM53

Title : A homozygous ABHD16A variant causes a complex hereditary spastic paraplegia with developmental delay, absent speech, and characteristic face - Miyake_2021_Clin.Genet__
Author(s) : Miyake N , Silva S , Troncoso M , Okamoto N , Andachi Y , Kato M , Iwabuchi C , Hirose M , Fujita A , Uchiyama Y , Matsumoto N
Ref : Clin Genet , : , 2021
Abstract : Miyake_2021_Clin.Genet__
ESTHER : Miyake_2021_Clin.Genet__
PubMedSearch : Miyake_2021_Clin.Genet__
PubMedID: 34866177
Gene_locus related to this paper: human-ABHD16A

Title : The second point mutation in PREPL: a case report and literature review - Silva_2018_J.Hum.Genet_63_677
Author(s) : Silva S , Miyake N , Tapia C , Matsumoto N
Ref : J Hum Genet , 63 :677 , 2018
Abstract : Silva_2018_J.Hum.Genet_63_677
ESTHER : Silva_2018_J.Hum.Genet_63_677
PubMedSearch : Silva_2018_J.Hum.Genet_63_677
PubMedID: 29483676
Gene_locus related to this paper: human-PREPL

Title : [Preheparin lipoprotein lipase mass and apolipoproteinC-III ratio helps identify postprandial triglyceride metabolic marker] - Miyake_2007_Rinsho.Byori_55_1019
Author(s) : Miyake N , Miyake K , Higurashi H , Ohsaka A
Ref : Rinsho Byori , 55 :1019 , 2007
Abstract : Miyake_2007_Rinsho.Byori_55_1019
ESTHER : Miyake_2007_Rinsho.Byori_55_1019
PubMedSearch : Miyake_2007_Rinsho.Byori_55_1019
PubMedID: 18154034