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Analysis of the genes responsible for steroid-resistant nephrotic syndrome and/or focal segmental glomerulosclerosis in Japanese patients by whole-exome sequencing analysis

Journal of human genetics, 2016-02, Vol.61 (2), p.137-141

2016

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Careful Clinical Surveillance Is Important for the Identification of Parechovirus Type A3-Associated Myalgia/Myositis: a Sporadic Case Found in a Season with a Low Level of Its Activity in Yamagata, Japan in 2017

Japanese Journal of Infectious Diseases, 2019/01/31, Vol.72(1), pp.71-72

2019

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Inheritance of polyalanine expansion mutation of PHOX2B in congenital central hypoventilation syndrome

Journal of human genetics, 2012-05, Vol.57 (5), p.335-337

2012

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Association of breast-fed neonatal hyperbilirubinemia with UGT1A1 polymorphisms: 211G>A (G71R) mutation becomes a risk factor under inadequate feeding

Journal of human genetics, 2013-01, Vol.58 (1), p.7-10

2013

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Association of neonatal hyperbilirubinemia in breast-fed infants with UGT1A1 or SLCOs polymorphisms

Journal of human genetics, 2015-01, Vol.60 (1), p.35-40

2015

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A founder haplotype of APOE-Sendai mutation associated with lipoprotein glomerulopathy

Journal of human genetics, 2013-05, Vol.58 (5), p.254-258

2013

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Correction: Corrigendum: Analysis of the genes responsible for steroid-resistant nephrotic syndrome and/or focal segmental glomerulosclerosis in Japanese patients by whole-exome sequencing analysis

Journal of human genetics, 2016-08, Vol.61 (8), p.771-772

2016

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Expression profiling of starch metabolism-related plastidic translocator genes in rice

Planta, 2006-01, Vol.223 (2), p.248-257

2006

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An Elderly Japanese Patient with Adult-onset Type II Citrullinemia with a Novel D493G Mutation in the SLC25A13 Gene

Internal Medicine, 2012, Vol.51(16), pp.2131-2134

2012

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Medium-chain triglyceride supplementation under a low-carbohydrate formula is a promising therapy for adult-onset type II citrullinemia

Molecular genetics and metabolism reports, 2014-01, Vol.1 (C), p.42-50

2014

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The double-stranded break-forming activity of plant SPO11s and a novel rice SPO11 revealed by a Drosophila bioassay

BMC molecular biology, 2012-01, Vol.13 (1), p.1-1, Article 1

2012

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Careful clinical surveillance is important for the identification of human parechovirus type A3-associated myalgia/myositis: a sporadic case found in a season with a low level of its activity in Yamagata, Japan in 2017

Japanese Journal of Infectious Diseases, 2018, pp.JJID.2018.341

2018

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Corrigendum: Analysis of the genes responsible for steroid-resistant nephrotic syndrome and/or focal segmental glomerulosclerosis in Japanese patients by whole-exome sequencing analysis

Journal of human genetics, 2016-08, Vol.61 (8), p.771-772

2016

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"Genomic structure and promoter analysis of phosphoenolpyruvate carboxylase in a C3 plant, Nicotiana sylvestris."

Bioscience, biotechnology, and biochemistry, 2002-08, Vol.66 (8), p.1691-1696

2002

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INF2 mutations in Charcot-Marie-Tooth disease complicated with focal segmental glomerulosclerosis

Journal of the peripheral nervous system, 2013-03, Vol.18 (1), p.97-98

2013

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Sweetness Sensor with Lipid/Polymer Membranes: Sweet-Responsive Substances

Sensors and materials, 2011, p.465

2011

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Sweetness Sensor with Lipid/Polymer Membranes: Response to Various Sugars

Sensors and materials, 2011, Vol.23 (8), p.475-482

2011

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A second pediatric patient with lipoprotein glomerulopathy carrying a heterozygous APOE-Sendai mutation

Japanese journal of pediatric nephrology, 2011/11/15, Vol.24(2), pp.218-223

2011

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P-52 A second pediatric patient with lipoprotein glomerulopathy carring a heterozygous ApoE Sendai mutation

Japanese Journal of Pediatric Nephrology, 2011, Vol.24 (suppl), p.212-212

2011

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A second pediatric patient with lipoprotein glomerulopathy carrying a heterozygous APOE-Sendai mutation

Nihon Shōni Jinzōbyō Gakkai zasshi, 2011, Vol.24 (2), p.218-223

2011

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Transcriptional activation of phosphoenolpyruvate carboxylase by phosphorus deficiency in tobacco

Journal of experimental botany, 2003-03, Vol.54 (384), p.961-969

2003

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SO-28 Dilemma of erythropoietin therapy for renal anemia in a patient with high-risk neuroblastoma

Japanese Journal of Pediatric Nephrology, 2011, Vol.24 (suppl), p.175-175

2011

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Genomic Structure and Promoter Analysis of Phospho enol pyruvate Carboxylase in a C3 Plant, Nicotiana sylvestris

Bioscience, biotechnology, and biochemistry, 2002-01, Vol.66 (8), p.1691-1696, Article 1691

2002

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山形県における2例目の小児リポ蛋白糸球体症

日本小児腎臓病学会雑誌, 2011/11/15, Vol.24(2), pp.218-223

2011

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INF2 mutations in Charcot-Marie-Tooth disease complicated with focal segmental glomerulosclerosis

Journal of the peripheral nervous system : JPNS, 2013, Vol.18 (1), p.97-98

2013

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Analysis of the genes responsible for steroid-resistant nephrotic syndrome and/or focal segmental glomerulosclerosis in Japanese patients by whole-exome sequencing analysis

Careful Clinical Surveillance Is Important for the Identification of Parechovirus Type A3-Associated Myalgia/Myositis: a Sporadic Case Found in a Season with a Low Level of Its Activity in Yamagata, Japan in 2017

Inheritance of polyalanine expansion mutation of PHOX2B in congenital central hypoventilation syndrome

Association of breast-fed neonatal hyperbilirubinemia with UGT1A1 polymorphisms: 211G>A (G71R) mutation becomes a risk factor under inadequate feeding

Association of neonatal hyperbilirubinemia in breast-fed infants with UGT1A1 or SLCOs polymorphisms

A founder haplotype of APOE-Sendai mutation associated with lipoprotein glomerulopathy

Correction: Corrigendum: Analysis of the genes responsible for steroid-resistant nephrotic syndrome and/or focal segmental glomerulosclerosis in Japanese patients by whole-exome sequencing analysis

Expression profiling of starch metabolism-related plastidic translocator genes in rice

An Elderly Japanese Patient with Adult-onset Type II Citrullinemia with a Novel D493G Mutation in the SLC25A13 Gene

Medium-chain triglyceride supplementation under a low-carbohydrate formula is a promising therapy for adult-onset type II citrullinemia

The double-stranded break-forming activity of plant SPO11s and a novel rice SPO11 revealed by a Drosophila bioassay

Careful clinical surveillance is important for the identification of human parechovirus type A3-associated myalgia/myositis: a sporadic case found in a season with a low level of its activity in Yamagata, Japan in 2017

Corrigendum: Analysis of the genes responsible for steroid-resistant nephrotic syndrome and/or focal segmental glomerulosclerosis in Japanese patients by whole-exome sequencing analysis

"Genomic structure and promoter analysis of phosphoenolpyruvate carboxylase in a C3 plant, Nicotiana sylvestris."

INF2 mutations in Charcot-Marie-Tooth disease complicated with focal segmental glomerulosclerosis

Sweetness Sensor with Lipid/Polymer Membranes: Sweet-Responsive Substances

Sweetness Sensor with Lipid/Polymer Membranes: Response to Various Sugars

A second pediatric patient with lipoprotein glomerulopathy carrying a heterozygous APOE-Sendai mutation

P-52 A second pediatric patient with lipoprotein glomerulopathy carring a heterozygous ApoE Sendai mutation

A second pediatric patient with lipoprotein glomerulopathy carrying a heterozygous APOE-Sendai mutation

Transcriptional activation of phosphoenolpyruvate carboxylase by phosphorus deficiency in tobacco

SO-28 Dilemma of erythropoietin therapy for renal anemia in a patient with high-risk neuroblastoma

Genomic Structure and Promoter Analysis of Phospho enol pyruvate Carboxylase in a C3 Plant, Nicotiana sylvestris

山形県における2例目の小児リポ蛋白糸球体症

INF2 mutations in Charcot-Marie-Tooth disease complicated with focal segmental glomerulosclerosis

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