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Publications by Hideki Hidaka

Two Genes That Map to the STSL Locus Cause Sitosterolemia: Genomic Structure and Spectrum of Mutations Involving Sterolin-1 and Sterolin-2, Encoded by ABCG5 and ABCG8, Respectively

American Journal of Human Genetics

Genetics

2001

English

A Case of Primary Gastric Natural Killer/T-Cell Lymphoma, Nasal Type

Japanese Journal of Gastroenterological Surgery

Surgery

Gastroenterology

2007

English

Related publications

Dietary Xenosterols Lead to Infertility and Loss of Abdominal Adipose Tissue in Sterolin-Deficient Mice

Journal of Lipid Research

English

GRP78 Rescues the ABCG5 ABCG8 Sterol Transporter in Db/Db Mice

Metabolism: Clinical and Experimental

English

Cholesterol Absorption Is Mainly Regulated by the Jejunal and Ileal ATP-binding Cassette Sterol Efflux Transporters Abcg5 and Abcg8 in Mice

Journal of Lipid Research

English

Overexpression of ABCG5 and ABCG8 Promotes Biliary Cholesterol Secretion and Reduces Fractional Absorption of Dietary Cholesterol

Journal of Clinical Investigation

Medicine

2002

English

Mutations in the LHX3 Gene Cause Dysregulation of Pituitary and Neural Target Genes That Reflect Patient Phenotypes

English

Mapping of the Human Genes (SLC23A2 and SLC23A1) Coding for Vitamin C Transporters 1 and 2 (SVCT1 and SVCT2) to 5q23 and 20p12, Respectively

Journal of Medical Genetics

Genetics

2000

English

Mutations in NCAPG2 Cause a Severe Neurodevelopmental Syndrome That Expands the Phenotypic Spectrum of Condensinopathies

American Journal of Human Genetics

Genetics

2019

English

Sequences in the Nonconsensus Nucleotide-Binding Domain of ABCG5/ABCG8 Required for Sterol Transport

Journal of Biological Chemistry

English

Mutations of the P53 Gene and Other Genes Involving in Human Colorectal Carcinogenesis.

Tohoku Journal of Experimental Medicine

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Hideki Hidaka

Two Genes That Map to the STSL Locus Cause Sitosterolemia: Genomic Structure and Spectrum of Mutations Involving Sterolin-1 and Sterolin-2, Encoded by ABCG5 and ABCG8, Respectively

A Case of Primary Gastric Natural Killer/T-Cell Lymphoma, Nasal Type

Related publications

Dietary Xenosterols Lead to Infertility and Loss of Abdominal Adipose Tissue in Sterolin-Deficient Mice

GRP78 Rescues the ABCG5 ABCG8 Sterol Transporter in Db/Db Mice

Cholesterol Absorption Is Mainly Regulated by the Jejunal and Ileal ATP-binding Cassette Sterol Efflux Transporters Abcg5 and Abcg8 in Mice

Overexpression of ABCG5 and ABCG8 Promotes Biliary Cholesterol Secretion and Reduces Fractional Absorption of Dietary Cholesterol

Mutations in the LHX3 Gene Cause Dysregulation of Pituitary and Neural Target Genes That Reflect Patient Phenotypes

Mapping of the Human Genes (SLC23A2 and SLC23A1) Coding for Vitamin C Transporters 1 and 2 (SVCT1 and SVCT2) to 5q23 and 20p12, Respectively

Mutations in NCAPG2 Cause a Severe Neurodevelopmental Syndrome That Expands the Phenotypic Spectrum of Condensinopathies

Sequences in the Nonconsensus Nucleotide-Binding Domain of ABCG5/ABCG8 Required for Sterol Transport

Mutations of the P53 Gene and Other Genes Involving in Human Colorectal Carcinogenesis.