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Sidt2 regulates hepatocellular lipid metabolism through autophagy

Journal of lipid research, 2018-03, Vol.59 (3), p.404-415

2018

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Successful newborn screening for Gaucher disease using fluorometric assay in China

Journal of human genetics, 2017-08, Vol.62 (8), p.763-768

2017

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X-ray induced photodynamic therapy (PDT) with a mitochondria-targeted liposome delivery system

Journal of nanobiotechnology, 2020-06, Vol.18 (1), p.87-13, Article 87

2020

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Reinforcement of the diagnosis and treatment of hyperphenylalaninemia and prognostic study

Zhonghua er ke za zhi, 2014-06, Vol.52 (6), p.401

Gu, Xuefan

2014

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Aggregation of Gold Nanoparticles Caused in Two Different Ways Involved in 4-Mercaptophenylboronic Acidand Hydrogen Peroxide

Materials, 2019-06, Vol.12 (11), p.1802

2019

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Late-onset cblC defect: clinical, biochemical and molecular analysis

Orphanet journal of rare diseases, 2023-09, Vol.18 (1), p.1-306, Article 306

2023

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Synthesis and Evaluation of Hydroxymethyl Tetramides as Flow Improvers for Crude Oil

Journal of the Chemical Society of Pakistan, 2020-08, Vol.42 (4), p.488-488

2020

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Determination of 7-ketocholesterol in plasma by LC-MS for rapid diagnosis of acid SMase-deficient Niemann-Pick disease

Journal of lipid research, 2014-02, Vol.55 (2), p.338-343

2014

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Lubricity and Rheological Properties of Highly Dispersed Graphite in Clay-Water-Based Drilling Fluids

Materials, 2022-01, Vol.15 (3), p.1083

2022

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Gene expression profiles in the brain of phenylketonuria mouse model reversed by the low phenylalanine diet therapy

Metabolic brain disease, 2021-12, Vol.36 (8), p.2405-2414

2021

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SID1 transmembrane family, member 2 (Sidt2): A novel lysosomal membrane protein

Biochemical and biophysical research communications, 2010-11, Vol.402 (4), p.588-594

2010

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Clinical, biochemical, and genetic analysis of 28 Chinese patients with holocarboxylase synthetase deficiency

Orphanet journal of rare diseases, 2023-03, Vol.18 (1), p.48-48, Article 48

2023

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Novel PYGL mutations in Chinese children leading to glycogen storage disease type VI: two case reports

BMC medical genetics, 2020-04, Vol.21 (1), p.74-74, Article 74

2020

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Diagnostic yield of additional exome sequencing after the detection of long continuous stretches of homozygosity (LCSH) in SNP arrays

Journal of human genetics, 2021-04, Vol.66 (4), p.409-417

2021

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Characteristics of Pompe disease in China: a report from the Pompe registry

Orphanet journal of rare diseases, 2019-04, Vol.14 (1), p.78-78, Article 78

2019

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Synthesis of New Hydrazone Compounds from Natural Grease and Investigation as Flow Improver for Crude Oil

Petroleum chemistry, 2023-05, Vol.63 (5), p.553-560

2023

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Demographic characteristics and distribution of lysosomal storage disorder subtypes in Eastern China

Journal of human genetics, 2016-04, Vol.61 (4), p.345-349

2016

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Next-generation sequencing analysis of twelve known causative genes in congenital hypothyroidism

Clinica chimica acta, 2017-05, Vol.468, p.76-80

2017

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Performance and Mechanism of Span Surfactants as Clean Flow Improvers for Crude Oil

Petroleum chemistry, 2020, Vol.60 (1), p.140-145

2020

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Three novel mutations of the FBN1 gene in Chinese children with acromelic dysplasia

Journal of human genetics, 2014-10, Vol.59 (10), p.563-567

2014

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Next-generation sequencing analysis of DUOX2 in 192 Chinese subclinical congenital hypothyroidism (SCH) and CH patients

Clinica chimica acta, 2016-07, Vol.458, p.30-34

2016

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Conformational Stability of Poly (N-Isopropylacrylamide) Anchored on the Surface of Gold Nanoparticles

Materials, 2021-01, Vol.14 (2), p.443

2021

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Value of amniotic fluid homocysteine assay in prenatal diagnosis of combined methylmalonic acidemia and homocystinuria, cobalamin C type

Orphanet journal of rare diseases, 2021-03, Vol.16 (1), p.125-125, Article 125

2021

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Impaired glucose tolerance in a mouse model of sidt2 deficiency

PloS one, 2013-06, Vol.8 (6), p.e66139-e66139

2013

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The Predictive Value of Genetic Analyses in the Diagnosis of Tetrahydrobiopterin (BH4)-Responsiveness in Chinese Phenylalanine Hydroxylase Deficiency Patients

Scientific reports, 2017-07, Vol.7 (1), p.6762-12, Article 6762

2017

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Sidt2 regulates hepatocellular lipid metabolism through autophagy

Successful newborn screening for Gaucher disease using fluorometric assay in China

X-ray induced photodynamic therapy (PDT) with a mitochondria-targeted liposome delivery system

Reinforcement of the diagnosis and treatment of hyperphenylalaninemia and prognostic study

Aggregation of Gold Nanoparticles Caused in Two Different Ways Involved in 4-Mercaptophenylboronic Acidand Hydrogen Peroxide

Late-onset cblC defect: clinical, biochemical and molecular analysis

Synthesis and Evaluation of Hydroxymethyl Tetramides as Flow Improvers for Crude Oil

Determination of 7-ketocholesterol in plasma by LC-MS for rapid diagnosis of acid SMase-deficient Niemann-Pick disease

Lubricity and Rheological Properties of Highly Dispersed Graphite in Clay-Water-Based Drilling Fluids

Gene expression profiles in the brain of phenylketonuria mouse model reversed by the low phenylalanine diet therapy

SID1 transmembrane family, member 2 (Sidt2): A novel lysosomal membrane protein

Clinical, biochemical, and genetic analysis of 28 Chinese patients with holocarboxylase synthetase deficiency

Novel PYGL mutations in Chinese children leading to glycogen storage disease type VI: two case reports

Diagnostic yield of additional exome sequencing after the detection of long continuous stretches of homozygosity (LCSH) in SNP arrays

Characteristics of Pompe disease in China: a report from the Pompe registry

Synthesis of New Hydrazone Compounds from Natural Grease and Investigation as Flow Improver for Crude Oil

Demographic characteristics and distribution of lysosomal storage disorder subtypes in Eastern China

Next-generation sequencing analysis of twelve known causative genes in congenital hypothyroidism

Performance and Mechanism of Span Surfactants as Clean Flow Improvers for Crude Oil

Three novel mutations of the FBN1 gene in Chinese children with acromelic dysplasia

Next-generation sequencing analysis of DUOX2 in 192 Chinese subclinical congenital hypothyroidism (SCH) and CH patients

Conformational Stability of Poly (N-Isopropylacrylamide) Anchored on the Surface of Gold Nanoparticles

Value of amniotic fluid homocysteine assay in prenatal diagnosis of combined methylmalonic acidemia and homocystinuria, cobalamin C type

Impaired glucose tolerance in a mouse model of sidt2 deficiency

The Predictive Value of Genetic Analyses in the Diagnosis of Tetrahydrobiopterin (BH4)-Responsiveness in Chinese Phenylalanine Hydroxylase Deficiency Patients

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