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O-GlcNAcylation of PGK1 coordinates glycolysis and TCA cycle to promote tumor growth

Nature communications, 2020-01, Vol.11 (1), p.36-14, Article 36

2020

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The influence of Nav1.9 channels on intestinal hyperpathia and dysmotility

Channels (Austin, Tex.), 2023-12, Vol.17 (1), p.2212350-2212350

2023

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Case Report: Three novel pathogenic ABCC2 mutations identified in two patients with Dubin–Johnson syndrome

Frontiers in genetics, 2022-08, Vol.13

2022

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Four Variants of SLCO2A1 Identified in Three Chinese Patients with Chronic Enteropathy Associated with the SLCO2A1 Gene

Digestive diseases and sciences, 2021-09, Vol.66 (9), p.2992-3001

2021

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Preliminary Findings on Proline-Rich Protein 14 as a Diagnostic Biomarker for Parkinson’s Disease

Neuromolecular medicine, 2021-06, Vol.23 (2), p.285-291

2021

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The Gain-of-Function R222S Variant in Scn11a Contributes to Visceral Hyperalgesia and Intestinal Dysmotility in Scn11aR222S/R222S Mice

Frontiers in neurology, 2022-05, Vol.13

2022

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Development of an informational support questionnaire of transitional care for aged patients with chronic disease

BMJ open, 2020-11, Vol.10 (11), p.e036573-e036573

2020

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Myotonia congenita and periodic hypokalemia paralysis in a consanguineous marriage pedigree: Coexistence of a novel CLCN1 mutation and an SCN4A mutation

PloS one, 2020-05, Vol.15 (5), p.e0233017

2020

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Factors associated with instrumental support in transitional care among older people with chronic disease: a cross-sectional study

BMC nursing, 2022-08, Vol.21 (1), p.1-230, Article 230

2022

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Myasthenia gravis coexisting with HINT1-related motor axonal neuropathy without neuromyotonia: a case report

BMC neurology, 2022-05, Vol.22 (1), p.168-168, Article 168

2022

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Novel compound heterozygous mutations in the CYP4F22 gene in a patient with autosomal recessive congenital ichthyosis

Clinical case reports, 2021-12, Vol.9 (12), p.e05082-n/a

2021

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Two different pathogenic gene mutations coexisted in the same hereditary spherocytosis family manifested with heterogeneous phenotypes

BMC medical genetics, 2019-05, Vol.20 (1), p.90-90, Article 90

2019

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Clinical Presentations and Genetic Characteristics of Late-Onset MADD Due to ETFDH Mutations in Five Patients: A Case Series

Frontiers in neurology, 2021-11, Vol.12

2021

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The Spider Venom Peptide Lycosin-II Has Potent Antimicrobial Activity against Clinically Isolated Bacteria

Toxins, 2016-04, Vol.8 (5), p.119-119

2016

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Omalizumab for STAT3 Hyper-IgE Syndromes in Adulthood: A Case Report and Literature Review

Frontiers in medicine, 2022-05, Vol.9, p.835257

2022

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Electrophysiological and Pharmacological Analyses of Nav1.9 Voltage-Gated Sodium Channel by Establishing a Heterologous Expression System

Frontiers in pharmacology, 2017-11, Vol.8, p.852-852

2017

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A novel splicing mutation of PTCH1 in a Chinese family with nevoid basal cell carcinoma syndrome

Medical molecular morphology, 2019-12, Vol.52 (4), p.235-237

2019

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Study protocol: A cross‐sectional study on instrumental support for transitional care among older adults with chronic diseases

Nursing open, 2021-07, Vol.8 (4), p.1990-1997

2021

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Molecular analysis of 53 Chinese families with Wilson's disease: Six novel mutations identified

Molecular genetics & genomic medicine, 2021-09, Vol.9 (9), p.e1735-n/a

2021

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Synthesis and analgesic effects of μ-TRTX-Hhn1b on models of inflammatory and neuropathic pain

Toxins, 2014-08, Vol.6 (8), p.2363-2378

2014

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Interleukin-6, tumor necrosis factor-alpha and receptor activator of nuclear factor kappa ligand are elevated in hypertrophic gastric mucosa of pachydermoperiostosis

Scientific reports, 2017-08, Vol.7 (1), p.9686-9, Article 9686

2017

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Next-Generation Sequencing in Early Diagnosis of Dent Disease 1: Two Case Reports

Frontiers in medicine, 2018-12, Vol.5, p.347

2018

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A novel SLC37A4 missense mutation in GSD‐Ib without hepatomegaly causes enhanced leukocytes endoplasmic reticulum stress and apoptosis

Molecular genetics & genomic medicine, 2021-01, Vol.9 (1), p.e1568-n/a

2021

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Beneficial effects of trypsin inhibitors derived from a spider venom peptide in L-arginine-induced severe acute pancreatitis in mice

PloS one, 2013-04, Vol.8 (4), p.e61049

2013

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EP88 THE GAIN-OF-FUNCTION R222S VARIANT IN SCN11A CONTRIBUTES TO VISCERAL HYPERALGESIA AND INTESTINAL DYSMOTILITY IN SAN11AR222S/R222S MICE

Gastroenterology (New York, N.Y. 1943), 2024-05, Vol.166 (5), p.S-1527-S-1527

2024

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O-GlcNAcylation of PGK1 coordinates glycolysis and TCA cycle to promote tumor growth

The influence of Nav1.9 channels on intestinal hyperpathia and dysmotility

Case Report: Three novel pathogenic ABCC2 mutations identified in two patients with Dubin–Johnson syndrome

Four Variants of SLCO2A1 Identified in Three Chinese Patients with Chronic Enteropathy Associated with the SLCO2A1 Gene

Preliminary Findings on Proline-Rich Protein 14 as a Diagnostic Biomarker for Parkinson’s Disease

The Gain-of-Function R222S Variant in Scn11a Contributes to Visceral Hyperalgesia and Intestinal Dysmotility in Scn11aR222S/R222S Mice

Development of an informational support questionnaire of transitional care for aged patients with chronic disease

Myotonia congenita and periodic hypokalemia paralysis in a consanguineous marriage pedigree: Coexistence of a novel CLCN1 mutation and an SCN4A mutation

Factors associated with instrumental support in transitional care among older people with chronic disease: a cross-sectional study

Myasthenia gravis coexisting with HINT1-related motor axonal neuropathy without neuromyotonia: a case report

Novel compound heterozygous mutations in the CYP4F22 gene in a patient with autosomal recessive congenital ichthyosis

Two different pathogenic gene mutations coexisted in the same hereditary spherocytosis family manifested with heterogeneous phenotypes

Clinical Presentations and Genetic Characteristics of Late-Onset MADD Due to ETFDH Mutations in Five Patients: A Case Series

The Spider Venom Peptide Lycosin-II Has Potent Antimicrobial Activity against Clinically Isolated Bacteria

Omalizumab for STAT3 Hyper-IgE Syndromes in Adulthood: A Case Report and Literature Review

Electrophysiological and Pharmacological Analyses of Nav1.9 Voltage-Gated Sodium Channel by Establishing a Heterologous Expression System

A novel splicing mutation of PTCH1 in a Chinese family with nevoid basal cell carcinoma syndrome

Study protocol: A cross‐sectional study on instrumental support for transitional care among older adults with chronic diseases

Molecular analysis of 53 Chinese families with Wilson's disease: Six novel mutations identified

Synthesis and analgesic effects of μ-TRTX-Hhn1b on models of inflammatory and neuropathic pain

Interleukin-6, tumor necrosis factor-alpha and receptor activator of nuclear factor kappa ligand are elevated in hypertrophic gastric mucosa of pachydermoperiostosis

Next-Generation Sequencing in Early Diagnosis of Dent Disease 1: Two Case Reports

A novel SLC37A4 missense mutation in GSD‐Ib without hepatomegaly causes enhanced leukocytes endoplasmic reticulum stress and apoptosis

Beneficial effects of trypsin inhibitors derived from a spider venom peptide in L-arginine-induced severe acute pancreatitis in mice

EP88 THE GAIN-OF-FUNCTION R222S VARIANT IN SCN11A CONTRIBUTES TO VISCERAL HYPERALGESIA AND INTESTINAL DYSMOTILITY IN SAN11AR222S/R222S MICE

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