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Investigating a Needle-Based Epidural Procedure in Obstetric Anesthesia

AMIA ... Annual Symposium proceedings, 2018, Vol.2018, p.720-729

2018

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Health-promoting school development in Zhejiang Province, China

Health promotion international, 2008-09, Vol.23 (3), p.220-230

2008

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A C-Means Clustering Approach Based on Cloud Model

2008 IEEE International Conference on Fuzzy Systems (IEEE World Congress on Computational Intelligence), 2008, p.965-968

2008

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The impact of diet and ethnicity on gut microbiota variation in irritable bowel syndrome: A multi‐center study

Journal of gastroenterology and hepatology, 2023-08, Vol.38 (8), p.1259-1268

2023

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Effects of DAPT and Atoh1 overexpression on hair cell production and hair bundle orientation in cultured Organ of Corti from neonatal rats

PloS one, 2011-10, Vol.6 (10), p.e23729-e23729

2011

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Bioactive Constituents from the Bryophyta Hypnum plumaeforme

Chemistry & biodiversity, 2020-12, Vol.17 (12), p.e2000552-n/a

2020

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Maternally Inherited Aminoglycoside-Induced and Nonsyndromic Deafness Is Associated with the Novel C1494T Mutation in the Mitochondrial 12S rRNA Gene in a Large Chinese Family

American journal of human genetics, 2004-01, Vol.74 (1), p.139-152

2004

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Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing loss

Nucleic acids research, 2005-01, Vol.33 (3), p.1132-1139

2005

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Coexistence of mitochondrial 12S rRNA C1494T and CO1/tRNA(Ser(UCN)) G7444A mutations in two Han Chinese pedigrees with aminoglycoside-induced and non-syndromic hearing loss

Biochemical and biophysical research communications, 2007-10, Vol.362 (1), p.94-100

2007

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The mitochondrial tRNA(Ala) T5628C variant may have a modifying role in the phenotypic manifestation of the 12S rRNA C1494T mutation in a large Chinese family with hearing loss

Biochemical and biophysical research communications, 2007-06, Vol.357 (2), p.554-560

2007

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Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA mutation in 16 Chinese families: Implication for early detection and prevention of deafness

Biochemical and biophysical research communications, 2006-02, Vol.340 (1), p.194-199

2006

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Peripheral Blood miR-937 May Serve as a Biomarker for Metabolic Disorders by Targeting AMPKα

Clinical laboratory (Heidelberg), 2019-01, Vol.65 (6)

2019

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May Measurement Month 2017 blood pressure screening: findings from Malaysia-South-East Asia and Australasia

European heart journal supplements, 2019-04, Vol.21 (Suppl D), p.D77-D79

2019

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Cosegregation of the G7444A mutation in the mitochondrial COI/tRNA(Ser(UCN)) genes with the 12S rRNA A1555G mutation in a Chinese family with aminoglycoside-induced and nonsyndromic hearing loss

American journal of medical genetics. Part A, 2005-10, Vol.138A (2), p.133

2005

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Extremely low penetrance of hearing loss in four Chinese families with the mitochondrial 12S rRNA A1555G mutation

Biochemical and biophysical research communications, 2005-03, Vol.328 (4), p.1244-1251

2005

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An effective and simplified scale-up strategy for acarbose fermentation based on the carbon source control

World journal of microbiology & biotechnology, 2012-02, Vol.28 (2), p.749-753

2012

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Mutations at position 7445 in the precursor of mitochondrial tRNA(Ser(UCN)) gene in three maternal Chinese pedigrees with sensorineural hearing loss

Mitochondrion, 2008-09, Vol.8 (4), p.285-292

2008

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Clinical and molecular characterization of a Chinese patient with auditory neuropathy associated with mitochondrial 12S rRNA T1095C mutation

American journal of medical genetics, 2005-02, Vol.133A (1), p.27-30

2005

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Clinical evaluation and sequence analysis of the complete mitochondrial genome of three Chinese patients with hearing impairment associated with the 12S rRNA T1095C mutation

Biochemical and biophysical research communications, 2004-12, Vol.325 (4), p.1503-1508

2004

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Comparison between chemoembolization combined with radiotherapy and chemoembolization alone for large hepatocellular carcinoma

World journal of gastroenterology : WJG, 2003-08, Vol.9 (8), p.1697

2003

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Clinical and molecular analysis of a four-generation Chinese family with aminoglycoside-induced and nonsyndromic hearing loss associated with the mitochondrial 12S rRNA C1494T mutation

Biochemical and biophysical research communications, 2006-02, Vol.340 (2), p.583-588

2006

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Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA T1095C mutation in three Chinese families

Biochemical and biophysical research communications, 2006-09, Vol.348 (1), p.200-205

2006

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Transverse Ising Model with a Crystal Field for the Spin-2

physica status solidi (b), 2001-05, Vol.225 (1), p.215-221

2001

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Clinical evaluation and mitochondrial DNA sequence analysis in two Chinese families with aminoglycoside-induced and non-syndromic hearing loss

Biochemical and biophysical research communications, 2005-10, Vol.336 (3), p.967-973

2005

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The mitochondrial tRNAAla T5628C variant may have a modifying role in the phenotypic manifestation of the 12S rRNA C1494T mutation in a large Chinese family with hearing loss

Biochemical and biophysical research communications, 2007-06, Vol.357 (2), p.554-560

2007

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Investigating a Needle-Based Epidural Procedure in Obstetric Anesthesia

Health-promoting school development in Zhejiang Province, China

A C-Means Clustering Approach Based on Cloud Model

The impact of diet and ethnicity on gut microbiota variation in irritable bowel syndrome: A multi‐center study

Effects of DAPT and Atoh1 overexpression on hair cell production and hair bundle orientation in cultured Organ of Corti from neonatal rats

Bioactive Constituents from the Bryophyta Hypnum plumaeforme

Maternally Inherited Aminoglycoside-Induced and Nonsyndromic Deafness Is Associated with the Novel C1494T Mutation in the Mitochondrial 12S rRNA Gene in a Large Chinese Family

Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing loss

Coexistence of mitochondrial 12S rRNA C1494T and CO1/tRNA(Ser(UCN)) G7444A mutations in two Han Chinese pedigrees with aminoglycoside-induced and non-syndromic hearing loss

The mitochondrial tRNA(Ala) T5628C variant may have a modifying role in the phenotypic manifestation of the 12S rRNA C1494T mutation in a large Chinese family with hearing loss

Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA mutation in 16 Chinese families: Implication for early detection and prevention of deafness

Peripheral Blood miR-937 May Serve as a Biomarker for Metabolic Disorders by Targeting AMPKα

May Measurement Month 2017 blood pressure screening: findings from Malaysia-South-East Asia and Australasia

Cosegregation of the G7444A mutation in the mitochondrial COI/tRNA(Ser(UCN)) genes with the 12S rRNA A1555G mutation in a Chinese family with aminoglycoside-induced and nonsyndromic hearing loss

Extremely low penetrance of hearing loss in four Chinese families with the mitochondrial 12S rRNA A1555G mutation

An effective and simplified scale-up strategy for acarbose fermentation based on the carbon source control

Mutations at position 7445 in the precursor of mitochondrial tRNA(Ser(UCN)) gene in three maternal Chinese pedigrees with sensorineural hearing loss

Clinical and molecular characterization of a Chinese patient with auditory neuropathy associated with mitochondrial 12S rRNA T1095C mutation

Clinical evaluation and sequence analysis of the complete mitochondrial genome of three Chinese patients with hearing impairment associated with the 12S rRNA T1095C mutation

Comparison between chemoembolization combined with radiotherapy and chemoembolization alone for large hepatocellular carcinoma

Clinical and molecular analysis of a four-generation Chinese family with aminoglycoside-induced and nonsyndromic hearing loss associated with the mitochondrial 12S rRNA C1494T mutation

Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA T1095C mutation in three Chinese families

Transverse Ising Model with a Crystal Field for the Spin-2

Clinical evaluation and mitochondrial DNA sequence analysis in two Chinese families with aminoglycoside-induced and non-syndromic hearing loss

The mitochondrial tRNAAla T5628C variant may have a modifying role in the phenotypic manifestation of the 12S rRNA C1494T mutation in a large Chinese family with hearing loss

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