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Acta Pharmacologica Sinica (9)
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Showing 1–27 of 27 results

Advanced filters: Author: Yao-Hua Zhang Clear advanced filters

Nature’s 10: Ten people who mattered in science in 2018

Picks include a rogue gene-editor, a wunderkind physicist and a DNA detective who helped catch a serial killer.

Elizabeth Gibney
Ewen Callaway
Davide Castelvecchi
News18 Dec 2018
Nature

Volume: 564, P: 325-335
Genotypic Confirmation from the Original Dried Blood Specimens in a Neonatal Hemoglobinopathy Screening Program

Maria Descartes
Ying Huang
Edward R B McCabe
Research01 Mar 1992
Pediatric Research

Volume: 31, P: 217-221
Genomic scanning for expressed sequences in Xp21 identifies the glycerol kinase gene

Weiwen Guo
Kim Worley
Edward R.B. McCabe
Research01 Aug 1993
Nature Genetics

Volume: 4, P: 367-372
Early onset Paget's disease of bone caused by a novel mutation (78dup27) of the TNFRSF11A gene in a Chinese family

Yao-hua Ke
Hua Yue
Zhen-lin Zhang
Research06 Jul 2009
Acta Pharmacologica Sinica

Volume: 30, P: 1204-1210
Association of serum 25-hydroxyvitamin D with insulin resistance and β-cell function in a healthy Chinese female population

Min-fang Tao
Zeng Zhang
Zhen-lin Zhang
Research17 Jun 2013
Acta Pharmacologica Sinica

Volume: 34, P: 1070-1074
Association of ALOX15 gene polymorphisms with obesity-related phenotypes in Chinese nuclear families with male offspring

Yao-hua Ke
Wen-jin Xiao
Zhen-lin Zhang
Research03 Feb 2012
Acta Pharmacologica Sinica

Volume: 33, P: 201-207
Serum osteocalcin levels are inversely associated with plasma glucose and body mass index in healthy Chinese women

Wei-wei Hu
Yao-hua Ke
Zhen-lin Zhang
Research20 Oct 2014
Acta Pharmacologica Sinica

Volume: 35, P: 1521-1526
No association between LRP5 gene polymorphisms and bone and obesity phenotypes in Chinese male-offspring nuclear families

Jin-bo Yu
Yao-hua Ke
Zhen-lin Zhang
Research18 Oct 2010
Acta Pharmacologica Sinica

Volume: 31, P: 1464-1469
Association of single nucleotide polymorphism Rs2236518 in PRDM16 gene with BMI in Chinese males

Hua Yue
Jin-wei He
Zhen-lin Zhang
Research25 Mar 2013
Acta Pharmacologica Sinica

Volume: 34, P: 710-716
Association between VDR and ESR1 gene polymorphisms with bone and obesity phenotypes in Chinese male nuclear families

Jie-mei Gu
Wen-jin Xiao
Zhen-lin Zhang
Research04 Dec 2009
Acta Pharmacologica Sinica

Volume: 30, P: 1634-1642
Contribution of Myostatin gene polymorphisms to normal variation in lean mass, fat mass and peak BMD in Chinese male offspring

Hua Yue
Jin-wei He
Zhen-lin Zhang
Research19 Mar 2012
Acta Pharmacologica Sinica

Volume: 33, P: 660-667
Social regulation of aggression by pheromonal activation of Or65a olfactory neurons in Drosophila

Adding to previous findings on Drosophila pheromone cVA and its receptor Or65a in regulating male-male aggression, this study finds that prior activation Or65a-positive olfactory receptor neurons before encountering other male flies is needed to mitigate social aggression.

Weiwei Liu
Xinhua Liang
Yi Rao
Research19 Jun 2011
Nature Neuroscience

Volume: 14, P: 896-902
No association between polymorphisms and haplotypes of COL1A1 and COL1A2 genes and osteoporotic fracture in postmenopausal Chinese women

Wei-wei Hu
Jin-wei He
Zhen-lin Zhang
Research23 May 2011
Acta Pharmacologica Sinica

Volume: 32, P: 947-955
BACTERIAL SPECIES IDENTIFICATION AFTER AMPLIFICATION WITH A UNIVERSAL PRIMER PAIR. † 1059

Kevin M McCabe
Yao-Hua Zhang
Edward R.B McCabe
Research01 Apr 1996
Pediatric Research

Volume: 39, P: 179
Adrenal Hypoplasia Congenita and Male Pseudohermaphroditism: New Syndromic Association Association Additional Sex Determining Gene(s)

Eric J Vilain
Charmain A Quigley
Edward R McCabe
Research01 Apr 1999
Pediatric Research

Volume: 45, P: 142
PAX2 mutation in a patient with coloboma-ureteral-renal syndrome. • 623

Lisa A Schimmenti
Kyna A Byerly
Heather H Shim
Research01 Apr 1997
Pediatric Research

Volume: 41, P: 106
Xp22.1-p21.3 Mental Retardation: Identification of CNS-Expressed Genes in Patients' Deletions • 715

Weiwen Guo
Hamid Kalhor
Edward RB McCabe
Research01 Apr 1998
Pediatric Research

Volume: 43, P: 124
Glycerol Kinase Missense Mutations Provide Structure-Function But Not Genotype-Phenotype Insights. † 641

Yao-Hua Zhang
Bing-Ling Huang
Edward R.B. McCabe
Research01 Apr 1997
Pediatric Research

Volume: 41, P: 109
Glycerol Kinase (GK) Point Mutations in Patients with Isolated GK Deficiency: Possible Genotype-Phenotype Relationships

Katrina M Dipple
Yao-Hua Zhang
Edward R McCabe
Research01 Apr 1999
Pediatric Research

Volume: 45, P: 137
Enhanced osteogenesis and angiogenesis by mesoporous hydroxyapatite microspheres-derived simvastatin sustained release system for superior bone regeneration

Wei-Lin Yu
Tuan-Wei Sun
Yao-Hua He
ResearchOpen Access13 Mar 2017
Scientific Reports

Volume: 7, P: 1-16
Author Correction: Quantitative inheritance of volatile pheromones and darcin and their interaction in olfactory preferences of female mice

Ying-Juan Liu
Hui-Fen Guo
Yao-Hua Zhang
Amendments and CorrectionsOpen Access06 Mar 2018
Scientific Reports

Volume: 8, P: 1
Quantitative inheritance of volatile pheromones and darcin and their interaction in olfactory preferences of female mice

Ying-Juan Liu
Hui-Fen Guo
Yao-Hua Zhang
ResearchOpen Access18 May 2017
Scientific Reports

Volume: 7, P: 1-9
Asymptomatic Isolated Human Glycerol Kinase Deficiency Associated with Splice-Site Mutations and Nonsense-Mediated Decay of Mutant RNA

Yao-Hua Zhang
Bing-Ling Huang
Katrina M Dipple
Research01 Apr 2006
Pediatric Research

Volume: 59, P: 590-592
Non-linear association of anthropometric measurements and pulmonary function

Rui-Heng Zhang
Jian-Bo Zhou
Albert Lecube
ResearchOpen Access16 Jul 2021
Scientific Reports

Volume: 11, P: 1-10
Ribosome biogenesis in disease: new players and therapeutic targets

Lijuan Jiao
Yuzhe Liu
Yangxin Li
ReviewsOpen Access09 Jan 2023
Signal Transduction and Targeted Therapy

Volume: 8, P: 1-22
Membraneless organelles in health and disease: exploring the molecular basis, physiological roles and pathological implications

Yangxin Li
Yuzhe Liu
Zhenya Shen
ReviewsOpen Access18 Nov 2024
Signal Transduction and Targeted Therapy

Volume: 9, P: 1-26
Inflammasomes as therapeutic targets in human diseases

Yangxin Li
Hui Huang
Yao-Hua Song
ReviewsOpen Access02 Jul 2021
Signal Transduction and Targeted Therapy

Volume: 6, P: 1-14

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Nature’s 10: Ten people who mattered in science in 2018

Genotypic Confirmation from the Original Dried Blood Specimens in a Neonatal Hemoglobinopathy Screening Program

Genomic scanning for expressed sequences in Xp21 identifies the glycerol kinase gene

Early onset Paget's disease of bone caused by a novel mutation (78dup27) of the TNFRSF11A gene in a Chinese family

Association of serum 25-hydroxyvitamin D with insulin resistance and β-cell function in a healthy Chinese female population

Association of ALOX15 gene polymorphisms with obesity-related phenotypes in Chinese nuclear families with male offspring

Serum osteocalcin levels are inversely associated with plasma glucose and body mass index in healthy Chinese women

No association between LRP5 gene polymorphisms and bone and obesity phenotypes in Chinese male-offspring nuclear families

Association of single nucleotide polymorphism Rs2236518 in PRDM16 gene with BMI in Chinese males

Association between VDR and ESR1 gene polymorphisms with bone and obesity phenotypes in Chinese male nuclear families

Contribution of Myostatin gene polymorphisms to normal variation in lean mass, fat mass and peak BMD in Chinese male offspring

Social regulation of aggression by pheromonal activation of Or65a olfactory neurons in Drosophila

No association between polymorphisms and haplotypes of COL1A1 and COL1A2 genes and osteoporotic fracture in postmenopausal Chinese women

BACTERIAL SPECIES IDENTIFICATION AFTER AMPLIFICATION WITH A UNIVERSAL PRIMER PAIR. † 1059

Adrenal Hypoplasia Congenita and Male Pseudohermaphroditism: New Syndromic Association Association Additional Sex Determining Gene(s)

PAX2 mutation in a patient with coloboma-ureteral-renal syndrome. • 623

Xp22.1-p21.3 Mental Retardation: Identification of CNS-Expressed Genes in Patients' Deletions • 715

Glycerol Kinase Missense Mutations Provide Structure-Function But Not Genotype-Phenotype Insights. † 641

Glycerol Kinase (GK) Point Mutations in Patients with Isolated GK Deficiency: Possible Genotype-Phenotype Relationships

Enhanced osteogenesis and angiogenesis by mesoporous hydroxyapatite microspheres-derived simvastatin sustained release system for superior bone regeneration

Author Correction: Quantitative inheritance of volatile pheromones and darcin and their interaction in olfactory preferences of female mice

Quantitative inheritance of volatile pheromones and darcin and their interaction in olfactory preferences of female mice

Asymptomatic Isolated Human Glycerol Kinase Deficiency Associated with Splice-Site Mutations and Nonsense-Mediated Decay of Mutant RNA

Non-linear association of anthropometric measurements and pulmonary function

Ribosome biogenesis in disease: new players and therapeutic targets

Membraneless organelles in health and disease: exploring the molecular basis, physiological roles and pathological implications

Inflammasomes as therapeutic targets in human diseases

Search

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