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CO2 Dominated Bifunctional Catalytic Sites for Efficient Industrial Exhaust Conversion

Advanced functional materials, 2022-02, Vol.32 (8), p.n/a

2022

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Multiregion WES of metastatic pancreatic neuroendocrine tumors revealed heterogeneity in genomic alterations, immune microenvironment and evolutionary patterns

Cell communication and signaling, 2024-03, Vol.22 (1), p.164-164, Article 164

2024

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MPZL2-a common autosomal recessive deafness gene related to moderate sensorineural hearing loss in the Chinese population

BMC medical genomics, 2024-01, Vol.17 (1), p.32-10, Article 32

2024

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Correction: Multiregion WES of metastatic pancreatic neuroendocrine tumors revealed heterogeneity in genomic alterations, immune microenvironment and evolutionary patterns

Cell communication and signaling, 2024-03, Vol.22 (1), p.181-181, Article 181

2024

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Primary and secondary consolidation compression for saturated soil considering coupling effect of loading and heating

Journal of Central South University, 2021-08, Vol.28 (8), p.2514-2526

2021

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The effects of fibroblast growth factor-2 delivered via a Gelfoam patch on the regeneration of myringosclerotic traumatic eardrum perforations lying close to the malleus

American journal of otolaryngology, 2017-09, Vol.38 (5), p.582-587

2017

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The effect of thermal consolidation on bearing characteristics of static drilling rooted energy pile

IOP conference series. Earth and environmental science, 2021-10, Vol.861 (7), p.72137

2021

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A novel mutation in the TECTA gene in a Chinese family with autosomal dominant nonsyndromic hearing loss

PloS one, 2014-02, Vol.9 (2), p.e89240-e89240

2014

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The functional verification of EGFR-CAR T-cells targeted to hypopharyngeal squamous cell carcinoma

OncoTargets and therapy, 2018-01, Vol.11, p.7053-7059

2018

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Newborn hearing concurrent gene screening can improve care for hearing loss: A study on 14,913 Chinese newborns

International journal of pediatric otorhinolaryngology, 2011-04, Vol.75 (4), p.535-542

2011

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Role of AQP1 in inner ear in motion sickness

Physiology & behavior, 2011-10, Vol.104 (5), p.749-753

2011

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Identification of SLC26A4 c.919-2A>G compound heterozygosity in hearing-impaired patients to improve genetic counseling

Journal of translational medicine, 2012-11, Vol.10 (1), p.225-225, Article 225

2012

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Chondrocyte‐specific Smad4 gene conditional knockout results in hearing loss and inner ear malformation in mice

Developmental dynamics, 2009-08, Vol.238 (8), p.1897-1908

2009

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The Advances in Hearing Rehabilitation and Cochlear Implants in China

Ear and hearing, 2017-11, Vol.38 (6), p.647-652

2017

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A Novel Mutation of POU3F4 Causes Congenital Profound Sensorineural Hearing Loss in a Large Chinese Family

The Laryngoscope, 2006-06, Vol.116 (6), p.944-950

2006

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Corrigendum to “The role of Smad4 in vestibular development in mice” [Int. J. Dev. Neurosci. 29 (2011) 15–23]

International journal of developmental neuroscience, 2011-11, Vol.29 (7), p.783-783

2011

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The role of Smad4 in vestibular development in mice

International journal of developmental neuroscience, 2011-02, Vol.29 (1), p.15-23

2011

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Effect of Drought Stress During Flowering Stage on Starch Accumulation and Starch Synthesis Enzymes in Sorghum Grains

Journal of Integrative Agriculture, 2014-11, Vol.13 (11), p.2399-2406

YI Bing, ZHOU Yu-fei, GAO Ming-yue, ZHANG Zhuang, HAN Yi, YANG Guang-dong, XU Wenjuan, HUANG Rui-dong (1State Key Laboratory of Crop Biology, Shandong Agricultural University, Tai'an 271018, P.R.China 2Bio-Tech Research Center, Shandong Academy of Agricultural Sciences, Ji'nan 250100, P.R.China 3Shandong Rice Research Institute, Ji'nan 250100, P.R.China)

2014

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Congenital middle ear abnormalities with absence of the oval window: diagnosis, surgery, and audiometric outcomes

Otology & neurotology, 2014-08, Vol.35 (7), p.1191-1195

2014

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Nonsense mutations in the PAX3 gene cause Waardenburg syndrome type I in two Chinese patients

Chinese medical journal, 2007-01, Vol.120 (1), p.46-49

2007

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Basic fibroblast growth factor protects auditory neurons and hair cells from glutamate neurotoxicity and noise exposure

Acta oto-laryngologica, 2004-03, Vol.124 (2), p.124-129

2004

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Pulsatile tinnitus in perimenopausal period

Acta oto-laryngologica, 2011-08, Vol.131 (8), p.896-904

2011

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Vibrant Soundbridge implantation via the third window in two Chinese patients with severe bilateral congenital aural atresia

Acta oto-laryngologica, 2014-01, Vol.134 (1), p.1-6

2014

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ossicular reconstruction with sheehy porp

Journal of otology (Beijing), 2009-06, Vol.4 (1), p.50-54

2009

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Microstructure and Abrasive Wear Behavior of Medium Carbon Low Alloy Martensitic Abrasion Resistant Steel

Journal of iron and steel research, international, 2014, Vol.21 (1), p.98-103

2014

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CO2 Dominated Bifunctional Catalytic Sites for Efficient Industrial Exhaust Conversion

Multiregion WES of metastatic pancreatic neuroendocrine tumors revealed heterogeneity in genomic alterations, immune microenvironment and evolutionary patterns

MPZL2-a common autosomal recessive deafness gene related to moderate sensorineural hearing loss in the Chinese population

Correction: Multiregion WES of metastatic pancreatic neuroendocrine tumors revealed heterogeneity in genomic alterations, immune microenvironment and evolutionary patterns

Primary and secondary consolidation compression for saturated soil considering coupling effect of loading and heating

The effects of fibroblast growth factor-2 delivered via a Gelfoam patch on the regeneration of myringosclerotic traumatic eardrum perforations lying close to the malleus

The effect of thermal consolidation on bearing characteristics of static drilling rooted energy pile

A novel mutation in the TECTA gene in a Chinese family with autosomal dominant nonsyndromic hearing loss

The functional verification of EGFR-CAR T-cells targeted to hypopharyngeal squamous cell carcinoma

Newborn hearing concurrent gene screening can improve care for hearing loss: A study on 14,913 Chinese newborns

Role of AQP1 in inner ear in motion sickness

Identification of SLC26A4 c.919-2A>G compound heterozygosity in hearing-impaired patients to improve genetic counseling

Chondrocyte‐specific Smad4 gene conditional knockout results in hearing loss and inner ear malformation in mice

The Advances in Hearing Rehabilitation and Cochlear Implants in China

A Novel Mutation of POU3F4 Causes Congenital Profound Sensorineural Hearing Loss in a Large Chinese Family

Corrigendum to “The role of Smad4 in vestibular development in mice” [Int. J. Dev. Neurosci. 29 (2011) 15–23]

The role of Smad4 in vestibular development in mice

Effect of Drought Stress During Flowering Stage on Starch Accumulation and Starch Synthesis Enzymes in Sorghum Grains

Congenital middle ear abnormalities with absence of the oval window: diagnosis, surgery, and audiometric outcomes

Nonsense mutations in the PAX3 gene cause Waardenburg syndrome type I in two Chinese patients

Basic fibroblast growth factor protects auditory neurons and hair cells from glutamate neurotoxicity and noise exposure

Pulsatile tinnitus in perimenopausal period

Vibrant Soundbridge implantation via the third window in two Chinese patients with severe bilateral congenital aural atresia

ossicular reconstruction with sheehy porp

Microstructure and Abrasive Wear Behavior of Medium Carbon Low Alloy Martensitic Abrasion Resistant Steel

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