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Nature and evolution of the Late Cretaceous lithospheric mantle beneath the eastern Jiangnan orogenic belt: constraints from peridotite xenoliths

Contributions to mineralogy and petrology, 2022-02, Vol.177 (2), Article 25

2022

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Characteristics and patterns of residential energy consumption for space cooling in China: Evidence from appliance-level data

Energy (Oxford), 2023-02, Vol.265, p.126395, Article 126395

2023

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Mechanistic Basis for the High Enantioselectivity and Activity in the Multichiral Bimetallic Complex-Mediated Enantioselective Copolymerization of meso-Epoxides

ACS catalysis, 2022-10, Vol.12 (19), p.12268-12280

2022

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Recommendations for Acupuncture in Clinical Practice Guidelines of the National Guideline Clearinghouse

Chinese journal of integrative medicine, 2017-11, Vol.23 (11), p.864-870

2017

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Identification of a Novel Mutation in Solute Carrier Family 29, Member 3 in a Chinese Patient with H Syndrome

Chinese medical journal, 2015-05, Vol.128 (10), p.1336-1339

2015

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Surface Tension Model Based on Implicit Incompressible Smoothed Particle Hydrodynamics for Fluid Simulation

Journal of computer science and technology, 2017-11, Vol.32 (6), p.1186-1197

2017

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Surface Tension Model Based on Implicit Incompressible Smoothed Particle Hydrodynamics for Fluid Simulation

计算机科学技术学报：英文版, 2017, Vol.32 (6), p.1186-1197

Xiao-Kun Wang Xiao-Juan Ban Ya-Lan Zhang Si-Nuo Liu Peng-Fei Ye

2017

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Transcriptomic analysis of the upper lip and primary palate development in mice

Frontiers in genetics, 2023-01, Vol.13, p.1039850-1039850

2023

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WDSPdb: an updated resource for WD40 proteins

Bioinformatics, 2019-11, Vol.35 (22), p.4824-4826

2019

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Generation of an induced pluripotent stem cell line from a congenital microtia patient with 4p16.1 microduplication involving the long-range enhancer of HMX1

Stem cell research, 2021-05, Vol.53, p.102357-102357, Article 102357

2021

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Keratin 5-Cre-driven deletion of Ncstn in an acne inversa-like mouse model leads to a markedly increased IL-36a and Sprr2 expression

Frontiers of medicine, 2020-06, Vol.14 (3), p.305-317

2020

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Duplications involving the long range HMX1 enhancer are associated with human isolated bilateral concha-type microtia

Journal of translational medicine, 2020-06, Vol.18 (1), p.244-244, Article 244

2020

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Molecular analysis of inherited cardiomyopathy using next generation semiconductor sequencing technologies

Journal of translational medicine, 2018-08, Vol.16 (1), p.241-241, Article 241

2018

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De novo 22q11.2 deletions and auricular findings in two Chinese patients with microtia

Molecular genetics & genomic medicine, 2022-01, Vol.10 (1), p.e1862-n/a

2022

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Identification of a Novel TP63 Variant in a Chinese Patient with Orofacial Clefts and Ectrodactyly: Case Report and Literature Review

The Cleft palate-craniofacial journal, 2024-05, p.10556656241241132-10556656241241132

2024

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Functional Pathway and Process Enrichment Analysis of Genes Associated With Morphological Abnormalities of the Outer Ear

The Journal of craniofacial surgery, 2023-03, Vol.34 (2), p.489

2023

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Heterogeneity of Accompanying Phenotypes and Genomic Variants Involved in Microtia

The Journal of craniofacial surgery, 2022-03, Vol.33 (2), p.432

2022

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Identification of loss-of-function HOXA2 mutations in Chinese families with dominant bilateral microtia

Gene, 2020-10, Vol.757, p.144945-144945, Article 144945

2020

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Gross deletions in FBN1 results in variable phenotypes of Marfan syndrome

Clinica chimica acta, 2017-11, Vol.474, p.54-59

2017

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Application of next-generation sequencing to screen for pathogenic mutations in 123 unrelated Chinese patients with Marfan syndrome or a related disease

Science China. Life sciences, 2019-12, Vol.62 (12), p.1630-1637

2019

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Model development and validation of noninvasive parameters based on coronary computed tomography angiography to predict culprit lesions in acute coronary syndromes within 3 years: value of plaque characteristics, hemodynamics and pericoronary adipose tissue

Quantitative imaging in medicine and surgery, 2023-07, Vol.13 (7), p.4325-4338

2023

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Identification of patients with acute coronary syndrome and representation of their degree of inflammation: application of pericoronary adipose tissue within different radial distances of the proximal coronary arteries

Quantitative imaging in medicine and surgery, 2023-06, Vol.13 (6), p.3644-3659

2023

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Steroid sulfatase and filaggrin mutations in a boy with severe ichthyosis, elevated serum IgE level and moyamoya syndrome

Gene, 2017-09, Vol.628, p.103-108

2017

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A Novel COL4A5 Splicing Mutation Causes Skipping of Exon 14 in a Chinese Family with Alport Syndrome

Kidney diseases, 2020-01, Vol.6 (1), p.43-49

2020

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Novel TRPM6 Mutations in Familial Hypomagnesemia with Secondary Hypocalcemia

American journal of nephrology, 2013-06, Vol.37 (6), p.541-548

2013

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Nature and evolution of the Late Cretaceous lithospheric mantle beneath the eastern Jiangnan orogenic belt: constraints from peridotite xenoliths

Characteristics and patterns of residential energy consumption for space cooling in China: Evidence from appliance-level data

Mechanistic Basis for the High Enantioselectivity and Activity in the Multichiral Bimetallic Complex-Mediated Enantioselective Copolymerization of meso-Epoxides

Recommendations for Acupuncture in Clinical Practice Guidelines of the National Guideline Clearinghouse

Identification of a Novel Mutation in Solute Carrier Family 29, Member 3 in a Chinese Patient with H Syndrome

Surface Tension Model Based on Implicit Incompressible Smoothed Particle Hydrodynamics for Fluid Simulation

Surface Tension Model Based on Implicit Incompressible Smoothed Particle Hydrodynamics for Fluid Simulation

Transcriptomic analysis of the upper lip and primary palate development in mice

WDSPdb: an updated resource for WD40 proteins

Generation of an induced pluripotent stem cell line from a congenital microtia patient with 4p16.1 microduplication involving the long-range enhancer of HMX1

Keratin 5-Cre-driven deletion of Ncstn in an acne inversa-like mouse model leads to a markedly increased IL-36a and Sprr2 expression

Duplications involving the long range HMX1 enhancer are associated with human isolated bilateral concha-type microtia

Molecular analysis of inherited cardiomyopathy using next generation semiconductor sequencing technologies

De novo 22q11.2 deletions and auricular findings in two Chinese patients with microtia

Identification of a Novel TP63 Variant in a Chinese Patient with Orofacial Clefts and Ectrodactyly: Case Report and Literature Review

Functional Pathway and Process Enrichment Analysis of Genes Associated With Morphological Abnormalities of the Outer Ear

Heterogeneity of Accompanying Phenotypes and Genomic Variants Involved in Microtia

Identification of loss-of-function HOXA2 mutations in Chinese families with dominant bilateral microtia

Gross deletions in FBN1 results in variable phenotypes of Marfan syndrome

Application of next-generation sequencing to screen for pathogenic mutations in 123 unrelated Chinese patients with Marfan syndrome or a related disease

Model development and validation of noninvasive parameters based on coronary computed tomography angiography to predict culprit lesions in acute coronary syndromes within 3 years: value of plaque characteristics, hemodynamics and pericoronary adipose tissue

Identification of patients with acute coronary syndrome and representation of their degree of inflammation: application of pericoronary adipose tissue within different radial distances of the proximal coronary arteries

Steroid sulfatase and filaggrin mutations in a boy with severe ichthyosis, elevated serum IgE level and moyamoya syndrome

A Novel COL4A5 Splicing Mutation Causes Skipping of Exon 14 in a Chinese Family with Alport Syndrome

Novel TRPM6 Mutations in Familial Hypomagnesemia with Secondary Hypocalcemia

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