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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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Cyanobacterial‐ and moss‐forming biocrusts consistently decrease the temperature sensitivity of microbial respiration along a continental precipitation gradient

Functional ecology, 2022-12, Vol.36 (12), p.3107-3119

2022

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Assessing the Content Quality of Industry Technology Roadmaps

Sustainability, 2023-06, Vol.15 (11), p.9058

2023

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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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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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Patterns of organic carbon and nitrogen stocks in soil particle-size fractions along an aridity gradient in Northern China’s deserts

Catena (Giessen), 2023-02, Vol.221, p.106785, Article 106785

2023

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Dexamethasone protects against asthma via regulating Hif-1α-glycolysis-lactate axis and protein lactylation

International immunopharmacology, 2024-04, Vol.131, p.111791-111791, Article 111791

2024

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A novel mutation in the CRYAA gene associated with congenital cataract and microphthalmia in a Chinese family

BMC medical genetics, 2018-10, Vol.19 (1), p.190-190, Article 190

2018

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Clinical and genetic findings in patients with congenital cataract and heart diseases

Orphanet journal of rare diseases, 2021-05, Vol.16 (1), p.1-242, Article 242

2021

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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 a human induced pluripotent stem cell line (PSHi002-A) from a Treacher-Collins syndrome patient carrying a TCOF1 gene mutation (c.1966_1969dup)

Stem cell research, 2021-08, Vol.55, p.102437-102437, Article 102437

2021

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Identification of novel mutations in EYA3 and EFTUD2 in a family with craniofacial microsomia: evidence of digenic inheritance

Frontiers of medicine, 2023-10, Vol.17 (5), p.1006-1009

2023

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Melatonin regulates circadian clock proteins expression in allergic airway inflammation

Heliyon, 2024-03, Vol.10 (6), p.e27471-e27471, Article e27471

2024

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A 105 kb interstitial insertion in the Xq27.1 palindrome from pseudoautosomal region PAR1 causes a novel X-linked recessive compound phenotype

Journal of translational medicine, 2019-04, Vol.17 (1), p.138-138, Article 138

2019

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Cu-catalyzed decarboxylative annulation of proline derivatives: multi-component synthesis of functionalized chromeno[2,3- c ]-pyrrol-9(1 H )-one derivatives

Organic Chemistry Frontiers, 2023-06, Vol.10 (12), p.2994-2999

2023

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Genetic Screening of Targeted Region on the Chromosome 22q11.2 in Patients with Microtia and Congenital Heart Defect

Genes, 2023-04, Vol.14 (4), p.879

2023

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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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Slc20a2 -Deficient Mice Exhibit Multisystem Abnormalities and Impaired Spatial Learning Memory and Sensorimotor Gating but Normal Motor Coordination Abilities

Frontiers in genetics, 2021-04, Vol.12, p.639935-639935

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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17p13.3 genomic rearrangement in a Chinese family with split-hand/foot malformation with long bone deficiency: report of a complicated duplication with marked variation in phenotype

Orphanet journal of rare diseases, 2018-07, Vol.13 (1), p.106-106, Article 106

2018

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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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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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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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Research progress of temperature, humidity and pressure detection technology using raman lidar

Chinese Optics, 2023, Vol.16 (2), p.243-257

2023

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

Cyanobacterial‐ and moss‐forming biocrusts consistently decrease the temperature sensitivity of microbial respiration along a continental precipitation gradient

Assessing the Content Quality of Industry Technology Roadmaps

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

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

Patterns of organic carbon and nitrogen stocks in soil particle-size fractions along an aridity gradient in Northern China’s deserts

Dexamethasone protects against asthma via regulating Hif-1α-glycolysis-lactate axis and protein lactylation

A novel mutation in the CRYAA gene associated with congenital cataract and microphthalmia in a Chinese family

Clinical and genetic findings in patients with congenital cataract and heart diseases

WDSPdb: an updated resource for WD40 proteins

Generation of a human induced pluripotent stem cell line (PSHi002-A) from a Treacher-Collins syndrome patient carrying a TCOF1 gene mutation (c.1966_1969dup)

Identification of novel mutations in EYA3 and EFTUD2 in a family with craniofacial microsomia: evidence of digenic inheritance

Melatonin regulates circadian clock proteins expression in allergic airway inflammation

A 105 kb interstitial insertion in the Xq27.1 palindrome from pseudoautosomal region PAR1 causes a novel X-linked recessive compound phenotype

Cu-catalyzed decarboxylative annulation of proline derivatives: multi-component synthesis of functionalized chromeno[2,3- c ]-pyrrol-9(1 H )-one derivatives

Genetic Screening of Targeted Region on the Chromosome 22q11.2 in Patients with Microtia and Congenital Heart Defect

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

Slc20a2 -Deficient Mice Exhibit Multisystem Abnormalities and Impaired Spatial Learning Memory and Sensorimotor Gating but Normal Motor Coordination Abilities

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

17p13.3 genomic rearrangement in a Chinese family with split-hand/foot malformation with long bone deficiency: report of a complicated duplication with marked variation in phenotype

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

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

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

Research progress of temperature, humidity and pressure detection technology using raman lidar

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