Found: 15
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Therapeutic inhibition of CXC chemokine receptor 2 by SB225002 attenuates LPS-induced acute lung injury in mice.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Rh-CXCL-12 Attenuates Neuronal Pyroptosis after Subarachnoid Hemorrhage in Rats via Regulating the CXCR4/NLRP1 Pathway.
- Published in:
- Oxidative Medicine & Cellular Longevity, 2021, p. 1, doi. 10.1155/2021/6966394
- By:
- Publication type:
- Article
gene variation is associated with the risk for conotruncal heart defects in Chinese population.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Familial congenital heart disease: data collection and preliminary analysis.
- Published in:
- Cardiology in the Young, 2013, v. 23, n. 3, p. 394, doi. 10.1017/S1047951112001035
- By:
- Publication type:
- Article
Identification of two CUL7 variants in two Chinese families with 3-M syndrome by whole-exome sequencing.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Further delineation of autosomal recessive intellectual disability syndrome caused by homozygous variant of the NSUN2 gene in a chinese pedigree.
- Published in:
- Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 12, p. 1, doi. 10.1002/mgg3.1518
- By:
- Publication type:
- Article
Therapeutic inhibition of CXC chemokine receptor 2 by SB225002 attenuates LPS-induced acute lung injury in mice.
- Published in:
- Archives of Medical Science, 2018, v. 14, n. 3, p. 635, doi. 10.5114/aoms.2017.64980
- By:
- Publication type:
- Article
Corrigendum to: A 55-Day-Old Female Infant Infected With 2019 Novel Coronavirus Disease: Presenting With Pneumonia, Liver Injury, and Heart Damage.
- Published in:
- 2020
- By:
- Publication type:
- journal article
A 55-Day-Old Female Infant Infected With 2019 Novel Coronavirus Disease: Presenting With Pneumonia, Liver Injury, and Heart Damage.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Novel TRAPPC11 Mutations in a Chinese Pedigree of Limb Girdle Muscular Dystrophy.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
A Potential Relationship among Beta-Defensins Haplotype, SOX7 Duplication and Cardiac Defects.
- Published in:
- PLoS ONE, 2013, v. 8, n. 8, p. 1, doi. 10.1371/journal.pone.0072515
- By:
- Publication type:
- Article
Exome Sequencing Identifies a Novel MYH7 p.G407C Mutation Responsible for Familial Hypertrophic Cardiomyopathy.
- Published in:
- DNA & Cell Biology, 2014, v. 33, n. 10, p. 699, doi. 10.1089/dna.2014.2483
- By:
- Publication type:
- Article
Genetic variation in folate metabolism is associated with the risk of conotruncal heart defects in a Chinese population.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Identification of two novel GATA6 mutations in patients with nonsyndromic conotruncal heart defects.
- Published in:
- Molecular Medicine Reports, 2014, v. 10, n. 2, p. 743, doi. 10.3892/mmr.2014.2247
- By:
- Publication type:
- Article
Influence of genes and the environment in familial congenital heart defects.
- Published in:
- Molecular Medicine Reports, 2014, v. 9, n. 2, p. 695, doi. 10.3892/mmr.2013.1847
- By:
- Publication type:
- Article