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Multiple gene variations contributed to congenital heart disease via GATA family transcriptional regulation.
- Published in:
- 2017
- By:
- Publication type:
- journal article
microRNA expression profiling of heart tissue during fetal development.
- Published in:
- International Journal of Molecular Medicine, 2014, v. 33, n. 5, p. 1250, doi. 10.3892/ijmm.2014.1691
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- Publication type:
- Article
Association between mRNA levels of DNMT1, DNMT3A, DNMT3B, MBD2 and LINE-1 methylation status in infants with tetralogy of Fallot.
- Published in:
- International Journal of Molecular Medicine, 2013, v. 32, n. 3, p. 694, doi. 10.3892/ijmm.2013.1427
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- Publication type:
- Article
Construction of P‐Chiral Alkenylphosphine Oxides through Highly Chemo‐, Regio‐, and Enantioselective Hydrophosphinylation of Alkynes.
- Published in:
- Angewandte Chemie International Edition, 2020, v. 59, n. 46, p. 20645, doi. 10.1002/anie.202009358
- By:
- Publication type:
- Article
Enantioselective Dicarbofunctionalization of Unactivated Alkenes by Palladium‐Catalyzed Tandem Heck/Suzuki Coupling Reaction.
- Published in:
- Angewandte Chemie International Edition, 2019, v. 58, n. 41, p. 14653, doi. 10.1002/anie.201907840
- By:
- Publication type:
- Article
Palladium‐Catalyzed Enantioselective Reductive Heck Reactions: Convenient Access to 3,3‐Disubstituted 2,3‐Dihydrobenzofuran.
- Published in:
- Angewandte Chemie International Edition, 2018, v. 57, n. 32, p. 10373, doi. 10.1002/anie.201806372
- By:
- Publication type:
- Article
H3K9me3, H3K36me3, and H4K20me3 Expression Correlates with Patient Outcome in Esophageal Squamous Cell Carcinoma as Epigenetic Markers.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Novel PAK3 gene missense variant associated with two Chinese siblings with intellectual disability: a case report.
- Published in:
- BMC Medical Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s12881-020-0957-x
- By:
- Publication type:
- Article
Construction of P‐Chiral Alkenylphosphine Oxides through Highly Chemo‐, Regio‐, and Enantioselective Hydrophosphinylation of Alkynes.
- Published in:
- Angewandte Chemie, 2020, v. 132, n. 46, p. 20826, doi. 10.1002/ange.202009358
- By:
- Publication type:
- Article
Enantioselective Dicarbofunctionalization of Unactivated Alkenes by Palladium‐Catalyzed Tandem Heck/Suzuki Coupling Reaction.
- Published in:
- Angewandte Chemie, 2019, v. 131, n. 41, p. 14795, doi. 10.1002/ange.201907840
- By:
- Publication type:
- Article
Thirteen New Patients of PPP2R5D Gene Mutation and the Fine Profile of Genotype–Phenotype Correlation Unraveling the Pathogenic Mechanism Underlying Macrocephaly Phenotype.
- Published in:
- Children, 2024, v. 11, n. 8, p. 897, doi. 10.3390/children11080897
- By:
- Publication type:
- Article
Optimized trio genome sequencing (OTGS) as a first-tier genetic test in critically ill infants: practice in China.
- Published in:
- Human Genetics, 2020, v. 139, n. 4, p. 473, doi. 10.1007/s00439-019-02103-8
- By:
- Publication type:
- Article
A primary role of TET proteins in establishment and maintenance of De Novo bivalency at CpG islands.
- Published in:
- Nucleic Acids Research, 2016, v. 44, n. 18, p. 8682, doi. 10.1093/nar/gkw529
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- Publication type:
- Article
Genetic spectrum of renal disease for 1001 Chinese children based on a multicenter registration system.
- Published in:
- Clinical Genetics, 2019, v. 96, n. 5, p. 402, doi. 10.1111/cge.13606
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- Publication type:
- Article
How disentangled sense of agency and sense of ownership can interact with different emotional events on stress feelings.
- Published in:
- Psicologia: Reflexão e Critica, 2017, v. 30, n. 1, p. 1, doi. 10.1186/s41155-017-0071-y
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- Publication type:
- Article
Influences of Extraction Methods on Physicochemical and Functional Characteristics of Three New Bulbil Starches from Dioscorea opposita Thunb. cv. Tiegun.
- Published in:
- Molecules, 2019, v. 24, n. 12, p. 2232, doi. 10.3390/molecules24122232
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- Publication type:
- Article
Hypomethylation and decreased expression of BRG1 in the myocardium of patients with congenital heart disease.
- Published in:
- Birth Defects Research, 2017, v. 109, n. 15, p. 1183, doi. 10.1002/bdr2.1053
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- Publication type:
- Article
HBx increases chromatin accessibility and ETV4 expression to regulate dishevelled-2 and promote HCC progression.
- Published in:
- Cell Death & Disease, 2022, v. 13, n. 2, p. 1, doi. 10.1038/s41419-022-04563-9
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- Publication type:
- Article
A world renowned psychophysiologist: Kaoliang Chow.
- Published in:
- Protein & Cell, 2022, v. 13, n. 12, p. 873, doi. 10.1007/s13238-020-00797-5
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- Publication type:
- Article
Tsai Chiao: The founder of physiology and aviation, aerospace and navigation medicine in China.
- Published in:
- Protein & Cell, 2022, v. 13, n. 11, p. 779, doi. 10.1007/s13238-020-00737-3
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- Publication type:
- Article
Te-Pei Feng: a pioneer of neuromuscular physiology in China.
- Published in:
- Protein & Cell, 2022, v. 13, n. 6, p. 387, doi. 10.1007/s13238-021-00850-x
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- Publication type:
- Article
Correction to: A world renowned psychophysiologist: Kaoliang Chow.
- Published in:
- 2022
- By:
- Publication type:
- Correction Notice
Kuo-Hua Sun: The founder of physiologic psychology and child psychology in China.
- Published in:
- Protein & Cell, 2021, v. 12, n. 8, p. 593, doi. 10.1007/s13238-019-00666-w
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- Publication type:
- Article
Zing-Yang Kuo and behavior epigenesis based on animal experiments.
- Published in:
- Protein & Cell, 2020, v. 11, n. 6, p. 387, doi. 10.1007/s13238-018-0516-9
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- Publication type:
- Article
Chi-Nan Hu—Pioneer of Chinese neuroscience and cognitive science.
- Published in:
- Protein & Cell, 2020, v. 11, n. 7, p. 465, doi. 10.1007/s13238-019-00658-w
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- Publication type:
- Article
Jiao Shao: A forerunner of physiological psychology and comparative psychology in China.
- Published in:
- Protein & Cell, 2019, v. 10, n. 9, p. 623, doi. 10.1007/s13238-018-0592-x
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- Publication type:
- Article
Yu-Tao Loo and the development of neuropsychology in China.
- Published in:
- Protein & Cell, 2017, v. 8, n. 7, p. 473, doi. 10.1007/s13238-017-0376-8
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- Publication type:
- Article
Novel Variants of the SMARCA4 Gene Associated with Autistic Features Rather Than Typical Coffin-Siris Syndrome in Eight Chinese Pediatric Patients.
- Published in:
- Journal of Autism & Developmental Disorders, 2022, v. 52, n. 11, p. 5033, doi. 10.1007/s10803-021-05365-2
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- Publication type:
- Article
Phenotypic spectrum and genetics of PAX2-related disorder in the Chinese cohort.
- Published in:
- BMC Medical Genomics, 2021, v. 14, n. 1, p. 1, doi. 10.1186/s12920-021-01102-x
- By:
- Publication type:
- Article
Association of Promoter Methylation Statuses of Congenital Heart Defect Candidate genes with Tetralogy of Fallot.
- Published in:
- Journal of Translational Medicine, 2014, v. 12, n. 1, p. 1, doi. 10.1186/1479-5876-12-31
- By:
- Publication type:
- Article
Association of promoter methylation statuses of congenital heart defect candidate genes with Tetralogy of Fallot.
- Published in:
- 2014
- By:
- Publication type:
- journal article
miRNA‑mRNA network contributes to HBV‑related hepatocellular carcinoma via immune infiltration induced by GRB2.
- Published in:
- Biomedical Reports, 2024, v. 20, n. 6, p. N.PAG, doi. 10.3892/br.2024.1777
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- Publication type:
- Article
COQ8B nephropathy: Early detection and optimal treatment.
- Published in:
- Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 8, p. 1, doi. 10.1002/mgg3.1360
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- Publication type:
- Article
Cover.
- Published in:
- Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 8, p. 1, doi. 10.1002/mgg3.1458
- By:
- Publication type:
- Article
Clinical exome sequencing identifies novel CREBBP variants in 18 Chinese Rubinstein–Taybi Syndrome kids with high frequency of polydactyly.
- Published in:
- Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 12, p. N.PAG, doi. 10.1002/mgg3.1009
- By:
- Publication type:
- Article
LncRNA TRERNA1 facilitates hepatocellular carcinoma metastasis by dimethylating H3K9 in the CDH1 promoter region via the recruitment of the EHMT2/SNAI1 complex.
- Published in:
- Cell Proliferation, 2019, v. 52, n. 4, p. N.PAG, doi. 10.1111/cpr.12621
- By:
- Publication type:
- Article
Novel Variants of PPP2R1A in Catalytic Subunit Binding Domain and Genotype–Phenotype Analysis in Neurodevelopmentally Delayed Patients.
- Published in:
- Genes, 2023, v. 14, n. 9, p. 1750, doi. 10.3390/genes14091750
- By:
- Publication type:
- Article
MicroRNA expression signature for Satb2-induced osteogenic differentiation in bone marrow stromal cells.
- Published in:
- Molecular & Cellular Biochemistry, 2014, v. 387, n. 1/2, p. 227, doi. 10.1007/s11010-013-1888-z
- By:
- Publication type:
- Article
Genome-wide methylation analysis reveals differentially methylated CpG sites and altered expression of heart development-associated genes in fetuses with cardiac defects.
- Published in:
- Experimental & Therapeutic Medicine, 2021, v. 22, n. 3, p. N.PAG, doi. 10.3892/etm.2021.10464
- By:
- Publication type:
- Article
CUL4B activates Wnt/β-catenin signalling in hepatocellular carcinoma by repressing Wnt antagonists.
- Published in:
- Journal of Pathology, 2015, v. 235, n. 5, p. 784, doi. 10.1002/path.4492
- By:
- Publication type:
- Article
Lack of CUL4B leads to increased abundance of GFAP-positive cells that is mediated by PTGDS in mouse brain.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 16, p. 4686, doi. 10.1093/hmg/ddv200
- By:
- Publication type:
- Article
Lack of Cul4b, an E3 Ubiquitin Ligase Component, Leads to Embryonic Lethality and Abnormal Placental Development.
- Published in:
- PLoS ONE, 2012, v. 7, n. 5, p. 1, doi. 10.1371/journal.pone.0037070
- By:
- Publication type:
- Article
Palladium‐Catalyzed Enantioselective Reductive Heck Reactions: Convenient Access to 3,3‐Disubstituted 2,3‐Dihydrobenzofuran.
- Published in:
- Angewandte Chemie, 2018, v. 130, n. 32, p. 10530, doi. 10.1002/ange.201806372
- By:
- Publication type:
- Article
Clinical utility of 24-h rapid trio-exome sequencing for critically ill infants.
- Published in:
- NPJ Genomic Medicine, 2020, v. 5, n. 1, p. 1, doi. 10.1038/s41525-020-0129-0
- By:
- Publication type:
- Article
Case Report: Complete Maternal Uniparental Isodisomy of Chromosome 5 (iUPD(5)mat) With PCSK1 Nonsense Variant in an Infant With Recurrent Diarrhea.
- Published in:
- Frontiers in Genetics, 2021, v. 11, p. N.PAG, doi. 10.3389/fgene.2021.668326
- By:
- Publication type:
- Article
Lentiviral-mediated expression of SATB2 promotes osteogenic differentiation of bone marrow stromal cells in vitro and in vivo.
- Published in:
- European Journal of Oral Sciences, 2014, v. 122, n. 3, p. 190, doi. 10.1111/eos.12122
- By:
- Publication type:
- Article
The roles of SMYD4 in epigenetic regulation of cardiac development in zebrafish.
- Published in:
- PLoS Genetics, 2018, v. 14, n. 8, p. 1, doi. 10.1371/journal.pgen.1007578
- By:
- Publication type:
- Article
First‐Principles Investigation About Different Sequence of Stereochemical Activity and Birefringence in Antimony Halides.
- Published in:
- Physica Status Solidi (B), 2022, v. 259, n. 7, p. 1, doi. 10.1002/pssb.202100576
- By:
- Publication type:
- Article
WDR62 variants contribute to congenital heart disease by inhibiting cardiomyocyte proliferation.
- Published in:
- Clinical & Translational Medicine, 2022, v. 12, n. 7, p. 1, doi. 10.1002/ctm2.941
- By:
- Publication type:
- Article
LINC00673 Represses CDKN2C and Promotes the Proliferation of Esophageal Squamous Cell Carcinoma Cells by EZH2-Mediated H3K27 Trimethylation.
- Published in:
- Frontiers in Oncology, 2020, v. 10, p. N.PAG, doi. 10.3389/fonc.2020.01546
- By:
- Publication type:
- Article