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Prenatal Nutritional Deficiency Reprogrammed Postnatal Gene Expression in Mammal Brains: Implications for Schizophrenia.
- Published in:
- International Journal of Neuropsychopharmacology, 2015, p. 1, doi. 10.1093/ijnp/pyu054
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- Publication type:
- Article
The relationship between the therapeutic response to risperidone and the dopamine D<sub>2</sub> receptor polymorphism in Chinese schizophrenia patients.
- Published in:
- International Journal of Neuropsychopharmacology, 2007, v. 10, n. 5, p. 631, doi. 10.1017/S146114570600719X
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- Publication type:
- Article
Pharmacogenomics can improve antipsychotic treatment in schizophrenia.
- Published in:
- Frontiers of Medicine, 2013, v. 7, n. 2, p. 180, doi. 10.1007/s11684-013-0249-3
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- Publication type:
- Article
Modulating neuroinflammation and cognitive function in postoperative cognitive dysfunction via CCR5‐GPCRs‐Ras‐MAPK pathway targeting with microglial EVs.
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- CNS Neuroscience & Therapeutics, 2024, v. 30, n. 8, p. 1, doi. 10.1111/cns.14924
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- Publication type:
- Article
Association of HTR2A Polymorphisms with Risperidone Efficacy in Chinese Han Schizophrenia Patients.
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- Klinik Psikofarmakoloji Bulteni, 2015, v. 25, n. 1, p. 4, doi. 10.5455/bcp.20140802124158
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- Publication type:
- Article
Methylenetetrahydrofolate reductase gene polymorphisms and cerebral palsy in Chinese infants.
- Published in:
- Journal of Human Genetics, 2011, v. 56, n. 1, p. 17, doi. 10.1038/jhg.2010.127
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- Publication type:
- Article
SePreSA: a server for the prediction of populations susceptible to serious adverse drug reactions implementing the methodology of a chemical–protein interactome.
- Published in:
- Nucleic Acids Research, 2009, v. 37, n. suppl_2, p. W406, doi. 10.1093/nar/gkp312
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- Publication type:
- Article
DNA methylome profiling of maternal peripheral blood and placentas reveal potential fetal DNA markers for non-invasive prenatal testing.
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- Molecular Human Reproduction, 2014, v. 20, n. 9, p. 875, doi. 10.1093/molehr/gau048
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- Publication type:
- Article
Promoter hypomethylation of TIMP3 is associated with pre-eclampsia in a Chinese population.
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- Molecular Human Reproduction, 2013, v. 19, n. 3, p. 153, doi. 10.1093/molehr/gas054
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- Publication type:
- Article
A common polymorphism in the human aromatase gene alters the risk for polycystic ovary syndrome and modifies aromatase activity in vitro.
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- Molecular Human Reproduction, 2011, v. 17, n. 11, p. 720, doi. 10.1093/molehr/gar046
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- Publication type:
- Article
A common polymorphism in the human aromatase gene alters the risk for polycystic ovary syndrome and modifies aromatase activity in vitro.
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- Molecular Human Reproduction, 2011, v. 17, n. 6, p. 386, doi. 10.1093/molehr/gar007
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- Publication type:
- Article
Promoter hypomethylation of COMT in human placenta is not associated with the development of pre-eclampsia.
- Published in:
- Molecular Human Reproduction, 2011, v. 17, n. 3, p. 199, doi. 10.1093/molehr/gaq092
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- Publication type:
- Article
A Possible New Mechanism in the Pathophysiology of Polycystic Ovary Syndrome (PCOS): The Discovery That Leukocyte Telomere Length Is Strongly Associated With PCOS.
- Published in:
- 2014
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- Publication type:
- Journal Article
Identification of microRNAs in human follicular fluid: characterization of microRNAs that govern steroidogenesis in vitro and are associated with polycystic ovary syndrome in vivo.
- Published in:
- 2013
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- Publication type:
- Journal Article
Role of microRNA‐145 in protection against myocardial ischemia/reperfusion injury in mice by regulating expression of GZMK with the treatment of sevoflurane.
- Published in:
- Journal of Cellular Physiology, 2019, v. 234, n. 9, p. 16526, doi. 10.1002/jcp.28323
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- Publication type:
- Article
The association of apolipoprotein E gene polymorphisms with cerebral palsy in Chinese infants.
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- Molecular Genetics & Genomics, 2014, v. 289, n. 3, p. 411, doi. 10.1007/s00438-014-0818-4
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- Publication type:
- Article
The aberrantly expressed miR-193b-3p contributes to preeclampsia through regulating transforming growth factor-β signaling.
- Published in:
- Scientific Reports, 2016, p. 19910, doi. 10.1038/srep19910
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- Publication type:
- Article
Quantitative Methylation Level of the <i>EPHX1</i> Promoter in Peripheral Blood DNA Is Associated with Polycystic Ovary Syndrome.
- Published in:
- PLoS ONE, 2014, v. 9, n. 2, p. 1, doi. 10.1371/journal.pone.0088013
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- Publication type:
- Article
Large-Scale Screens of miRNA-mRNA Interactions Unveiled That the 3′UTR of a Gene Is Targeted by Multiple miRNAs.
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- PLoS ONE, 2013, v. 8, n. 7, p. 1, doi. 10.1371/journal.pone.0068204
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- Publication type:
- Article
Up-Regulated Expression and Aberrant DNA Methylation of <i>LEP</i> and <i>SH3PXD2A</i> in Pre-Eclampsia.
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- PLoS ONE, 2013, v. 8, n. 3, p. 1, doi. 10.1371/journal.pone.0059753
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- Publication type:
- Article
No Correlation of hsa-miR-148a with Expression of <i>PXR</i> or <i>CYP3A4</i> in Human Livers from Chinese Han Population.
- Published in:
- PLoS ONE, 2013, v. 8, n. 3, p. 1, doi. 10.1371/journal.pone.0059141
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- Publication type:
- Article
Identification and Functional Study of a New Missense Mutation in the Motor Head Domain of Myosin VIIA in a Family with Autosomal Dominant Hearing Impairment (DFNA11).
- Published in:
- PLoS ONE, 2013, v. 8, n. 1, p. 1, doi. 10.1371/journal.pone.0055178
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- Publication type:
- Article
A Functional Alternative Splicing Mutation in AIRE Gene Causes Autoimmune Polyendocrine Syndrome Type 1.
- Published in:
- PLoS ONE, 2013, v. 8, n. 1, p. 1, doi. 10.1371/journal.pone.0053981
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- Publication type:
- Article
Dynamic Network of Transcription and Pathway Crosstalk to Reveal Molecular Mechanism of MGd-Treated Human Lung Cancer Cells.
- Published in:
- PLoS ONE, 2012, v. 7, n. 5, p. 1, doi. 10.1371/journal.pone.0031984
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- Publication type:
- Article
An association study of IL2RA polymorphisms with cerebral palsy in a Chinese population.
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- BMC Medical Genomics, 2022, v. 15, n. 1, p. 1, doi. 10.1186/s12920-022-01350-5
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- Publication type:
- Article
Identification of a novel ADAR mutation in a Chinese family with dyschromatosis symmetrica hereditaria (DSH).
- Published in:
- Archives of Dermatological Research, 2005, v. 297, n. 3, p. 139, doi. 10.1007/s00403-005-0589-1
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- Publication type:
- Article
Common genetic variation in the 3′-untranslated region of gonadotropin-releasing hormone receptor regulates gene expression in cella and is associated with thyroid function, insulin secretion as well as insulin sensitivity in polycystic ovary syndrome patients
- Published in:
- Human Genetics, 2011, v. 129, n. 5, p. 553, doi. 10.1007/s00439-011-0954-4
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- Publication type:
- Article
A locus for familial generalized lentiginosis without systemic involvement maps to chromosome 4q21.1–q22.3.
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- Human Genetics, 2005, v. 117, n. 2/3, p. 154, doi. 10.1007/s00439-005-1284-1
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- Publication type:
- Article
Genetic variants in the BDNF gene and therapeutic response to risperidone in schizophrenia patients: a pharmacogenetic study.
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- European Journal of Human Genetics, 2010, v. 18, n. 6, p. 707, doi. 10.1038/ejhg.2009.238
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- Publication type:
- Article
A Variant of the Autophagy-Related 5 Gene Is Associated with Child Cerebral Palsy.
- Published in:
- Frontiers in Cellular Neuroscience, 2017, p. 1, doi. 10.3389/fncel.2017.00407
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- Publication type:
- Article
The Association Study of IL-23R Polymorphisms With Cerebral Palsy in Chinese Population.
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- Frontiers in Neuroscience, 2020, v. 14, p. N.PAG, doi. 10.3389/fnins.2020.590098
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- Article
Comprehensive Transcriptomic Analysis of Mouse Gonadal Development Involving Sexual Differentiation, Meiosis and Gametogenesis.
- Published in:
- Biological Procedures Online, 2019, v. 21, n. 1, p. N.PAG, doi. 10.1186/s12575-019-0108-y
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- Article
Genetic association study of adaptor protein complex 4 with cerebral palsy in a Han Chinese population.
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- Molecular Biology Reports, 2013, v. 40, n. 11, p. 6459, doi. 10.1007/s11033-013-2761-6
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- Publication type:
- Article
Common genetic variation in CYP1B1 is associated with concentrations of T, FT and FT in the sera of polycystic ovary syndrome patients.
- Published in:
- Molecular Biology Reports, 2013, v. 40, n. 4, p. 3315, doi. 10.1007/s11033-012-2406-1
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- Publication type:
- Article
Effects of the Dopamine D<sub>3</sub> Receptor (DRD3) Gene Polymorphisms on Risperidone Response: A Pharmacogenetic Study.
- Published in:
- Neuropsychopharmacology, 2008, v. 33, n. 2, p. 305, doi. 10.1038/sj.npp.1301418
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- Publication type:
- Article
Long non‐coding RNA ESCCAL‐1/miR‐590/LRP6 signaling pathway participates in the progression of esophageal squamous cell carcinoma.
- Published in:
- Cancer Medicine, 2023, v. 12, n. 1, p. 445, doi. 10.1002/cam4.4915
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- Publication type:
- Article
Identification of circular RNA biomarkers for Pien Tze Huang treatment of CCl<sub>4</sub>-induced liver fibrosis using RNA-sequencing.
- Published in:
- Molecular Medicine Reports, 2022, v. 26, n. 4, p. N.PAG, doi. 10.3892/mmr.2022.12825
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- Publication type:
- Article
Association of <italic>NOS1</italic> gene polymorphisms with cerebral palsy in a Han Chinese population: a case-control study.
- Published in:
- 2018
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- Publication type:
- Case Study
Variants of the OLIG2 Gene are Associated with Cerebral Palsy in Chinese Han Infants with Hypoxic-Ischemic Encephalopathy.
- Published in:
- NeuroMolecular Medicine, 2019, v. 21, n. 1, p. 75, doi. 10.1007/s12017-018-8510-1
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- Publication type:
- Article
Association Between Osteopontin Gene Polymorphisms and Cerebral Palsy in a Chinese Population.
- Published in:
- NeuroMolecular Medicine, 2016, v. 18, n. 2, p. 232, doi. 10.1007/s12017-016-8397-7
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- Publication type:
- Article
p53 regulates ERK1/2/ CREB cascade via a novel SASH1/ MAP2K2 crosstalk to induce hyperpigmentation.
- Published in:
- Journal of Cellular & Molecular Medicine, 2017, v. 21, n. 10, p. 2465, doi. 10.1111/jcmm.13168
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- Publication type:
- Article
A novel P53/ POMC/Gαs/ SASH1 autoregulatory feedback loop activates mutated SASH1 to cause pathologic hyperpigmentation.
- Published in:
- Journal of Cellular & Molecular Medicine, 2017, v. 21, n. 4, p. 802, doi. 10.1111/jcmm.13022
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- Publication type:
- Article
The DNA methylation status of genes encoding Matrix metalloproteinases and tissue inhibitors of Matrix metalloproteinases in endometriosis.
- Published in:
- Molecular Reproduction & Development, 2018, v. 85, n. 1, p. 17, doi. 10.1002/mrd.22931
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- Publication type:
- Article
Serum CD203c+ Extracellular Vesicle Serves as a Novel Diagnostic and Prognostic Biomarker for Succinylated Gelatin Induced Perioperative Hypersensitive Reaction.
- Published in:
- Frontiers in Immunology, 2021, v. 12, p. 1, doi. 10.3389/fimmu.2021.732209
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- Publication type:
- Article
Establishment of a mathematical prediction model for voriconazole stable maintenance dose: a prospective study.
- Published in:
- Frontiers in Cellular & Infection Microbiology, 2023, p. 1, doi. 10.3389/fcimb.2023.1157944
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- Publication type:
- Article
Clinical, Viral and Genetic Characteristics of Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS) in Shanghai, China.
- Published in:
- Acta Dermato-Venereologica, 2018, v. 98, n. 4, p. 401, doi. 10.2340/00015555-2867
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- Publication type:
- Article
Regulation of cytochrome P450 3A4 by small vault RNAb derived from the non-coding vault RNA1 of multidrug resistance-linked vault particle.
- Published in:
- Molecular Medicine Reports, 2016, v. 14, n. 1, p. 387, doi. 10.3892/mmr.2016.5228
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- Publication type:
- Article
Ildr1b is essential for semicircular canal development, migration of the posterior lateral line primordium and hearing ability in zebrafish: implications for a role in the recessive hearing impairment DFNB42.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 23, p. 6201, doi. 10.1093/hmg/ddu340
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- Publication type:
- Article
Lack of the brain-specific isoform of apoptosis-inducing factor aggravates cerebral damage in a model of neonatal hypoxia–ischemia.
- Published in:
- Cell Death & Disease, 2019, v. 10, n. 1, p. 1, doi. 10.1038/s41419-018-1250-1
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- Publication type:
- Article
Gain‐of‐Function KIDINS220 Variants Disrupt Neuronal Development and Cause Cerebral Palsy.
- Published in:
- Movement Disorders, 2024, v. 39, n. 3, p. 498, doi. 10.1002/mds.29694
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- Publication type:
- Article