Found: 107
Select item for more details and to access through your institution.
PBX1, EMCN and ERG are associated with the sub-clusters and the prognosis of VHL mutant clear cell renal cell carcinoma.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-13148-7
- By:
- Publication type:
- Article
Classifying and Evaluating Fetuses With Ventriculomegaly in Genetic Etiologic Studies.
- Published in:
- Frontiers in Genetics, 2021, v. 11, p. 1, doi. 10.3389/fgene.2021.682707
- By:
- Publication type:
- Article
Serum peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 in combination with C-reactive protein and white blood cell as novel predictors for infants with community-acquired pneumonia.
- Published in:
- European Journal of Inflammation, 2020, v. 18, p. 1, doi. 10.1177/2058739220942343
- By:
- Publication type:
- Article
Serum peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 in combination with C-reactive protein and white blood cell as novel predictors for infants with community-acquired pneumonia.
- Published in:
- European Journal of Inflammation, 2020, p. 1, doi. 10.1177/2058739220942343
- By:
- Publication type:
- Article
Application of the Single-Molecule Real-Time Technology (SMRT) for Identification of HKαα Thalassemia Allele.
- Published in:
- Laboratory Medicine, 2023, v. 54, n. 1, p. 65, doi. 10.1093/labmed/lmac065
- By:
- Publication type:
- Article
Fetal mosaicism, should conventional karyotype always be performed?
- Published in:
- Journal of Obstetrics & Gynaecology Research, 2023, v. 49, n. 12, p. 2836, doi. 10.1111/jog.15804
- By:
- Publication type:
- Article
Prenatal diagnosis and genetic study of 22q11.2 microduplication in Chinese fetuses: A series of 31 cases and literature review.
- Published in:
- 2024
- By:
- Publication type:
- Case Study
Prenatal diagnosis of BACs‐on‐Beads assay in 1520 cases from Fujian Province, China.
- Published in:
- Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 10, p. 1, doi. 10.1002/mgg3.1446
- By:
- Publication type:
- Article
Using single nucleotide polymorphism array for prenatal diagnosis in a large multicenter study in Southern China.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-33668-0
- By:
- Publication type:
- Article
Prenatal genetic analysis of fetal aberrant right subclavian artery with or without additional ultrasound anomalies in a third level referral center.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-30598-9
- By:
- Publication type:
- Article
Peripheral blood circular RNA circ-0008102 may serve as a novel clinical biomarker in beta-thalassemia patients.
- Published in:
- European Journal of Pediatrics, 2024, v. 183, n. 3, p. 1367, doi. 10.1007/s00431-023-05398-y
- By:
- Publication type:
- Article
The clinical value of hsa-miR-190b-5p in peripheral blood of pediatric β-thalassemia and its regulation on BCL11A expression.
- Published in:
- PLoS ONE, 2023, v. 18, n. 10, p. 1, doi. 10.1371/journal.pone.0292031
- By:
- Publication type:
- Article
Transforming growth factor-induced gene TGFBI is correlated with the prognosis and immune infiltrations of breast cancer.
- Published in:
- World Journal of Surgical Oncology, 2024, v. 22, n. 1, p. 1, doi. 10.1186/s12957-024-03301-z
- By:
- Publication type:
- Article
Fetal growth restriction: associated genetic etiology and pregnancy outcomes in a tertiary referral center.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Identification of transcription factors MYC and C/EBPβ mediated regulatory networks in heart failure based on gene expression omnibus datasets.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Genetic analysis, ultrasound phenotype, and pregnancy outcomes of fetuses with Xp22.33 or Yp11.32 microdeletions.
- Published in:
- Journal of Perinatal Medicine, 2024, v. 52, n. 1, p. 96, doi. 10.1515/jpm-2023-0190
- By:
- Publication type:
- Article
Prenatal diagnosis of non-mosaic sex chromosome abnormalities: a 10-year experience from a tertiary referral center.
- Published in:
- Journal of Perinatal Medicine, 2023, v. 51, n. 7, p. 904, doi. 10.1515/jpm-2022-0552
- By:
- Publication type:
- Article
Prenatal diagnosis and genetic analysis of small supernumerary marker chromosomes in the eastern chinese han population: A retrospective study of 36 cases.
- Published in:
- Chromosome Research, 2024, v. 32, n. 3, p. 1, doi. 10.1007/s10577-024-09754-y
- By:
- Publication type:
- Article
Application of the prenatal BACs-on-Beads™ assay for rapid prenatal detection of sex chromosome mosaicism.
- Published in:
- Molecular Genetics & Genomics, 2022, v. 297, n. 5, p. 1423, doi. 10.1007/s00438-022-01931-0
- By:
- Publication type:
- Article
Genetic disorders and pregnancy outcomes of non-immune hydrops fetalis in a tertiary referral center.
- Published in:
- BMC Medical Genomics, 2023, v. 16, n. 1, p. 1, doi. 10.1186/s12920-023-01505-y
- By:
- Publication type:
- Article
Clinical findings and genetic analysis of patients with copy number variants involving 17p13.3 using a single nucleotide polymorphism array: a single-center experience.
- Published in:
- BMC Medical Genomics, 2022, v. 15, n. 1, p. 1, doi. 10.1186/s12920-022-01423-5
- By:
- Publication type:
- Article
Evaluation of genetic variants using chromosomal microarray analysis for fetuses with polyhydramnios.
- Published in:
- BMC Medical Genomics, 2022, v. 15, n. 1, p. 1, doi. 10.1186/s12920-022-01224-w
- By:
- Publication type:
- Article
Comparison and Agreement Analysis of ARCHITECT i2000SR and i-CHROMA™ Reader for Detecting Human Chorionic Gonadotropin Beta Subunit in Plasma.
- Published in:
- Clinical Laboratory, 2019, v. 65, n. 9, p. 1589, doi. 10.7754/Clin.Lab.2019.181237
- By:
- Publication type:
- Article
Antimicrobial Resistance, Genetic Diversity and Virulence Genes of Salmonella Typhimurium Isolated in Infant with Acute Diarrhea in Fuzhou, China, 2015 - 2017.
- Published in:
- Clinical Laboratory, 2019, v. 65, n. 5, p. 779, doi. 10.7754/Clin.Lab.2018.181010
- By:
- Publication type:
- Article
Activating transcription factor 4 in erythroid development and β-thalassemia: a powerful regulator with therapeutic potential.
- Published in:
- Annals of Hematology, 2024, v. 103, n. 8, p. 2659, doi. 10.1007/s00277-023-05508-8
- By:
- Publication type:
- Article
Intrauterine ultrasound phenotyping, molecular characteristics, and postnatal follow-up of fetuses with the 15q11.2 BP1-BP2 microdeletion syndrome: a single-center, retrospective clinical study.
- Published in:
- BMC Pregnancy & Childbirth, 2024, v. 24, n. 1, p. 1, doi. 10.1186/s12884-023-06223-y
- By:
- Publication type:
- Article
Intrauterine ultrasound phenotyping, molecular characteristics, and postnatal follow-up of fetuses with the 15q11.2 BP1-BP2 microdeletion syndrome: a single-center, retrospective clinical study.
- Published in:
- BMC Pregnancy & Childbirth, 2024, v. 24, n. 1, p. 1, doi. 10.1186/s12884-023-06223-y
- By:
- Publication type:
- Article
Prenatal genetic diagnosis of fetuses with dextrocardia using whole exome sequencing in a tertiary center.
- Published in:
- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-67164-w
- By:
- Publication type:
- Article
Comprehensive analysis of early pregnancy loss based on cytogenetic findings from a tertiary referral center.
- Published in:
- Molecular Cytogenetics (17558166), 2021, v. 14, n. 1, p. 1, doi. 10.1186/s13039-021-00577-8
- By:
- Publication type:
- Article
Copy number variations associated with fetal congenital kidney malformations.
- Published in:
- Molecular Cytogenetics (17558166), 2020, v. 13, n. 1, p. 1, doi. 10.1186/s13039-020-00481-7
- By:
- Publication type:
- Article
Submicroscopic aberrations of chromosome 16 in prenatal diagnosis.
- Published in:
- Molecular Cytogenetics (17558166), 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s13039-019-0448-y
- By:
- Publication type:
- Article
Molecular cytogenetic identification of small supernumerary marker chromosomes using chromosome microarray analysis.
- Published in:
- Molecular Cytogenetics (17558166), 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s13039-019-0425-5
- By:
- Publication type:
- Article
Chromosomal abnormalities and copy number variations in fetal ventricular septal defects.
- Published in:
- Molecular Cytogenetics (17558166), 2018, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13039-018-0408-y
- By:
- Publication type:
- Article
Screening primary carnitine deficiency in 10 million Chinese newborns: a systematic review and meta-analysis.
- Published in:
- Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03267-x
- By:
- Publication type:
- Article
Biochemical and molecular features of chinese patients with glutaric acidemia type 1 from Fujian Province, southeastern China.
- Published in:
- Orphanet Journal of Rare Diseases, 2023, v. 18, n. 1, p. 1, doi. 10.1186/s13023-023-02833-z
- By:
- Publication type:
- Article
Prognostic analysis of E2F transcription factors E2F1 and E2F3 in four independent pediatric neuroblastoma cohorts.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Co‐amplified with PDGFRA, IGFBP7 is a prognostic biomarker correlated with the immune infiltrations of glioma.
- Published in:
- Cancer Medicine, 2023, v. 12, n. 4, p. 4951, doi. 10.1002/cam4.5187
- By:
- Publication type:
- Article
Analysis of the EGFR Amplification and CDKN2A Deletion Regulated Transcriptomic Signatures Reveals the Prognostic Significance of SPATS2L in Patients With Glioma.
- Published in:
- Frontiers in Oncology, 2021, v. 11, p. N.PAG, doi. 10.3389/fonc.2021.551160
- By:
- Publication type:
- Article
The Clinical Values of Afamin, Triglyceride and PLR in Predicting Risk of Gestational Diabetes During Early Pregnancy.
- Published in:
- Frontiers in Endocrinology, 2021, v. 12, p. 1, doi. 10.3389/fendo.2021.723650
- By:
- Publication type:
- Article
Ferroptosis contributes to hemolytic hyperbilirubinemia‑induced brain damage in vivo and in vitro.
- Published in:
- Molecular Medicine Reports, 2023, v. 28, n. 6, p. N.PAG, doi. 10.3892/mmr.2023.13123
- By:
- Publication type:
- Article
LKB1 alleviates high glucose- and high fat-induced inflammation and the expression of GnRH and sexual precocity-related genes, in mouse hypothalamic cells by activating the AMPK/FOXO1 signaling pathway.
- Published in:
- Molecular Medicine Reports, 2022, v. 25, n. 4, p. N.PAG, doi. 10.3892/mmr.2022.12659
- By:
- Publication type:
- Article
Choroid Plexus Cysts: Single Nucleotide Polymorphism Array Analysis of Associated Genetic Anomalies and Resulting Obstetrical Outcomes.
- Published in:
- Risk Management & Healthcare Policy, 2021, n. 14, p. 2491, doi. 10.2147/RMHP.S312813
- By:
- Publication type:
- Article
Performance of Chromosomal Microarray Analysis for Detection of Copy Number Variations in Fetal Echogenic Bowel.
- Published in:
- Risk Management & Healthcare Policy, 2021, v. 14, p. 1431, doi. 10.2147/RMHP.S299806
- By:
- Publication type:
- Article
Chromosomal Microarray Analysis for the Prenatal Diagnosis in Fetuses with Nasal Bone Hypoplasia: A Retrospective Cohort Study.
- Published in:
- Risk Management & Healthcare Policy, 2021, v. 14, p. 1533, doi. 10.2147/RMHP.S286038
- By:
- Publication type:
- Article
SNP Array as a Tool for Prenatal Diagnosis of Congenital Heart Disease Screened by Echocardiography: Implications for Precision Assessment of Fetal Prognosis.
- Published in:
- Risk Management & Healthcare Policy, 2021, v. 14, p. 345, doi. 10.2147/RMHP.S286001
- By:
- Publication type:
- Article
Prenatal diagnosis of Pallister‐Killian syndrome and literature review.
- Published in:
- Journal of Cellular & Molecular Medicine, 2021, v. 25, n. 18, p. 8929, doi. 10.1111/jcmm.16853
- By:
- Publication type:
- Article
Chromosomal microarray analysis for pregnancies with abnormal maternal serum screening who undergo invasive prenatal testing.
- Published in:
- Journal of Cellular & Molecular Medicine, 2021, v. 25, n. 13, p. 6271, doi. 10.1111/jcmm.16589
- By:
- Publication type:
- Article
Comparative clinical genetic testing in spontaneous miscarriage: Insights from a study in Southern Chinese women.
- Published in:
- Journal of Cellular & Molecular Medicine, 2021, v. 25, n. 12, p. 5721, doi. 10.1111/jcmm.16588
- By:
- Publication type:
- Article
A pan-cancer perspective analysis reveals the opposite prognostic significance of CD133 in lower grade glioma and papillary renal cell carcinoma.
- Published in:
- Science Progress, 2021, v. 104, p. 1, doi. 10.1177/00368504211010938
- By:
- Publication type:
- Article
Application of the BACs‐on‐Beads™ assay for rapid prenatal detection application of BoBs™ for PND of aneuploidies and microdeletions.
- Published in:
- Molecular Reproduction & Development, 2018, v. 85, n. 2, p. 146, doi. 10.1002/mrd.22945
- By:
- Publication type:
- Article