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Analysis of rare thalassemia genetic variants based on third-generation sequencing.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-14038-8
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- Publication type:
- Article
Natural phytochemicals prevent side effects in BRCA-mutated ovarian cancer and PARP inhibitor treatment.
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- Frontiers in Pharmacology, 2022, v. 13, p. 1, doi. 10.3389/fphar.2022.1078303
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- Article
Correction: Surgical margins and prognosis of borderline and malignant phyllodes tumors.
- Published in:
- 2024
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- Publication type:
- Correction Notice
Surgical margins and prognosis of borderline and malignant phyllodes tumors.
- Published in:
- Clinical & Translational Oncology, 2024, v. 26, n. 7, p. 1613, doi. 10.1007/s12094-023-03377-1
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- Publication type:
- Article
The Neuroprotective Effect of Byu d Mar 25 in LPS-Induced Alzheimer's Disease Mice Model.
- Published in:
- Evidence-based Complementary & Alternative Medicine (eCAM), 2021, p. 1, doi. 10.1155/2021/8879014
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- Publication type:
- Article
HIV-1-related factors interact with p53 to influence cellular processes.
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- AIDS Research & Therapy, 2023, v. 20, n. 1, p. 1, doi. 10.1186/s12981-023-00563-7
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- Publication type:
- Article
A case of congenital cataracts with hypotrichosis caused by compound heterozygous variants in the LSS gene.
- Published in:
- 2024
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- Publication type:
- Case Study
Identification of a novel LMX1B nonsense variant associated with congenital talipes equinovarus by prenatal exome sequencing: A case report.
- Published in:
- 2024
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- Publication type:
- Case Study
A novel splicing variation in L1CAM is responsible for recurrent fetal hydrocephalus.
- Published in:
- 2023
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- Publication type:
- Case Study
A novel heterozygous PKD1 variant causing alternative splicing in a Chinese family with autosomal dominant polycystic kidney disease.
- Published in:
- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 8, p. 1, doi. 10.1002/mgg3.2217
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- Publication type:
- Article
Compound heterozygous splicing variants in KIAA0586 cause fetal short‐rib thoracic dysplasia and cerebellar malformation: Use of exome sequencing in prenatal diagnosis.
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- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 3, p. 1, doi. 10.1002/mgg3.2124
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- Publication type:
- Article
A novel CLCNKB variant in a Chinese family with classic Bartter syndrome and prenatal genetic diagnosis.
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- Molecular Genetics & Genomic Medicine, 2022, v. 10, n. 10, p. 1, doi. 10.1002/mgg3.2027
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- Publication type:
- Article
Copy number variation of GATA4 and NKX2-5 in Chinese fetuses with congenital heart disease.
- Published in:
- Pediatrics International, 2015, v. 57, n. 2, p. 234, doi. 10.1111/ped.12489
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- Publication type:
- Article
Human papillomavirus types 16 and 33, herpes simplex virus type 2 and other risk factors for cervical cancer in sichuan province, china.
- Published in:
- International Journal of Cancer, 1991, v. 47, n. 5, p. 711, doi. 10.1002/ijc.2910470515
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- Publication type:
- Article
Correlation Analysis of the Therapy Adherence to Long-Acting Inhalers Among Patients with Stable COPD.
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- Patient Preference & Adherence, 2023, v. 17, p. 1467, doi. 10.2147/PPA.S413948
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- Publication type:
- Article
Paris saponin II of Rhizoma Paridis - A novel inducer of apoptosis in human ovarian cancer cells.
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- BioScience Trends, 2012, v. 6, n. 4, p. 201, doi. 10.5582/bst.2012.v6.4.201
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- Publication type:
- Article
Perinatal outcomes in vanishing twin pregnancies following assisted reproductive technology (ART) – a systematic review and meta-analysis.
- Published in:
- Journal of Perinatal Medicine, 2020, v. 48, n. 7, p. 639, doi. 10.1515/jpm-2020-0088
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- Publication type:
- Article
A Clinicopathologic Analysis of Decidual Polyps: A Potentially Problematic Diagnosis.
- Published in:
- 2022
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- Publication type:
- journal article
Carrying both COL1A2 and FBN2 gene heterozygous mutations results in a severe skeletal clinical phenotype: an affected family.
- Published in:
- BMC Medical Genomics, 2022, v. 15, n. 1, p. 1, doi. 10.1186/s12920-022-01296-8
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- Publication type:
- Article
Preimplantation genetic testing in couples with balanced chromosome rearrangement: a four-year period real world retrospective cohort study.
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- BMC Pregnancy & Childbirth, 2024, v. 24, n. 1, p. 1, doi. 10.1186/s12884-023-06237-6
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- Publication type:
- Article
A new contingent screening strategy increased detection rate of trisomy 21 in the first trimester.
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- BMC Pregnancy & Childbirth, 2023, v. 23, n. 1, p. 1, doi. 10.1186/s12884-023-06115-1
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- Publication type:
- Article
The risk factors of procedure-related complications after amniocentesis in twin pregnancies: a retrospective analysis.
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- BMC Pregnancy & Childbirth, 2023, v. 23, n. 1, p. 1, doi. 10.1186/s12884-023-05884-z
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- Publication type:
- Article
Rapid Detection of Aneuploidy and Unbalanced Chromosomal Rearrangements by Subtelomeric Multiplex Ligation-Dependent Probe Amplification in Fetuses with Congenital Heart Disease.
- Published in:
- Fetal Diagnosis & Therapy, 2013, v. 34, n. 2, p. 110, doi. 10.1159/000350272
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- Publication type:
- Article
Comparison of Intercostal Block and Epidural Analgesia for Post-thoracotomy: A Systematic Review and Meta-analysis of Randomized Controlled Trials.
- Published in:
- Pain Physician, 2023, v. 26, n. 3, p. 219
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- Publication type:
- Article
The Relevance of the OPRM1 118A>G Genetic Variant for Opioid Requirement in Pain Treatment: A Meta-Analysis.
- Published in:
- 2019
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- Publication type:
- journal article
The Relevance of the OPRM1 118A>G Genetic Variant for Opioid Requirement in Pain Treatment: A Meta-Analysis.
- Published in:
- Pain Physician, 2019, v. 22, n. 4, p. 331
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- Publication type:
- Article
A novel deletion mutation in the BCOR gene is associated with oculo-facio-cardio-dental syndrome: a case report.
- Published in:
- 2022
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- Publication type:
- journal article
A long-read sequencing and SNP haplotype-based novel preimplantation genetic testing method for female ADPKD patient with de novo PKD1 mutation.
- Published in:
- BMC Genomics, 2023, v. 24, n. 1, p. 1, doi. 10.1186/s12864-023-09593-x
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- Publication type:
- Article
Chromosomal Aberrations in Pediatric Patients with Developmental Delay/Intellectual Disability: A Single-Center Clinical Investigation.
- Published in:
- BioMed Research International, 2019, p. 1, doi. 10.1155/2019/9352581
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- Publication type:
- Article
Prenatal Diagnostic Value of Chromosomal Microarray in Fetuses with Nuchal Translucency Greater than 2.5 mm.
- Published in:
- BioMed Research International, 2019, p. 1, doi. 10.1155/2019/6504159
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- Publication type:
- Article
GTSE1 promotes the growth of NSCLC by regulating microtubule‐associated proteins through the ERK/MAPK pathway.
- Published in:
- Thoracic Cancer, 2023, v. 14, n. 17, p. 1624, doi. 10.1111/1759-7714.14908
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- Publication type:
- Article
1-calcium phosphate-uracil, a synthesized pyrimidine derivative agent, has anti-proliferative, pro-apoptotic and anti-invasion effects on multiple tumor cell lines.
- Published in:
- Molecular Medicine Reports, 2014, v. 10, n. 5, p. 2271, doi. 10.3892/mmr.2014.2489
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- Publication type:
- Article
Functional characterization of inactivating ABCC8 variants causing congenital hyperinsulinism.
- Published in:
- Clinical Genetics, 2024, v. 105, n. 5, p. 549, doi. 10.1111/cge.14484
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- Publication type:
- Article
Case report: A novel de novo deletion mutation of DYRK1A is associated with intellectual developmental disorder, autosomal dominant 7.
- Published in:
- Frontiers in Neuroscience, 2023, p. 01, doi. 10.3389/fnins.2023.1174925
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- Publication type:
- Article
Accumulation of invariant NKT cells with increased IFN-γ production in persistent high-risk HPV-infected high-grade cervical intraepithelial neoplasia.
- Published in:
- Diagnostic Pathology, 2015, v. 10, n. 1, p. 1, doi. 10.1186/s13000-015-0254-8
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- Publication type:
- Article
Accumulation of invariant NKT cells with increased IFN-γ production in persistent high-risk HPV-infected high-grade cervical intraepithelial neoplasia
- Published in:
- Diagnostic Pathology, 2015, v. 10, n. 1, p. 20, doi. 10.1186/s13000-015-0254-8
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- Publication type:
- Article
Expression of serum amyloid A in uterine cervical cancer.
- Published in:
- Diagnostic Pathology, 2014, v. 9, n. 1, p. 1, doi. 10.1186/1746-1596-9-16
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- Publication type:
- Article
USP9X expression correlates with tumor progression and poor prognosis in esophageal squamous cell carcinoma.
- Published in:
- Diagnostic Pathology, 2013, v. 8, n. 1, p. 1, doi. 10.1186/1746-1596-8-177
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- Publication type:
- Article
Genomic amplification of the human telomerase gene (hTERC) associated with human papillomavirus is related to the progression of uterine cervical dysplasia to invasive cancer.
- Published in:
- Diagnostic Pathology, 2012, v. 7, n. 1, p. 147, doi. 10.1186/1746-1596-7-147
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- Publication type:
- Article
Enhanced antifungal activity of bovine lactoferrin-producing probiotic Lactobacillus casei in the murine model of vulvovaginal candidiasis.
- Published in:
- BMC Microbiology, 2019, v. 19, n. 1, p. N.PAG, doi. 10.1186/s12866-018-1370-x
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- Publication type:
- Article
Identification of a novel EXT2 frameshift mutation in a family with hereditary multiple exostoses by whole‐exome sequencing.
- Published in:
- Journal of Clinical Laboratory Analysis, 2021, v. 35, n. 9, p. 1, doi. 10.1002/jcla.23968
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- Publication type:
- Article
Paris Saponin II suppresses the growth of human ovarian cancer xenografts via modulating VEGF-mediated angiogenesis and tumor cell migration.
- Published in:
- Cancer Chemotherapy & Pharmacology, 2014, v. 73, n. 4, p. 807, doi. 10.1007/s00280-014-2408-x
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- Publication type:
- Article
Long non-coding RNAs in HBV-related hepatocellular carcinoma (Review).
- Published in:
- International Journal of Oncology, 2020, v. 56, n. 1, p. 18, doi. 10.3892/ijo.2019.4909
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- Publication type:
- Article
Infertility in a man with oligoasthenozoospermia associated with mosaic chromosome 22q11 deletion.
- Published in:
- Molecular Genetics & Genomic Medicine, 2018, v. 6, n. 6, p. 1249, doi. 10.1002/mgg3.487
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- Publication type:
- Article
Prenatal diagnosis of chromosomal aberrations by chromosomal microarray analysis in foetuses with ventriculomegaly.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41598-020-77400-8
- By:
- Publication type:
- Article
Embryonic organizer formation disorder leads to multiorgan dysplasia in Down syndrome.
- Published in:
- Cell Death & Disease, 2022, v. 13, n. 12, p. 1, doi. 10.1038/s41419-022-05517-x
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- Publication type:
- Article
A novel USH2A variant in a patient with hearing loss and prenatal diagnosis of a familial fetus: a case report.
- Published in:
- BMC Medical Genomics, 2021, v. 14, n. 1, p. 1, doi. 10.1186/s12920-021-01052-4
- By:
- Publication type:
- Article
427. Adenovirus Mediated GRP94/gp96 Expression in Treatment of Neuroblastoma.
- Published in:
- Molecular Therapy, 2006, v. 13, p. S164, doi. 10.1016/j.ymthe.2006.08.492
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- Publication type:
- Article
Clinical experience of noninvasive prenatal testing for rare chromosome abnormalities in singleton pregnancies.
- Published in:
- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.955694
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- Publication type:
- Article
Potentials and challenges of chromosomal microarray analysis in prenatal diagnosis.
- Published in:
- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.938183
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- Publication type:
- Article