Found: 41
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Upregulation of CD22 by Chidamide promotes CAR T cells functionality.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-00227-4
- By:
- Publication type:
- Article
Genetic causes of isolated and severe fetal growth restriction in normal chromosomal microarray analysis.
- Published in:
- International Journal of Gynecology & Obstetrics, 2023, v. 161, n. 3, p. 1004, doi. 10.1002/ijgo.14620
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- Publication type:
- Article
Prenatal diagnosis in the fetal hyperechogenic kidneys: assessment using chromosomal microarray analysis and exome sequencing.
- Published in:
- Human Genetics, 2023, v. 142, n. 6, p. 835, doi. 10.1007/s00439-023-02545-1
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- Publication type:
- Article
Whole exome sequencing improves genetic diagnosis of fetal clubfoot.
- Published in:
- Human Genetics, 2023, v. 142, n. 3, p. 407, doi. 10.1007/s00439-022-02516-y
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- Publication type:
- Article
Application of exome sequencing for prenatal diagnosis of fetal structural anomalies: clinical experience and lessons learned from a cohort of 1618 fetuses.
- Published in:
- Genome Medicine, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13073-022-01130-x
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- Publication type:
- Article
Anti-Hyperuricemic and Nephroprotective Effects of Dihydroberberine in Potassium Oxonate- and Hypoxanthine-Induced Hyperuricemic Mice.
- Published in:
- Frontiers in Pharmacology, 2021, v. 11, p. N.PAG, doi. 10.3389/fphar.2021.645879
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- Publication type:
- Article
Research on the Transient Characteristics of a Three-Stream Adaptive Cycle Engine.
- Published in:
- Energies (19961073), 2023, v. 16, n. 24, p. 8076, doi. 10.3390/en16248076
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- Publication type:
- Article
A Double Heterozygous Mutation of TNNI3 Causes Hypertrophic Cardiomyopathy in a Han Chinese Family.
- Published in:
- Cardiology, 2016, v. 133, n. 2, p. 91, doi. 10.1159/000440877
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- Publication type:
- Article
Analysis of human upstream open reading frames and impact on gene expression.
- Published in:
- Human Genetics, 2015, v. 134, n. 6, p. 605, doi. 10.1007/s00439-015-1544-7
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- Publication type:
- Article
Prenatal diagnosis in fetal right aortic arch using chromosomal microarray analysis and whole exome sequencing: a Chinese single-center retrospective study.
- Published in:
- Molecular Cytogenetics (17558166), 2024, v. 17, n. 1, p. 1, doi. 10.1186/s13039-024-00691-3
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- Publication type:
- Article
Association of prenatal Cleft Lip and Palate ultrasound abnormalities with copy number variants at a single Chinese tertiary center.
- Published in:
- Italian Journal of Pediatrics, 2024, v. 50, n. 1, p. 1, doi. 10.1186/s13052-024-01720-y
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- Publication type:
- Article
Analysis of Mutation Spectra of 28 Pathogenic Genes Associated With Congenital Hypothyroidism in the Chinese Han Population.
- Published in:
- Frontiers in Endocrinology, 2021, v. 12, p. 1, doi. 10.3389/fendo.2021.695426
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- Publication type:
- Article
A novel two-step administration of XPO-1 inhibitor may enhance the effect of anti-BCMA CAR-T in relapsed/refractory extramedullary multiple myeloma.
- Published in:
- Journal of Translational Medicine, 2023, v. 21, n. 1, p. 1, doi. 10.1186/s12967-023-04655-w
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- Publication type:
- Article
MicroRNA Let-7i Regulates Innate TLR4 Pathways in Peripheral Blood Mononuclear Cells of Patients with Ankylosing Spondylitis.
- Published in:
- International Journal of General Medicine, 2023, v. 16, p. 1393, doi. 10.2147/IJGM.S397160
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- Publication type:
- Article
Prenatal exome sequencing in fetuses with congenital heart defects.
- Published in:
- Clinical Genetics, 2020, v. 98, n. 3, p. 215, doi. 10.1111/cge.13774
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- Publication type:
- Article
Altered expression of circular RNAs in human placental chorionic plate-derived mesenchymal stem cells pretreated with hypoxia.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Abnormal Expression of Dysferlin in Blood Monocytes Supports Primary Dysferlinopathy in Patients Confirmed by Genetic Analyses.
- Published in:
- Frontiers in Neurology, 2021, v. 11, p. N.PAG, doi. 10.3389/fneur.2020.540098
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- Publication type:
- Article
Anti-Inflammatory Activation of Phellodendri Chinensis Cortex is Mediated by Berberine Erythrocytes Self-Assembly Targeted Delivery System.
- Published in:
- Drug Design, Development & Therapy, 2022, v. 16, p. 4365, doi. 10.2147/DDDT.S385301
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- Publication type:
- Article
Prenatal diagnosis of 21 fetuses with balanced chromosomal abnormalities (BCAs) using whole-genome sequencing.
- Published in:
- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.951829
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- Publication type:
- Article
Case Report: Two Novel L1CAM Mutations in Two Unrelated Chinese Families With X-Linked Hydrocephalus.
- Published in:
- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.810853
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- Publication type:
- Article
Nonalcoholic fatty liver disease experiences accumulation of hepatic liquid crystal associated with increasing lipophagy.
- Published in:
- Cell & Bioscience, 2020, v. 10, n. 1, p. 1, doi. 10.1186/s13578-020-00414-2
- By:
- Publication type:
- Article
Primary Testicular and Cutaneous Philadelphia Chromosome Positive B-Cell Lymphoblastic Lymphoma: A Rare Case and Review.
- Published in:
- 2022
- By:
- Publication type:
- Case Study
Primary Testicular and Cutaneous Philadelphia Chromosome Positive B-Cell Lymphoblastic Lymphoma: A Rare Case and Review.
- Published in:
- Cancer Management & Research, 2022, v. 14, p. 1507, doi. 10.2147/CMAR.S353022
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- Publication type:
- Article
Evaluation of the Z‐score accuracy of noninvasive prenatal testing for fetal trisomies 13, 18 and 21 at a single center.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 6, p. 690, doi. 10.1002/pd.5908
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- Publication type:
- Article
Evaluation of the Z‐score accuracy of noninvasive prenatal testing for fetal trisomies 13, 18 and 21 at a single center.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 6, p. 690, doi. 10.1002/pd.5908
- By:
- Publication type:
- Article
Genetic tests aid in counseling of fetuses with cerebellar vermis defects.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Nonimmune hydrops fetalis: Genetic analysis and clinical outcome.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Pregnancy outcome of autosomal aneuploidies other than common trisomies detected by noninvasive prenatal testing in routine clinical practice.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Mutation in SSUH2 Causes Autosomal-Dominant Dentin Dysplasia Type I.
- Published in:
- Human Mutation, 2017, v. 38, n. 1, p. 95, doi. 10.1002/humu.23130
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- Publication type:
- Article
Case report: Light-chain amyloidosis responsive to selinexor in combination with daratumumab and dexamethasone (SDd) therapy.
- Published in:
- Frontiers in Medicine, 2024, p. 1, doi. 10.3389/fmed.2024.1363805
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- Publication type:
- Article
Primary gastrointestinal stromal tumor of the prostate: A case report and literature review.
- Published in:
- 2014
- By:
- Publication type:
- Case Study
CD19/CD22 CAR-T-cell cocktail therapy following autologous transplantation is an optimizing strategy for treating relapsed/refractory central nervous system lymphoma.
- Published in:
- 2024
- By:
- Publication type:
- Letter
Case report: Germline RECQL mutation potentially involved in hereditary predisposition to acute leukemia.
- Published in:
- Frontiers in Oncology, 2023, v. 13, p. 1, doi. 10.3389/fonc.2023.1066083
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- Publication type:
- Article
Exome sequencing improves genetic diagnosis of congenital orofacial clefts.
- Published in:
- Frontiers in Genetics, 2023, p. 1, doi. 10.3389/fgene.2023.1252823
- By:
- Publication type:
- Article
Genetic diagnosis of fetal microcephaly at a single tertiary center in China.
- Published in:
- Frontiers in Genetics, 2023, p. 1, doi. 10.3389/fgene.2023.1112153
- By:
- Publication type:
- Article
Dynamics expression of DmFKBP12/Calstabin during embryonic early development of Drosophila melanogaster.
- Published in:
- Cell & Bioscience, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1186/s13578-019-0270-6
- By:
- Publication type:
- Article
Genetic Analysis and Sonography Characteristics in Fetus with SHOX Haploinsufficiency.
- Published in:
- Genes, 2023, v. 14, n. 1, p. 140, doi. 10.3390/genes14010140
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- Publication type:
- Article
Prenatal Diagnosis of Chromosome 16p11.2 Microdeletion.
- Published in:
- Genes, 2022, v. 13, n. 12, p. 2315, doi. 10.3390/genes13122315
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- Publication type:
- Article
Prenatal Diagnosis and Outcomes in Fetuses with Hemivertebra.
- Published in:
- Genes, 2022, v. 13, n. 9, p. 1623, doi. 10.3390/genes13091623
- By:
- Publication type:
- Article
CS1 Expression Pattern in NK Cells and Correlated Factors in Plasma Cell dyscrasias: Implications for Elotuzumab Therapy and CAR-T Efficacy.
- Published in:
- Journal of Cancer, 2024, v. 15, n. 10, p. 3065, doi. 10.7150/jca.93637
- By:
- Publication type:
- Article
Mutations in immunodeficiency-related genes may increase the risk of infection after CAR-T-cell therapy: a report of two cases.
- Published in:
- 2023
- By:
- Publication type:
- Case Study