Works matching IS 00180661 AND DT 2021 AND VI 158 AND IP 1
Results: 49
Altered microRNAs in C3H10T1/2 cells induced by p.E95K mutant IHH signaling.
- Published in:
- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-021-00207-8
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- Publication type:
- Article
TGF-β1/SMOC2/AKT and ERK axis regulates proliferation, migration, and fibroblast to myofibroblast transformation in lung fibroblast, contributing with the asthma progression.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-021-00213-w
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- Publication type:
- Article
Identification of crucial genes involved in pathogenesis of regional weakening of the aortic wall.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-021-00200-1
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- Publication type:
- Article
Identification and validation of hub genes of synovial tissue for patients with osteoarthritis and rheumatoid arthritis.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-021-00201-0
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- Publication type:
- Article
IFNAR1 gene mutation may contribute to developmental stuttering in the Chinese population.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-021-00211-y
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- Publication type:
- Article
Establishment and validation of a logistic regression model for prediction of septic shock severity in children.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-021-00206-9
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- Publication type:
- Article
The role of ceRNA-mediated diagnosis and therapy in hepatocellular carcinoma.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-021-00208-7
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- Publication type:
- Article
Monocytic THP-1 cells diverge significantly from their primary counterparts: a comparative examination of the chromosomal conformations and transcriptomes.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-021-00205-w
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- Publication type:
- Article
Functional analysis of enhancer elements regulating the expression of the Drosophila homeodomain transcription factor DRx by gene targeting.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-021-00210-z
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- Publication type:
- Article
Enhancer analysis of the Drosophila zinc finger transcription factor Earmuff by gene targeting.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-021-00209-6
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- Publication type:
- Article
Multiomics landscape of the autosomal dominant osteopetrosis type II disease-specific induced pluripotent stem cells.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-021-00204-x
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- Publication type:
- Article
RNA-Seq based transcriptome analysis in oral lichen planus.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-021-00202-z
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- Publication type:
- Article
Comprehensive characterization and clinical relevance of the SWI/SNF copy number aberrations across human cancers.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-021-00203-y
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- Publication type:
- Article
The unidirectional phylogeny of Homo sapiens anchors the origin of modern humans in Eurasia.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-021-00197-7
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- Publication type:
- Article
Leopard syndrome: the potential cardiac defect underlying skin phenotypes.
- Published in:
- 2021
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- Publication type:
- Case Study
Favorable function of Ectonucleoside triphosphate diphosphohydrolase 1 high expression in thyroid carcinoma.
- Published in:
- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-021-00198-6
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- Publication type:
- Article
RNA sequencing analyses in infants patients with coarctation of the aorta.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-021-00194-w
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- Publication type:
- Article
Dynamic co-expression modular network analysis in nonalcoholic fatty liver disease.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-021-00196-8
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- Publication type:
- Article
Identification of glioblastoma immune subtypes and immune landscape based on a large cohort.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-021-00193-x
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- Publication type:
- Article
Modulating the bicoid gradient in space and time.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-021-00192-y
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- Publication type:
- Article
Regulation of DNA methylation on key parasitism genes of Cysticercus cellulosae revealed by integrative epigenomic-transcriptomic analyses.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-021-00195-9
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- Publication type:
- Article
FBXW7 gene polymorphism is associated with type 2 diabetes in the Uygur population in Xinjiang, China.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-021-00191-z
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- Publication type:
- Article
Identification and characterization of miRNAs associated with sterile flower buds in the tea plant based on small RNA sequencing.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-021-00188-8
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- Publication type:
- Article
Bioinformatics analysis of differentially expressed genes and identification of an miRNA–mRNA network associated with entorhinal cortex and hippocampus in Alzheimer's disease.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-021-00190-0
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- Publication type:
- Article
Association of pigmentation related-genes polymorphisms and geographic environmental variables in the Chinese population.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-021-00189-7
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- Publication type:
- Article
Identification of potential biomarkers for pathogenesis of Alzheimer's disease.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-021-00187-9
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- Publication type:
- Article
RTP4 is a novel prognosis-related hub gene in cutaneous melanoma.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-021-00183-z
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- Publication type:
- Article
Network analysis of potential risk genes for psoriasis.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-021-00186-w
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- Publication type:
- Article
An Axin2 mutation and perinatal risk factors contribute to sagittal craniosynostosis: evidence from a Chinese female monochorionic diamniotic twin family.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-021-00182-0
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- Publication type:
- Article
Correction to: Genetic polymorphism of IDOL gene was associated with the susceptibility of coronary artery disease in Han population in Xinjiang, China.
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- 2021
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- Publication type:
- Correction Notice
Somatic frameshift mutation in PIK3CA causes CLOVES syndrome by provoking PI3K/AKT/mTOR pathway.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-021-00184-y
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- Publication type:
- Article
Up-regulated RFC2 predicts unfavorable progression in hepatocellular carcinoma.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-021-00179-9
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- Publication type:
- Article
Association between CCN1 gene polymorphism and acute coronary syndrome in Chinese Han and Uygur populations.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-021-00180-2
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- Publication type:
- Article
Prognostic biomarkers and therapeutic targets in oral squamous cell carcinoma: a study based on cross-database analysis.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-021-00181-1
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- Publication type:
- Article
Identification of metabolism genes related to hepatocarcinogenesis and progression in type 2 diabetes mellitus via co-expression networks analysis.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-021-00177-x
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- Publication type:
- Article
Bioinformatic analysis identifies potential biomarkers and therapeutic targets of septic-shock-associated acute kidney injury.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-021-00176-y
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- Publication type:
- Article
Genetic polymorphism of IDOL gene was associated with the susceptibility of coronary artery disease in Han population in Xinjiang, China.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-021-00178-w
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- Publication type:
- Article
Nucleo-cytoplasmic shuttling of murine RBPJ by Hairless protein matches that of Su(H) protein in the model system Drosophila melanogaster.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-021-00175-z
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- Publication type:
- Article
Development and analysis of long non-coding RNA-associated competing endogenous RNA network for osteosarcoma metastasis.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-021-00174-0
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- Publication type:
- Article
Performance comparison of four types of target enrichment baits for exome DNA sequencing.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-021-00171-3
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- Publication type:
- Article
Development and analysis of long non-coding RNA-associated competing endogenous RNA network for osteosarcoma metastasis.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-021-00174-0
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- Publication type:
- Article
Correction to: A century of Hereditas: from local publication to international journal.
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- 2021
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- Publication type:
- Correction Notice
PeakMatcher facilitates updated Aedes aegypti embryonic cis-regulatory element map.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-021-00172-2
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- Publication type:
- Article
A novel intron mutation in FBN-1 gene identified in a pregnant woman with Marfan syndrome.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-020-00170-w
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- Publication type:
- Article
Identification of differentially expressed genes, signaling pathways and immune infiltration in rheumatoid arthritis by integrated bioinformatics analysis.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-020-00169-3
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- Publication type:
- Article
Mediators of SARS-CoV-2 entry are preferentially enriched in cardiomyocytes.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-020-00168-4
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- Publication type:
- Article
IFI27 may predict and evaluate the severity of respiratory syncytial virus infection in preterm infants.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-020-00167-5
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- Publication type:
- Article
Immunological analysis and differential genes screening of venous thromboembolism.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-020-00166-6
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- Publication type:
- Article
Defining muscle-invasive bladder cancer immunotypes by introducing tumor mutation burden, CD8+ T cells, and molecular subtypes.
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- Hereditas, 2021, v. 158, n. 1, p. 1, doi. 10.1186/s41065-020-00165-7
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- Publication type:
- Article