Works about HUMAN genes
Results: 1586
Difference Analysis Among Six Kinds of Acceptor Splicing Sequences by the Dispersion Features of 6-mer Subsets in Human Genes.
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- Biology (2079-7737), 2025, v. 14, n. 2, p. 206, doi. 10.3390/biology14020206
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- Article
Molecular Evolution of the Fusion (F) Genes in Human Parainfluenza Virus Type 2.
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- Microorganisms, 2025, v. 13, n. 2, p. 399, doi. 10.3390/microorganisms13020399
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- Article
Phylogenomic Analyses of the Hemagglutinin-Neuraminidase (HN) Gene in Human Parainfluenza Virus Type 4 Isolates in Japan.
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- Microorganisms, 2025, v. 13, n. 2, p. 384, doi. 10.3390/microorganisms13020384
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- Article
A genome-wide arrayed CRISPR screen identifies PLSCR1 as an intrinsic barrier to SARS-CoV-2 entry that recent virus variants have evolved to resist.
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- PLoS Biology, 2024, v. 22, n. 9, p. 1, doi. 10.1371/journal.pbio.3002767
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- Article
Recurrent gene mutations detected in canine mast cell tumours by next generation sequencing.
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- Veterinary & Comparative Oncology, 2020, v. 18, n. 4, p. 509, doi. 10.1111/vco.12572
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- Article
Binding‐Mediated Formation of Ribonucleoprotein Corona for Efficient Delivery and Control of CRISPR/Cas9.
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- Angewandte Chemie, 2021, v. 133, n. 20, p. 11204, doi. 10.1002/ange.202014162
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- Article
Human Rho guanine nucleotide exchange factor 11 gene is associated with schizophrenia in a Japanese population.
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- Human Psychopharmacology: Clinical & Experimental, 2014, v. 29, n. 6, p. 552, doi. 10.1002/hup.2435
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- Article
Functional analysis of suspected splicing variants in CLCN5 gene in Dent disease 1.
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- Clinical & Experimental Nephrology, 2020, v. 24, n. 7, p. 606, doi. 10.1007/s10157-020-01876-x
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- Article
Cytochrome P450 expression patterns in human osteoblasts during osteogenic differentiation with or without TNFα treatment.
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- Biopharmaceutics & Drug Disposition, 2020, v. 41, n. 4/5, p. 184, doi. 10.1002/bdd.2227
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- Article
Intracellular Binding of Terfenadine Competes with Its Access to Pancreatic ß-cell ATP-Sensitive K<sup>+</sup> Channels and Human ether-à-go-go-Related Gene Channels.
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- Journal of Membrane Biology, 2023, v. 256, n. 1, p. 63, doi. 10.1007/s00232-022-00252-y
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- Article
Novel mechanism of conjoined gene formation in the human genome.
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- Functional & Integrative Genomics, 2012, v. 12, n. 1, p. 45, doi. 10.1007/s10142-011-0260-1
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- Article
Ichthyin/NIPAL4 localizes to keratins and desmosomes in epidermis and Ichthyin mutations affect epidermal lipid metabolism.
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- Archives of Dermatological Research, 2012, v. 304, n. 5, p. 377, doi. 10.1007/s00403-012-1207-7
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- Article
Evidence for zoonotic transmission of species A rotavirus from goat and cattle in nomadic herds in Morocco, 2012–2014.
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- Virus Genes, 2020, v. 56, n. 5, p. 582, doi. 10.1007/s11262-020-01778-w
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- Article
Inherited chromosomally integrated HHV-6 possibly modulates human gene expression.
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- Virus Genes, 2020, v. 56, n. 3, p. 386, doi. 10.1007/s11262-020-01745-5
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- Article
Determinants of Platelet-Leukocyte Aggregation and Platelet Activation in Stroke.
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- Cerebrovascular Diseases, 2015, v. 39, n. 3/4, p. 176, doi. 10.1159/000375396
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- Article
Human genes for U2 small nuclear RNA map to a major adenovirus 12 modification site on chromosome 17.
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- Nature, 1985, p. 115
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- Article
Correction to "Retraction".
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- 2024
- Publication type:
- Correction Notice
Retraction Statement: Inhibition of GPR137 suppresses proliferation of medulloblastoma cells in vitro.
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- 2023
- Publication type:
- Correction Notice
Ethical and regulatory issues in human gene editing: Chinese perspective.
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- Biotechnology & Applied Biochemistry, 2020, v. 67, n. 6, p. 880, doi. 10.1002/bab.2032
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- Article
企业基因视角下企业成长影响因素荟萃回归分析.
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- Journal of Changzhou University (Social Science Edition), 2022, n. 4, p. 60, doi. 10.3969/j.issn.2095-042X.2022.04.007
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- Article
El porqué de la cooperación al desarrollo. Aproximación a los factores determinantes a partir de la técnica "Iceberg".
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- Terra: Revista de Desarrollo Local, 2022, n. 11, p. 164, doi. 10.7203/terra.11.25447
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- Article
Analysis of histone variant constraint and tissue expression suggests five potential novel human disease genes: H2AFY2, H2AFZ, H2AFY, H2AFV, H1F0.
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- Human Genetics, 2022, v. 141, n. 8, p. 1409, doi. 10.1007/s00439-022-02432-1
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- Article
Genetic testing for pediatric hearing loss: no time to waste.
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- Human Genetics, 2022, v. 141, n. 3/4, p. 315, doi. 10.1007/s00439-021-02333-9
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- Article
A network-based machine-learning framework to identify both functional modules and disease genes.
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- Human Genetics, 2021, v. 140, n. 6, p. 897, doi. 10.1007/s00439-020-02253-0
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- Article
The X chromosome and male infertility.
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- Human Genetics, 2021, v. 140, n. 1, p. 203, doi. 10.1007/s00439-019-02101-w
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- Article
Second-tier trio exome sequencing after negative solo clinical exome sequencing: an efficient strategy to increase diagnostic yield and decipher molecular bases in undiagnosed developmental disorders.
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- Human Genetics, 2020, v. 139, n. 11, p. 1381, doi. 10.1007/s00439-020-02178-8
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- Article
The Human Gene Mutation Database (HGMD<sup>®</sup>): optimizing its use in a clinical diagnostic or research setting.
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- Human Genetics, 2020, v. 139, n. 10, p. 1197, doi. 10.1007/s00439-020-02199-3
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- Article
MS/MS in silico subtraction-based proteomic profiling as an approach to facilitate disease gene discovery: application to lens development and cataract.
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- Human Genetics, 2020, v. 139, n. 2, p. 151, doi. 10.1007/s00439-019-02095-5
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- Article
Paired involvement of human-specific Olduvai domains and NOTCH2NL genes in human brain evolution.
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- Human Genetics, 2019, v. 138, n. 7, p. 715, doi. 10.1007/s00439-019-02018-4
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- Article
利用 CRISPR/ Cas9 系统构建 LMNA 基因突变 AC16 人心肌细胞系.
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- Journal of Guangxi Normal University - Natural Science Edition, 2023, v. 41, n. 3, p. 163, doi. 10.16088/j.issn.1001-6600.2022040602
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- Article
Transcriptomics reveals the effects of NTRK1 on endoplasmic reticulum stress response-associated genes in human neuronal cell lines.
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- PeerJ, 2023, p. 1, doi. 10.7717/peerj.15219
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- Article
Further evaluation of differential expression of keratoconus candidate genes in human corneas.
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- PeerJ, 2020, p. 1, doi. 10.7717/peerj.9793
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- Article
Identification of key genes of human bone marrow stromal cells adipogenesis at an early stage.
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- PeerJ, 2020, p. 1, doi. 10.7717/peerj.9484
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- Article
Computational analysis of microRNA-mediated interactions in SARS-CoV-2 infection.
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- PeerJ, 2020, p. 1, doi. 10.7717/peerj.9369
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- Article
Identification of key gene modules and hub genes of human mantle cell lymphoma by coexpression network analysis.
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- PeerJ, 2020, p. 1, doi. 10.7717/peerj.8843
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- Article
Divergent and convergent evolution of housekeeping genes in human–pig lineage.
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- PeerJ, 2019, p. 1, doi. 10.7717/peerj.4840
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- Article
OsteoporosAtlas: a human osteoporosis-related gene database.
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- PeerJ, 2019, p. 1, doi. 10.7717/peerj.6778
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- Article
The expression of chondrogenesis-related and arthritis-related genes in human ONFH cartilage with different Ficat stages.
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- PeerJ, 2019, p. 1, doi. 10.7717/peerj.6306
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- Article
Using novel chimeric gonadotropins with single (FSH) or dual (LH and FSH) activity to induce follicle development in sheep.
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- Journal of Animal Science, 2006, v. 84, p. 434
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- Article
Predictive QSAR models development and validation for human ether-a-go-go related gene (hERG) blockers using newer tools.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2014, v. 29, n. 3, p. 317, doi. 10.3109/14756366.2013.779264
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- Article
An integrated analysis of multiple datasets reveals novel gene signatures in human granulosa cells.
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- Scientific Data, 2024, v. 11, n. 1, p. 1, doi. 10.1038/s41597-024-03715-0
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- Article
Human SERPINA3 induces neocortical folding and improves cognitive ability in mice.
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- Cell Discovery, 2022, v. 8, n. 1, p. 1, doi. 10.1038/s41421-022-00469-0
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- Article
Neurofascin antibodies in chronic inflammatory demyelinating polyradiculoneuropathy: from intrinsic genetic background to clinical manifestations.
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- 2021
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- Publication type:
- journal article
Chimeric Genes in Deletions and Duplications Associated with Intellectual Disability.
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- International Journal of Genomics, 2017, p. 1, doi. 10.1155/2017/4798474
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- Article
Human phenotypes caused by <italic>PIEZO1</italic> mutations; one gene, two overlapping phenotypes?
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- Journal of Physiology, 2018, v. 596, n. 6, p. 985, doi. 10.1113/JP275718
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- Article
Triadin regulation of the ryanodine receptor complex.
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- Journal of Physiology, 2015, v. 593, n. 15, p. 3261, doi. 10.1113/jphysiol.2014.281147
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- Article
Teleost fish models in membrane transport research: the PEPT1(SLC15A1) H<sup>+</sup>-oligopeptide transporter as a case study.
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- Journal of Physiology, 2014, v. 592, n. 5, p. 881, doi. 10.1113/jphysiol.2013.259622
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- Article
Potential Use of Zebrafish as Danon Disease Model: Comparative Computational Modeling and Protein-Protein Interaction Analysis on the LAMP2 Gene of Human, Mouse and Zebrafish.
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- Malaysian Journal of Medicine & Health Sciences, 2023, v. 19, p. 85
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- Article
Xenotransplantation literature update, March-April 2016.
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- Xenotransplantation, 2016, v. 23, n. 3, p. 249, doi. 10.1111/xen.12241
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- Article
Understanding the heterogeneous performance of variant effect predictors across human protein-coding genes.
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- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-76202-6
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- Article