Works matching DE "GLOBIN genes"
Results: 985
Sequencing of Hemoglobin Gene 4 (dmhb4) and Southern Blot Analysis Provide Evidence of More Than Four members of the Daphnia magna Globin Family.
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- Bioscience, Biotechnology & Biochemistry, 2005, v. 69, n. 6, p. 1193, doi. 10.1271/bbb.69.1193
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- Article
Characterization of the enhancer element of the Danio rerio minor globin gene locus.
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- Histochemistry & Cell Biology, 2016, v. 145, n. 4, p. 463, doi. 10.1007/s00418-016-1413-z
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- Article
Genetic engineering of the pancreatic β-cell line MIN6 to express bacterial globin proteins protects cells from nitrosative stress.
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- Biotechnology & Applied Biochemistry, 2011, v. 58, n. 2, p. 84, doi. 10.1002/bab.4
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- Publication type:
- Article
Translocation and neuroprotective properties of transactivator-of-transcription protein-transduction domain–neuroglobin fusion protein in primary cultured cortical neurons.
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- Biotechnology & Applied Biochemistry, 2008, v. 049, n. 1, p. 25, doi. 10.1042/ba20070061
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- Article
Isolation and Characterization of Fibroblast from Normal and Thalassemia Foreskin.
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- Trends in Sciences, 2024, v. 21, n. 6, p. 1, doi. 10.48048/tis.2024.7672
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- Article
CRISPR/Cas-based gene editing in therapeutic strategies for beta-thalassemia.
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- Human Genetics, 2023, v. 142, n. 12, p. 1677, doi. 10.1007/s00439-023-02610-9
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- Article
Epimutation in inherited metabolic disorders: the influence of aberrant transcription in adjacent genes.
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- Human Genetics, 2022, v. 141, n. 7, p. 1309, doi. 10.1007/s00439-021-02414-9
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- Article
An aerotaxis receptor influences invasion of Agrobacterium tumefaciens into its host.
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- PeerJ, 2024, p. 1, doi. 10.7717/peerj.16898
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- Article
Molecular basis of a high Hb A<sub>2</sub>/Hb Fβ-thalassemia trait: a retrospective analysis, genotype-phenotype interaction, diagnostic implication, and identification of a novel interaction with α-globin gene triplication.
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- PeerJ, 2023, p. 1, doi. 10.7717/peerj.15308
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- Publication type:
- Article
Effect of Iron on Some Parameters Recombinant Pseudomonas aeruginosa Carrying Vitreoscilla Hemoglobin Gene.
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- Sakarya University Journal of Science (SAUJS) / Sakarya Üniversitesi Fen Bilimleri Enstitüsü Dergisi, 2022, v. 26, n. 4, p. 805, doi. 10.16984/saufenbilder.1096293
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- Article
Molecular and Hematological Analysis of Alpha Thalassemia in Middle East Patients; A Cross-Sectional Retrospective Study.
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- Egyptian Academic Journal of Biological Sciences, C Physiology & Molecular Biology, 2024, v. 16, n. 2, p. 455, doi. 10.21608/EAJBSC.2024.397463
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- Publication type:
- Article
Haematologic Profile of Haemoglobin Constant Spring and Its Co-inheritance With Alpha and Beta Thalassaemia Among Form Four Students in Negeri Sembilan.
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- Malaysian Journal of Medicine & Health Sciences, 2022, v. 18, p. 23, doi. 10.47836/mjmhs18.s21.5
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- Publication type:
- Article
Effects of Transfusion and Splenectomy on Globin Chain Expression in NTDT HbE/β-thalassaemia.
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- Malaysian Journal of Medicine & Health Sciences, 2021, v. 17, p. 39
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- Publication type:
- Article
Molecular Interactions between Neuroglobin and Cytochrome c: Possible Mechanisms of Antiapoptotic Defense in Neuronal Cells.
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- Biomolecules (2218-273X), 2023, v. 13, n. 8, p. 1233, doi. 10.3390/biom13081233
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- Article
MiR-144 Regulates Hemoglobin Expression in Human Erythroid Cell Line.
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- Walailak Journal of Science & Technology, 2020, v. 17, n. 11, p. 1221, doi. 10.48048/wjst.2020.10712
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- Article
Preliminary Study of Alpha-Globin mRNA as a Molecular Tool for Age Estimation of Human Bloodstains.
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- Walailak Journal of Science & Technology, 2016, v. 13, n. 4, p. 281
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- Publication type:
- Article
Expression of α- and β-globin genes occurs within different nuclear domains in haemopoietic cells.
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- Nature Cell Biology, 2001, v. 3, n. 6, p. 602, doi. 10.1038/35078577
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- Article
Oral Oncology/Microbiology Detection of human papillomaviruses of high oncogenic potential in oral squamous cell carcinoma in a Venezuelan population.
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- Oral Diseases, 2004, v. 10, n. 3, p. 163, doi. 10.1046/j.1601-0825.2003.00989.x
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- Publication type:
- Article
Thalassemia and Nanotheragnostics: Advanced Approaches for Diagnosis and Treatment.
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- Biosensors (2079-6374), 2023, v. 13, n. 4, p. 450, doi. 10.3390/bios13040450
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- Publication type:
- Article
Metabolic sensor O-GlcNAcylation regulates erythroid differentiation and globin production via BCL11A.
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- Stem Cell Research & Therapy, 2022, v. 13, n. 1, p. 1, doi. 10.1186/s13287-022-02954-5
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- Publication type:
- Article
CRISPR-mediated gene modification of hematopoietic stem cells with beta-thalassemia IVS-1-110 mutation.
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- Stem Cell Research & Therapy, 2020, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13287-020-01876-4
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- Publication type:
- Article
A Novel Frameshift Mutation, Deletion of HBB:c.199_202delAAAG [Codon 66/67 (-AAAG)] in β-Thalassemia Major Patients from the Western Region of Uttar Pradesh, India.
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- Application of Clinical Genetics, 2021, v. 14, p. 77, doi. 10.2147/TACG.S294891
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- Publication type:
- Article
Alpha Globin Gene Mutation: A Major Determinant of Hydroxyurea Response in Transfusion-Dependent HbE-β-Thalassaemia.
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- Acta Haematologica, 2019, v. 142, n. 3, p. 132, doi. 10.1159/000495453
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- Article
A Severe Case of Hemoglobin H Disease due to Compound Heterozygosity for Deletion of the Major α-Globin Regulatory Element (MCS-R2) and α<sup>0</sup>-Thalassemia.
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- 2017
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- Publication type:
- Case Study
The Problem of Borderline Hemoglobin A2 Levels in the Screening for β-Thalassemia Carriers in Sardinia.
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- Acta Haematologica, 2016, v. 135, n. 4, p. 193, doi. 10.1159/000442194
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- Article
Investigating the Alpha1NcoI Mutation.
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- Acta Haematologica, 2015, v. 133, n. 2, p. 145, doi. 10.1159/000363440
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- Publication type:
- Article
α-Globin Gene Quadruplication and Heterozygous β-Thalassemia: A Not So Rare Cause of Thalassemia Intermedia.
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- Acta Haematologica, 2014, v. 131, n. 3, p. 162, doi. 10.1159/000353410
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- Publication type:
- Article
Five Hemoglobin Variants in a Double Heterozygote for α- and β-Globin Chain Defects.
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- Acta Haematologica, 2014, v. 131, n. 2, p. 71, doi. 10.1159/000353123
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- Article
Beta-Globin Gene Cluster Haplotypes in Yemeni Children with Sickle Cell Disease.
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- Acta Haematologica, 2010, v. 123, n. 3, p. 182, doi. 10.1159/000294965
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- Publication type:
- Article
Accurate Prenatal Diagnosis of Hb Bart’s Hydrops Fetalis in Daily Practice with a Double-Check PCR System.
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- Acta Haematologica, 2009, v. 121, n. 4, p. 227, doi. 10.1159/000225930
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- Publication type:
- Article
A Novel Frameshift Mutation (+A) at Codon 18 of the β-Globin Gene Associated with High Persistence of Fetal Hemoglobin Phenotype and δβ-Thalassemia.
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- Acta Haematologica, 2008, v. 119, n. 1, p. 28, doi. 10.1159/000114204
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- Publication type:
- Article
Everolimus Is a Potent Inducer of Erythroid Differentiation and γ-Globin Gene Expression in Human Erythroid Cells.
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- Acta Haematologica, 2007, v. 117, n. 3, p. 168, doi. 10.1159/000097465
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- Article
Molecular Analysis of Beta-Thalassemia and Sickle Cell Anemia in Antalya.
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- Acta Haematologica, 2004, v. 111, n. 4, p. 205, doi. 10.1159/000077567
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- Publication type:
- Article
The Delta-Globin RNA Transcript Level in Beta-Thalassemia Carriers.
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- Acta Haematologica, 1999, v. 102, n. 1, p. 1, doi. 10.1159/000040959
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- Publication type:
- Article
Peripheral blood gene expression: it all boils down to the RNA collection tubes.
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- BMC Research Notes, 2012, v. 5, n. 1, p. 1, doi. 10.1186/1756-0500-5-1
- Publication type:
- Article
Cytoglobin functions as a redox regulator of melanogenesis in normal epidermal melanocytes.
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- Pigment Cell & Melanoma Research, 2024, v. 37, n. 2, p. 276, doi. 10.1111/pcmr.13146
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- Publication type:
- Article
Richard A. Spritz.
- Published in:
- 2011
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- Publication type:
- Other
Clinical utility of combined preimplantation genetic testing methods in couples at risk of passing on beta thalassemia/hemoglobin E disease: A retrospective review from a single center.
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- PLoS ONE, 2019, v. 14, n. 11, p. 1, doi. 10.1371/journal.pone.0225457
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- Publication type:
- Article
An intergenic non-coding RNA promoter required for histone modifications in the human β-globin chromatin domain.
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- PLoS ONE, 2019, v. 14, n. 8, p. 1, doi. 10.1371/journal.pone.0217532
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- Publication type:
- Article
Genomic safe harbors permit high β-globin transgene expression in thalassemia induced pluripotent stem cells.
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- Nature Biotechnology, 2011, v. 29, n. 1, p. 73, doi. 10.1038/nbt.1717
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- Article
Research highlights.
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- Nature Biotechnology, 2010, v. 28, n. 2, p. 148, doi. 10.1038/nbt0210-148
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- Publication type:
- Article
Alloimmunization among transfusion-dependent thalassemia patients.
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- Asian Journal of Transfusion Science, 2009, v. 3, n. 2, p. 95, doi. 10.4103/0973-6247.53884
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- Publication type:
- Article
The Alpha Thalassaemias.
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- Cellular & Molecular Life Sciences, 2009, v. 66, n. 7, p. 1154, doi. 10.1007/s00018-008-8529-9
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- Publication type:
- Article
Function and evolution of vertebrate globins.
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- Acta Physiologica, 2014, v. 211, n. 3, p. 501, doi. 10.1111/apha.12312
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- Publication type:
- Article
GLOBIN-5-Dependent O<sub>2</sub> Responses Are Regulated by PDL-1/PrBP That Targets Prenylated Soluble Guanylate Cyclases to Dendritic Endings.
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- Journal of Neuroscience, 2014, v. 34, n. 50, p. 16726, doi. 10.1523/JNEUROSCI.5368-13.2014
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- Publication type:
- Article
A new deletion defect leading to α-thalassaemia in a large Dutch Caucasian family.
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- British Journal of Haematology, 2007, v. 136, n. 4, p. 662, doi. 10.1111/j.1365-2141.2006.06475.x
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- Publication type:
- Article
A novel beta-delta globin gene fusion, anti-Lepore Hong Kong, leads to overexpression of delta globin chain and a mild thalassaemia intermedia phenotype when co-inherited with β°- thalassaemia.
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- British Journal of Haematology, 2007, v. 136, n. 1, p. 158, doi. 10.1111/j.1365-2141.2006.06383.x
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- Publication type:
- Article
Effects of human γ-globin in murine β-thalassaemia.
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- British Journal of Haematology, 2006, v. 134, n. 1, p. 100, doi. 10.1111/j.1365-2141.2006.06102.x
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- Publication type:
- Article
Human α2-globin nonsense-mediated mRNA decay induced by a novel α-thalassaemia frameshift mutation at codon 22.
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- British Journal of Haematology, 2006, v. 133, n. 1, p. 98, doi. 10.1111/j.1365-2141.2006.05971.x
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- Publication type:
- Article
Thalassaemia-like carriers not linked to the β-globin gene cluster.
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- British Journal of Haematology, 2006, v. 132, n. 5, p. 640, doi. 10.1111/j.1365-2141.2005.05915.x
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- Publication type:
- Article