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Loss of distal 11q is associated with DNA repair deficiency and reduced sensitivity to ionizing radiation in head and neck squamous cell carcinoma.
- Published in:
- Genes, Chromosomes & Cancer, 2007, v. 46, n. 8, p. 761, doi. 10.1002/gcc.20462
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- Publication type:
- Article
Gebelikte HBsAg Pozitifliği Saptanarak Doğumda Aşı+HBIG Yapılan Bebeklerin ve Annelerin Güncel Durumları ve İzlem Sonuçları.
- Published in:
- Mediterranean Journal of Infection, Microbes & Antimicrobials, 2024, v. 13, p. 127
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- Publication type:
- Article
Altitude is a phenotypic modifier in hereditary paraganglioma type 1: evidence for an oxygen-sensing defect.
- Published in:
- Human Genetics, 2003, v. 113, n. 3, p. 228, doi. 10.1007/s00439-003-0969-6
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- Publication type:
- Article
Germ line insertion of mtDNA at the breakpoint junction of a reciprocal constitutional translocation.
- Published in:
- Human Genetics, 2001, v. 109, n. 2, p. 216, doi. 10.1007/s004390100564
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- Publication type:
- Article
Impact of Maternal Ketogenic Diet on NLRP3 Inflammasome Response in the Offspring Brain.
- Published in:
- Nutrients, 2023, v. 15, n. 8, p. 1994, doi. 10.3390/nu15081994
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- Publication type:
- Article
A Phenotypic Perspective on Mammalian Oxygen Sensor Candidates.
- Published in:
- Annals of the New York Academy of Sciences, 2006, v. 1073, n. 1, p. 221, doi. 10.1196/annals.1353.024
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- Publication type:
- Article
A prospective cohort study on the prediction of fetal distress and neonatal status with arterial and venous Doppler measurements in appropriately grown term fetuses.
- Published in:
- 2017
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- Publication type:
- journal article
The implications of APOBEC3-mediated C-to-U RNA editing for human disease.
- Published in:
- Communications Biology, 2024, v. 7, n. 1, p. 1, doi. 10.1038/s42003-024-06239-w
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- Publication type:
- Article
Identification of a 4.9-kilo base-pair Alu-mediated founder SDHD deletion in two extended paraganglioma families from Austria.
- Published in:
- Journal of Human Genetics, 2010, v. 55, n. 3, p. 182, doi. 10.1038/jhg.2009.142
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- Publication type:
- Article
Genomic imprinting at a boundary element flanking the SDHD locus.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 22, p. 4452, doi. 10.1093/hmg/ddr376
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- Publication type:
- Article
APOBEC3A cytidine deaminase induces RNA editing in monocytes and macrophages.
- Published in:
- Nature Communications, 2015, v. 6, n. 4, p. 6881, doi. 10.1038/ncomms7881
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- Publication type:
- Article
Role of mitochondrial mutations in cancer.
- Published in:
- Endocrine Pathology, 2006, v. 17, n. 3, p. 203, doi. 10.1385/EP:17:3:203
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- Publication type:
- Article
Novel mutations in the SDHD gene in pedigrees with familial carotid body paraganglioma and sensorineural hearing loss.
- Published in:
- Genes, Chromosomes & Cancer, 2001, v. 31, n. 3, p. 255, doi. 10.1002/gcc.1142
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- Publication type:
- Article
Nearly all hereditary paragangliomas in The Netherlands are caused by two founder mutations in the SDHD gene.
- Published in:
- Genes, Chromosomes & Cancer, 2001, v. 31, n. 3, p. 274, doi. 10.1002/gcc.1144
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- Publication type:
- Article
A high-resolution integrated map spanning the SDHD gene at 11q23: a 1.1-Mb BAC contig, a partial transcript map and 15 new repeat polymorphisms in a tumour-suppressor region.
- Published in:
- European Journal of Human Genetics, 2001, v. 9, n. 2, p. 121, doi. 10.1038/sj.ejhg.5200585
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- Publication type:
- Article
Proportion of Heritable Paraganglioma Cases and Associated Clinical Characteristics.
- Published in:
- Laryngoscope, 2001, v. 111, n. 10, p. 1822, doi. 10.1097/00005537-200110000-00029
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- Publication type:
- Article
Genetic Analysis in the Diagnosis of Familial Paragangliomas.
- Published in:
- Laryngoscope, 2000, v. 110, n. 7, p. 1225, doi. 10.1097/00005537-200007000-00030
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- Publication type:
- Article
A Case Series of Neonatal Supraventricular Tachycardia: A Review of Different Management and Clinical Outcomes.
- Published in:
- Journal of Tepecik Education & Research Hospital / İzmir Tepecik Eğitim ve Araştırma Hastanesi Dergisi, 2020, v. 30, n. 2, p. 117, doi. 10.5222/terh.2020.87609
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- Publication type:
- Article
Miniseminar: contemporary management of paragangliomas
- Published in:
- 2003
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- Publication type:
- Abstract
Yenidoğan yoğun bakım ünitesinde doğumsal kalp hastalığı sıklık ve dağılımı: Tek merkez deneyimi.
- Published in:
- Ortadogu Medical Journal / Ortadogu Tip Dergisi, 2019, v. 11, n. 4, p. 446, doi. 10.21601/ortadogutipdergisi.525745
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- Publication type:
- Article
Mitochondrial hypoxic stress induces widespread RNA editing by APOBEC3G in natural killer cells.
- Published in:
- Genome Biology, 2019, v. 20, n. 1, p. N.PAG, doi. 10.1186/s13059-019-1651-1
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- Publication type:
- Article
Ofatumumab plus HyperCVAD/HD‐MA induction leads to high rates of minimal residual disease negativity in patients with newly diagnosed mantle cell lymphoma: Results of a phase 2 study.
- Published in:
- Cancer (0008543X), 2022, v. 128, n. 8, p. 1595, doi. 10.1002/cncr.34106
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- Publication type:
- Article
Genetics of Carney Triad: Recurrent Losses at Chromosome 1 but Lack of Germline Mutations in Genes Associated with Paragangliomas and Gastrointestinal Stromal Tumors.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2007, v. 92, n. 8, p. 2938, doi. 10.1210/jc.2007-0797
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- Publication type:
- Article
Mitochondria: More than Mitochondrial DNA in Cancer.
- Published in:
- 2006
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- Publication type:
- Letter
Stem-loop structure preference for site-specific RNA editing by APOBEC3A and APOBEC3G.
- Published in:
- PeerJ, 2017, p. 1, doi. 10.7717/peerj.4136
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- Publication type:
- Article
The double-domain cytidine deaminase APOBEC3G is a cellular site-specific RNA editing enzyme.
- Published in:
- Scientific Reports, 2016, p. 39100, doi. 10.1038/srep39100
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- Publication type:
- Article
Mitochondria: More than Mitochondrial DNA in Cancer.
- Published in:
- 2006
- By:
- Publication type:
- Letter
Unusual B-Lymphoid Blastic Crisis as Initial Presentation of Chronic Myeloid Leukemia Imposes Diagnostic Challenges.
- Published in:
- 2022
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- Publication type:
- Case Study
Coordinate up-regulation of TMEM97 and cholesterol biosynthesisgenes in normal ovarian surface epithelial cells treated withprogesterone: implications for pathogenesis of ovarian cancer.
- Published in:
- BMC Cancer, 2007, v. 7, p. 223, doi. 10.1186/1471-2407-7-223
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- Publication type:
- Article
Phenotypic dichotomy in mitochondrial complex II genetic disorders.
- Published in:
- Journal of Molecular Medicine, 2001, v. 79, n. 9, p. 495, doi. 10.1007/s001090100267
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- Publication type:
- Article
RNA editing enzyme APOBEC3A promotes pro-inflammatory M1 macrophage polarization.
- Published in:
- Communications Biology, 2021, v. 4, n. 1, p. 1, doi. 10.1038/s42003-020-01620-x
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- Publication type:
- Article
Pregnant and Newborn Health in COVID-19 Pandemic: Knowledge level, Attitude and Perspective of Obstetricians & Gynecologists and Pediatricians in Turkey (A Survey-based Study).
- Published in:
- Electronic Journal of General Medicine, 2021, v. 18, n. 3, p. 1, doi. 10.29333/ejgm/10831
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- Publication type:
- Article
Is European Medicines Agency (EMA) sepsis criteria accurate for neonatal sepsis diagnosis or do we need new criteria?
- Published in:
- PLoS ONE, 2019, v. 14, n. 6, p. 1, doi. 10.1371/journal.pone.0218002
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- Publication type:
- Article
Mitochondrial complex II regulates a distinct oxygen sensing mechanism in monocytes.
- Published in:
- Human Molecular Genetics, 2017, v. 26, n. 7, p. 1328, doi. 10.1093/hmg/ddx041
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- Publication type:
- Article
Etiopathogenesis and clinical presentation of carotid body tumors.
- Published in:
- Microscopy Research & Technique, 2002, v. 59, n. 3, p. 256, doi. 10.1002/jemt.10200
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- Publication type:
- Article
Neurodevelopmental outcome of children with congenital hypothyroidism diagnosed in a national screening program in Turkey.
- Published in:
- Indian Pediatrics, 2017, v. 54, n. 5, p. 381, doi. 10.1007/s13312-017-1111-5
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- Publication type:
- Article