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Association between adenomatosis polyposis coli functional status and microsomal prostaglandin E synthase-1 expression in colorectal cancer.
- Published in:
- Molecular Carcinogenesis, 2009, v. 48, n. 5, p. 401, doi. 10.1002/mc.20500
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- Publication type:
- Article
Association between ulcerative growth and hypoxia inducible factor‐1α polymorphisms in colorectal cancer patients.
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- Molecular Carcinogenesis, 2006, v. 45, n. 11, p. 833, doi. 10.1002/mc.20209
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- Publication type:
- Article
Mutation analysis of the human homologue of drosophila patched and the xeroderma pigmentosum complementation group A genes in squamous cell carcinomas of the skin.
- Published in:
- Molecular Carcinogenesis, 1998, v. 21, n. 2, p. 87, doi. 10.1002/(SICI)1098-2744(199802)21:2<87::AID-MC2>3.0.CO;2-L
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- Publication type:
- Article
A genome-wide linkage scan in Tunisian families identifies a novel locus for non-syndromic posterior microphthalmia to chromosome 2q37.1.
- Published in:
- Human Genetics, 2009, v. 126, n. 4, p. 575, doi. 10.1007/s00439-009-0688-8
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- Publication type:
- Article
Genetic Alterations in Mitochondrial DNA Are Complementary to Nuclear DNA Mutations in Pheochromocytomas.
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- Cancers, 2022, v. 14, n. 2, p. 269, doi. 10.3390/cancers14020269
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- Publication type:
- Article
Deletions on Chromosome Y and Downregulation of the SRY Gene in Tumor Tissue Are Associated with Worse Survival of Glioblastoma Patients.
- Published in:
- Cancers, 2021, v. 13, n. 7, p. 1619, doi. 10.3390/cancers13071619
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- Publication type:
- Article
S100B polymorphisms are associated with age of onset of Parkinson’s disease.
- Published in:
- BMC Medical Genetics, 2018, v. 19, p. 1, doi. 10.1186/s12881-018-0547-3
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- Article
NOTCH1 mutations influence survival in chronic lymphocytic leukemia patients.
- Published in:
- 2013
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- Publication type:
- journal article
Bcl11b mutations identified in murine lymphomas increase theproliferation rate of hematopoietic progenitor cells.
- Published in:
- BMC Cancer, 2007, v. 7, p. 195, doi. 10.1186/1471-2407-7-195
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- Publication type:
- Article
Methylation associated with long- or short-term survival in glioblastoma patients from the Nordic phase 3 trial.
- Published in:
- Frontiers in Genetics, 2022, v. 13, p. 01, doi. 10.3389/fgene.2022.934519
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- Publication type:
- Article
TP53 mutations and MDM2<sup>SNP309</sup> identify subgroups of AML patients with impaired outcome.
- Published in:
- European Journal of Haematology, 2015, v. 94, n. 4, p. 355, doi. 10.1111/ejh.12438
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- Publication type:
- Article
MDM2 SNP309 promoter polymorphism, an independent prognostic factor in chronic lymphocytic leukemia.
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- European Journal of Haematology, 2010, v. 85, n. 3, p. 251, doi. 10.1111/j.1600-0609.2010.01470.x
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- Publication type:
- Article
Absence of hot spot mutations of the PIK3CA gene in acute myeloid leukaemia.
- Published in:
- 2006
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- Publication type:
- Letter
Identification of two new mutations in the GPR98 and the PDE6B genes segregating in a Tunisian family.
- Published in:
- European Journal of Human Genetics, 2009, v. 17, n. 4, p. 474, doi. 10.1038/ejhg.2008.167
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- Publication type:
- Article
Human Gene Variants Linked to Enhanced NLRP3 Activity Limit Intramacrophage Growth of Mycobacterium tuberculosis.
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- Journal of Infectious Diseases, 2014, v. 209, n. 5, p. 749, doi. 10.1093/infdis/jit572
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- Publication type:
- Article
Rare germline mutations identified by targeted next-generation sequencing of susceptibility genes in pheochromocytoma and paraganglioma.
- Published in:
- 2014
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- Publication type:
- journal article
Germline SDHA Mutation Detected by Next-Generation Sequencing in a Young Index Patient With Large Paraganglioma.
- Published in:
- 2013
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- Publication type:
- Journal Article
Real-time RT-PCR methodology for quantification of thiopurine methyltransferase gene expression.
- Published in:
- European Journal of Clinical Pharmacology, 2003, v. 59, n. 3, p. 207, doi. 10.1007/s00228-003-0617-z
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- Publication type:
- Article
Evolution of DNA repair defects during malignant progression of low-grade gliomas after temozolomide treatment.
- Published in:
- Acta Neuropathologica, 2015, v. 129, n. 4, p. 597, doi. 10.1007/s00401-015-1403-6
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- Publication type:
- Article
Pharmacogenetic Studies of Paclitaxel in the Treatment of Ovarian Cancer.
- Published in:
- Basic & Clinical Pharmacology & Toxicology, 2009, v. 104, n. 2, p. 130, doi. 10.1111/j.1742-7843.2008.00351.x
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- Publication type:
- Article
Polymorphisms in CARD8 and NLRP3 are associated with extrapulmonary TB and poor clinical outcome in active TB in Ethiopia.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41598-019-40121-8
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- Publication type:
- Article
Exploring the two-gene ratio in breast cancer-independent roles for HOXB13 and IL17BR in prediction of clinical outcome.
- Published in:
- Breast Cancer Research & Treatment, 2008, v. 107, n. 2, p. 225, doi. 10.1007/s10549-007-9541-8
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- Publication type:
- Article
Corrigendum to “G/A polymorphism in intronic sequence affects the processing of MAO-B gene in patients with Parkinson disease” [FEBS Lett. 586 (2012) 3698–3704]
- Published in:
- 2013
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- Publication type:
- Correction notice
G/A polymorphism in intronic sequence affects the processing of MAO-B gene in patients with Parkinson disease
- Published in:
- FEBS Letters, 2012, v. 586, n. 20, p. 3698, doi. 10.1016/j.febslet.2012.08.028
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- Publication type:
- Article
Expression of mRNA for Phospholipase A[sub 2] , Cyclooxygenases, and Lipoxygenases in Cultured Human Umbilical Vascular Endothelial and Smooth Muscle Cells and in Biopsies from Umbilical Arteries and Veins.
- Published in:
- Journal of Vascular Research, 1998, v. 35, n. 3, p. 150, doi. 10.1159/000025578
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- Publication type:
- Article
SLC7A9 cDNA cloning and mutational analysis of SLC3A1 and SLC7A9 in canine cystinuria.
- Published in:
- Mammalian Genome, 2006, v. 17, n. 7, p. 769, doi. 10.1007/s00335-005-0146-4
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- Publication type:
- Article
Sex Disparities in MGMT Promoter Methylation and Survival in Glioblastoma: Further Evidence from Clinical Cohorts.
- Published in:
- Journal of Clinical Medicine, 2021, v. 10, n. 4, p. 556, doi. 10.3390/jcm10040556
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- Publication type:
- Article
Increased diagnostic sensitivity of palpation‐guided thyroid nodule fine‐needle aspiration cytology by BRAF V600E‐mutation analysis.
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- Journal of Pathology: Clinical Research, 2021, v. 7, n. 6, p. 556, doi. 10.1002/cjp2.231
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- Publication type:
- Article
Do we really know who has an MGMT methylated glioma? Results of an international survey regarding use of MGMT analyses for glioma.
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- Neuro-Oncology Practice, 2020, v. 7, n. 1, p. 68, doi. 10.1093/nop/npz039
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- Publication type:
- Article
Novel BEST1 gene mutations associated with two different forms of macular dystrophy in Tunisian families.
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- Clinical & Experimental Ophthalmology, 2019, v. 47, n. 8, p. 1063, doi. 10.1111/ceo.13577
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- Publication type:
- Article
Integrative genomics reveals frequent somatic NF1 mutations in sporadic pheochromocytomas.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 26, p. 5406, doi. 10.1093/hmg/dds402
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- Publication type:
- Article
Hypoxia Signaling and Circadian Disruption in and by Pheochromocytoma.
- Published in:
- Frontiers in Endocrinology, 2018, p. N.PAG, doi. 10.3389/fendo.2018.00612
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- Publication type:
- Article
Caffeine Interaction with Glutamate Receptor Gene GRIN2A: Parkinson's Disease in Swedish Population.
- Published in:
- PLoS ONE, 2014, v. 9, n. 6, p. 1, doi. 10.1371/journal.pone.0099294
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- Publication type:
- Article
The Q705K Polymorphism in NLRP3 Is a Gain-of-Function Alteration Leading to Excessive Interleukin-1β and IL-18 Production.
- Published in:
- PLoS ONE, 2012, v. 7, n. 4, p. 1, doi. 10.1371/journal.pone.0034977
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- Publication type:
- Article
Common Genetic Variations in the NALP3 Inflammasome Are Associated with Delayed Apoptosis of Human Neutrophils.
- Published in:
- PLoS ONE, 2012, v. 7, n. 3, p. 1, doi. 10.1371/journal.pone.0031326
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- Publication type:
- Article
The Notch-2 Gene Is Regulated by Wnt Signaling in Cultured Colorectal Cancer Cells.
- Published in:
- PLoS ONE, 2011, v. 6, n. 3, p. 1, doi. 10.1371/journal.pone.0017957
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- Publication type:
- Article
Activating FGFR1 Mutations in Sporadic Pheochromocytomas.
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- World Journal of Surgery, 2018, v. 42, n. 2, p. 482, doi. 10.1007/s00268-017-4320-0
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- Publication type:
- Article
Role of SDHAF2 and SDHD in von Hippel-Lindau Associated Pheochromocytomas.
- Published in:
- World Journal of Surgery, 2014, v. 38, n. 3, p. 724, doi. 10.1007/s00268-013-2373-2
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- Publication type:
- Article
Characterization of sequence variations in human histone H1.2 and H1.4 subtypes.
- Published in:
- FEBS Journal, 2005, v. 272, n. 14, p. 3673, doi. 10.1111/j.1742-4658.2005.04793.x
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- Publication type:
- Article
HRAS Mutation Prevalence and Associated Expression Patterns in Pheochromocytoma.
- Published in:
- Genes, Chromosomes & Cancer, 2016, v. 55, n. 5, p. 452, doi. 10.1002/gcc.22347
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- Publication type:
- Article
Whole-exome sequencing defines the mutational landscape of pheochromocytoma and identifies KMT2 D as a recurrently mutated gene.
- Published in:
- Genes, Chromosomes & Cancer, 2015, v. 54, n. 9, p. 542, doi. 10.1002/gcc.22267
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- Publication type:
- Article
X-chromosome variants are associated with aldosterone producing adenomas.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-89986-8
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- Publication type:
- Article
Case report: Two sisters with a germline CHEK2 variant and distinct endocrine neoplasias.
- Published in:
- Frontiers in Endocrinology, 2022, v. 13, p. 1, doi. 10.3389/fendo.2022.1024108
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- Publication type:
- Article
Nlrp3-inflammasome activation in non-myeloid-derived cells aggravates diabetic nephropathy.
- Published in:
- Kidney International, 2015, v. 87, n. 1, p. 74, doi. 10.1038/ki.2014.271
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- Publication type:
- Article
Alteration of the serine protease PRSS56 causes angle-closure glaucoma in mice and posterior microphthalmia in humans and mice.
- Published in:
- Nature Genetics, 2011, v. 43, n. 6, p. 579, doi. 10.1038/ng.813
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- Publication type:
- Article
MDM2 SNP309 promoter polymorphism and p53 mutations in urinary bladder carcinoma stage T1.
- Published in:
- BMC Urology, 2013, v. 13, n. 1, p. 1, doi. 10.1186/1471-2490-13-5
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- Publication type:
- Article
MDM2 SNP309 promoter polymorphism and p53 mutations in urinary bladder carcinoma stage T1.
- Published in:
- 2013
- By:
- Publication type:
- journal article
Identification of 12 novel mutations in the SLC3A1 gene in Swedish cystinuria patients.
- Published in:
- Human Mutation, 2001, v. 18, n. 6, p. 516, doi. 10.1002/humu.1228
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- Publication type:
- Article
Association of Protective HLA-A With HLA-B<sup>∗</sup>27 Positive Ankylosing Spondylitis.
- Published in:
- Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.659042
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- Publication type:
- Article
Inactivations of p16<sup>INK4a</sup>-α, p16<sup>INK4a</sup>-β and p15<sup>INK4b</sup> genes in 2′, 3′-dideoxycytidine- and 1,3-butadiene-induced murine lymphomas.
- Published in:
- Oncogene, 1998, v. 16, n. 6, p. 803, doi. 10.1038/sj.onc.1201600
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- Publication type:
- Article