Found: 29
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Genome-wide analysis of primary plasma cell leukemia identifies recurrent imbalances associated with changes in transcriptional profiles.
- Published in:
- American Journal of Hematology, 2013, v. 88, n. 1, p. 16, doi. 10.1002/ajh.23339
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- Publication type:
- Article
Violence against Women and Stress-Related Disorders: Seeking for Associated Epigenetic Signatures, a Pilot Study.
- Published in:
- Healthcare (2227-9032), 2023, v. 11, n. 1, p. 173, doi. 10.3390/healthcare11020173
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- Publication type:
- Article
The Mammary Gland and the Homeobox Gene Otx1 PAGANI ET AL. Otx1 Expression in Breast Cancer.
- Published in:
- Breast Journal, 2010, v. 16, p. S53, doi. 10.1111/j.1524-4741.2010.01006.x
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- Publication type:
- Article
Evidence of epigenetic changes affecting the chromatin state of the retinoic acid receptor β2 promoter in breast cancer cells.
- Published in:
- Oncogene, 2000, v. 19, n. 12, p. 1556, doi. 10.1038/sj.onc.1203456
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- Publication type:
- Article
gDNA qPCR is statistically more reliable than mRNA analysis in detecting leukemic cells to monitor CML.
- Published in:
- Cell Death & Disease, 2018, v. 9, n. 3, p. 1, doi. 10.1038/s41419-018-0387-2
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- Publication type:
- Article
ESX1 mRNA expression in seminal fluid is an indicator of residual spermatogenesis in non-obstructive azoospermic men.
- Published in:
- Human Reproduction, 2014, v. 29, n. 12, p. 2620, doi. 10.1093/humrep/deu261
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- Publication type:
- Article
Germline oncopharmacogenetics, a promising field in cancer therapy.
- Published in:
- Cellular Oncology (2211-3428), 2015, v. 38, n. 1, p. 65, doi. 10.1007/s13402-014-0214-4
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- Publication type:
- Article
Non-invasive biomarkers for sperm retrieval in non-obstructive patients: a comprehensive review.
- Published in:
- Frontiers in Endocrinology, 2024, p. 1, doi. 10.3389/fendo.2024.1349000
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- Publication type:
- Article
A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver-Russell and Beckwith-Wiedemann syndromes.
- Published in:
- Clinical Epigenetics, 2016, v. 8, p. 1, doi. 10.1186/s13148-016-0183-8
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- Publication type:
- Article
Molecular profiling of lung cancer specimens and liquid biopsies using MALDI-TOF mass spectrometry.
- Published in:
- Diagnostic Pathology, 2018, v. 13, p. 1, doi. 10.1186/s13000-017-0683-7
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- Publication type:
- Article
Dysfunction in IGF2R Pathway and Associated Perturbations in Autophagy and WNT Processes in Beckwith–Wiedemann Syndrome Cell Lines.
- Published in:
- International Journal of Molecular Sciences, 2024, v. 25, n. 7, p. 3586, doi. 10.3390/ijms25073586
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- Publication type:
- Article
Primary TSC2 -/meth Cells Induce Follicular Neogenesis in an Innovative TSC Mouse Model.
- Published in:
- International Journal of Molecular Sciences, 2022, v. 23, n. 17, p. 9713, doi. 10.3390/ijms23179713
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- Publication type:
- Article
Correction: Rondinone et al. Extensive Placental Methylation Profiling in Normal Pregnancies. Int. J. Mol. Sci. 2021, 22 , 2136.
- Published in:
- 2022
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- Publication type:
- Correction Notice
Clinical and Molecular Diagnosis of Beckwith-Wiedemann Syndrome with Single- or Multi-Locus Imprinting Disturbance.
- Published in:
- International Journal of Molecular Sciences, 2021, v. 22, n. 7, p. 3445, doi. 10.3390/ijms22073445
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- Publication type:
- Article
Extensive Placental Methylation Profiling in Normal Pregnancies.
- Published in:
- International Journal of Molecular Sciences, 2021, v. 22, n. 4, p. 2136, doi. 10.3390/ijms22042136
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- Publication type:
- Article
Sequence variants identification at the KCNQ1OT1:TSS differentially Methylated region in isolated omphalocele cases.
- Published in:
- BMC Medical Genetics, 2017, v. 18, p. 1, doi. 10.1186/s12881-017-0470-z
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- Publication type:
- Article
DNA Methylation in the Diagnosis of Monogenic Diseases.
- Published in:
- Genes, 2020, v. 11, n. 4, p. 355, doi. 10.3390/genes11040355
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- Publication type:
- Article
Biparental expression of ESX1L gene in placentas from normal and intrauterine growth-restricted pregnancies.
- Published in:
- European Journal of Human Genetics, 2004, v. 12, n. 4, p. 272, doi. 10.1038/sj.ejhg.5201121
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- Publication type:
- Article
Role of epigenetics in human aging and longevity: genome-wide DNA methylation profile in centenarians and centenarians' offspring.
- Published in:
- Age, 2013, v. 35, n. 5, p. 1961, doi. 10.1007/s11357-012-9463-1
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- Publication type:
- Article
A HS6ST2 gene variant associated with X‐linked intellectual disability and severe myopia in two male twins.
- Published in:
- Clinical Genetics, 2019, v. 95, n. 3, p. 368, doi. 10.1111/cge.13485
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- Publication type:
- Article
Profound alterations of the chromatin architecture at chromosome 11p15.5 in cells from Beckwith-Wiedemann and Silver-Russell syndromes patients.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-65082-1
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- Publication type:
- Article
Misbehaviour of XIST RNA in Breast Cancer Cells.
- Published in:
- PLoS ONE, 2009, v. 4, n. 5, p. 1, doi. 10.1371/journal.pone.0005559
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- Publication type:
- Article
Cohesin Mutations Induce Chromatin Conformation Perturbation of the H19 / IGF2 Imprinted Region and Gene Expression Dysregulation in Cornelia de Lange Syndrome Cell Lines.
- Published in:
- Biomolecules (2218-273X), 2021, v. 11, n. 11, p. 1622, doi. 10.3390/biom11111622
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- Publication type:
- Article
Preferential expression of mutant ABCD1 allele is common in adrenoleukodystrophy female carriers but unrelated to clinical symptoms.
- Published in:
- 2012
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- Publication type:
- journal article
Loss of heterozygosity on chromosome 4q32–35 in sporadic basal cell carcinomas: evidence for the involvement of p33ING2/ING1L and SAP30 genes.
- Published in:
- Journal of Cutaneous Pathology, 2004, v. 31, n. 4, p. 318, doi. 10.1111/j.0303-6987.2004.0187.x
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- Publication type:
- Article
Constitutive BRCA1 Promoter Hypermethylation Can Be a Predisposing Event in Isolated Early-Onset Breast Cancer.
- Published in:
- Cancers, 2019, v. 11, n. 1, p. 58, doi. 10.3390/cancers11010058
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- Publication type:
- Article
TSC2 epigenetic defect in primary LAM cells. Evidence of an anchorage-independent survival.
- Published in:
- Journal of Cellular & Molecular Medicine, 2014, v. 18, n. 5, p. 766, doi. 10.1111/jcmm.12237
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- Publication type:
- Article
A novel splice site variant in ITPR1 gene underlying recessive Gillespie syndrome.
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- American Journal of Medical Genetics. Part A, 2018, v. 176, n. 6, p. 1427, doi. 10.1002/ajmg.a.38704
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- Publication type:
- Article
(Epi)genetic profiling of extraembryonic and postnatal tissues from female monozygotic twins discordant for Beckwith–Wiedemann syndrome.
- Published in:
- Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 9, p. 1, doi. 10.1002/mgg3.1386
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- Publication type:
- Article