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A new childhood ALL case with an extremely complex karyotype and acute spontaneous tumor lysis syndrome.
- Published in:
- Molecular Cytogenetics (17558166), 2020, v. 13, n. 1, p. N.PAG, doi. 10.1186/s13039-020-00512-3
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- Publication type:
- Article
An acquired stable variant of a dicentric dic(9;20) and complex karyotype in a Syrian childhood B-acute lymphoblastic leukemia case.
- Published in:
- Molecular Cytogenetics (17558166), 2020, v. 13, n. 1, p. 1, doi. 10.1186/s13039-020-00499-x
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- Publication type:
- Article
Human plasma metabolomics in age-related macular degeneration (AMD) using nuclear magnetic resonance spectroscopy.
- Published in:
- PLoS ONE, 2017, v. 12, n. 5, p. 1, doi. 10.1371/journal.pone.0177749
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- Publication type:
- Article
Can nuclear magnetic resonance (NMR) spectroscopy reveal different metabolic signatures for lung tumours?
- Published in:
- 2010
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- Publication type:
- journal article
Stroma-derived IL-6, G-CSF and Activin-A mediated dedifferentiation of lung carcinoma cells into cancer stem cells.
- Published in:
- Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-29947-w
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- Publication type:
- Article
Isochromosome 17q in Chronic Lymphocytic Leukemia.
- Published in:
- Leukemia Research & Treatment, 2015, p. 1, doi. 10.1155/2015/489592
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- Publication type:
- Article
A Novel Cryptic Three-Way Translocation t(2;9;18)(p23.2;p21.3;q21.33) with Deletion of Tumor Suppressor Genes in 9p21.3 and 13q14 in a T-Cell Acute Lymphoblastic Leukemia.
- Published in:
- Leukemia Research & Treatment, 2014, p. 1, doi. 10.1155/2014/357123
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- Publication type:
- Article
Maternal plasma phospholipids are altered in trisomy 21 cases and prior to preeclampsia and preterm outcomes.
- Published in:
- Rapid Communications in Mass Spectrometry: RCM, 2014, v. 28, n. 14, p. 1635, doi. 10.1002/rcm.6941
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- Publication type:
- Article
A unique phenotype in a patient with a rare triplication of the 22q11.2 region and new clinical insights of the 22q11.2 microduplication syndrome: a report of two cases.
- Published in:
- BMC Pediatrics, 2015, v. 15, n. 1, p. 1, doi. 10.1186/s12887-015-0417-5
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- Publication type:
- Article
A unique phenotype in a patient with a rare triplication of the 22q11.2 region and new clinical insights of the 22q11.2 microduplication syndrome: a report of two cases.
- Published in:
- BMC Pediatrics, 2015, v. 15, n. 1, p. 95, doi. 10.1186/s12887-015-0417-5
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- Publication type:
- Article
A unique phenotype in a patient with a rare triplication of the 22q11.2 region and new clinical insights of the 22q11.2 microduplication syndrome: a report of two cases.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Complex karyotype with cryptic FUS gene rearrangement and deletion of NR3C1 and VPREB1 genes in childhood B-cell acute lymphoblastic leukemia: A case report.
- Published in:
- Oncology Letters, 2020, v. 19, n. 4, p. 2957, doi. 10.3892/ol.2020.11387
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- Publication type:
- Article
BIRC3 alterations in chronic and B-cell acute lymphocytic leukemia patients.
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- Oncology Letters, 2016, v. 11, n. 5, p. 3240, doi. 10.3892/ol.2016.4388
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- Publication type:
- Article
A novel IGH@ gene rearrangement associated with CDKN2A/B deletion in young adult B-cell acute lymphoblastic leukemia.
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- Oncology Letters, 2016, v. 11, n. 3, p. 2117, doi. 10.3892/ol.2016.4169
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- Publication type:
- Article
MLLT10 and IL3 rearrangement together with a complex four-way translocation and trisomy 4 in a patient with early T-cell precursor acute lymphoblastic leukemia: A case report.
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- Oncology Reports, 2015, v. 33, n. 2, p. 625, doi. 10.3892/or.2014.3624
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- Publication type:
- Article
Human Gingival Fibroblasts Response to Different Endodontic Sealers: An In Vitro Study.
- Published in:
- Applied Sciences (2076-3417), 2023, v. 13, n. 19, p. 10976, doi. 10.3390/app131910976
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- Publication type:
- Article
Screening of copy number variants in the 22q11.2 region of congenital heart disease patients from the Sao Miguel Island, Azores, revealed the second patient with a triplication.
- Published in:
- BMC Genetics, 2014, v. 15, n. 1, p. 1, doi. 10.1186/s12863-014-0115-6
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- Publication type:
- Article
Probability distribution of copy number alterations along the genome: an algorithm to distinguish different tumour profiles.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41598-020-71859-1
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- Publication type:
- Article
Genetic and epigenetic characterization of the tumors in a patient with a tongue primary tumor, a recurrence and a pharyngoesophageal second primary tumor.
- Published in:
- 2017
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- Publication type:
- Case Study
MLPA analysis in a cohort of patients with autism.
- Published in:
- Molecular Cytogenetics (17558166), 2017, v. 10, p. 1, doi. 10.1186/s13039-017-0302-z
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- Publication type:
- Article
High rates of submicroscopic aberrations in karyotypically normal acute lymphoblastic leukemia.
- Published in:
- Molecular Cytogenetics (17558166), 2015, v. 8, n. 1, p. 1, doi. 10.1186/s13039-015-0153-4
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- Publication type:
- Article
Cutis Aplasia as a clinical hallmark for the syndrome associated with 19q13.11 deletion: the possible role for UBA2 gene.
- Published in:
- Molecular Cytogenetics (17558166), 2015, v. 8, n. 1, p. 1, doi. 10.1186/s13039-015-0123-x
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- Publication type:
- Article
Interstitial 287 kb deletion of 4p16.3 including FGFRL1 gene associated with language impairment and overgrowth.
- Published in:
- 2014
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- Publication type:
- Case Study
X-chromosome terminal deletion in a female with premature ovarian failure: Haploinsufficiency of X-linked genes as a possible explanation.
- Published in:
- Molecular Cytogenetics (17558166), 2010, v. 3, p. 14, doi. 10.1186/1755-8166-3-14
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- Publication type:
- Article
Insertional translocation leading to a 4q13 duplication including the EPHA5 gene in two siblings with attention-deficit hyperactivity disorder.
- Published in:
- American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 8, p. 1923, doi. 10.1002/ajmg.a.36032
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- Publication type:
- Article
Cryptic 7q36.2q36.3 deletion causes multiple congenital eye anomalies and craniofacial dysmorphism.
- Published in:
- American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 3, p. 589, doi. 10.1002/ajmg.a.35713
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- Publication type:
- Article
A New Complex Karyotype Involving a KMT2A-r Variant Three-Way Translocation in a Rare Clinical Presentation of a Pediatric Patient with Acute Myeloid Leukemia.
- Published in:
- Cytogenetic & Genome Research, 2019, v. 157, n. 3, p. 213, doi. 10.1159/000499640
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- Publication type:
- Article
NMR metabolomics of human lung tumours reveals distinct metabolic signatures for adenocarcinoma and squamous cell carcinoma.
- Published in:
- Carcinogenesis, 2015, v. 36, n. 1, p. 68, doi. 10.1093/carcin/bgu226
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- Publication type:
- Article
Genomic profile of oral squamous cell carcinomas with an adjacent leukoplakia or with an erythroleukoplakia that evolved after the treatment of primary tumor: A report of two cases.
- Published in:
- 2017
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- Publication type:
- Case Study
NMR metabonomic study of lung cancer: metabolic profiling of tissues.
- Published in:
- 2010
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- Publication type:
- Abstract
NMR metabonomic study of lung cancer: metabolic profiling of urine and blood plasma.
- Published in:
- 2010
- By:
- Publication type:
- Abstract
Metabolic responses of A549 lung cells to cisplatin and radiation exposure studied by 1H NMR spectroscopy.
- Published in:
- 2010
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- Publication type:
- Abstract
Cytogenetic, genomic, and epigenetic characterization of the HSC-3 tongue cell line with lymph node metastasis.
- Published in:
- 2018
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- Publication type:
- journal article