Výsledky vyhledávání - "M. Zielenska"

Akademický článek

The Role of RUNX2 in Osteosarcoma Oncogenesis

Autor: J. W. Martin, M. Zielenska, G. S. Stein, A. J. van Wijnen, J. A. Squire

Publikováno v: Sarcoma, Vol 2011 (2011)

Osteosarcoma is an aggressive but ill-understood cancer of bone that predominantly affects adolescents. Its rarity and biological heterogeneity have limited studies of its molecular basis. In recent years, an important role has emerged for the RUNX2

Externí odkaz: https://doaj.org/article/74bcab7dcdfb40fa90f8737ba35fdfd2

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Akademický článek

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Integrated cytogenetic and high-resolution array CGH analysis of genomic alterations associated with MYCN amplification

Autor: A, Pandita, J, Bayani, J, Paderova, P, Marrano, C, Graham, M, Barrett, M, Prasad, M, Zielenska, J A, Squire

Publikováno v: Cytogenetic and genome research. 134(1)

Amplification of oncogenes and closely linked flanking genes is common in some types of cancer and can be associated with complex chromosome rearrangements and/or co-amplification of non-syntenic chromosomal regions. To better understand the etiology

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::19e319b5bb31c7c9830fba58325a12df
https://pubmed.ncbi.nlm.nih.gov/21508638

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Akademický článek

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High-resolution cDNA microarray CGH mapping of genomic imbalances in osteosarcoma using formalin-fixed paraffin-embedded tissue

Autor: M. Zielenska, Paula Marrano, Michael Ho, Y. Liu, Ben Beheshti, X.-S. Hao, J. Pei, Paul S. Thorner, B.C. Sun, Jeremy A. Squire, Jane Bayani

Publikováno v: Cytogenetic and genome research. 107(1-2)

Formalin-fixed paraffin embedded (FFPE) tumor tissue provides an opportunity to perform retrospective genomic studies of tumors in which chromosomal imbalances are strongly associated with oncogenesis. The application of comparative genomic hybridiza

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72a3aab1db21e1a111a4bbace21eebd1
https://pubmed.ncbi.nlm.nih.gov/15305059

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[Skin-to-skin contact after birth as a factor determining breastfeeding duration]

Autor: K, Mikiel-Kostyra, I, Boltruszko, J, Mazur, M, Zielenska

Publikováno v: Medycyna wieku rozwojowego. 5(2)

Using prospective cohort study design the influence of skin-to-skin contact after birth on breastfeeding was analyzed in a group of 1250 three years old Polish children. The implementation of this practice significantly increased the mean exclusive b

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::69b19fef98efd147eeab51d8bd50ae6e
https://pubmed.ncbi.nlm.nih.gov/11679683

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[Molecular diagnosis of lymphomas and leukaemias]

Autor: M, Jurkowska, C, Zekanowski, I, Malinowska, M, Zielenska

Publikováno v: Medycyna wieku rozwojowego. 5(2)

In the last years molecular diagnosis has become a routine method m the evaluation of haematological malignancies. Various techniques are used to assess B- and T-cell clonality, chromosomal rearrangements involving protooncogenes, monitoring of minim

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::43be6c9258b4ddc7c0c1bea8e2560846
https://pubmed.ncbi.nlm.nih.gov/11679676

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Acquisition of secondary structural chromosomal changes in pediatric ewing sarcoma is a probable prognostic factor for tumor response and clinical outcome

Autor: M, Zielenska, Z M, Zhang, K, Ng, P, Marrano, J, Bayani, O C, Ramirez, P, Sorensen, P, Thorner, M, Greenberg, J A, Squire

Publikováno v: Cancer. 91(11)

The Ewing sarcoma (ES) group of tumors commonly have the t(11;22)(q24;q12) or other rearrangements involving 22q12. In addition to these consistent aberrations, both numeric and structural aberrations have been reported: namely gains of chromosomes 8

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::223bdec28a7a2be715a246f6147ac7ff
https://pubmed.ncbi.nlm.nih.gov/11391597

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Chromosome 22q a frequent site of allele loss in head and neck carcinoma

Autor: R C, Poli-Frederico, N A, Bergamo, P P, Reis, L P, Kowalski, M, Zielenska, J A, Squire, S R, Rogatto

Publikováno v: Headneck. 22(6)

Loss of heterozygosity (LOH) correlates with inactivated tumor suppressor genes. LOH at chromosome arm 22q has been found in a variety of human neoplasms, suggesting that this region contains a tumor suppressor gene(s) other than NF2 important to tum

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::36d195b50e73b6a9460019e0e0381337
https://pubmed.ncbi.nlm.nih.gov/10941160

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Intractable seizure disorder associated with chronic herpes infection. HSV1 detection in tissue by the polymerase chain reaction

Autor: V, Jay, P, Hwang, H J, Hoffman, L E, Becker, M, Zielenska

Publikováno v: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery. 14(1-2)

We describe the pathological findings and report the detection of herpes simplex virus 1 (HSV1) in the brain in three patients who presented with intractable seizures. All three patients had a previous history of HSV1 encephalitis and went on to deve

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::045da54fce469b813c68ae09836db3f7
https://pubmed.ncbi.nlm.nih.gov/9548334

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