Zobrazeno 1 - 10
of 314
pro vyhledávání: '"Virtual karyotype"'
Autor:
Mami Miyado, Maki Fukami
Publikováno v:
Annals of Pediatric Endocrinology & Metabolism
Annals of Pediatric Endocrinology & Metabolism, Vol 22, Iss 2, Pp 90-94 (2017)
Annals of Pediatric Endocrinology & Metabolism, Vol 22, Iss 2, Pp 90-94 (2017)
Next-generation sequencing (NGS) and array-based comparative genomic hybridization (array CGH) have enabled us to perform high-throughput mutation screening and genome-wide copy number analysis, respectively. These methods can be used for molecular d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::135329f4c8807541d2a91dd54ef7014d
http://europepmc.org/articles/PMC5495984
http://europepmc.org/articles/PMC5495984
Autor:
Eline M. P. Cremers, Saskia K. Klein, Petra Muus, Marian Stevens-Kroef, Georgine E. de Greef, Theresia M. Westers, Canan Alhan, Daniel Olde Weghuis, Pierre W. Wijermans, Sonia M Cunha, Najat ElIdrissi-Zaynoun, M Ron Schaafsma, Edo Vellenga, Gert J. Ossenkoppele, Arjan A. van de Loosdrecht, Bert A. van der Reijden, Dana A. Chitu, Heleen Visser-Wisselaar, Joop H. Jansen
Publikováno v:
Genes, Chromosomes and Cancer. 56:524-534
Karyotyping is considered as the gold standard in the genetic subclassification of myelodysplastic syndrome (MDS). Oligo/SNP-based genomic array profiling is a high-resolution tool that also enables genome wide analysis. We compared karyotyping with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f4b0464314cf046abda92350ec5abc02
https://doi.org/10.1002/gcc.22455
https://doi.org/10.1002/gcc.22455
Autor:
Jennifer B. Gordetsky, Denise A.S. Batista, Diana Morlote, Shuko Harada, Soroush Rais-Bahrami
Publikováno v:
Human pathology. 91
Clear cell papillary renal cell carcinoma (CCP-RCC) is a recently recognized tumor that shares morphologic features of both clear cell renal cell carcinoma and papillary renal cell carcinoma but behaves in a more indolent fashion. To date, there is l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da34cb9dca1e37be5b901f8e0cf4d1ec
https://pubmed.ncbi.nlm.nih.gov/31175917
https://pubmed.ncbi.nlm.nih.gov/31175917
Autor:
Marian Stevens-Kroef, Javier Suela, H. Berna Beverloo, Katrina Rack, Dominique Muehlematter, Eva van den Berg, Ros Hastings, Jacqueline Schoumans
Publikováno v:
Genes, Chromosomes and Cancer. 55:480-491
Genetic profiling is important for disease evaluation and prediction of prognosis or responsiveness to therapy in neoplasia. Microarray technologies, including array comparative genomic hybridization and single-nucleotide polymorphism-detecting array
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ebdabc8186fdbad9f51e21280b3fb64
https://doi.org/10.1002/gcc.22350
https://doi.org/10.1002/gcc.22350
Autor:
Cristina Cavaliere, Simonetta Kerim, Guido Valente, Ilaria Coro, Paolo Spina, Federica Morani, Alessandra Galetto, Matteo Vidali, Alessia De Donno
Publikováno v:
Applied Immunohistochemistry & Molecular Morphology. 24:120-127
Oligonucleotide array-based comparative genomic hybridization (oaCGH) was used to investigate 60 cases of hematologic malignancies, mainly acute myeloid leukemias and myelodysplastic syndromes, in order to evaluate its sensitivity and specificity and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c53c633cf757dfcaa1fcafbf170b244f
https://doi.org/10.1097/pai.0000000000000159
https://doi.org/10.1097/pai.0000000000000159
Autor:
Zuzana Majtánová, Radka Symonová, Muhammet Gaffaroğlu, Sevgi Ünal, Šárka Pelikánová, Zdeněk Lajbner, Petr Ráb
Publikováno v:
Genes
Genes, Vol 11, Iss 1462, p 1462 (2020)
GENES
Volume 11
Issue 12
Genes, Vol 11, Iss 1462, p 1462 (2020)
GENES
Volume 11
Issue 12
Salmonids are extremely important economically and scientifically
therefore, dynamic developments in their research have occurred and will continue occurring in the future. At the same time, their complex phylogeny and taxonomy are challenging f
therefore, dynamic developments in their research have occurred and will continue occurring in the future. At the same time, their complex phylogeny and taxonomy are challenging f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::16984095f1bec04625e10340a27e26af
https://doi.org/10.3390/genes11121462
https://doi.org/10.3390/genes11121462
Publikováno v:
Human Chromosome Variation: Heteromorphism, Polymorphism and Pathogenesis ISBN: 9789811030345
Two revolutionary advances in molecular biology have enabled scanning of the entire human genome for genetic variation: 1. Array-comparative genomic hybridization-microarray analysis (aCGH, CMA, microarray analysis, referred to henceforth as aCGH) th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::15fd4f41ffaf1f4ed933f80e647992a4
https://doi.org/10.1007/978-981-10-3035-2_9
https://doi.org/10.1007/978-981-10-3035-2_9
Publikováno v:
Journal of Genetic Disorders & Genetic Reports.
Pallister-Killian Syndrome (PKS) is a rare sporadic genetic disorder and tissue-limited characteristics of i(12p) mosaicism. We report a boy who is diagnosed with PKS until the age of 2 years and 3 months. Amniocentesis at 18 weeks of gestation due t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5962867c31af5f5ece6944b7195a2936
https://doi.org/10.4172/2327-5790.1000153
https://doi.org/10.4172/2327-5790.1000153
Publikováno v:
Journal of Clinical Pathology
Aim To evaluate the role of whole genome comparative genomic hybridisation microarray (array-CGH) in detecting genomic imbalances as compared to conventional karyotype (GTG-analysis) or myeloma specific fluorescence in situ hybridisation (FISH) panel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35bba0409284e88b9857e59d5051788e
https://doi.org/10.1136/jclinpath-2013-201691
https://doi.org/10.1136/jclinpath-2013-201691