Detalles de la búsqueda
1.
Identification of potential novel drug resistance mechanisms by genomic and transcriptomic profiling of colon cancer cells with p53 deletion.
Arch Toxicol
; 95(3): 959-974, 2021 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-33515271
2.
Novel Unbalanced Translocations Affecting the Long Arms of Chromosomes 10 and 22 Cause Complex Syndromes with Very Severe Neurodevelopmental Delay, Speech Impairment, Autistic Behavior, and Epilepsy.
Cytogenet Genome Res
; 151(4): 171-178, 2017.
Artículo
en Inglés
| MEDLINE | ID: mdl-28486223
3.
Comprehensive Analyses of White-Handed Gibbon Chromosomes Enables Access to 92 Evolutionary Conserved Breakpoints Compared to the Human Genome.
Cytogenet Genome Res
; 145(1): 42-9, 2015.
Artículo
en Inglés
| MEDLINE | ID: mdl-25926034
4.
Analysis of SYCP3 encoding synaptonemal complex protein 3 in human aneuploidies.
Arch Gynecol Obstet
; 288(5): 1153-8, 2013 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-23677416
5.
Common fragile sites: genomic hotspots of DNA damage and carcinogenesis.
Int J Mol Sci
; 13(9): 11974-11999, 2012.
Artículo
en Inglés
| MEDLINE | ID: mdl-23109895
6.
Acute myeloid leukemia due to germline CEBPA mutation in a Syrian family.
Mol Genet Genomic Med
; 10(2): e1854, 2022 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-35032366
7.
Identification of novel drug resistance mechanisms by genomic and transcriptomic profiling of glioblastoma cells with mutation-activated EGFR.
Life Sci
; 284: 119601, 2021 Nov 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-33991550
8.
Preferred co-localization of chromosome 8 and 21 in myeloid bone marrow cells detected by three dimensional molecular cytogenetics.
Int J Mol Med
; 24(3): 335-41, 2009 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-19639225
9.
Recombinant Chromosomes Resulting From Parental Pericentric Inversions-Two New Cases and a Review of the Literature.
Front Genet
; 10: 1165, 2019.
Artículo
en Inglés
| MEDLINE | ID: mdl-31798640
10.
Molecular definition of high-resolution multicolor banding probes: first within the human DNA sequence anchored FISH banding probe set.
J Histochem Cytochem
; 56(5): 487-93, 2008 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-18256020
11.
Thirty-two new cases with small supernumerary marker chromosomes detected in connection with fertility problems: detailed molecular cytogenetic characterization and review of the literature.
Int J Mol Med
; 21(6): 705-14, 2008 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-18506363
12.
Parental origin of deletions and duplications - about the necessity to check for cryptic inversions.
Mol Cytogenet
; 11: 20, 2018.
Artículo
en Inglés
| MEDLINE | ID: mdl-29541160
13.
New immortalized cell lines of patients with small supernumerary marker chromosome: towards the establishment of a cell bank.
J Histochem Cytochem
; 55(6): 651-60, 2007 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-17341473
14.
Molecular cytogenetic characterization of eight small supernumerary marker chromosomes originating from chromosomes 2, 4, 8, 18, and 21 in three patients.
J Appl Genet
; 48(2): 167-75, 2007.
Artículo
en Inglés
| MEDLINE | ID: mdl-17495351
15.
Intrachromosomal amplification of BCR expressed as homogenously staining region (hsr) in a case of acute myeloid leukemia with myelodysplasia-related changes.
Int J Lab Hematol
; 44(6): 993-994, 2022 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-35534180
16.
Molecular cytogenetic characterization of the mouse cell line WMP2 by spectral karyotyping and multicolor banding applying murine probes.
Int J Mol Med
; 17(2): 209-13, 2006 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-16391817
17.
Genomic and transcriptomic profiling of resistant CEM/ADR-5000 and sensitive CCRF-CEM leukaemia cells for unravelling the full complexity of multi-factorial multidrug resistance.
Sci Rep
; 6: 36754, 2016 11 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-27824156
18.
First molecular-cytogenetic characterization of Fanconi anemia fragile sites in primary lymphocytes of FA-D2 patients in different stages of the disease.
Mol Cytogenet
; 9(1): 70, 2016.
Artículo
en Inglés
| MEDLINE | ID: mdl-27625703
19.
S100A11 plays a role in homologous recombination and genome maintenance by influencing the persistence of RAD51 in DNA repair foci.
Cell Cycle
; 15(20): 2766-79, 2016 Oct 17.
Artículo
en Inglés
| MEDLINE | ID: mdl-27590262
20.
Three cases with enlarged acrocentric p-arms and two cases with cryptic partial trisomies.
J Histochem Cytochem
; 53(3): 359-60, 2005 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-15750019