Results 21 to 30 of about 88,181 (213)

Discrepancy of Cytogenetic Analysis in Western and Eastern Taiwan

open access: yesPediatrics and Neonatology, 2013
This study aimed at investigating the results of second-trimester amniocyte karyotyping in western and eastern Taiwan, and identifying any regional differences in the prevalence of fetal chromosomal anomalies.
Yu-Hsun Chang   +6 more
doaj   +1 more source

Daratumumab, lenalidomide, and dexamethasone in relapsed/refractory myeloma: a cytogenetic subgroup analysis of POLLUX

open access: yes, 2020
High cytogenetic risk abnormalities confer poor outcomes in multiple myeloma patients. In POLLUX, daratumumab/lenalidomide/dexamethasone (D-Rd) demonstrated significant clinical benefit versus lenalidomide/dexamethasone (Rd) in relapsed/refractory ...
Magen, H   +14 more
core   +1 more source

Translocation (8;21) in acute nonlymphocytic leukemia delineated by chromosomal in situ suppression hybridization [PDF]

open access: yes, 1991
In situ suppression hybridization with recombinant bacteriophage DNA libraries for chromosomes 8 and 21 was performed in two cases of acute nonlymphocytic leukemia, type FAB M2.
Cremer, Thomas   +5 more
core   +1 more source

Cytogenetic Analysis for Suspected Chromosomal Abnormalities; A Five Years Experience [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2016
Introduction: Chromosomal abnormalities are the results of alterations in the number or structure of chromosomes causing significant human morbidity and mortality.
Sunil Kumar Polipalli   +6 more
doaj   +1 more source

Medical Implementation of Microarray Technology

open access: yesKorean Journal of Clinical Laboratory Science, 2020
Microarray technology represents a critical new advance in molecular cytogenetics. The de-velopment of this approach has provided fundamental insights into the molecular pathogenesis in clinical cytogenetics and has provided a clue to many unidentified ...
Ji Un Kang
doaj   +1 more source

Serum biochemical parameters in pregnant women with and without fetal chromosomal abnornalities

open access: yesФундаментальная и клиническая медицина, 2022
Aim. To analyse the levels of serum beta-human chorionic gonadotropin (β-hCG) and pregnancy-associated plasma protein A (PAPP-A) in pregnant women without fetal chromosomal abnormalities and with fetal trisomy 21 (Down syndrome) or 18 (Edwards syndrome ...
A. N. Volkov   +4 more
doaj   +1 more source

Chromosomal variations and genetic diversity in subpopulations of Senna alexandrina Mill. from Western Thar, India

open access: yesCaryologia
Homologous recombination promotes genetic diversity by exchanging genetic material between homologs, ensuring unique combinations of alleles in offspring.
Sunita Arora, Monika Vyas, Meena Barupal
doaj   +1 more source

A Semi-Closed Device for Chromosome Spreading for Cytogenetic Analysis

open access: yesMicromachines, 2014
Metaphase chromosome spreading is the most crucial step required for successful karyotyping and FISH analysis. These two techniques are routinely used in cytogenetics to assess the chromosome abnormalities.
Dorota Kwasny   +7 more
doaj   +1 more source

Prognostic Implications of Cytogenetic Features in Myelodysplastic Syndromes [PDF]

open access: yes, 2013
Myelodysplastic Syndromes (MDS) are a heterogeneous group of hematological diseases characterized by refractory cytopenia(s) and variable risk of leukemic progression.
Belli, Carolina Bárbara   +3 more
core   +1 more source

Immunophenotypic characterisation and cytogenetic analysis of mesenchymal stem cells from equine bone marrow and foal umbilical cords during in vitro culture

open access: yesJournal of Veterinary Research, 2016
Introduction: The objective of the study was immunophenotypic and cytogenetic analysis of mesenchymal stem cells from equine bone marrow and foal umbilical cords during in vitro culture.
Mazurkevych Anatoliy   +7 more
doaj   +1 more source

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