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Mostrando ítems 11-20 de 33
Ataxia telangiectasia. Diagnosis and monitoring in a series of four cases [Ataxia telangiectasia. Diagnóstico y seguimiento en una serie de cuatro casos]
(2013)
Ataxia telangiectasia (AT) is a chromosomal instability syndrome with autosomal recessive inheritance, it is caused by more than 500 mutations of the ATM gene, which is involved in the cellular response to DNA damage. The ...
Pediatric donor cell leukemia after allogeneic hematopoietic stem cell transplantation in AML patient from related donor
(2015)
Here we present a male patient with acute myeloid leukemia (AML) initially diagnosed as M5 and with karyotype 46, XY. After induction therapy, he underwent a HLA-matched allogeneic hematopoietic stem cell transplantation, ...
Secondary chromosomal changes in 34 Philadelphia-chromosome-positive chronic myelocytic leukemia patients from the Mexican West
(2004)
The clonal evolution in t(9;22)-positive chronic myelocytic leukemia (CML) is well established. Four major changes occur in more than 70% of patients: +8, i(17q), +19, and an extra Philadelphia chromosome. The frequencies ...
A t(1;9)(q23.3∼q25;q34) affecting the ABL1 gene in a biphenotypic leukemia
(2004)
Recurring chromosome translocations, which are found in leukemia, can result in the inappropriate expression of oncogenes or in the formation of chimeric genes that code for structurally and functionally abnormal proteins. ...
Cell cycle and centromere FISH studies in premature centromere division
(2005)
Background: Mitotic configurations consistent in split centromeres and splayed chromatids in all or most of the chromosomes or premature centromere division (PCD) have been described in three categories. (1) Low frequency ...
Cell cycle and centromere FISH studies in premature centromere division
(2005)
Background: Mitotic configurations consistent in split centromeres and splayed chromatids in all or most of the chromosomes or premature centromere division (PCD) have been described in three categories. (1) Low frequency ...
Pediatric donor cell leukemia after allogeneic hematopoietic stem cell transplantation in AML patient from related donor
(2008)
Functional cortical organization is not dependent on cognition only, but also reflects basic intrinsic individual characteristics stable over time and across physiological conditions that suggest the existence of ...
Self adaptive high pass filtering using photochromic glass
(2004)
The clonal evolution in t(9;22)-positive chronic myelocytic leukemia (CML) is well established. Four major changes occur in more than 70% of patients: +8, i(17q), +19, and an extra Philadelphia chromosome. The frequencies ...
Molecular cytogenetic characterization of two cases with constitutional distal 11q duplication/triplication
(2004)
Recurring chromosome translocations, which are found in leukemia, can result in the inappropriate expression of oncogenes or in the formation of chimeric genes that code for structurally and functionally abnormal proteins. ...
Pediatric donor cell leukemia after allogeneic hematopoietic stem cell transplantation in AML patient from related donor
(2015)
Here we present a male patient with acute myeloid leukemia (AML) initially diagnosed as M5 and with karyotype 46, XY. After induction therapy, he underwent a HLA-matched allogeneic hematopoietic stem cell transplantation, ...