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Alterações no número de cópias genômicas em carcinomas de mama
(Universidade Estadual Paulista (UNESP), 2014)
Alterações no número de cópias genômicas em carcinomas de mama
(Universidade Estadual Paulista (Unesp), 2014)
Quantum q-field theory: Q-Schrödinger and q-Klein-Gordon fields
(Europhysics Letters, 2017-06)
We show how to deal with the generalized q-Schrödinger and q-Klein-Gordon fields in a variety of scenarios. These q-fields are meaningful at very high energies (TeVs) for high ones (GeVs) for and at low energies (MeVs) for ...
Contribution of Mitochondrial DNA Heteroplasmy to the Congenital Cardiac and Palatal Phenotypic Variability in Maternally Transmitted 22q11.2 Deletion Syndrome
(2021)
Congenital heart disease (CHD) and palatal anomalies (PA), are among the most common
characteristics of 22q11.2 deletion syndrome (22q11.2DS), but they show incomplete penetrance, suggesting the presence of additional ...
Conectividades no Modelo de Q-Potts crítico bidimensional
(Universidade Federal do Rio Grande do NorteBrasilUFRNPROGRAMA DE PÓS-GRADUAÇÃO EM FÍSICA, 2020-03-12)
The conformal field theory has been show as a valuable asset in theoretical physics over
the course of the last decades. In this work such theory was used as a way to evaluate
four-point boundary connectivities in a ...
Genes candidatos a marcadores tumorais na progressão do adenocarcinoma de próstata indentificados por análise de HR-CGH e CGH-ARRAY
(Universidade Estadual Paulista (Unesp), 2009-02-01)
O câncer de próstata (CaP) é a neoplasia mais comumente diagnosticada entre homens no ocidente. Embora tratamentos efetivos para a doença localizada estejam disponíveis atualmente, não há terapia curativa para tumores ...
Aplicación de Hibridación In Situ Fluorescente (FISH) en pacientes con sospecha clínica de Síndrome de Deleción 22q11.2 (SD22q11.2)Applying Fluorescent in situ hybridization (FISH) in patients with suspected clinical signs of 22q11.2 deletion syndrome (DS22q11.2)
(Hospital de Niños "Ricardo Gutiérrez", 2019-05)
El SD22q11.2 está asociado a síndromes de DiGeorge, velocardiofacial, facioconotruncal y Cayler, reconocidos con la misma etiología: microdeleción 22q11.2. El fenotipo es variable y presenta cardiopatía conotruncal (CC), ...
Genomic imbalances in esophageal squamous cell carcinoma identified by molecular cytogenetic techniques
(Sociedade Brasileira de Genética, 2014)
Alterações no número de cópias genômicas em carcinomas de mama
(Universidade Estadual Paulista (Unesp), 2013-12-18)
Breast cancer (BC) is a heterogeneous both at molecular and clinical level. Patients with similar clinical and histopathological findings can present different prognosis. Analysis of large scale genomic changes have helped ...
Biallelic deletion 13q14.3 in patients with chronic lymphocytic leukemia: Cytogenetic, FISH and clinical studies
(Wiley Blackwell Publishing, Inc, 2008-08)
Background and objective: Monoallelic deletion of 13q14.3 (13q14x1) is the most common abnormality in chronic lymphocytic leukemia (CLL). As a sole alteration, it predicts a favorable outcome. Biallelic 13q14.3 (13q14x2) ...