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Associated anomalies among infants with oral clefts at birth and during a 1-year follow-up
(Wiley-liss, Div John Wiley & Sons Inc, 2011-07)
Reports of birth defects rates may focus on defects observed in the newborn period or include defects diagnosed at older ages. However, little information is available on the rates of additional anomalies detected after ...
Recurrent miscarriage in a novel translocation 7:9 carriers with no infertility
(Somil Shah, 2017-12-04)
A balanced translocation between the short arm of chromosome 7 and the long arm ofchromosome 9 was observed in a pedigree of three carriers (proband, his daugtherand first cousin). In this study, the proband and first ...
Estudos moleculares de doenças genéticas humanas
(Universidade Federal de Minas GeraisUFMG, 2014-01-20)
The molecular study of human genetic diseases has an important role in the detection, prevention, treatment and/or counseling genetic of diseases which are caused by chromosomal abnormalities and DNA sequence variants. The ...
PLA and Organoclays Nanocomposites: Degradation Process and Evaluation of ecotoxicity Using Allium cepa as Test Organism
(2013-07-17)
In this study, nanocomposites of PLA and organoclays Cloisite 20A and Cloisite 30B were prepared by the melt intercalation method and the obtained samples were characterized by transmission electron microscopy (TEM). Since ...
Análise cromossômica por microarranjos aplicada à identificação de alterações genômicas em pacientes com fissura lábio palatina
(BrasilUFRNPROGRAMA DE PÓS-GRADUAÇÃO EM CIÊNCIAS DA SAÚDE, 2019-11-12)
Non-syndromic orofacial clefts (OFC) consist of craniofacial malformations
characterized by the presence of abnormal spaces or gaps in the upper lip, alveolus
and/or palate, which may have effects on speech, hearing, ...
Características del primer hemograma, al momento del diagnóstico de leucemia linfoblástica aguda, en los niños del Instituto del Cáncer SOLCA-Cuenca
(Universidad de Cuenca. Facultad de Ciencias Médicas, 2016-12)
BACKGROUND: The acute lymphoblastic leukemia (ALL)
is the most common type of childhood cancer that
affects the blood and bone marrow as a result of abnormal
clonal proliferation of a cell group, and contrary
to what ...
Localização subcelular da DSCR2, uma proteína relacionada à síndrome de Down.
(Universidade Federal de São CarlosBRUFSCarPrograma de Pós-Graduação em Genética Evolutiva e Biologia Molecular - PPGGEv, 2003-10-17)
Down Syndrome (DS) is the major cause of mental retardation with a high incidence among human beings. Main features in DS include facial and
dermatological features, congenital heart defects as well as immunological, ...
Predominant Rab-GTPase amplicons contributing to oral squamous cell carcinoma progression to metastasis
(Oncotarget, 2015-09-08)
Metastatic oral squamous cell carcinoma (OSCC) is frequently associated with recurrent gene abnormalities at specific chromosomal loci. Here, we utilized array comparative genomic hybridization and genome-wide screening ...
Centrosome amplification in chondrosarcomas: A primary cell culture and cryopreserved tumor sample study
(Spandidos Publ Ltd, 2017-03-01)
The genetics background underlying the aggressiveness of chondrosarcoma (CS) is poorly understood. One possible cause of malignant transformation is chromosomal instability, which involves an error in mitotic segregation ...
Biomonitoreo de células bucales a partir de micronúcleos en soldadores de metales en Cartagena (Bolívar)
(2011)
En el mundo moderno, la soldadura es un proceso que permite la fundición de algunos metales pesados como hierro, cobre, estaño, aluminio, plomo, zinc, arsénico y cadmio. Estos elementos pueden ocasionar efectos genotóxicos ...