Genome-wide differentially methylated genes in prostate cancer tissues from African-American and Caucasian men
JM Devaney, S Wang, P Furbert-Harris, V Apprey… - Epigenetics, 2015 - Taylor & Francis
Increasing evidence suggests that aberrant DNA methylation changes may contribute to
prostate cancer (PCa) ethnic disparity. To comprehensively identify DNA methylation …
prostate cancer (PCa) ethnic disparity. To comprehensively identify DNA methylation …
Monoallelic expression of the human FOXP2 speech gene
AA Adegbola, GF Cox, EM Bradshaw… - Proceedings of the …, 2015 - National Acad Sciences
The recent descriptions of widespread random monoallelic expression (RMAE) of genes
distributed throughout the autosomal genome indicate that there are more genes subject to …
distributed throughout the autosomal genome indicate that there are more genes subject to …
[PDF][PDF] SÍNDROME DE ANGELMAN
IVP Rodrigues, B Genética - APOSTILA DE GENÉTICA MÉDICA - lagemufma.com
A prevalência da Síndrome de Angelman está estimada em 1: 10.000 a 1: 40.000 nativivos
em todo o mundo.(CLAYTON-SMITH; LAAN, 2003) e atinge homens, mulheres e todos os …
em todo o mundo.(CLAYTON-SMITH; LAAN, 2003) e atinge homens, mulheres e todos os …
Detection of Loss of Imprinting by Pyrosequencing®
S Tabano, E Bonaparte, M Miozzo - Pyrosequencing: Methods and …, 2015 - Springer
Genomic imprinting is an epigenetically regulated process determining allele-specific
expression in a parent-of-origin dependent manner. Altered expression of imprinted genes …
expression in a parent-of-origin dependent manner. Altered expression of imprinted genes …
Prader-Willi syndrome with a long-contiguous stretch of homozygosity not covering the critical region
X Yingjun, Z Yi, W Jianzhu, S Yunxia… - Journal of Child …, 2015 - journals.sagepub.com
Prader-Willi syndrome is a common and complex disorder affecting multiple systems. Its
main manifestations are infantile hypotonia with a poor sucking reflex, a characteristic facial …
main manifestations are infantile hypotonia with a poor sucking reflex, a characteristic facial …
Estudo da expressão diferencial de genes localizados no segmento cromossômico 15q11-q13 em pacientes com as síndromes de Angelman e Prader-Willi
EM Cruvinel - 2015 - teses.usp.br
A síndrome de Prader Willi (PWS) é uma doença de neurodesenvolvimento; a principal
hipótese de causa de PWS é a ausência da expressão de SNORD116. O SNORD116 fica …
hipótese de causa de PWS é a ausência da expressão de SNORD116. O SNORD116 fica …