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The upstream sequence of the phycocyanin b subunit gene from Arthrospira platensis regulates expression of gfp gene in response to light intensity
(Pontificia Universidad Católica de Valparaíso, 2005)
Testis development in the absence of SRY: chromosomal rearrangements at SOX9 and SOX3
(Nature Publishing, 2015)
Duplications in the similar to 2 Mb desert region upstream of SOX9 at 17q24.3 may result in familial 46, XX disorders of sex development (DSD) without any effects on the XY background. A balanced translocation with its ...
Regulation of human alpha-globin gene expression and alpha-thalassemia
(Funpec-editoraRibeirao PretoBrasil, 2008)
Clinical And Molecular Characterization Of A Brazilian Cohort Of Campomelic Dysplasia Patients, And Identification Of Seven New Sox9 Mutations
(SOC BRASIL GENETICARIBEIRAO PRET, 2015)
Polymorphism in the bovine BOLA-DRB3 upstream regulatory regions detected through PCR-SSCP and DNA sequencing
(Elsevier Science, 2004-09)
In the present work, we describe through polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP) and DNA sequencing the polymorphism within the URR-BoLA-DRB3 in 15 cattle breeds. In total, seven PCR-SSCP ...
Deletion Of The Single Ureg Urease Activation Gene In Soybean Nil Lines: Characterization And Pleiotropic Effects
(Brazilian Soc Plant PhysiologyCampinas, 2016)
Promoter-specific alterations of APC are a rare cause for mutation-negative familial adenomatous polyposis
(Wiley-liss, Div John Wiley & Sons Inc, 2014-06)
In familial adenomatous polyposis (FAP), 20% of classical and 70% of attenuated/atypical (AFAP) cases remain mutation-negative after routine testing; yet, allelic expression imbalance may suggest an APC alteration. Our aim ...
Psychophysical measurements of luminance and chromatic spatial and temporal contrast sensitivity in Duchenne muscular dystrophy
(Pontificia Universidade Católica do Rio de JaneiroUniversidade de BrasíliaUniversidade de São Paulo, 2011)
In children with Duchenne muscular dystrophy, color vision losses have been related to dystrophin deletions downstream of exon 30, which affect a dystrophin isoform, Dp260, present in the retina. To further evaluate visual ...