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A naturally occurring deletion in the SRY promoter region affecting the Sp1 binding site is associated with sex reversal
(Editrice Kurtis S R LMilanItália, 2005)
Mutations in SRY and WT1 genes required for gonadal development are not responsible for XY partial gonadal dysgenesis
(Associação Brasileira de Divulgação Científica, 2005)
Similarities and differences of X and Y chromosome homologous genes, SRY and SOX3, in regulating the renin-angiotensin system promoters
(Amer Physiological Soc, 2015-05-01)
The renin-angiotensin system (RAS) is subject to sex-specific modulation by hormones and gene products. However, sex differences in the balance between the vasoconstrictor/proliferative ACE/ANG II/AT1 axis, and the ...
Regulação da região promotora de genes do sistema renina-angiotensina pelas proteínas SRY e SOX3
(Universidade Federal de Minas GeraisUFMG, 2015-04-01)
The renin-angiotensin system (RAS) is subject to sex-specific modulation by hormones and gene products. However, sex-differences in the balance between the vasoconstrictor/proliferative ACE (angiotensin-converting enzyme)/Ang ...
Avaliação da função dos genes Gata-1 e Sry na fisiologia testicular de camundongos adultos
(Universidade Federal de Minas GeraisBrasilICB - DEPARTAMENTO DE MORFOLOGIAPrograma de Pós-Graduação em Biologia CelularUFMG, 2021-11-30)
The present work proposed to analyze the function of two genes, Gata-1 and Sry, expressed in the
testis. Gata-1 is a transcription factor of the GATA family that was initially identified as a crucial
regulator of ...
Disorders of Sex Development with Testicular Differentiation in SRY-Negative 46,XX Individuals: Clinical and Genetic Aspects
(Karger, 2016-05)
Virilisation of the XX foetus is the result of androgen excess, resulting most frequently from congenital adrenal hyperplasia in individuals with typical ovarian differentiation. In rare cases, 46,XX gonads may differentiate ...
Complete gonadal dysgenesis in clinical practice: the 46,XY karyotype accounts for more than one third of cases
(Elsevier Science IncNew YorkEUA, 2011)
Recurrence of a nonsense mutation in the conserved domain of SRY in a Brazilian patient with 46,XY gonadal dysgenesis
(Freund Publishing House LtdLondonInglaterra, 1999)