[PDF] from peerproject.euM Taulan, E Lopez, V Viart, C Guittard, C Templin… - 2011 - repository.peerproject.eu ... Page 2. 2 Abstract Background: CBAVD (Congenital Bilateral Absence of the VasDeferens), a frequent cause ... Genetic investigations of CFTR mutations in congenital absence of vasdeferens, uterus, and vagina as a cause of infertility. J Androl 2008;29(5):506-13. ... Related articles
[PDF] from cnrs.frE Lopez, V Viart, C Guittard, C Templin… - Journal of medical …, 2011 - jmg.bmj.com Methods and results Mutation scanning analysis of microsatellite variability in the CFTR gene identified two undescribed 4 bp sequence repeats (TAAA) 6 and (TAAA) 8 in intron 9 in two CBAVD patients heterozygote for either the −33G→A promoter transition or the classical [TG12T5] ... Cited by 1 - Related articles - All 5 versions
P Marcorelles, D Gillet, G Friocourt, F Ledé… - Human Pathology, 2011 - Elsevier ... [4] R. Radpour, H. Gourabi, A. Vosough Dizaj, W. Holzgreve and XY Zhong, Genetics investigations of CFTR mutations in congenital absence of vasdeferens, uterus, vagina as a cause of infertility, J Androl 29 (2008), pp. 506–513. ...
P Medina, G Segarra, MD Mauricio, JM Vila… - Biochemical …, 2011 - Elsevier ... Figure 1A shows representative tracings of the effects of PGE1 (10-8-10-6 M) on EFS-evoked contractions of the vasdeferens rings in the absence (control) and in the presence of K+ channel blockers and Figure 1B and C summarizes the results from all the experiments. ... All 2 versions
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