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J Buratini Jr, A B Teixeira1, I B Costa2, V F Glapinski2, M G Pinto1, I C Giometti1, C M Barros2, M Cao3, E S Nicola3 and C A Price3
Departamento de Fisiologia, Instituto de Biociências, Universidade Estadual Paulista, Botucatu, São Paulo, Brazil, 1Departamento de Reprodução Animal, Faculdade de Medicina Veterinária, Universidade Estadual Paulista, Botucatu, São Paulo, Brazil, 2Departmento de Farmacologia, Instituto de Biociências, Universidade Estadual Paulista, Botucatu, São Paulo Brazil and 3Centre de Recherche en Reproduction Animale, Faculté de Médecine Vétérinaire, Université de Montréal, St-Hyacinthe, Québec, Canada
Correspondence should be addressed to J Buratini; Email: buratini{at}ibb.unesp.bra
The authors and journal apologize for an error in the above paper, which appeared in volume 130 part 3, page 347. The legend to Figure 3 should read "Developmental regulation of Fgfr3c expression in bovine antral follicles. (A) Gels showing target and housekepping (Gapd) PCR products in granulose and in theca cells of two representative follicles with low (<5 ng/ml) and high (>100 ng/ml) estradiol concentrations in follicular fluid (FF). Positive (Pos; fetal brain) and negative (Neg; water) PCR controls are also shown. (B) Mean ± S.E.M. relative Fgfr3c mRNA levels in granulose (GC) and theca (TC) cells from non-atretic follicles classed according to FF estradiol content (n = 16, 10, 10 and 6 follicles grouped by diameter. Means with different letters are significantly different (P < 0.05). Data for atretic follicles were derived from theca samples only, as insufficient granulose cell RNA was recovered from atretic follicles."
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