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Summary Expression Phenotypes Gene Literature (16) GO Terms (2) Nucleotides (51) Proteins (33) Interactants (51) Wiki
XB-GENEPAGE-484694

Papers associated with fshb



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Developmental profiles of progesterone receptor transcripts and molecular responses to gestagen exposure during Silurana tropicalis early development., Thomson P, Langlois VS., Gen Comp Endocrinol. September 1, 2018; 265 4-14.          


Asymmetrical allocation of JAK1 mRNA during spermatogonial stem cell division in Xenopus laevis., Hyakutake K, Kawasaki T, Zhang J, Kubota H, Abe SI, Takamune K., Dev Growth Differ. June 1, 2015; 57 (5): 389-399.                  


Steroid exposure during larval development of Xenopus laevis affects mRNA expression of the reproductive pituitary-gonadal axis in a sex- and stage-dependent manner., Urbatzka R, Lorenz C, Wiedemann C, Lutz I, Kloas W., Comp Biochem Physiol C Toxicol Pharmacol. March 1, 2014; 160 1-8.


Physiological responses of Xenopus laevis tadpoles exposed to cyanobacterial biomass containing microcystin-LR., Ziková A, Lorenz C, Lutz I, Pflugmacher S, Kloas W., Aquat Toxicol. March 15, 2013; 128-129 25-33.


Ionotropic glutamate receptor AMPA 1 is associated with ovulation rate., Sugimoto M, Sasaki S, Watanabe T, Nishimura S, Ideta A, Yamazaki M, Matsuda K, Yuzaki M, Sakimura K, Aoyagi Y, Sugimoto Y., PLoS One. November 3, 2010; 5 (11): e13817.          


Expression profiles of LHbeta, FSHbeta and their gonadal receptor mRNAs during sexual differentiation of Xenopus laevis tadpoles., Urbatzka R, Lorenz C, Lutz I, Kloas W., Gen Comp Endocrinol. September 1, 2010; 168 (2): 239-44.


Exposure of Xenopus laevis tadpoles to finasteride, an inhibitor of 5-alpha reductase activity, impairs spermatogenesis and alters hypophyseal feedback mechanisms., Urbatzka R, Watermann B, Lutz I, Kloas W., J Mol Endocrinol. November 1, 2009; 43 (5): 209-19.


Differential regulation of gonadotropins (FSH and LH) and growth hormone (GH) by neuroendocrine, endocrine, and paracrine factors in the zebrafish--an in vitro approach., Lin SW, Ge W., Gen Comp Endocrinol. January 15, 2009; 160 (2): 183-93.


Electrophysiological and pharmacological characterization of the K(ATP) channel involved in the K+-current responses to FSH and adenosine in the follicular cells of Xenopus oocyte., Fujita R, Kimura S, Kawasaki S, Watanabe S, Watanabe N, Hirano H, Matsumoto M, Sasaki K., J Physiol Sci. February 1, 2007; 57 (1): 51-61.


Functional demonstration of the ability of a primary spermatogonium as a stem cell by tracing a single cell destiny in Xenopus laevis., Kawasaki T, Imura F, Nakada A, Kubota H, Sakamaki K, Abe S, Takamune K., Dev Growth Differ. October 1, 2006; 48 (8): 525-35.            


Luteinizing hormone, follicle stimulating hormone, and gonadotropin releasing hormone mRNA expression of Xenopus laevis in response to endocrine disrupting compounds affecting reproductive biology., Urbatzka R, Lutz I, Opitz R, Kloas W., Gen Comp Endocrinol. April 1, 2006; 146 (2): 119-25.        


Atrial natriuretic peptide inhibits the actions of FSH and forskolin in meiotic maturation of pig oocytes via different signalling pathways., Zhang M, Tao Y, Zhou B, Xie H, Wang F, Lei L, Huo L, Sun Q, Xia G., J Mol Endocrinol. April 1, 2005; 34 (2): 459-72.


ATP suppresses the K(+) current responses to FSH and adenosine in the follicular cells of Xenopus oocyte., Fujita R, Kimura S, Kawasaki S, Takashima K, Matsumoto M, Hirano H, Sasaki K., Jpn J Physiol. August 1, 2001; 51 (4): 491-500.


Characterization of FSH-regulated genes isolated by mRNA differential display from pig ovarian granulosa cells., Clouscard-Martinato C, Mulsant P, Robic A, Bonnet A, Gasser F, Hatey F., Anim Genet. April 1, 1998; 29 (2): 98-106.


Xenopus oocyte K+ current. I. FSH and adenosine stimulate follicle cell-dependent currents., Greenfield LJ, Hackett JT, Linden J., Am J Physiol. November 1, 1990; 259 (5 Pt 1): C775-83.


Follicle-stimulating hormone (FSH) receptors in the testis of the newt, Cynops pyrrhogaster, and comparison of temperature dependency of the receptors with those of the other vertebrates., Kubokawa K, Ishii S., Gen Comp Endocrinol. April 1, 1980; 40 (4): 425-33.

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