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Sex-specifically expressed

Rojas DC, Teale P, Sheeder J, Simon J, Reite M. 1997. Sex-specific expression of Heschl s gyrus functional and structural abnormalities in paranoid schizophrenia. Am J Psychiatry 154(12) 1655-1662. [Pg.379]

Shan, Z. Nanda, L Wang, Y. Schmid, M. Vortkamp, A. Haaf, T. (2000). Sex-specific expression of an evolutionarily conserved male regulatory gene, DMRTL, in birds. Cytogenetics and Cell Genetics, Vol.89, No.3-4, pp. 252-257, ISSN 0301-0171... [Pg.63]

Developmentally regulated and non-sex-specific expression of autosomal dmrt genes in embryos of Medaka fish (Oryzias latipes). Mechanism of Development, Vol.121, No.7-8, pp. 997-1005, ISSN 0925-4773... [Pg.65]

Thavathiru E., Jana N. and De P.K. (1999). Abundant secretory lipocalins displaying male and lactation-specific expression in adult hamster submandibular gland cDNA cloning and sex hormone-regulated repression. Eur J Biochem 266, 467-476. [Pg.252]

Saito, K., Nishikawa, J., Imagawa, M., Nishihara, T. and Matsuo, M. (2000) Molecular evidence of complex tissue- and sex-specific mRNA expression of the rat alpha(2u)-globulin multigene family. Biochem. Biophys. Res. Commun. 272, 337 44. [Pg.49]

M and F denote male- and female-specific expression differences, and C denotes significant differences in transcript abundance pooled across sexes. [Pg.62]

BRUGIERE, N., CUI, Y. H., BI, Y. M., ROTHSTEIN, S. J., The AtPP gene of the Brassica napus S locus region is specifically expressed in the stigma and encodes a protein similar to a methyltransferase involved in plant defense., Sex. Plant Reprod., 2001,13, 309-314. [Pg.282]

CYP subfamilies can display complex sex-, tissue-, and development-specific expression patterns. In addition, CYP expression and activity can be influenced by genetic polymorphism. [Pg.148]

Pfohl-Leszkowicz, A., Pinelli, E., Bartsch, H., Mohr, U. and Castegnaro, M. (1998) Sex- and strain-specific expression of cytochrome P450s in ochratoxin A-induced genotoxicity and carcinogenicity in rats, Mol. Carcinogen., 23 (2), 76-85. [Pg.170]

Kimoto H, Haga S, Sato K, Touhara K (2005) Sex-specific peptides from exocrine glands stimulate mouse vomeronasal sensory neurons. Nature 437 898-901 Kimoto H, Sato K, Nodari F, Haga S, Holy TE, Touhara K (2007) Sex- and strain-specific expression and vomeronasal activity of mouse ESP family peptides. Curr Biol 17 1879-1884 Kobayakawa K, Kobayakawa R, Matsumoto H, Oka Y, Imai T, Ikawa M, Okabe M, Ikeda T, Itohara S, Kikusui T, Mori K, Sakano H (2007) Innate versus learned odour processing in the mouse olfactory bulb. Nature 450 503-508... [Pg.106]

Waxman, D.J. Dannan, G.A. and Guengerich, F.P. Regulation of rat hepatic cytochrome P-450 Age-dependent expression, hormonal imprinting, and xenobiotic inducibility of sex-specific isozymes. Biochemistry 24 4409-4417, 1985. [Pg.271]

Kamoshida S, Tsutsumi Y. Extraprostatic localization of prostatic acid phosphatase and prostate-specific antigen distribution in cloacogenic glandular epithelium and sex-dependent expression in human anal gland. Hum Pathol. 1990 21 1108. [Pg.650]

Mil. McLellan, L. L, and Hayes, J. D., Sex-specific constitutive expression of the pre-neoplastic marker glutathione S-transferase, YfYf, in mouse liver. Biochem. J. 245, 399-406 (1987). McLellan, L. I., Kerr, L. A., Cronshaw, A. D., and Hayes, J. D., Regulation of mouse glutathione S-transferases by chemoprotectors. Molecular evidence for the existence of three distinct alpha-class glutathione S-transferase subunits, Yal, Ya2 and Ya3, in mouse liver. Biochem. J. 276, 461 69 (1991). [Pg.372]

The response of the class 11 male P450 genes to hypophysectomy of female rats, which derepresses, that is, increases liver enzyme levels to near-normal intact male liver levels, demonstrates that the class II male liver P450s are subject to negative pituitary regulation in female rat liver, where their expression is strongly repressed by the near continuous pattern of plasma GH exposure. These patterns of hormonal regulation are summarized in Table 9.2, which presents the responses of representative sex-specific liver CYPs to continuous and intermittent GH treatment applied to intact, hypo-physectomized and neonatal MSG-treated rats. [Pg.354]


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See also in sourсe #XX -- [ Pg.137 ]




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