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Orchidopexy restores morphometric-stereologic changes in the caput epididymis and daily sperm production in cryptorchidic mice, although sperm transit time and fertility parameters remain impaired
(Elsevier B.V., 2011-09-01)
Objective: To evaluate the changes in the caput epididymis following cryptorchidism and orchidopexy.Design: Experimental study in a research laboratory.Setting: Reproductive biology research laboratory.Animal(s): Immature ...
Atrogin-1 and MuRF1 regulate cardiac MyBP-C levels via different mechanisms
(OXFORD UNIV PRESS, 2010)
Familial hypertrophic cardiomyopathy (FHC) is frequently caused by cardiac myosin-binding protein C (cMyBP-C) gene mutations, which should result in C-terminal truncated mutants. However, truncated mutants were not detected ...
Fiber Type Composition in Semitendinous Muscle of Wistar Rats and Effects of Intermittent Training on its Hypertrophy
(Soc Chilena AnatomiaTemucoChile, 2008)
Effects of Recession versus Tenotomy Surgery without Recession in Adult Rabbit Extraocular Muscle
(ASSOC RESEARCH VISION OPHTHALMOLOGY INC, 2010)
PURPOSE. Surgical recession of an extraocular muscle (EOM) posterior to its original insertion is a common form of strabismus surgery, weakening the rotational force exerted by the muscle on the globe and improving eye ...
Thyrotropin-Releasing Hormone Overexpression induces structural changes of the Left Ventricle in the normal Rat heart
(American Physiological Society, 2014-10)
Thyrotropin-releasing hormone (TRH) hyperactivity has been observed in the left ventricle of spontaneously hypertensive rats. Its long-term inhibition suppresses the development of hypertrophy, specifically preventing ...
MYH9-related disease: Five novel mutations expanding the spectrum of causative mutations and confirming genotype/phenotype correlations
(Elsevier Masson, 2013-01)
MYH9-related disease (MYH9-RD) is a rare autosomal dominant syndromic disorder caused by mutations in MYH9, the gene encoding for the heavy chain of non-muscle myosin IIA (myosin-9). MYH9-RD is characterized by congenital ...
Low triioothyronine (T-3) or reverse triioothyronine (rT(3)) syndrome modifies gene expression in rats with congestive heart failure
(Taylor & Francis Inc, 2005-01-01)
Heart failure (NF) is frequently associated with euthyroid sicksyndrome (low T-3 and elevated rT(3)). We investigated if altered thyroid hormone in HF could affect expression of the TH receptor (TR alpha 1), and alpha and ...
Proteasome activity is altered in skeletal muscle tissue of tumour-bearing rats fed a leucine-rich diet
(Soc EndocrinologyBristolInglaterra, 2004)
Neuronal nitric oxide synthase is heterogeneously distributed in equine myofibers and highly expressed in endurance trained horses
(Canadian Vet Med AssocOttawaCanadá, 2005)
Estudo de mutações causadoras de cardiomiopatia hipertrófica em um grupo de pacientes no Espírito Santo, Brasil
(Sociedade Brasileira de Cardiologia - SBC, 2010)
FUNDAMENTO: A cardiomiopatia hipertrófica (CH) é a doença cardíaca hereditária mais frequente, causada por mutações nos genes codificadores para proteínas do sarcômero. Embora mais de 430 mutações tenham sido identificadas ...