Výsledky vyhledávání

Clinical and biochemical implications of low thyroid hormone levels (total and free forms) in euthyroid patients with chronic kidney disease

Autor: Abdul Rashid Qureshi, Peter Stenvinkel, Jonas Axelsson, Peter Bárány, Olof Heimbürger, Juan Jesus Carrero, M. R. Witt, Mohamed E. Suliman, Mahmut Ilker Yilmaz, Bengt Lindholm, S. Rehnmark, Anders Alvestrand

Publikováno v: Journal of Internal Medicine. 262:690-701

Carrero JJ, Qureshi AR, Axelsson J, Yilmaz MI, Rehnmark S, Witt MR, Barany P, Heimburger O, Suliman ME, Alvestrand A, Lindholm B, Stenvinkel P (Karolinska Institutet, Stockholm; and Karo Bio AB, Novum, Huddinge; Sweden). Clinical and biochemical impl

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::3de969f971163fe5a0d947e5ccb22484
https://doi.org/10.1111/j.1365-2796.2007.01865.x

Zobrazit plný text záznamu

Akademický článek

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Clinical and biochemical implications of low thyroid hormone levels (total and free forms) in euthyroid patients with chronic kidney disease

Autor: J J, Carrero, A R, Qureshi, J, Axelsson, M I, Yilmaz, S, Rehnmark, M R, Witt, P, Bárány, O, Heimbürger, M E, Suliman, A, Alvestrand, B, Lindholm, P, Stenvinkel

Publikováno v: Journal of internal medicine. 262(6)

In this study, we explore the associations of decreased thyroid hormone levels with inflammation, wasting and survival in biochemically euthyroid patients with end-stage renal disease (ESRD).After exclusion of 23 patients with thyroid-stimulating hor

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::850b0aaf2e791d1ea931dcbb58974550
https://pubmed.ncbi.nlm.nih.gov/17908160

Zobrazit plný text záznamu

Instantaneous Bearing Discriminators with Omnidirectional Coverageand High Accuracy

Autor: S. Rehnmark

Publikováno v: MTT-S International Microwave Symposium Digest.

Monopulse Bearing Discriminators, with full omniazimuthal coverage, designed specifically for high probability of detection in dense signal environments are presented. S-band (2-4 GHz) developmental models give angle of arrival information on a singl

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b3c9c5ab3e4de3812641d0e0a5f3f9be
https://doi.org/10.1109/mwsym.1980.1124203

Zobrazit plný text záznamu

Ambient temperature regulation of apoptosis in brown adipose tissue. Erk1/2 promotes norepinephrine-dependent cell survival

Autor: J M, Lindquist, S, Rehnmark

Publikováno v: The Journal of biological chemistry. 273(46)

Brown adipose tissue hyperplasia is a fundamental response to low ambient temperature. We show here that cold exposure of an animal markedly increased the phosphorylation of mitogen-activated protein kinase (p42/p44) Erk1 and Erk2 in brown adipose ti

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::fdf94b7d8266835de5dad86c6ed0f4a4
https://pubmed.ncbi.nlm.nih.gov/9804770

Zobrazit plný text záznamu

The fatty liver dystrophy mutant mouse: microvesicular steatosis associated with altered expression levels of peroxisome proliferator-regulated proteins

Autor: S, Rehnmark, C S, Giometti, B G, Slavin, M H, Doolittle, K, Reue

Publikováno v: Journal of lipid research. 39(11)

Fatty liver dystrophy ( fld) is an autosomal recessive mutation in mice characterized by hypertriglyceridemia and fatty liver during neonatal development. The fatty liver in fld/fld mice spontaneously resolves between the age of 14-18 days, at which

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::32375e5518db217c46d5b85d469f37ba
https://pubmed.ncbi.nlm.nih.gov/9799807

Zobrazit plný text záznamu

The fatty liver dystrophy (fld) mutation: Developmentally related alterations in hepatic triglyceride metabolism and protein expression

Autor: R.D. Cohen, Karen Reue, K. Mishler, S. Rehnmark, B.G. Slavin, T.H. Leete, Mark H. Doolittle, C.S. Giometti

Fatty liver dystrophy (fld) is an autosomal recessive mutation in mice characterized by hypertriglyceridemia and development of a fatty liver in the early neonatal period. Also associated with the fld phenotype is a tissue-specific deficiency in the

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::0d799d0dca65f6e6bc3b1e364cbf1895
https://doi.org/10.2172/505325

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání