Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Ingrid Kalev"'
Publikováno v:
World Journal of Cardiovascular Diseases. :545-556
Background: Chronic kidney disease (CKD) is an irreversible decline in the glomerular filtration due to nephrosclerosis and glomerular loss. Rat remnant kidney model enables to assess the benefits of different treatment possibilities. Aim: The aim of
Autor:
Ingrid Kalev, Erkki Juronen, Alar Sünter, Andres Piirsoo, Aavo-Valdur Mikelsaar, Peeter Toomik, Ruth Mikelsaar, Anu Kõiveer, Kalmer Karpson
Publikováno v:
Hybridoma. 29:391-401
We report the development of a new mouse anti-titin monoclonal antibody, named MAb Tit1 5H1.1, using the synthetic peptide corresponding to an amino acid sequence in the A-band of the titin molecule as immunogen. In the human skeletal muscle, MAb Tit
Publikováno v:
Molecular Syndromology. 1:307-310
Holt-Oram syndrome (HOS) is an autosomal dominant developmental defect involving preaxial radial ray upper limb deformity and variable cardiac defects. It has been demonstrated that HOS is caused by mutations in the T-box transcription factor gene TB
Publikováno v:
European Journal of Pediatrics. 169:469-473
LEOPARD syndrome (LS) is a heterogeneous disease characterised mainly by cutaneous manifestations. LEOPARD is the acronym for its major features-multiple lentigines, electrocardiographic conduction defects, ocular hypertelorism, pulmonary stenosis, a
Autor:
Mihkel Zilmer, Tarvo Rajasalu, Kersti Oselin, Aavo Valdur Mikelsaar, Piret Pärlist, Toomas Podar, Ingrid Kalev
Publikováno v:
Journal of Diabetes and its Complications. 17:387-391
The purpose of this study was to determine the CCR5-del32 allele frequency in type I (insulin-dependent) and type II (noninsulin-dependent) diabetes patients, and to test whether and how this mutation is associated with both types of diabetes. Thirty
Publikováno v:
European Journal of Epidemiology. 16:1107-1109
In previous studies, the highest frequencies (16%) of the CCR5 Δ32 deletion have been found in populations of Finno-Ugric origin. We here report a high CCR5 Δ32 frequency (15%) in another Finno-Ugric populations, the Estonians. The highest frequenc
Publikováno v:
Neuroscience letters. 394(1)
We have studied the expression of CC-chemokine receptor 5 (CCR5) at the protein level in human fetal neural stem/progenitor and glioblastoma cells in differentiation, using immunocytochemistry, routine fluorescence microscopy and confocal laser micro
Autor:
Begić, Fatima1, Tahirović, Husref2 husref.tahirovic@gmail.com, Kardašević, Mediha1, Kalev, Ingrid3, Muru, Kai4
Publikováno v:
European Journal of Pediatrics. Jun2014, Vol. 173 Issue 6, p819-822. 4p.
Autor:
Kalev, Ingrid1 ingrid.kalev@ut.ee, Muru, Kai2,3, Teek, Rita2,4, Zordania, Riina5, Reimand, Tiia2,3, Köbas, Kristel6, Õunap, Katrin2,3
Publikováno v:
European Journal of Pediatrics. Apr2010, Vol. 169 Issue 4, p469-473. 5p. 1 Black and White Photograph, 2 Charts, 1 Graph.
Publikováno v:
Scandinavian Journal of Immunology. Jul/Aug2001 Supplement 1, Vol. 54, p4-4. 1p.