Zobrazeno 1 - 8
of 8
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc0b0b2f6bb79d995d709cfccfe3169d
https://doi.org/10.4236/wjcd.2018.812054
https://doi.org/10.4236/wjcd.2018.812054
Publikováno v:
European Journal of Pediatrics. 173:819-822
This is the first reported family with Leopard syndrome (LS) from Bosnia and Herzegovina. We report five cases of LS from two generations of the same family. In the present series of patients from one family, all patients carry the same recurrent mut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ff9b95cbc24865653fe1f49ed1ee6ef
https://doi.org/10.1007/s00431-013-2243-9
https://doi.org/10.1007/s00431-013-2243-9
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dee26b85ae2fbaa084f8e3c449be5c2a
https://doi.org/10.1089/hyb.2009.0116
https://doi.org/10.1089/hyb.2009.0116
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b58f6d8581bbb59bc26b09bd2306828
https://doi.org/10.1159/000330109
https://doi.org/10.1159/000330109
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7da83c00f9440f429df2ebf5312cee50
https://doi.org/10.1007/s00431-009-1058-1
https://doi.org/10.1007/s00431-009-1058-1
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::975f466d7d7dbb2dff4168805e01aed0
https://doi.org/10.1016/s1056-8727(02)00242-8
https://doi.org/10.1016/s1056-8727(02)00242-8
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5d97a8ef81fa6e4ac10ede78e5f15f41
https://doi.org/10.1023/a:1010829816334
https://doi.org/10.1023/a:1010829816334
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76233a81af82d6df8838679e1ddda11e
https://pubmed.ncbi.nlm.nih.gov/16278045
https://pubmed.ncbi.nlm.nih.gov/16278045