Beltcheva O - Search Results

1

Alternatively used promoters and distinct elements direct tissue-specific expression of nephrin.

Beltcheva O, Kontusaari S, Fetissov S, Putaala H, Kilpeläinen P, Hökfelt T, Tryggvason K. Beltcheva O, et al. J Am Soc Nephrol. 2003 Feb;14(2):352-8. doi: 10.1097/01.asn.0000043081.65110.c4. J Am Soc Nephrol. 2003. PMID: 12538735

2

Sp1 specifically binds to an evolutionarily conserved DNA segment within a region necessary for podocyte-specific expression of nephrin.

Beltcheva O, Hjorleifsdottir EE, Kontusaari S, Tryggvason K. Beltcheva O, et al. Nephron Exp Nephrol. 2010;114(1):e15-22. doi: 10.1159/000245062. Epub 2009 Oct 9. Nephron Exp Nephrol. 2010. PMID: 19816048

3

Mutation spectrum in the nephrin gene (NPHS1) in congenital nephrotic syndrome.

Beltcheva O, Martin P, Lenkkeri U, Tryggvason K. Beltcheva O, et al. Hum Mutat. 2001 May;17(5):368-73. doi: 10.1002/humu.1111. Hum Mutat. 2001. PMID: 11317351

4

Wolf-Hirschhorn syndrome candidate 1-like 1 epigenetically regulates nephrin gene expression.

Ito Y, Katayama K, Nishibori Y, Akimoto Y, Kudo A, Kurayama R, Hada I, Takahashi S, Kimura T, Fukutomi T, Katada T, Suehiro J, Beltcheva O, Tryggvason K, Yan K. Ito Y, et al. Among authors: beltcheva o. Am J Physiol Renal Physiol. 2017 Jun 1;312(6):F1184-F1199. doi: 10.1152/ajprenal.00305.2016. Epub 2017 Feb 22. Am J Physiol Renal Physiol. 2017. PMID: 28228401 Free article.

5

Steroid-resistant nephrotic syndrome caused by novel WT1 mutation inherited from a mosaic parent.

Beltcheva O, Boueva A, Tzveova R, Roussinov D, Marinova S, Kaneva R, Mitev V. Beltcheva O, et al. Ren Fail. 2016;38(2):290-3. doi: 10.3109/0886022X.2015.1117906. Epub 2015 Dec 1. Ren Fail. 2016. PMID: 26627896 Free article.

6

Novel mutation in Wilms' tumour 1 gene associated with steroid-resistant nephrotic syndrome.

Beltcheva O, Boueva A, Morgunova E, Boiadjieva E, Marinova S, Kaneva R, Mitev V. Beltcheva O, et al. NDT Plus. 2011 Feb;4(1):17-9. doi: 10.1093/ndtplus/sfq173. Epub 2010 Oct 7. NDT Plus. 2011. PMID: 25984092 Free PMC article.

7

C283Y mutation and other C-terminal nucleotide changes in the gamma-sarcoglycan gene in the Bulgarian Gypsy population.

Todorova A, Ashikov A, Beltcheva O, Tournev I, Kremensky I. Todorova A, et al. Among authors: beltcheva o. Hum Mutat. 1999;14(1):40-4. doi: 10.1002/(SICI)1098-1004(1999)14:1<40::AID-HUMU5>3.0.CO;2-R. Hum Mutat. 1999. PMID: 10447257

8

Evaluation of the clinical value of the newly identified urine biomarker HIST1H4K for diagnosis and prognosis of prostate cancer in Bulgarian patients.

Kachakova D, Mitkova A, Popov E, Beltcheva O, Vlahova A, Dikov T, Hristova S, Mitev V, Slavov C, Kaneva R. Kachakova D, et al. Among authors: beltcheva o. J BUON. 2013 Jul-Sep;18(3):660-8. J BUON. 2013. PMID: 24065480 Free article.

9

The rs266729 single-nucleotide polymorphism in the adiponectin gene shows association with gestational diabetes.

Beltcheva O, Boyadzhieva M, Angelova O, Mitev V, Kaneva R, Atanasova I. Beltcheva O, et al. Arch Gynecol Obstet. 2014 Apr;289(4):743-8. doi: 10.1007/s00404-013-3029-z. Epub 2013 Sep 26. Arch Gynecol Obstet. 2014. PMID: 24068295

10

A familial case of severe infantile nephronophthisis explained by oligogenic inheritance.

Penchev V, Boueva A, Kamenarova K, Roussinov D, Tzveova R, Ivanova M, Dimitrova V, Kremensky I, Mitev V, Kaneva R, Beltcheva O. Penchev V, et al. Among authors: beltcheva o. Eur J Med Genet. 2017 Jun;60(6):321-325. doi: 10.1016/j.ejmg.2017.04.002. Epub 2017 Apr 6. Eur J Med Genet. 2017. PMID: 28392475

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