Borowiec M - Search Results

1

A family with the Arg103Pro mutation in the NEUROD1 gene detected by next-generation sequencing - Clinical characteristics of mutation carriers.

Szopa M, Ludwig-Galezowska AH, Radkowski P, Skupien J, Machlowska J, Klupa T, Wolkow P, Borowiec M, Mlynarski W, Malecki MT. Szopa M, et al. Among authors: borowiec m. Eur J Med Genet. 2016 Feb;59(2):75-9. doi: 10.1016/j.ejmg.2016.01.002. Epub 2016 Jan 8. Eur J Med Genet. 2016. PMID: 26773576

2

Examination of PPP1R3B as a candidate gene for the type 2 diabetes and MODY loci on chromosome 8p23.

Dunn JS, Mlynarski WM, Pezzolesi MG, Borowiec M, Powers C, Krolewski AS, Doria A. Dunn JS, et al. Among authors: borowiec m. Ann Hum Genet. 2006 Sep;70(Pt 5):587-93. doi: 10.1111/j.1469-1809.2005.00248.x. Ann Hum Genet. 2006. PMID: 16907705

3

Evaluation of Apolipoprotein M Serum Concentration as a Biomarker of HNF-1alpha MODY.

Skupien J, Kepka G, Gorczynska-Kosiorz S, Gebska A, Klupa T, Wanic K, Nowak N, Borowiec M, Sieradzki J, Malecki MT. Skupien J, et al. Among authors: borowiec m. Rev Diabet Stud. 2007 Winter;4(4):231-5. doi: 10.1900/RDS.2007.4.231. Epub 2008 Feb 10. Rev Diabet Stud. 2007. PMID: 18338076 Free PMC article.

4

Molecular background and clinical characteristics of HNF1A MODY in a Polish population.

Skupien J, Gorczynska-Kosiorz S, Klupa T, Cyganek K, Wanic K, Borowiec M, Sieradzki J, Malecki MT. Skupien J, et al. Among authors: borowiec m. Diabetes Metab. 2008 Nov;34(5):524-8. doi: 10.1016/j.diabet.2008.05.004. Epub 2008 Oct 1. Diabetes Metab. 2008. PMID: 18838325

5

Mutations at the BLK locus linked to maturity onset diabetes of the young and beta-cell dysfunction.

Borowiec M, Liew CW, Thompson R, Boonyasrisawat W, Hu J, Mlynarski WM, El Khattabi I, Kim SH, Marselli L, Rich SS, Krolewski AS, Bonner-Weir S, Sharma A, Sale M, Mychaleckyj JC, Kulkarni RN, Doria A. Borowiec M, et al. Proc Natl Acad Sci U S A. 2009 Aug 25;106(34):14460-5. doi: 10.1073/pnas.0906474106. Epub 2009 Aug 10. Proc Natl Acad Sci U S A. 2009. PMID: 19667185 Free PMC article.

6

Dipeptidyl peptidase-IV inhibitors are efficient adjunct therapy in HNF1A maturity-onset diabetes of the young patients--report of two cases.

Katra B, Klupa T, Skupien J, Szopa M, Nowak N, Borowiec M, Kozek E, Malecki MT. Katra B, et al. Among authors: borowiec m. Diabetes Technol Ther. 2010 Apr;12(4):313-6. doi: 10.1089/dia.2009.0159. Diabetes Technol Ther. 2010. PMID: 20210571

7

[Optimization of monogenic diabetes screening programme--initial report on recruitment efficacy of the TEAM project].

Borowiec M, Fendler W, Antosik K, Ciepiela A, Baranowska A, Hogendorf A, Mianowska B, Szadkowska A, Młynarski W. Borowiec M, et al. Pediatr Endocrinol Diabetes Metab. 2010;16(2):73-6. Pediatr Endocrinol Diabetes Metab. 2010. PMID: 20813082 Polish.

8

FOXP3, IL-10, and TGF-β genes expression in children with IgE-dependent food allergy.

Krogulska A, Borowiec M, Polakowska E, Dynowski J, Młynarski W, Wasowska-Królikowska K. Krogulska A, et al. Among authors: borowiec m. J Clin Immunol. 2011 Apr;31(2):205-15. doi: 10.1007/s10875-010-9487-1. Epub 2010 Nov 24. J Clin Immunol. 2011. PMID: 21107665 Free PMC article.

9

Paternally inherited proinsulin mutations may result in earlier onset of monogenic diabetes mutation identity effect in monogenic diabetes.

Fendler W, Borowiec M, Antosik K, Jaroszewska-Swiatek B, Szwalkiewicz-Warowicka E, Malecki M, Mysliwiec M, Mlynarski W. Fendler W, et al. Among authors: borowiec m. Diabetes Care. 2011 Jan;34(1):e9. doi: 10.2337/dc10-1142. Diabetes Care. 2011. PMID: 21193618 No abstract available.

10

Novel glucokinase mutations in patients with monogenic diabetes - clinical outline of GCK-MD and potential for founder effect in Slavic population.

Borowiec M, Antosik K, Fendler W, Deja G, Jarosz-Chobot P, Mysliwiec M, Zmyslowska A, Malecki M, Szadkowska A, Mlynarski W. Borowiec M, et al. Clin Genet. 2012 Mar;81(3):278-83. doi: 10.1111/j.1399-0004.2011.01656.x. Epub 2011 Mar 18. Clin Genet. 2012. PMID: 21348868

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