Borowiec M - Search Results

1

Evidence against RAB40AL being the locus for Martin-Probst X-linked deafness-intellectual disability syndrome.

Ołdak M, Ścieżyńska A, Młynarski W, Borowiec M, Ruszkowska E, Szulborski K, Pollak A, Kosińska J, Mueller-Malesińska M, Stawiński P, Szaflik JP, Płoski R. Ołdak M, et al. Among authors: borowiec m. Hum Mutat. 2014 Oct;35(10):1171-4. doi: 10.1002/humu.22620. Epub 2014 Aug 7. Hum Mutat. 2014. PMID: 25044830

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

Phenotype variability and neonatal diabetes in a large family with heterozygous mutation of the glucokinase gene.

Borowiec M, Mysliwiec M, Fendler W, Antosik K, Brandt A, Malecki M, Mlynarski W. Borowiec M, et al. Acta Diabetol. 2011 Sep;48(3):203-8. doi: 10.1007/s00592-011-0279-8. Epub 2011 Mar 25. Acta Diabetol. 2011. PMID: 21437567 Free PMC article.

4

Metabolic syndrome components among children born small for gestational age: analysis of the first decade of life.

Szałapska M, Stawerska R, Borowiec M, Młynarski W, Lewiński A, Hilczer M. Szałapska M, et al. Among authors: borowiec m. Pediatr Endocrinol Diabetes Metab. 2010;16(4):270-6. Pediatr Endocrinol Diabetes Metab. 2010. PMID: 21447268

5

Wolfram syndrome in the Polish population: novel mutations and genotype-phenotype correlation.

Zmyslowska A, Borowiec M, Antosik K, Szalecki M, Stefanski A, Iwaniszewska B, Jedrzejczyk M, Pietrzak I, Mlynarski W. Zmyslowska A, et al. Among authors: borowiec m. Clin Endocrinol (Oxf). 2011 Nov;75(5):636-41. doi: 10.1111/j.1365-2265.2011.04102.x. Clin Endocrinol (Oxf). 2011. PMID: 21564155

6

Doubling the referral rate of monogenic diabetes through a nationwide information campaign--update on glucokinase gene mutations in a Polish cohort.

Borowiec M, Fendler W, Antosik K, Baranowska A, Gnys P, Zmyslowska A, Malecki M, Mlynarski W. Borowiec M, et al. Clin Genet. 2012 Dec;82(6):587-90. doi: 10.1111/j.1399-0004.2011.01803.x. Epub 2011 Dec 30. Clin Genet. 2012. PMID: 22035297

7

Successful haploidentical PBSCT with subsequent T-cell addbacks in a boy with HyperIgM syndrome presenting as severe congenital neutropenia.

Jasinska A, Kalwak K, Trelinska J, Borowiec M, Piatosa B, Zeman K, Mlynarski W. Jasinska A, et al. Among authors: borowiec m. Pediatr Transplant. 2013 Feb;17(1):E37-40. doi: 10.1111/j.1399-3046.2012.01786.x. Epub 2012 Aug 29. Pediatr Transplant. 2013. PMID: 22928961

8

Serum tumor necrosis factor-α and interleukin-10 levels as markers to predict outcome of patients with chronic lymphocytic leukemia in different risk groups defined by the IGHV mutation status.

Lech-Maranda E, Grzybowska-Izydorczyk O, Wyka K, Mlynarski W, Borowiec M, Antosik K, Cebula-Obrzut B, Makuch-Lasica H, Nowak G, Klimkiewicz-Wojciechowska G, Wawrzyniak E, Bilinski P, Robak T, Warzocha K. Lech-Maranda E, et al. Among authors: borowiec m. Arch Immunol Ther Exp (Warsz). 2012 Dec;60(6):477-86. doi: 10.1007/s00005-012-0197-7. Epub 2012 Sep 4. Arch Immunol Ther Exp (Warsz). 2012. PMID: 22945689 Free article.

9

[Polymorphism of metalloproteinases MMP-1 and MMP-2 in risk of laryngeal cancer].

Olejniczak I, Fendler W, Borowiec M, Młynarski W, Pietruszewska W. Olejniczak I, et al. Among authors: borowiec m. Otolaryngol Pol. 2012 Sep;66(4 Suppl):30-5. doi: 10.1016/S0030-6657(12)70782-5. Otolaryngol Pol. 2012. PMID: 23164104 Polish.

10

Polymorphisms of TNF and IL-10 genes and clinical outcome of patients with chronic lymphocytic leukemia.

Lech-Maranda E, Mlynarski W, Grzybowska-Izydorczyk O, Borowiec M, Pastorczak A, Cebula-Obrzut B, Klimkiewicz-Wojciechowska G, Wcislo M, Majewski M, Kotkowska A, Robak T, Warzocha K. Lech-Maranda E, et al. Among authors: borowiec m. Genes Chromosomes Cancer. 2013 Mar;52(3):287-96. doi: 10.1002/gcc.22028. Epub 2012 Dec 8. Genes Chromosomes Cancer. 2013. PMID: 23225254

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