Lace B - Search Results

1

HFE-related hemochromatosis risk mutations in Latvian population.

Peculis R, Lace B, Putnina A, Nikitina-Zake L, Klovins J. Peculis R, et al. Among authors: lace b. Ann Hematol. 2015 Feb;94(2):343-4. doi: 10.1007/s00277-014-2157-2. Ann Hematol. 2015. PMID: 25015053 No abstract available.

2

Association studies of candidate genes and cleft lip and palate taking into consideration geographical origin.

Lace B, Kempa I, Piekuse L, Grinfelde I, Klovins J, Pliss L, Krumina A, Vieira AR. Lace B, et al. Eur J Oral Sci. 2011 Dec;119(6):413-7. doi: 10.1111/j.1600-0722.2011.00877.x. Epub 2011 Oct 15. Eur J Oral Sci. 2011. PMID: 22112025

3

Genetic linkage studies of a North Carolina macular dystrophy family.

Audere M, Rutka K, Inaskina I, Peculis R, Sepetiene S, Valeina S, Lāce B. Audere M, et al. Among authors: lace b. Medicina (Kaunas). 2016;52(3):180-6. doi: 10.1016/j.medici.2016.04.001. Epub 2016 Apr 19. Medicina (Kaunas). 2016. PMID: 27496188 Free article.

4

BCL3 gene role in facial morphology.

Lace B, Kempa I, Klovins J, Stavusis J, Krumina A, Akota I, Barkane B, Vieira AR, Nagle E, Grinfelde I, Maulina I. Lace B, et al. Birth Defects Res A Clin Mol Teratol. 2012 Nov;94(11):918-24. doi: 10.1002/bdra.23085. Epub 2012 Nov 1. Birth Defects Res A Clin Mol Teratol. 2012. PMID: 23115114

5

Variation in FGF1, FOXE1, and TIMP2 genes is associated with nonsyndromic cleft lip with or without cleft palate.

Nikopensius T, Kempa I, Ambrozaitytė L, Jagomägi T, Saag M, Matulevičienė A, Utkus A, Krjutškov K, Tammekivi V, Piekuse L, Akota I, Barkane B, Krumina A, Klovins J, Lace B, Kučinskas V, Metspalu A. Nikopensius T, et al. Among authors: lace b. Birth Defects Res A Clin Mol Teratol. 2011 Apr;91(4):218-25. doi: 10.1002/bdra.20791. Epub 2011 Apr 1. Birth Defects Res A Clin Mol Teratol. 2011. PMID: 21462296

6

Age of SERPINA1 gene PI Z mutation: Swedish and Latvian population analysis.

Lace B, Sveger T, Krams A, Cernevska G, Krumina A. Lace B, et al. Ann Hum Genet. 2008 May;72(Pt 3):300-4. doi: 10.1111/j.1469-1809.2008.00431.x. Epub 2008 Feb 23. Ann Hum Genet. 2008. PMID: 18294358

7

Duplication events downstream of IRX1 cause North Carolina macular dystrophy at the MCDR3 locus.

Cipriani V, Silva RS, Arno G, Pontikos N, Kalhoro A, Valeina S, Inashkina I, Audere M, Rutka K, Puech B, Michaelides M, van Heyningen V, Lace B, Webster AR, Moore AT. Cipriani V, et al. Among authors: lace b. Sci Rep. 2017 Aug 8;7(1):7512. doi: 10.1038/s41598-017-06387-6. Sci Rep. 2017. PMID: 28790370 Free PMC article.

8

Presentation of Complex Homozygous Allele in ABCA4 Gene in a Patient with Retinitis Pigmentosa.

Audere M, Rutka K, Šepetiene S, Lāce B. Audere M, et al. Among authors: lace b. Case Rep Ophthalmol Med. 2015;2015:452068. doi: 10.1155/2015/452068. Epub 2015 Jul 2. Case Rep Ophthalmol Med. 2015. PMID: 26229699 Free PMC article.

9

Complete mtDNA sequencing reveals mutations m.9185T>C and m.13513G>A in three patients with Leigh syndrome.

Pelnena D, Burnyte B, Jankevics E, Lace B, Dagyte E, Grigalioniene K, Utkus A, Krumina Z, Rozentale J, Adomaitiene I, Stavusis J, Pliss L, Inashkina I. Pelnena D, et al. Among authors: lace b. Mitochondrial DNA A DNA Mapp Seq Anal. 2018 Oct;29(7):1115-1120. doi: 10.1080/24701394.2017.1413365. Epub 2017 Dec 12. Mitochondrial DNA A DNA Mapp Seq Anal. 2018. PMID: 29228836

10

Dupuytren's Contracture Cosegregation with Limb-Girdle Muscle Dystrophy.

Lace B, Inashkina I, Micule I, Vasiljeva I, Naudina MS, Strautmanis J, Stavusis J, Jankevics E. Lace B, et al. Case Rep Neurol Med. 2013;2013:254950. doi: 10.1155/2013/254950. Epub 2013 Aug 19. Case Rep Neurol Med. 2013. PMID: 24024053 Free PMC article.

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