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Items: 14

1.

Evaluation of the role of STAP1 in Familial Hypercholesterolemia.

Danyel M, Ott CE, Grenkowitz T, Salewsky B, Hicks AA, Fuchsberger C, Steinhagen-Thiessen E, Bobbert T, Kassner U, Demuth I.

Sci Rep. 2019 Aug 19;9(1):11995. doi: 10.1038/s41598-019-48402-y.

2.

Exploring the Relationship of Relative Telomere Length and the Epigenetic Clock in the LipidCardio Cohort.

Banszerus VL, Vetter VM, Salewsky B, König M, Demuth I.

Int J Mol Sci. 2019 Jun 21;20(12). pii: E3032. doi: 10.3390/ijms20123032.

3.

The hSNM1B/Apollo variant rs11552449 is associated with cellular sensitivity towards mitomycin C and ionizing radiation.

Herwest S, Albers C, Schmiester M, Salewsky B, Hopfenmüller W, Meyer A, Bertram L, Demuth I.

DNA Repair (Amst). 2018 Dec;72:93-98. doi: 10.1016/j.dnarep.2018.09.004. Epub 2018 Sep 12.

PMID:
30262195
4.

Gene Therapy in Lipoprotein Lipase Deficiency: Case Report on the First Patient Treated with Alipogene Tiparvovec Under Daily Practice Conditions.

Kassner U, Hollstein T, Grenkowitz T, Wühle-Demuth M, Salewsky B, Demuth I, Dippel M, Steinhagen-Thiessen E.

Hum Gene Ther. 2018 Apr;29(4):520-527. doi: 10.1089/hum.2018.007.

PMID:
29641318
5.

Clinical characterization and mutation spectrum of German patients with familial hypercholesterolemia.

Grenkowitz T, Kassner U, Wühle-Demuth M, Salewsky B, Rosada A, Zemojtel T, Hopfenmüller W, Isermann B, Borucki K, Heigl F, Laufs U, Wagner S, Kleber ME, Binner P, März W, Steinhagen-Thiessen E, Demuth I.

Atherosclerosis. 2016 Oct;253:88-93. doi: 10.1016/j.atherosclerosis.2016.08.037. Epub 2016 Aug 26.

PMID:
27596133
6.

Relative Leukocyte Telomere Length, Hematological Parameters and Anemia - Data from the Berlin Aging Study II (BASE-II).

Meyer A, Salewsky B, Buchmann N, Steinhagen-Thiessen E, Demuth I.

Gerontology. 2016;62(3):330-6. doi: 10.1159/000430950. Epub 2016 Jan 29. Erratum in: Gerontology. 2016;62(3):336.

PMID:
26820977
7.

Leukocyte telomere length is related to appendicular lean mass: cross-sectional data from the Berlin Aging Study II (BASE-II).

Meyer A, Salewsky B, Spira D, Steinhagen-Thiessen E, Norman K, Demuth I.

Am J Clin Nutr. 2016 Jan;103(1):178-83. doi: 10.3945/ajcn.115.116806. Epub 2015 Dec 16.

PMID:
26675777
8.

Sports and Exercise at Different Ages and Leukocyte Telomere Length in Later Life--Data from the Berlin Aging Study II (BASE-II).

Saßenroth D, Meyer A, Salewsky B, Kroh M, Norman K, Steinhagen-Thiessen E, Demuth I.

PLoS One. 2015 Dec 2;10(12):e0142131. doi: 10.1371/journal.pone.0142131. eCollection 2015.

9.

Directed Alternative Splicing in Nijmegen Breakage Syndrome: Proof of Principle Concerning Its Therapeutical Application.

Salewsky B, Hildebrand G, Rothe S, Parplys AC, Radszewski J, Kieslich M, Wessendorf P, Krenzlin H, Borgmann K, Nussenzweig A, Sperling K, Digweed M.

Mol Ther. 2016 Feb;24(1):117-24. doi: 10.1038/mt.2015.144. Epub 2015 Aug 12.

10.

Severe hypertriglyceridemia in a patient heterozygous for a lipoprotein lipase gene allele with two novel missense variants.

Kassner U, Salewsky B, Wühle-Demuth M, Szijarto IA, Grenkowitz T, Binner P, März W, Steinhagen-Thiessen E, Demuth I.

Eur J Hum Genet. 2015 Sep;23(9):1259-61. doi: 10.1038/ejhg.2014.295. Epub 2015 Jan 14.

11.

Nijmegen breakage syndrome: the clearance pathway for mutant nibrin protein is allele specific.

Salewsky B, Wessendorf P, Hirsch D, Krenzlin H, Digweed M.

Gene. 2013 May 1;519(2):217-21. doi: 10.1016/j.gene.2013.02.033. Epub 2013 Feb 28.

PMID:
23458873
12.

The nuclease hSNM1B/Apollo is linked to the Fanconi anemia pathway via its interaction with FANCP/SLX4.

Salewsky B, Schmiester M, Schindler D, Digweed M, Demuth I.

Hum Mol Genet. 2012 Nov 15;21(22):4948-56. doi: 10.1093/hmg/dds338. Epub 2012 Aug 19.

PMID:
22907656
13.

DNA damage in Nijmegen Breakage Syndrome cells leads to PARP hyperactivation and increased oxidative stress.

Krenzlin H, Demuth I, Salewsky B, Wessendorf P, Weidele K, Bürkle A, Digweed M.

PLoS Genet. 2012;8(3):e1002557. doi: 10.1371/journal.pgen.1002557. Epub 2012 Mar 1.

14.

Dosage effect of zero to three functional LBR-genes in vivo and in vitro.

Gravemann S, Schnipper N, Meyer H, Vaya A, Nowaczyk MJ, Rajab A, Hofmann WK, Salewsky B, Tönnies H, Neitzel H, Stassen HH, Sperling K, Hoffmann K.

Nucleus. 2010 Mar-Apr;1(2):179-89. doi: 10.4161/nucl.1.2.11113. Epub 2010 Jan 3.

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