Kind B - Search Results

1

Intracellular ROS level is increased in fibroblasts of triple A syndrome patients.

Kind B, Koehler K, Krumbholz M, Landgraf D, Huebner A. Kind B, et al. J Mol Med (Berl). 2010 Dec;88(12):1233-42. doi: 10.1007/s00109-010-0661-y. Epub 2010 Aug 13. J Mol Med (Berl). 2010. PMID: 20706703

2

Changes in differential gene expression in fibroblast cells from patients with triple A syndrome under oxidative stress.

Koehler K, End K, Kind B, Landgraf D, Mitzscherling P, Huebner A. Koehler K, et al. Among authors: kind b. Horm Metab Res. 2013 Feb;45(2):102-8. doi: 10.1055/s-0032-1331196. Epub 2013 Jan 11. Horm Metab Res. 2013. PMID: 23315990

3

Axonal neuropathy with unusual pattern of amyotrophy and alacrima associated with a novel AAAS mutation p.Leu430Phe.

Koehler K, Brockmann K, Krumbholz M, Kind B, Bönnemann C, Gärtner J, Huebner A. Koehler K, et al. Among authors: kind b. Eur J Hum Genet. 2008 Dec;16(12):1499-506. doi: 10.1038/ejhg.2008.132. Epub 2008 Jul 16. Eur J Hum Genet. 2008. PMID: 18628786

4

The nuclear pore complex protein ALADIN is anchored via NDC1 but not via POM121 and GP210 in the nuclear envelope.

Kind B, Koehler K, Lorenz M, Huebner A. Kind B, et al. Biochem Biophys Res Commun. 2009 Dec 11;390(2):205-10. doi: 10.1016/j.bbrc.2009.09.080. Epub 2009 Sep 24. Biochem Biophys Res Commun. 2009. PMID: 19782045

5

Deficiency of ferritin heavy-chain nuclear import in triple a syndrome implies nuclear oxidative damage as the primary disease mechanism.

Storr HL, Kind B, Parfitt DA, Chapple JP, Lorenz M, Koehler K, Huebner A, Clark AJ. Storr HL, et al. Among authors: kind b. Mol Endocrinol. 2009 Dec;23(12):2086-94. doi: 10.1210/me.2009-0056. Epub 2009 Oct 23. Mol Endocrinol. 2009. PMID: 19855093 Free PMC article.

6

Role of ALADIN in human adrenocortical cells for oxidative stress response and steroidogenesis.

Jühlen R, Idkowiak J, Taylor AE, Kind B, Arlt W, Huebner A, Koehler K. Jühlen R, et al. Among authors: kind b. PLoS One. 2015 Apr 13;10(4):e0124582. doi: 10.1371/journal.pone.0124582. eCollection 2015. PLoS One. 2015. PMID: 25867024 Free PMC article.

7

Clinical and molecular genetic findings in a 6-year-old Bosnian boy with triple A syndrome.

Toromanovic A, Tahirovic H, Milenkovic T, Koehler K, Kind B, Zdravkovic D, Hasanhodzic M, Huebner A. Toromanovic A, et al. Among authors: kind b. Eur J Pediatr. 2009 Mar;168(3):317-20. doi: 10.1007/s00431-008-0758-2. Epub 2008 Jun 13. Eur J Pediatr. 2009. PMID: 18551317

8

Single-stranded nucleic acids promote SAMHD1 complex formation.

Tüngler V, Staroske W, Kind B, Dobrick M, Kretschmer S, Schmidt F, Krug C, Lorenz M, Chara O, Schwille P, Lee-Kirsch MA. Tüngler V, et al. Among authors: kind b. J Mol Med (Berl). 2013 Jun;91(6):759-70. doi: 10.1007/s00109-013-0995-3. Epub 2013 Jan 31. J Mol Med (Berl). 2013. PMID: 23371319

9

Tert expression and telomerase activity in gonads and somatic cells of the Japanese medaka (Oryzias latipes).

Pfennig F, Kind B, Zieschang F, Busch M, Gutzeit HO. Pfennig F, et al. Among authors: kind b. Dev Growth Differ. 2008 Mar;50(3):131-41. doi: 10.1111/j.1440-169X.2008.00986.x. Epub 2008 Feb 27. Dev Growth Differ. 2008. PMID: 18312429

10

Therapeutic Approaches to Type I Interferonopathies.

Bienias M, Brück N, Griep C, Wolf C, Kretschmer S, Kind B, Tüngler V, Berner R, Lee-Kirsch MA. Bienias M, et al. Among authors: kind b. Curr Rheumatol Rep. 2018 Apr 20;20(6):32. doi: 10.1007/s11926-018-0743-3. Curr Rheumatol Rep. 2018. PMID: 29679241 Review.

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