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Items: 41

1.

A homozygous DSC2 deletion associated with arrhythmogenic cardiomyopathy is caused by uniparental isodisomy.

Brodehl A, Weiss J, Debus JD, Stanasiuk C, Klauke B, Deutsch MA, Fox H, Bax J, Ebbinghaus H, Gärtner A, Tiesmeier J, Laser T, Peterschröder A, Gerull B, Gummert J, Paluszkiewicz L, Milting H.

J Mol Cell Cardiol. 2020 Mar 19. pii: S0022-2828(20)30068-7. doi: 10.1016/j.yjmcc.2020.03.006. [Epub ahead of print]

2.

The role of stigma during the course of inpatient psychotherapeutic treatment in a German sample.

Deres AT, Bürkner PC, Klauke B, Buhlmann U.

Clin Psychol Psychother. 2020 Jan 7. doi: 10.1002/cpp.2423. [Epub ahead of print]

PMID:
31910308
3.

Facial Emotion Recognition Abilities in Women Experiencing Eating Disorders.

Wyssen A, Lao J, Rodger H, Humbel N, Lennertz J, Schuck K, Isenschmid B, Milos G, Trier S, Whinyates K, Assion HJ, Ueberberg B, Müller J, Klauke B, Teismann T, Margraf J, Juckel G, Kossmann C, Schneider S, Caldara R, Munsch S.

Psychosom Med. 2019 Feb/Mar;81(2):155-164. doi: 10.1097/PSY.0000000000000664.

PMID:
30702549
4.

Facial Emotion Recognition Abilities in Women Suffering from Eating Disorders.

Wyssen A, Junpeng L, Rodger H, Humbel N, Lennertz J, Schuck K, Isenschmid B, Milos G, Trier S, Whinyates K, Assion HJ, Ueberberg B, Müller J, Klauke B, Teismann T, Margraf J, Juckel G, Kossmann C, Schneider S, Caldara R, Munsch S.

Psychosom Med. 2019 Jan 4. doi: 10.1097/PSY.0000000000000664. [Epub ahead of print]

PMID:
30614960
5.

Functional analysis of DES-p.L398P and RBM20-p.R636C.

Brodehl A, Ebbinghaus H, Gaertner-Rommel A, Stanasiuk C, Klauke B, Milting H.

Genet Med. 2019 May;21(5):1246-1247. doi: 10.1038/s41436-018-0291-2. Epub 2018 Sep 28. No abstract available.

PMID:
30262925
6.

Self-reported emotion regulation difficulties are associated with mood but not with the biological stress response to thin ideal exposure.

Humbel N, Messerli-Bürgy N, Schuck K, Wyssen A, Garcia-Burgos D, Biedert E, Lennertz J, Meyer AH, Whinyates K, Isenschmid B, Milos G, Trier S, Adolph D, Cwik J, Margraf J, Assion HJ, Teismann T, Ueberberg B, Juckel G, Müller J, Klauke B, Schneider S, Munsch S.

PLoS One. 2018 Jun 27;13(6):e0199769. doi: 10.1371/journal.pone.0199769. eCollection 2018.

7.

A novel desmin (DES) indel mutation causes severe atypical cardiomyopathy in combination with atrioventricular block and skeletal myopathy.

Schirmer I, Dieding M, Klauke B, Brodehl A, Gaertner-Rommel A, Walhorn V, Gummert J, Schulz U, Paluszkiewicz L, Anselmetti D, Milting H.

Mol Genet Genomic Med. 2018 Mar;6(2):288-293. doi: 10.1002/mgg3.358. Epub 2017 Dec 23.

8.

High proportion of genetic cases in patients with advanced cardiomyopathy including a novel homozygous Plakophilin 2-gene mutation.

Klauke B, Gaertner-Rommel A, Schulz U, Kassner A, Zu Knyphausen E, Laser T, Kececioglu D, Paluszkiewicz L, Blanz U, Sandica E, van den Bogaerdt AJ, van Tintelen JP, Gummert J, Milting H.

PLoS One. 2017 Dec 18;12(12):e0189489. doi: 10.1371/journal.pone.0189489. eCollection 2017.

9.

Molecular autopsy of sudden unexplained deaths reveals genetic predispositions for cardiac diseases among young forensic cases.

Hellenthal N, Gaertner-Rommel A, Klauke B, Paluszkiewicz L, Stuhr M, Kerner T, Farr M, Püschel K, Milting H.

Europace. 2017 Nov 1;19(11):1881-1890. doi: 10.1093/europace/euw247.

PMID:
29016939
10.

The novel αB-crystallin (CRYAB) mutation p.D109G causes restrictive cardiomyopathy.

Brodehl A, Gaertner-Rommel A, Klauke B, Grewe SA, Schirmer I, Peterschröder A, Faber L, Vorgerd M, Gummert J, Anselmetti D, Schulz U, Paluszkiewicz L, Milting H.

Hum Mutat. 2017 Aug;38(8):947-952. doi: 10.1002/humu.23248. Epub 2017 Jun 21.

PMID:
28493373
11.

Functional characterization of the novel DES mutation p.L136P associated with dilated cardiomyopathy reveals a dominant filament assembly defect.

Brodehl A, Dieding M, Biere N, Unger A, Klauke B, Walhorn V, Gummert J, Schulz U, Linke WA, Gerull B, Vorgert M, Anselmetti D, Milting H.

J Mol Cell Cardiol. 2016 Feb;91:207-14. doi: 10.1016/j.yjmcc.2015.12.015. Epub 2015 Dec 23.

PMID:
26724190
12.

Allelic variation in CRHR1 predisposes to panic disorder: evidence for biased fear processing.

Weber H, Richter J, Straube B, Lueken U, Domschke K, Schartner C, Klauke B, Baumann C, Pané-Farré C, Jacob CP, Scholz CJ, Zwanzger P, Lang T, Fehm L, Jansen A, Konrad C, Fydrich T, Wittmann A, Pfleiderer B, Ströhle A, Gerlach AL, Alpers GW, Arolt V, Pauli P, Wittchen HU, Kent L, Hamm A, Kircher T, Deckert J, Reif A.

Mol Psychiatry. 2016 Jun;21(6):813-22. doi: 10.1038/mp.2015.125. Epub 2015 Sep 1.

PMID:
26324098
13.

RGS2 ggenetic variation: association analysis with panic disorder and dimensional as well as intermediate phenotypes of anxiety.

Hohoff C, Weber H, Richter J, Domschke K, Zwanzger PM, Ohrmann P, Bauer J, Suslow T, Kugel H, Baumann C, Klauke B, Jacob CP, Fritze J, Bandelow B, Gloster AT, Gerlach AL, Kircher T, Lang T, Alpers GW, Ströhle A, Fehm L, Wittchen HU, Arolt V, Pauli P, Hamm A, Reif A, Deckert J.

Am J Med Genet B Neuropsychiatr Genet. 2015 Apr;168B(3):211-22. doi: 10.1002/ajmg.b.32299. Epub 2015 Mar 4.

PMID:
25740197
14.

The TMEM43 Newfoundland mutation p.S358L causing ARVC-5 was imported from Europe and increases the stiffness of the cell nucleus.

Milting H, Klauke B, Christensen AH, Müsebeck J, Walhorn V, Grannemann S, Münnich T, Šarić T, Rasmussen TB, Jensen HK, Mogensen J, Baecker C, Romaker E, Laser KT, zu Knyphausen E, Kassner A, Gummert J, Judge DP, Connors S, Hodgkinson K, Young TL, van der Zwaag PA, van Tintelen JP, Anselmetti D.

Eur Heart J. 2015 Apr 7;36(14):872-81. doi: 10.1093/eurheartj/ehu077. Epub 2014 Mar 4.

PMID:
24598986
15.

The novel desmin mutant p.A120D impairs filament formation, prevents intercalated disk localization, and causes sudden cardiac death.

Brodehl A, Dieding M, Klauke B, Dec E, Madaan S, Huang T, Gargus J, Fatima A, Saric T, Cakar H, Walhorn V, Tönsing K, Skrzipczyk T, Cebulla R, Gerdes D, Schulz U, Gummert J, Svendsen JH, Olesen MS, Anselmetti D, Christensen AH, Kimonis V, Milting H.

Circ Cardiovasc Genet. 2013 Dec;6(6):615-23. doi: 10.1161/CIRCGENETICS.113.000103. Epub 2013 Nov 7.

PMID:
24200904
16.

The interaction of early life experiences with COMT val158met affects anxiety sensitivity.

Baumann C, Klauke B, Weber H, Domschke K, Zwanzger P, Pauli P, Deckert J, Reif A.

Genes Brain Behav. 2013 Nov;12(8):821-9. doi: 10.1111/gbb.12090. Epub 2013 Oct 25.

17.

[Experience of loss and complicated grief in depressive inpatients].

Klinitzke G, Domschke K, Wagner B, Klauke B, Kersting A.

Psychiatr Prax. 2014 Sep;41(6):313-8. doi: 10.1055/s-0033-1349467. Epub 2013 Aug 13. German.

PMID:
23943078
18.

Epigenetic signature of panic disorder: a role of glutamate decarboxylase 1 (GAD1) DNA hypomethylation?

Domschke K, Tidow N, Schrempf M, Schwarte K, Klauke B, Reif A, Kersting A, Arolt V, Zwanzger P, Deckert J.

Prog Neuropsychopharmacol Biol Psychiatry. 2013 Oct 1;46:189-96. doi: 10.1016/j.pnpbp.2013.07.014. Epub 2013 Jul 29.

PMID:
23906988
19.

In vitro functional analyses of arrhythmogenic right ventricular cardiomyopathy-associated desmoglein-2-missense variations.

Gaertner A, Klauke B, Stork I, Niehaus K, Niemann G, Gummert J, Milting H.

PLoS One. 2012;7(10):e47097. doi: 10.1371/journal.pone.0047097. Epub 2012 Oct 10.

20.

Functional characterization of desmin mutant p.P419S.

Brodehl A, Dieding M, Cakar H, Klauke B, Walhorn V, Gummert J, Anselmetti D, Milting H.

Eur J Hum Genet. 2013 Jun;21(6):589-90. doi: 10.1038/ejhg.2012.212. Epub 2012 Oct 3. No abstract available.

21.

Meta-analysis argues for a female-specific role of MAOA-uVNTR in panic disorder in four European populations.

Reif A, Weber H, Domschke K, Klauke B, Baumann C, Jacob CP, Ströhle A, Gerlach AL, Alpers GW, Pauli P, Hamm A, Kircher T, Arolt V, Wittchen HU, Binder EB, Erhardt A, Deckert J.

Am J Med Genet B Neuropsychiatr Genet. 2012 Oct;159B(7):786-93. doi: 10.1002/ajmg.b.32085. Epub 2012 Aug 22.

PMID:
22911667
22.

Affect-modulated startle: interactive influence of catechol-O-methyltransferase Val158Met genotype and childhood trauma.

Klauke B, Winter B, Gajewska A, Zwanzger P, Reif A, Herrmann MJ, Dlugos A, Warrings B, Jacob C, Mühlberger A, Arolt V, Pauli P, Deckert J, Domschke K.

PLoS One. 2012;7(6):e39709. doi: 10.1371/journal.pone.0039709. Epub 2012 Jun 22.

23.

Gender differences in associations of glutamate decarboxylase 1 gene (GAD1) variants with panic disorder.

Weber H, Scholz CJ, Domschke K, Baumann C, Klauke B, Jacob CP, Maier W, Fritze J, Bandelow B, Zwanzger PM, Lang T, Fehm L, Ströhle A, Hamm A, Gerlach AL, Alpers GW, Kircher T, Wittchen HU, Arolt V, Pauli P, Deckert J, Reif A.

PLoS One. 2012;7(5):e37651. doi: 10.1371/journal.pone.0037651. Epub 2012 May 25.

24.

Monoamine oxidase A gene DNA hypomethylation - a risk factor for panic disorder?

Domschke K, Tidow N, Kuithan H, Schwarte K, Klauke B, Ambrée O, Reif A, Schmidt H, Arolt V, Kersting A, Zwanzger P, Deckert J.

Int J Neuropsychopharmacol. 2012 Oct;15(9):1217-28. doi: 10.1017/S146114571200020X. Epub 2012 Mar 21.

25.

Neuropeptide S receptor gene (NPSR) and life events: G × E effects on anxiety sensitivity and its subdimensions.

Klauke B, Deckert J, Zwanzger P, Baumann C, Arolt V, Pauli P, Reif A, Domschke K.

World J Biol Psychiatry. 2014 Jan;15(1):17-25. doi: 10.3109/15622975.2011.646302. Epub 2012 Mar 9.

PMID:
22404660
26.

Dual color photoactivation localization microscopy of cardiomyopathy-associated desmin mutants.

Brodehl A, Hedde PN, Dieding M, Fatima A, Walhorn V, Gayda S, Šarić T, Klauke B, Gummert J, Anselmetti D, Heilemann M, Nienhaus GU, Milting H.

J Biol Chem. 2012 May 4;287(19):16047-57. doi: 10.1074/jbc.M111.313841. Epub 2012 Mar 8.

27.

Modification of caffeine effects on the affect-modulated startle by neuropeptide S receptor gene variation.

Domschke K, Klauke B, Winter B, Gajewska A, Herrmann MJ, Warrings B, Mühlberger A, Wosnitza K, Dlugos A, Naunin S, Nienhaus K, Fobker M, Jacob C, Arolt V, Pauli P, Reif A, Zwanzger P, Deckert J.

Psychopharmacology (Berl). 2012 Aug;222(3):533-41. doi: 10.1007/s00213-012-2678-0. Epub 2012 Mar 8.

PMID:
22399050
28.

A randomized, double-blind, placebo-controlled study of the safety and tolerance of regadenoson in subjects with stage 3 or 4 chronic kidney disease.

Ananthasubramaniam K, Weiss R, McNutt B, Klauke B, Feaheny K, Bukofzer S.

J Nucl Cardiol. 2012 Apr;19(2):319-29. doi: 10.1007/s12350-011-9508-3. Epub 2012 Jan 19.

29.

In vitro modeling of ryanodine receptor 2 dysfunction using human induced pluripotent stem cells.

Fatima A, Xu G, Shao K, Papadopoulos S, Lehmann M, Arnáiz-Cot JJ, Rosa AO, Nguemo F, Matzkies M, Dittmann S, Stone SL, Linke M, Zechner U, Beyer V, Hennies HC, Rosenkranz S, Klauke B, Parwani AS, Haverkamp W, Pfitzer G, Farr M, Cleemann L, Morad M, Milting H, Hescheler J, Saric T.

Cell Physiol Biochem. 2011;28(4):579-92. doi: 10.1159/000335753. Epub 2011 Dec 14.

30.

Serotonin transporter gene and childhood trauma--a G × E effect on anxiety sensitivity.

Klauke B, Deckert J, Reif A, Pauli P, Zwanzger P, Baumann C, Arolt V, Glöckner-Rist A, Domschke K.

Depress Anxiety. 2011 Dec 21;28(12):1048-57. doi: 10.1002/da.20840. Epub 2011 Jun 16.

PMID:
21681867
31.

De novo desmin-mutation N116S is associated with arrhythmogenic right ventricular cardiomyopathy.

Klauke B, Kossmann S, Gaertner A, Brand K, Stork I, Brodehl A, Dieding M, Walhorn V, Anselmetti D, Gerdes D, Bohms B, Schulz U, Zu Knyphausen E, Vorgerd M, Gummert J, Milting H.

Hum Mol Genet. 2010 Dec 1;19(23):4595-607. doi: 10.1093/hmg/ddq387. Epub 2010 Sep 9.

PMID:
20829228
32.

Neuropeptide S receptor gene -- converging evidence for a role in panic disorder.

Domschke K, Reif A, Weber H, Richter J, Hohoff C, Ohrmann P, Pedersen A, Bauer J, Suslow T, Kugel H, Heindel W, Baumann C, Klauke B, Jacob C, Maier W, Fritze J, Bandelow B, Krakowitzky P, Rothermundt M, Erhardt A, Binder EB, Holsboer F, Gerlach AL, Kircher T, Lang T, Alpers GW, Ströhle A, Fehm L, Gloster AT, Wittchen HU, Arolt V, Pauli P, Hamm A, Deckert J.

Mol Psychiatry. 2011 Sep;16(9):938-48. doi: 10.1038/mp.2010.81. Epub 2010 Jul 6.

PMID:
20603625
33.

Life events in panic disorder-an update on "candidate stressors".

Klauke B, Deckert J, Reif A, Pauli P, Domschke K.

Depress Anxiety. 2010 Aug;27(8):716-30. doi: 10.1002/da.20667. Review.

PMID:
20112245
34.

New names for known things: on the association of novel word forms with existing semantic information.

Dobel C, Junghöfer M, Breitenstein C, Klauke B, Knecht S, Pantev C, Zwitserlood P.

J Cogn Neurosci. 2010 Jun;22(6):1251-61. doi: 10.1162/jocn.2009.21297.

PMID:
19583468
35.

Molecular genetics of arrhythmogenic right ventricular dysplasia/cardiomyopathy.

Milting H, Klauke B.

Nat Clin Pract Cardiovasc Med. 2008 Oct;5(10):E1; author reply E2. doi: 10.1038/ncpcardio1350. No abstract available.

PMID:
18813333
36.

No association between single nucleotide polymorphisms and the development of nephrotoxicity after orthotopic heart transplantation.

Klauke B, Wirth A, Zittermann A, Bohms B, Tenderich G, Körfer R, Milting H.

J Heart Lung Transplant. 2008 Jul;27(7):741-5. doi: 10.1016/j.healun.2008.04.001. Epub 2008 May 23.

PMID:
18582803
37.

Composite polymorphisms in the ryanodine receptor 2 gene associated with arrhythmogenic right ventricular cardiomyopathy.

Milting H, Lukas N, Klauke B, Körfer R, Perrot A, Osterziel KJ, Vogt J, Peters S, Thieleczek R, Varsányi M.

Cardiovasc Res. 2006 Aug 1;71(3):496-505. Epub 2006 Apr 18.

PMID:
16769042
38.

Influence of ACE-inhibition and mechanical unloading on the regulation of extracellular matrix proteins in the myocardium of heart transplantation candidates bridged by ventricular assist devices.

Milting H, Kassner A, Arusoglu L, Meyer HE, Morshuis M, Brendel R, Klauke B, El Banayosy A, Körfer R.

Eur J Heart Fail. 2006 May;8(3):278-83. Epub 2005 Nov 23.

39.
40.

Saturation mutagenesis in Escherichia coli of a cloned Xanthomonas campestris DNA fragment with the lux transposon Tn4431 using the delivery plasmid pDS1, thermosensitive in replication.

Steinmann D, Wiggerich HG, Klauke B, Schramm U, Pühler A, Priefer UB.

Appl Microbiol Biotechnol. 1993 Nov;40(2-3):356-60.

PMID:
7764391

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