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	<title>Wollnik, Bernd &#8211; MBExC</title>
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	<title>Wollnik, Bernd &#8211; MBExC</title>
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		<title>Targeting Interleukin-8-Mediated Cellular Crosstalk Reverses Hypertrophic Cardiomyopathy and Cardiac Fibrosis in Noonan Syndrome</title>
		<link>https://mbexc.de/targeting-interleukin-8-mediated-cellular-crosstalk-reverses-hypertrophic-cardiomyopathy-and-cardiac-fibrosis-in-noonan-syndrome/</link>
		
		<dc:creator><![CDATA[Susann Meyer]]></dc:creator>
		<pubDate>Thu, 16 Apr 2026 07:11:56 +0000</pubDate>
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		<category><![CDATA[Zimmermann, Wolfram-Hubertus]]></category>
		<category><![CDATA[Circulation]]></category>
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					<description><![CDATA[Fell J, Pavez-Giani M, Koitka F, Kensah G, Santos GL, van der Vorst EPC, Lenz C, Salinas G, Busley AV, Fedorenko A, Hindmarsh R, Wolf CM, Lutz S, Hasenfuss G, Zimmermann WH, Wollnik B, Cyganek L]]></description>
		
		
		
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		<title>Mitotic BLM functions are required to maintain genomic stability</title>
		<link>https://mbexc.de/mitotic-blm-functions-are-required-to-maintain-genomic-stability/</link>
		
		<dc:creator><![CDATA[Susann Meyer]]></dc:creator>
		<pubDate>Tue, 10 Mar 2026 09:07:17 +0000</pubDate>
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		<category><![CDATA[Nucleic Acids Research]]></category>
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					<description><![CDATA[Hamann TE, Wieland A, Mohseni F, Vukušić K, Tirincsi A, Wardenaar R, Losito M, Harmsen I, Gönenc II, Wollnik B, Foijer F, Tolić IM, Storchová Z, Räschle M]]></description>
		
		
		
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		<title>Generation of pluripotent stem cell line (IPWi001-A) and a corresponding CRISPR/Cas9 modified isogenic rescue control (IPWi001-A-1) from a patient with arrhythmia-induced cardiomyopathy harboring a KCNQ1 truncating mutation</title>
		<link>https://mbexc.de/generation-of-pluripotent-stem-cell-line-ipwi001-a-and-a-corresponding-crispr-cas9-modified-isogenic-rescue-control-ipwi001-a-1-from-a-patient-with-arrhythmia-induced-cardiomyopathy-harboring-a-kc/</link>
		
		<dc:creator><![CDATA[Susann Meyer]]></dc:creator>
		<pubDate>Tue, 03 Feb 2026 12:36:50 +0000</pubDate>
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		<category><![CDATA[Stem Cell Research]]></category>
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					<description><![CDATA[Anders M, Hoppe S, Eberl H, Rebs S, Seedorf A, Maurer W, Schill T, Zibat A, Unsöld JK, Yigit G, Wollnik B, Vollmann D, Sossalla S, Streckfuss-Bömeke K]]></description>
		
		
		
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		<title>Molecular genotype-phenotype correlation in ACTB- and ACTG1-related non-muscle actinopathies</title>
		<link>https://mbexc.de/molecular-genotype-phenotype-correlation-in-actb-and-actg1-related-non-muscle-actinopathies/</link>
		
		<dc:creator><![CDATA[Susann Meyer]]></dc:creator>
		<pubDate>Mon, 12 Jan 2026 12:06:47 +0000</pubDate>
				<category><![CDATA[2026]]></category>
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		<category><![CDATA[American Journal of Human Genetics]]></category>
		<category><![CDATA[Wollnik, Bernd]]></category>
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					<description><![CDATA[Di Donato N; NMA Consortium; Thom A, Rump A, Greve JN, Cadiñanos J, Calabro S, Cathey S, Chung B, Cope H, Costales M, Cuvertino S, Dinkel P, Erripi K, Fry AE, Garavelli L, Hoffjan S, Janzarik WG, Kreimer I, Mancini G, Marin-Reina P, Meinhardt A, Niehaus I, Pilz D, Ricca I, Simarro FS, Schrock E, Marquardt A, Taft MH, Tezcan K, Thunström S, Verhagen J, Verloes A, Wollnik B, Krawitz P, Hsieh TC, Seifert M, Heide M, Lawrence CB, Roberts NA, Manstein DJ, Woolf AS, Banka S]]></description>
		
		
		
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		<title>Mutations in the Key Autophagy Tethering Factor EPG5 Link Neurodevelopmental and Neurodegenerative Disorders Including Early-Onset Parkinsonism</title>
		<link>https://mbexc.de/mutations-in-the-key-autophagy-tethering-factor-epg5-link-neurodevelopmental-and-neurodegenerative-disorders-including-early-onset-parkinsonism/</link>
		
		<dc:creator><![CDATA[Susann Meyer]]></dc:creator>
		<pubDate>Mon, 06 Oct 2025 07:04:36 +0000</pubDate>
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					<description><![CDATA[Dafsari HS, Deneubourg C, Singh K, Maroofian R, Suprenant Z, Kho AL, Ingham NJ, Steel KP, Sheshadri P, Baur F, Hentrich L, Gerisch B, Zamani M, Alves C, Siddiqui A, Dafsari HS, Salari M, Lang AE, Harris M, Abdelaleem A, Sadeghian S, Azizimalamiri R, Galehdari H, Shariati G, Sedaghat A, Zeighami J, Calame D, Marafi D, Duan R, Boehnke A, Clark GD, Rosenfeld JA, Mohila CA, Steel D, Chopra S, Sharma S, Kohlschmidt N, Patzer S, Saffari A, Ebrahimi-Fakhari D, Çavdartepe BE, Chang IJ, Beckman E, Peters R, Fennell AP, Lo B, Averdunk L, Distelmaier F, Baethmann M, Elmslie F, Joost K, Nampoothiri S, Yesodharan D, Mandel H, Kimball A, Kline AD, Mignot C, Keren B, Laugel V, Õunap K, Devadathan K, van Berkestijn FMC, Silwal A, Koene S, Verma S, Karim MY, Boubidi C, Aziz M, ElGhazali G, Mattas L, Miryounesi M, Hashemi-Gorji F, Alavi S, Nouri N, Noruzinia M, Kavousi S, Kamath A, Jayawant S, Saneto R, Haridy NA, Kart PO, Cansu A, Joubert M, Beneteau C, Stuurman KE, Wilke M, Barakat TS, Tajsharghi H, Scardamaglia A, Vallian S, Hız S, Shoeibi A, Boostani R, Hashemi N, Babaei M, Alsaleh NS, Porter J, Attié-Bitach T, Marzin P, Wicher D, Gold JI, Schuler E, Kashgari A, Alanazi RF, Eyaid W, Engelen M, Langeveld M, Stüve B, Li Y, Yigit G, Wollnik B, Monje MHG, Krainc D, Mencacci NE, Bakhtiari S, Kruer M, Argilli E, Sherr E, Jamshidi Y, Karimiani EG, Cheung YWS, Karin I, Zifarelli G, Bauer P, Chung WK, Lupski JR, Kurian MA, Dötsch J, von Kleist-Retzow JC, Klopstock T, Wagner M, Yip C, Roos A, Carsetti R, Dionisi-Vici C, Gautel M, Duchen MR, Antebi A, Houlden H, Fanto M, Jungbluth H]]></description>
		
		
		
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		<title>Is CABP2-Associated Hearing Loss (DFNB93) a Gene Therapy Target? Preclinical Progress and Patient Registry</title>
		<link>https://mbexc.de/is-cabp2-associated-hearing-loss-dfnb93-a-gene-therapy-target-preclinical-progress-and-patient-registry/</link>
		
		<dc:creator><![CDATA[Susann Meyer]]></dc:creator>
		<pubDate>Mon, 08 Sep 2025 08:40:11 +0000</pubDate>
				<category><![CDATA[2025]]></category>
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		<category><![CDATA[Moser, Tobias]]></category>
		<category><![CDATA[Pangrsic Vilfan, Tina]]></category>
		<category><![CDATA[Vona, Barbara]]></category>
		<category><![CDATA[Wollnik, Bernd]]></category>
		<category><![CDATA[MedComm]]></category>
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					<description><![CDATA[Vona B, Wollnik B, Strenzke N, Pangrsic T, Moser T]]></description>
		
		
		
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		<title>Uncoupling of CSF biomarkers and clinical status in patients with a novel mutation of ATP13a2</title>
		<link>https://mbexc.de/uncoupling-of-csf-biomarkers-and-clinical-status-in-patients-with-a-novel-mutation-of-atp13a2/</link>
		
		<dc:creator><![CDATA[Susann Meyer]]></dc:creator>
		<pubDate>Fri, 05 Sep 2025 07:36:31 +0000</pubDate>
				<category><![CDATA[2025]]></category>
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		<category><![CDATA[Bähr, Mathias]]></category>
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		<category><![CDATA[MedRxiv]]></category>
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					<description><![CDATA[Stephani C, Ewers D, Stausberg D, Rasche D, Bahiraee A, Ahmad B, Baehr M, Downie B, Hirschel S, Pauli SJ, Riedel C, Sachkova A, Salinas G, Schneider A, van Riesen C, Wollnik B, Yigit G, Nave K, Zerr I, Eggert S, Sereda MW]]></description>
		
		
		
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		<title>SEC24C deficiency causes trafficking and glycosylation abnormalities in an epileptic encephalopathy with cataracts and dyserythropoeisis</title>
		<link>https://mbexc.de/sec24c-deficiency-causes-trafficking-and-glycosylation-abnormalities-in-an-epileptic-encephalopathy-with-cataracts-and-dyserythropoeisis/</link>
		
		<dc:creator><![CDATA[Susann Meyer]]></dc:creator>
		<pubDate>Thu, 08 May 2025 10:47:58 +0000</pubDate>
				<category><![CDATA[2025]]></category>
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		<category><![CDATA[Cyganek, Lukas]]></category>
		<category><![CDATA[Wollnik, Bernd]]></category>
		<category><![CDATA[JCI Insight]]></category>
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					<description><![CDATA[Bögershausen N, Cavdarli B, Nagai TH, Milev MP, Wolff A, Mehranfar M, Schmidt J, Choudhary D, Gutiérrez-Gutiérrez Ó, Cyganek L, Saint-Dic D, Zibat A, Köhrer K, Wollenweber TE, Wieczorek D, Altmüller J, Borodina T, Kaçar D, Haliloğlu G, Li Y, Thiel C, Sacher M, Knapik EW, Yigit G, Wollnik B]]></description>
		
		
		
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		<title>BTRR complex deficiency is a driver for genomic instability in Bloom syndrome</title>
		<link>https://mbexc.de/btrr-complex-deficiency-is-a-driver-for-genomic-instability-in-bloom-syndrome/</link>
		
		<dc:creator><![CDATA[Susann Meyer]]></dc:creator>
		<pubDate>Tue, 22 Apr 2025 07:39:46 +0000</pubDate>
				<category><![CDATA[2025]]></category>
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		<category><![CDATA[bioRxiv]]></category>
		<category><![CDATA[Wollnik, Bernd]]></category>
		<guid isPermaLink="false">https://mbexc.de/?p=22133</guid>

					<description><![CDATA[Gönenc II, Wolff A, Busley AV, Wieland A, Tijhuis A, Müller C, Wardenaar R, Argyriou L, Kaulfuß S, Räschle M, Spierings DCJ, Foijer F, Bastians H, Yigit G, Zibat A, Cyganek L, Wollnik B]]></description>
		
		
		
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		<title>Understanding inherited cardiomyopathies: clinical aspects and genetic determinants</title>
		<link>https://mbexc.de/understanding-inherited-cardiomyopathies-clinical-aspects-and-genetic-determinants/</link>
		
		<dc:creator><![CDATA[Susann Meyer]]></dc:creator>
		<pubDate>Tue, 08 Apr 2025 11:02:33 +0000</pubDate>
				<category><![CDATA[2025]]></category>
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		<category><![CDATA[Medizinische Genetik]]></category>
		<guid isPermaLink="false">https://mbexc.de/?p=21969</guid>

					<description><![CDATA[Yigit G, Kaulfuß S, Wollnik B]]></description>
		
		
		
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