Wissenschaftliche Publikationen Suche Suche Autor/in Forschungsgruppe Veröffentlichungsdatum Wirkungsfaktor Suchen Sortieren nach RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Reihenfolge AufsteigendAbsteigend Acevedo Ochoa, Ernesto (2) Adami, Eleonora Dr. (21) Ahmad, Ata Ul Wakeel (1) Aigner, Denise (1) Akalin, Altuna Dr. (75) Akmeric, Emir Bora (2) Albrecht, Jan Philipp (6) Alenina, Natalia Dr. (176) Ali, Mohammed Ahmed Khallaf Dr. (1) Alp, Keziban Merve (5) Anandakumar, Harithaa (6) Annibale, Paolo Dr. (28) Arnau Soler, Aleix Dr. (5) Bachtler, Barbara (1) Bader, Michael Prof. Dr. (691) Badillo Lisakowski, Victor Christian Dr. (3) Bahr, Lina Samira Dr. (3) Bähring, Sylvia Dr. (51) Bahry, Ella Dr. (3) Barke, Niclas (1) Bartels-Klein, Eireen (9) Bartolomaeus, Hendrik (25) Bartolomaeus, Theda (18) Bassot, Claudio Dr. (1) Bauersachs, Daniel (1) Baumann, Elisabeth (4) Bayram, Safak (4) Begay-Müller, Valerie Dr. (25) Beier, Christin (1) Beitnere, Ulrika Dr. (1) Bemmann, Franziska (1) Benlasfer, Nouhad (3) Berangi, Mostafa (5) Bernert, Carola (4) Berruezo Llacuna, Maria (3) Beule, Dieter Dr. (102) Biese, Charlotte (1) Birchmeier, Walter Prof. Dr. (209) Birchmeier-Kohler, Carmen Prof. Dr. (175) Birkner, Till (10) Birol, Melissa Dr. (12) Blachut, Susanne (7) Blankenstein, Thomas Prof. Dr. (180) Blume, Alexander Dr. (8) Blüthgen, Nils (24) Bock-Bierbaum, Tobias Dr. (5) Born, Gabriele (1) Borodina, Tatiana Dr. (12) Bosco, Bartolomeo Dr. (1) Braeuning, Caroline (7) Brouwer-Lehmitz, Antje Susan (1) Brüning, Ulrike Dr. (6) Bunina, Daria Dr. (12) Bunse, Mario Dr. (17) Cakmak-Görür, Nese Dr. (2) Cano Rincon, Elena Dr. (9) Carneiro Raimundo, Sandra Cristina Dr. (1) Carvalho, Silvia Filipa (3) Castilho de Barros, Carlos Prof. Dr. (6) Cerda Esteban, Nuria Dr. (3) Cerda Jara, Cledi Alicia (4) Cess, Colin (1) Cetin, Ali Osman (1) Chakrabarti, Sampurna Dr. (4) Chekulaeva, Marina Dr. (22) Chen, Chia-Yu (7) Chen, Wei Prof. Dr. (148) Chu, Van Trung Dr. (23) Chu, Xiaofeng (3) Cibin, Penelope (1) Clauß, Julian (2) Cöl Arslan, Seda Dr. (7) Collins, Russell Thomas Dr. (8) Conrad, Thomas Dr. (18) Coralluzzo, Violeta (1) Coscia, Fabian Dr. (27) Costanza, Mariantonia Dr. (5) Crocini, Claudia Dr. (4) Dahlmann, Mathias Dr. (29) Dang Ngoc, Tu Dr. (2) Daniel, Peter Prof. Dr. (99) Dartsch, Josephine (7) Daumke, Oliver Prof. Dr. (96) Dechend, Ralf Priv. 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Sortieren: Treffgenauigkeit Neueste nach älteste Älteste nach neueste April 2022 / J Am Soc Nephrol Claudin-10a deficiency shifts proximal tubular Cl(-) permeability to cation selectivity via claudin-2 redistribution T. Breiderhoff N. Himmerkus L. Meoli A. Fromm S. Sewerin N. Kriuchkova O. Nagel Y. Ladilov S. Krug C. Quintanova M. Stumpp D. Garbe-Schönberg U. Westernströer C. Merkel M. Brinkhus J. Altmüller M. Schweiger D. Mueller K. Mutig M. Morawski J. Halbritter S. Milatz M. Bleich D. Günzel Mai 2022 / Clin Genet Phenotypic spectrum of BLM- and RMI1-related Bloom syndrome I.I. Gönenc N.H. Elcioglu C. Martinez Grijalva S. Aras N. Großmann I. Praulich J. Altmüller S. Kaulfuß Y. Li P. Nürnberg P. Burfeind G. Yigit B. Wollnik 01. Mai 2022 / Cancer Res Noncanonical function of AGO2 augments T-cell receptor signaling in T-cell prolymphocytic leukemia T. Braun J. Stachelscheid N. Bley S. Oberbeck M. Otte T.A. Müller L. Wahnschaffe M. Glaß K. Ommer M. Franitza B. Gathof J. Altmüller M. Hallek D. Auguin S. Hüttelmaier A. Schrader M. Herling Oktober 2021 / Neurogenetics ANK3 related neurodevelopmental disorders: expanding the spectrum of heterozygous loss-of-function variants K. Kloth B. Lozic J. Tagoe M.J.V. Hoffer A. Van der Ven H. Thiele J. Altmüller C. Kubisch P.Y.B. Au J. Denecke E.K. Bijlsma D. Lessel November 2021 / Genet Med Biallelic variants in PCDHGC4 cause a novel neurodevelopmental syndrome with progressive microcephaly, seizures, and joint anomalies M. Iqbal R. Maroofian B. Çavdarlı F. Riccardi M. Field S. Banka D.K. Bubshait Y. Li J. Hertecant S.M. Baig D. Dyment S. Efthymiou U. Abdullah E.U.H. Makhdoom Z. Ali T Scherf de Almeida F. Molinari C. Mignon-Ravix B. Chabrol J. Antony L. Ades A.T. Pagnamenta A. Jackson S. Douzgou C. Beetz V. Karageorgou B. Vona A. Rad J.M. Baig T. Sultan J.R. Alvi S. Maqbool F. Rahman M.B. Toosi F. Ashrafzadeh S. Imannezhad E.G. Karimiani Y. Sarwar S. Khan M. Jameel A.A. Noegel B. Budde J. Altmüller S. Motameny W. Höhne H. Houlden P. Nürnberg B. Wollnik L. Villard F.S. Alkuraya M. Osmond M.S. Hussain G. Yigit Juli 2021 / Nat Cell Biol Niche stiffening compromises hair follicle stem cell potential during ageing by reducing bivalent promoter accessibility J. Koester Y.A. Miroshnikova S. Ghatak C.A. Chacón-Martínez J. Morgner X. Li I. Atanassov J. Altmüller D.E. Birk M. Koch W. Bloch M. Bartusel C.M. Niessen A. Rada-Iglesias S.A. Wickström 25. Juni 2021 / Nat Commun SMG5-SMG7 authorize nonsense-mediated mRNA decay by enabling SMG6 endonucleolytic activity V. Boehm S. Kueckelmann J.V. Gerbracht S. Kallabis T. Britto-Borges J. Altmüller M. Krüger C. Dieterich N.H. Gehring 09. August 2021 / EMBO Mol Med Long-lived macrophage reprogramming drives spike protein-mediated inflammasome activation in COVID-19 S.J. Theobald A. Simonis T. Georgomanolis C. Kreer M. Zehner H.S. Eisfeld M.C. Albert J. Chhen S. Motameny F. Erger J. Fischer J.J. Malin J. Gräb S. Winter A. Pouikli F. David B. Böll P. Koehler K. Vanshylla H. Gruell I. Suárez M. Hallek G. Fätkenheuer N. Jung O.A. Cornely C. Lehmann P. Tessarz J. Altmüller P. Nürnberg H. Kashkar F. Klein M. Koch J. Rybniker 20. Mai 2022 / J Med Genet Loss-of-function variants in DNM1 cause a specific form of developmental and epileptic encephalopathy only in biallelic state G. Yigit R. Sheffer M. Daana Y. Li E. Kaygusuz H. Mor-Shakad J. Altmüller P. Nürnberg L. Douiev S. Kaulfuss P. Burfeind B. Wollnik K. Brockmann 01. Juni 2021 / Mol Syst Biol HMGB1 coordinates SASP-related chromatin folding and RNA homeostasis on the path to senescence K. Sofiadis N. Josipovic M. Nikolic Y. Kargapolova N. Übelmesser V. Varamogianni-Mamatsi A. Zirkel I. Papadionysiou G. Loughran J. Keane A. Michel E.G. Gusmao C. Becker J. Altmüller T. Georgomanolis A. Mizi A. Papantonis Seitennummerierung Erste Seite « First Vorherige Seite ‹ Previous … Seite 32 Aktuelle Seite 33 Seite 34 Seite 35 Nächste Seite Next › Letzte Seite Last »
April 2022 / J Am Soc Nephrol Claudin-10a deficiency shifts proximal tubular Cl(-) permeability to cation selectivity via claudin-2 redistribution T. Breiderhoff N. Himmerkus L. Meoli A. Fromm S. Sewerin N. Kriuchkova O. Nagel Y. Ladilov S. Krug C. Quintanova M. Stumpp D. Garbe-Schönberg U. Westernströer C. Merkel M. Brinkhus J. Altmüller M. Schweiger D. Mueller K. Mutig M. Morawski J. Halbritter S. Milatz M. Bleich D. Günzel
Mai 2022 / Clin Genet Phenotypic spectrum of BLM- and RMI1-related Bloom syndrome I.I. Gönenc N.H. Elcioglu C. Martinez Grijalva S. Aras N. Großmann I. Praulich J. Altmüller S. Kaulfuß Y. Li P. Nürnberg P. Burfeind G. Yigit B. Wollnik
01. Mai 2022 / Cancer Res Noncanonical function of AGO2 augments T-cell receptor signaling in T-cell prolymphocytic leukemia T. Braun J. Stachelscheid N. Bley S. Oberbeck M. Otte T.A. Müller L. Wahnschaffe M. Glaß K. Ommer M. Franitza B. Gathof J. Altmüller M. Hallek D. Auguin S. Hüttelmaier A. Schrader M. Herling
Oktober 2021 / Neurogenetics ANK3 related neurodevelopmental disorders: expanding the spectrum of heterozygous loss-of-function variants K. Kloth B. Lozic J. Tagoe M.J.V. Hoffer A. Van der Ven H. Thiele J. Altmüller C. Kubisch P.Y.B. Au J. Denecke E.K. Bijlsma D. Lessel
November 2021 / Genet Med Biallelic variants in PCDHGC4 cause a novel neurodevelopmental syndrome with progressive microcephaly, seizures, and joint anomalies M. Iqbal R. Maroofian B. Çavdarlı F. Riccardi M. Field S. Banka D.K. Bubshait Y. Li J. Hertecant S.M. Baig D. Dyment S. Efthymiou U. Abdullah E.U.H. Makhdoom Z. Ali T Scherf de Almeida F. Molinari C. Mignon-Ravix B. Chabrol J. Antony L. Ades A.T. Pagnamenta A. Jackson S. Douzgou C. Beetz V. Karageorgou B. Vona A. Rad J.M. Baig T. Sultan J.R. Alvi S. Maqbool F. Rahman M.B. Toosi F. Ashrafzadeh S. Imannezhad E.G. Karimiani Y. Sarwar S. Khan M. Jameel A.A. Noegel B. Budde J. Altmüller S. Motameny W. Höhne H. Houlden P. Nürnberg B. Wollnik L. Villard F.S. Alkuraya M. Osmond M.S. Hussain G. Yigit
Juli 2021 / Nat Cell Biol Niche stiffening compromises hair follicle stem cell potential during ageing by reducing bivalent promoter accessibility J. Koester Y.A. Miroshnikova S. Ghatak C.A. Chacón-Martínez J. Morgner X. Li I. Atanassov J. Altmüller D.E. Birk M. Koch W. Bloch M. Bartusel C.M. Niessen A. Rada-Iglesias S.A. Wickström
25. Juni 2021 / Nat Commun SMG5-SMG7 authorize nonsense-mediated mRNA decay by enabling SMG6 endonucleolytic activity V. Boehm S. Kueckelmann J.V. Gerbracht S. Kallabis T. Britto-Borges J. Altmüller M. Krüger C. Dieterich N.H. Gehring
09. August 2021 / EMBO Mol Med Long-lived macrophage reprogramming drives spike protein-mediated inflammasome activation in COVID-19 S.J. Theobald A. Simonis T. Georgomanolis C. Kreer M. Zehner H.S. Eisfeld M.C. Albert J. Chhen S. Motameny F. Erger J. Fischer J.J. Malin J. Gräb S. Winter A. Pouikli F. David B. Böll P. Koehler K. Vanshylla H. Gruell I. Suárez M. Hallek G. Fätkenheuer N. Jung O.A. Cornely C. Lehmann P. Tessarz J. Altmüller P. Nürnberg H. Kashkar F. Klein M. Koch J. Rybniker
20. Mai 2022 / J Med Genet Loss-of-function variants in DNM1 cause a specific form of developmental and epileptic encephalopathy only in biallelic state G. Yigit R. Sheffer M. Daana Y. Li E. Kaygusuz H. Mor-Shakad J. Altmüller P. Nürnberg L. Douiev S. Kaulfuss P. Burfeind B. Wollnik K. Brockmann
01. Juni 2021 / Mol Syst Biol HMGB1 coordinates SASP-related chromatin folding and RNA homeostasis on the path to senescence K. Sofiadis N. Josipovic M. Nikolic Y. Kargapolova N. Übelmesser V. Varamogianni-Mamatsi A. Zirkel I. Papadionysiou G. Loughran J. Keane A. Michel E.G. Gusmao C. Becker J. Altmüller T. Georgomanolis A. Mizi A. Papantonis