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August 2023 / Cell Rep Structural insights into anion selectivity and activation mechanism of LRRC8 volume-regulated anion channels H. Liu M.M. Polovitskaya L. Yang M. Li H. Li Z. Han J. Wu Q. Zhang T.J. Jentsch J. Liao August 2022 / Nat Genet Origin and function of activated fibroblast states during zebrafish heart regeneration B. Hu S. Lelek B. Spanjaard H. El-Sammak M.G. Simões J. Mintcheva H. Aliee R. Schäfer A.M. Meyer F. Theis D.Y.R. Stainier D. Panáková J.P. Junker Oktober 2022 / Hum Mutat Biallelic variants in WARS1 cause a highly variable neurodevelopmental syndrome and implicate a critical exon for normal auditory function S.J. Lin B. Vona H.M. Porter M. Izadi K. Huang Y. Lacassie J.A. Rosenfeld S. Khan C. Petree T.A. Ali N. Muhammad S.A. Khan N. Muhammad P. Liu M.L. Haymon F. Rüschendorf I.K. Kong L. Schnapp N. Shur L. Chorich L. Layman T. Haaf E. Pourkarimi H.G. Kim G.K. Varshney 02. Februar 2022 / Sci Adv Gating choreography and mechanism of the human proton-activated chloride channel ASOR C. Wang M.M. Polovitskaya B.D. Delgado T.J. Jentsch S.B. Long 16. März 2022 / Int J Mol Sci Simultaneous genetic ablation of PD-1, LAG-3, and TIM-3 in CD8 T cells delays tumor growth and improves survival outcome E. Ciraolo S. Althoff J. Ruß S. Rosnev M. Butze M. Pühl M. Frentsch L. Bullinger I.K. Na 16. November 2021 / Nat Commun Rare variant analysis in eczema identifies exonic variants in DUSP1, NOTCH4 and SLC9A4 S. Grosche I. Marenholz J. Esparza-Gordillo A. Arnau-Soler E. Pairo-Castineira F. Rüschendorf T.S. Ahluwalia C. Almqvist A. Arnold H. Baurecht H. Bisgaard K. Bønnelykke S.J. Brown M. Bustamante J.A. Curtin A. Custovic S.C. Dharmage A. Esplugues M. Falchi D. Fernandez-Orth M.A.R. Ferreira A. Franke S. Gerdes C. Gieger H. Hakonarson P.G. Holt G. Homuth N. Hubner P.G. Hysi M.R. Jarvelin R. Karlsson G.H. Koppelman S. Lau M. Lutz P.K.E. Magnusson G.B. Marks M. Müller-Nurasyid M.M. Nöthen L. Paternoster C.E. Pennell A. Peters K. Rawlik C.F. Robertson E. Rodriguez S. Sebert A. Simpson P.M.A. Sleiman M. Standl D. Stölzl K. Strauch A. Szwajda A. Tenesa P.J. Thompson V. Ullemar A. Visconti J.M. Vonk C.A. Wang S. Weidinger M. Wielscher C.L. Sargent C.J. Xu Y.A. Lee März 2024 / Hypertension KCNQ5 controls perivascular adipose tissue–mediated vasodilation D. Tsvetkov J. Schleifenbaum Y. Wang M. Kassmann M.M. Polovitskaya M. Ali S. Schütze M. Rothe F.C. Luft T.J. Jentsch M. Gollasch 05. Januar 2024 / Hum Mutat Macrocephaly and digital anomalies expand the phenotypic spectrum of PGAP2 variants in hyperphosphatasia with impaired intellectual development syndrome 3 (HPMRS3) S. Susgun A. Ben-Mahmoud F. Rüschendorf B. Ku S.I. Hussain S. Schulz O. Puk S. Biskup J.D.J. Labonne D.W. Don V. Gupta T.I. Choi S. Khan N. Wasif Y. Lacassie L.C. Layman S.A. Ugur Iseri C.H. Kim H.G. Kim 12. September 2024 / Acta Physiol A gender perspective on diet, microbiome, and sex hormone interplay in cardiovascular disease N. Jovanovic V. Zach C. Crocini L.S. Bahr S.K. Forslund-Startceva K. Franz Seitennummerierung Erste Seite « First Vorherige Seite ‹ Previous … Seite 11 Seite 12 Seite 13 Aktuelle Seite 14
29. August 2023 / Cell Rep Structural insights into anion selectivity and activation mechanism of LRRC8 volume-regulated anion channels H. Liu M.M. Polovitskaya L. Yang M. Li H. Li Z. Han J. Wu Q. Zhang T.J. Jentsch J. Liao
August 2022 / Nat Genet Origin and function of activated fibroblast states during zebrafish heart regeneration B. Hu S. Lelek B. Spanjaard H. El-Sammak M.G. Simões J. Mintcheva H. Aliee R. Schäfer A.M. Meyer F. Theis D.Y.R. Stainier D. Panáková J.P. Junker
Oktober 2022 / Hum Mutat Biallelic variants in WARS1 cause a highly variable neurodevelopmental syndrome and implicate a critical exon for normal auditory function S.J. Lin B. Vona H.M. Porter M. Izadi K. Huang Y. Lacassie J.A. Rosenfeld S. Khan C. Petree T.A. Ali N. Muhammad S.A. Khan N. Muhammad P. Liu M.L. Haymon F. Rüschendorf I.K. Kong L. Schnapp N. Shur L. Chorich L. Layman T. Haaf E. Pourkarimi H.G. Kim G.K. Varshney
02. Februar 2022 / Sci Adv Gating choreography and mechanism of the human proton-activated chloride channel ASOR C. Wang M.M. Polovitskaya B.D. Delgado T.J. Jentsch S.B. Long
16. März 2022 / Int J Mol Sci Simultaneous genetic ablation of PD-1, LAG-3, and TIM-3 in CD8 T cells delays tumor growth and improves survival outcome E. Ciraolo S. Althoff J. Ruß S. Rosnev M. Butze M. Pühl M. Frentsch L. Bullinger I.K. Na
16. November 2021 / Nat Commun Rare variant analysis in eczema identifies exonic variants in DUSP1, NOTCH4 and SLC9A4 S. Grosche I. Marenholz J. Esparza-Gordillo A. Arnau-Soler E. Pairo-Castineira F. Rüschendorf T.S. Ahluwalia C. Almqvist A. Arnold H. Baurecht H. Bisgaard K. Bønnelykke S.J. Brown M. Bustamante J.A. Curtin A. Custovic S.C. Dharmage A. Esplugues M. Falchi D. Fernandez-Orth M.A.R. Ferreira A. Franke S. Gerdes C. Gieger H. Hakonarson P.G. Holt G. Homuth N. Hubner P.G. Hysi M.R. Jarvelin R. Karlsson G.H. Koppelman S. Lau M. Lutz P.K.E. Magnusson G.B. Marks M. Müller-Nurasyid M.M. Nöthen L. Paternoster C.E. Pennell A. Peters K. Rawlik C.F. Robertson E. Rodriguez S. Sebert A. Simpson P.M.A. Sleiman M. Standl D. Stölzl K. Strauch A. Szwajda A. Tenesa P.J. Thompson V. Ullemar A. Visconti J.M. Vonk C.A. Wang S. Weidinger M. Wielscher C.L. Sargent C.J. Xu Y.A. Lee
März 2024 / Hypertension KCNQ5 controls perivascular adipose tissue–mediated vasodilation D. Tsvetkov J. Schleifenbaum Y. Wang M. Kassmann M.M. Polovitskaya M. Ali S. Schütze M. Rothe F.C. Luft T.J. Jentsch M. Gollasch
05. Januar 2024 / Hum Mutat Macrocephaly and digital anomalies expand the phenotypic spectrum of PGAP2 variants in hyperphosphatasia with impaired intellectual development syndrome 3 (HPMRS3) S. Susgun A. Ben-Mahmoud F. Rüschendorf B. Ku S.I. Hussain S. Schulz O. Puk S. Biskup J.D.J. Labonne D.W. Don V. Gupta T.I. Choi S. Khan N. Wasif Y. Lacassie L.C. Layman S.A. Ugur Iseri C.H. Kim H.G. Kim
12. September 2024 / Acta Physiol A gender perspective on diet, microbiome, and sex hormone interplay in cardiovascular disease N. Jovanovic V. Zach C. Crocini L.S. Bahr S.K. Forslund-Startceva K. Franz