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SaveShare Save ADAM19 cleaves the PTH receptor and associates with brachydactyly type E
Aydin, Atakan; Klenk, Christoph; Nemec, Katarina; Isbilir, Ali; Martin, Lisa M.; Zauber, Henrik; Rrustemi, Trendelina; Toka, Hakan R.; Schuster, Herbert; Gong, Maolian; Stricker, Sigmar; Bock, Andreas; Baehring, Sylvia; Selbach, Matthias; Lohse, Martin J.; Luft, Friedrich C. Share Save Mutant Phosphodiesterase 3A Protects From Hypertension-Induced Cardiac DamageErcu, Maria; Muecke, Michael B.; Pallien, Tamara; Marko, Lajos; Sholokh, Anastasiia; Schaechterle, Carolin; Aydin, Atakan; Kidd, Alexa; Walter, Stephan; Esmati, Yasmin; McMurray, Brandon J.; Lato, Daniella F.; Yumi Sunaga-Franze, Daniele; Dierks, Philip H.; Flores, Barbara Isabel Montesinos; Walker-Gray, Ryan; Gong, Maolian; Merticariu, Claudia; Zuehlke, Kerstin; Russwurm, Michael; Liu, Tiannan; Batolomaeus, Theda U. P.; Pautz, Sabine; Schelenz, Stefanie; Taube, Martin; Napieczynska, Hanna; Heuser, Arnd; Eichhorst, Jenny; Lehmann, Martin; Miller, Duncan C.; Diecke, Sebastian; Qadri, Fatimunnisa; Popova, Elena; Langanki, Reika; Movsesian, Matthew A.; Herberg, Friedrich W.; Forslund, Sofia K.; Mueller, Dominik N.; Borodina, Tatiana; Maass, Philipp G.; Baehring, Sylvia; Huebner, Norbert; Bader, Michael; Klussmann, Enno Share Save Phosphatidylinositol 4-kinase β mutations cause nonsyndromic sensorineural deafness and inner ear malformationSu, Xiulan; Feng, Yufei; Rahman, Sofia A.; Wu, Shuilong; Li, Guoan; Ruschendorf, Franz; Zhao, Lei; Cui, Hongwei; Liang, Junqing; Fang, Liang; Hu, Hao; Froehler, Sebastian; Yu, Yong; Patone, Giannino; Hummel, Oliver; Chen, Qinghua; Raile, Klemens; Luft, Friedrich C.; Baehring, Sylvia; Hussain, Khalid; Chen, Wei; Zhang, Jingjing; Gong, Maolian Share Save Evaluation of a rare glucose-dependent insulinotropic polypeptide receptor variant in a patient with diabetesJacobi, Simon F.; Khajavi, Noushafarin; Kleinau, Gunnar; Teumer, Alexander; Scheerer, Patrick; Homuth, Georg; Voelzke, Henry; Wiegand, Susanna; Kuehnen, Peter; Krude, Heiko; Gong, Maolian; Raile, Klemens; Biebermann, Heike Share Save PDE3A mutations cause autosomal dominant hypertension with brachydactylyMaass, Philipp G.; Aydin, Atakan; Luft, Friedrich C.; Schaechterle, Carolin; Weise, Anja; Stricker, Sigmar; Lindschau, Carsten; Vaegler, Martin; Qadri, Fatimunnisa; Toka, Hakan R.; Schulz, Herbert; Krawitz, Peter M.; Parkhomchuk, Dmitri; Hecht, Jochen; Hollfinger, Irene; Wefeld-Neuenfeld, Yvette; Bartels-Klein, Eireen; Muehl, Astrid; Kann, Martin; Schuster, Herbert; Chitayat, David; Bialer, Martin G.; Wienker, Thomas F.; Ott, Juerg; Rittscher, Katharina; Liehr, Thomas; Jordan, Jens; Plessis, Ghislaine; Tank, Jens; Mai, Knut; Naraghi, Ramin; Hodge, Russell; Hopp, Maxwell; Hattenbach, Lars O.; Busjahn, Andreas; Rauch, Anita; Vandeput, Fabrice; Gong, Maolian; Rueschendorf, Franz; Huebner, Norbert; Haller, Hermann; Mundlos, Stefan; Bilginturan, Nihat; Movsesian, Matthew A.; Klussmann, Enno; Toka, Okan; Baehring, Sylvia Share Save Recessive Mutations in PCBD1 Cause a New Type of Early-Onset DiabetesSimaite, Deimante; Kofent, Julia; Gong, Maolian; Rueschendorf, Franz; Jia, Shiqi; Arn, Pamela; Bentler, Kristi; Ellaway, Carolyn; Kuehnen, Peter; Hoffmann, Georg F.; Blau, Nenad; Spagnoli, Francesca M.; Huebner, Norbert; Raile, Klemens Share Save Share Save Inversion region for hypertension and brachydactyly on chromosome 12p features multiple splicing and noncoding RNABaehring, Sylvia; Kann, Martin; Neuenfeld, Yvette; Gong, Maolian; Chitayat, David; Toka, Hakan R.; Toka, Okan; Plessis, Ghislaine; Maass, Philipp; Rauch, Anita; Aydin, Atakan; Luft, Friedrich C. Share Save Mutations in the gene encoding the 3′-5′ DNA exonuclease TREX1 are associated with systemic lupus erythematosusLee-Kirsch, Min Ae; Gong, Maolian; Chowdhury, Dipanjan; Senenko, Lydia; Engel, Kerstin; Lee, Young-Ae; de Silva, Udesh; Bailey, Suzanna L.; Witte, Torsten; Vyse, Timothy J.; Kere, Juha; Pfeiffer, Christiane; Harvey, Scott; Wong, Andrew; Koskenmies, Sari; Hummel, Oliver; Rohde, Klaus; Schmidt, Reinhold E.; Dominiczak, Anna F.; Gahr, Manfred; Hollis, Thomas; Perrino, Fred W.; Lieberman, Judy; Huebner, Norbert Share Save Familial chilblain lupus, a monogenic form of cutaneous lupus erythematosus, maps to chromosome 3pLee-Kirsch, Min Ae; Gong, Maolian; Schulz, Herbert; Rueschendorf, Franz; Stein, Annette; Pfeiffer, Christiane; Ballarini, Annalisa; Gahr, Manfred; Hubner, Norbert; Linne, Maja Share Save Share Save Genome-wide linkage reveals a locus for human essential (primary) hypertension on chromosome 12pGong, ML; Zhang, HY; Schulz, H; Lee, YA; Sun, K; Bähring, S; Luft, FC; Nürnberg, P; Reis, A; Rohde, K; Ganten, D; Hui, RT; Hübner, N Share Save 
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