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Grunwald, S. Scientific Reports 10 : Wenzel, J.

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Doll, J. International Journal of Molecular Sciences 21 1 : Journal of Endocrinology 1 : January Chothani, S.

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Current Protocols in Molecular Biology 1 : e December Disruption of PHF21A causes syndromic intellectual disability with craniofacial anomalies, epilepsy, hypotonia, and neurobehavioral problems including autism.

Kim, H. Molecular Autism 10 : Chothani, S. Circulation 11 : Chen, H. Nature Communications 10 1 : Siegerink, B. Gorvin, C. Journal of Bone and Mineral Research 34 7 : July The translational landscape of the human heart.

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Cell 1 : Frontiers in Neurology 10 : June SarcTrack: an adaptable software tool for efficient large-scale analysis of sarcomere function in hiPSC-cardiomyocytes. Toepfer, C. Circulation Research 8 : Blood harenda single track : Journal of Bone and Mineral Research 34 3 : March The Tug1 locus is essential for male fertility.

Lewandowski, J. Ferreira, M. Journal of Allergy and Clinical Immunology 2 : February Hemmer, M.

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Diabetes 68 1 : Pflugers Archiv 11 : November Translational control of cardiac fibrosis. Marenholz, I. Journal of Allergy and Clinical Immunology 4 : Kopp, S.

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Scientific Reports 8 1 : Lützenberg, R. Cellular Physiology and Biochemistry 47 4 : Kuda, O.

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Diabetes 67 6 : Günther, C. Journal of Investigative Dermatology 6 : June A Canadian genome-wide association study and meta-analysis confirm HLA as a risk factor for peanut allergy independent of asthma. Asai, Y. April Sharma, A. April Meckes, J.

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Schafer, S. Nature : Nature Genetics 49 12 : December Transmembrane helix connectivity in Orai1 harenda single track two gates for calcium-dependent transcription.

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Frischauf, I. Science Signaling 10 : eaao Sassi, Y. S and De Strooper, B.

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Nature Communications 8 erste bekanntschaft : Heinig, M. Genome Biology 18 1 : BMC Research Notes 10 1 : Ventura-Clapier, R. Cardiovascular Research 7 : Lorenz, C. Cell Stem Cell 20 5 : Kammertoens, T.

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Current Protocols in Molecular Biology : McDermott-Roe, C. February Molecular dissection of germline chromothripsis in a developmental context using patient-derived iPS cells. Middelkamp, S.

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