Browse by Journal Title

2024

The role of microRNAs in defining LSECs cellular identity and in regulating F8 gene expression.
Jamil, M. A., Al-Rifai, R., Nuesgen, N., Altmüller, J., Oldenburg, J. and El-Maarri, O.
Frontiers in Genetics 15 : 1302685. 19 February 2024

2023

Mesoangioblasts at 20: from the embryonic aorta to the patient bed.
Cossu, G., Tonlorenzi, R., Brunelli, S., Sampaolesi, M., Messina, G., Azzoni, E., Benedetti, S., Biressi, S., Bonfanti, C., Bragg, L., Camps, J., Cappellari, O., Cassano, M., Ciceri, F., Coletta, M., Covarello, D., Crippa, S., Cusella-De Angelis, M.G., De Angelis, L., Dellavalle, A., Diaz-Manera, J., Galli, D., Galli, F., Gargioli, C., Gerli, M.F.M., Giacomazzi, G., Galvez, B.G., Hoshiya, H., Guttinger, M., Innocenzi, A., Minasi, M.G., Perani, L., Previtali, S.C., Quattrocelli, M., Ragazzi, M., Roostalu, U., Rossi, G., Scardigli, R., Sirabella, D., Tedesco, F.S., Torrente, Y. and Ugarte, G.
Frontiers in Genetics 13 : 1056114. 4 January 2023

2022

Full-length spatial transcriptomics reveals the unexplored isoform diversity of the myocardium post-MI.
Boileau, E., Li, X., Naarmann-de Vries, I.S., Becker, C., Casper, R., Altmüller, J., Leuschner, F. and Dieterich, C.
Frontiers in Genetics 13 : 912572. 22 July 2022

Detection and validation of circular DNA fragments using nanopore sequencing.
Tüns, A.I., Hartmann, T., Magin, S., Chamorro González, R., Henssen, A.G., Rahmann, S., Schramm, A. and Köster, J.
Frontiers in Genetics 13 : 867018. 30 May 2022

Venn diagrams may indicate erroneous statistical reasoning in transcriptomics.
Weiner, J., Obermayer, B. and Beule, D.
Frontiers in Genetics 13 : 818683. 14 April 2022

2021

Myogenic cell transplantation in genetic and acquired diseases of skeletal muscle.
Boyer, O., Butler-Browne, G., Chinoy, H., Cossu, G., Galli, F., Lilleker, J.B., Magli, A., Mouly, V., Perlingeiro, R.R., Previtali, S.C., Sampaolesi, M., Smeets, H., Schoewel-Wolf, V., Spuler, S., Torrente, Y. and Van Tienen, F.
Frontiers in Genetics 12 : 702547. August 2021

Cystatin M/E variant causes autosomal dominant keratosis follicularis spinulosa decalvans by dysregulating cathepsins L and V.
Eckl, K.M., Gruber, R., Brennan, L., Marriott, A., Plank, R., Moosbrugger-Martinz, V., Blunder, S., Schossig, A., Altmüller, J., Thiele, H., Nürnberg, P., Zschocke, J., Hennies, H.C. and Schmuth, M.
Frontiers in Genetics 12 : 689940. July 2021

2019

Efficient and precise CRISPR/Cas9-mediated MECP2 modifications in human-induced pluripotent stem cells.
Le, T.T.H., Tran, N.T., Dao, T.M.L., Nguyen, D.D., Do, H.D., Ha, T.L., Kühn, R., Nguyen, T.L., Rajewsky, K. and Chu, V.T.
Frontiers in Genetics 10 : 625. July 2019

Enhancement of precise gene editing by the association of Cas9 with homologous recombination factors.
Tran, N.T., Bashir, S., Li, X., Rossius, J., Chu, V.T., Rajewsky, K. and Kühn, R.
Frontiers in Genetics 10 : 365. 30 April 2019

Live-imaging readouts and cell models for phenotypic profiling of mitochondrial function.
Iannetti, E.F., Prigione, A., Smeitink, J.A.M., Koopman, W.J.H., Beyrath, J. and Renkema, H.
Frontiers in Genetics 10 : 131. March 2019

2016

Dissecting the effect of genetic variation on the hepatic expression of drug disposition genes across the collaborative cross mouse strains.
Nachshon, A., Abu-Toamih Atamni, H.J., Steuerman, Y., Sheikh-Hamed, R., Dorman, A., Mott, R., Dohm, J.C., Lehrach, H., Sultan, M., Shamir, R., Sauer, S., Himmelbauer, H., Iraqi, F.A. and Gat-Viks, I.
Frontiers in Genetics 7 : 172. 5 October 2016

Anchoring a leviathan: how the nuclear membrane tethers the genome.
Czapiewski, R., Robson, M.I. and Schirmer, E.C.
Frontiers in Genetics 7 : 82. 6 May 2016

Current approaches toward quantitative mapping of the interactome.
Buntru, A., Trepte, P., Klockmeier, K., Schnoegl, S. and Wanker, E.E.
Frontiers in Genetics 7 : 74. 4 May 2016

2015

Quantitative affinity purification mass spectrometry: a versatile technology to study protein-protein interactions.
Meyer, K. and Selbach, M.
Frontiers in Genetics 6 : 237. July 2015

2013

Polymer models of chromatin organization.
Barbieri, M., Scialdone, A., Piccolo, A., Chiariello, A.M., di Lanno, C., Prisco, A., Pombo, A. and Nicodemi, M.
Frontiers in Genetics 4 : 113. June 2013