Human TGF-β1 deficiency causes severe inflammatory bowel disease and encephalopathy

Autor: Kotlarz, Daniel, Marquardt, Benjamin, Barøy, Tuva, Lee, Way S., Konnikova, Liza, Hollizeck, Sebastian, Magg, Thomas, Lehle, Anna S., Walz, Christoph, Borggraefe, Ingo, Hauck, Fabian, Bufler, Philip, Conca, Raffaele, Wall, Sarah M., Schumacher, Eva Margrethe, Misceo, Doriana, Frengen, Eirik, Bentsen, Beint Sigmund, Uhlig, Holm H., Hopfner, Karl-Peter, Muise, Aleixo M., Snapper, Scott B., Strømme, Petter, Klein, Christoph

Publikováno v: Kotlarz, Daniel Marquardt, Benjamin Barøy, Tuva Lee, Way S. Konnikova, Liza Hollizeck, Sebastian Magg, Thomas Lehle, Anna S. Walz, Christoph Borggraefe, Ingo Hauck, Fabian Bufler, Philip Conca, Raffaele Wall, Sarah M. Schumacher, Eva Margrethe Misceo, Doriana Frengen, Eirik Bentsen, Beint Sigmund Uhlig, Holm H. Hopfner, Karl-Peter Muise, Aleixo M. Snapper, Scott B. Strømme, Petter Klein, Christoph . Human TGF-β1 deficiency causes severe inflammatory bowel disease and encephalopathy. Nature Genetics. 2018, 50(3), 344-348
Nature Genetics

Externí odkaz: http://hdl.handle.net/10852/66399
https://www.duo.uio.no/bitstream/handle/10852/66399/2/KotlarzNatGenetFinal.pdf

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Enhanced TH17 Responses in Patients with IL10 Receptor Deficiency and Infantile-onset IBD.

Autor: Shouval, Dror S., Konnikova, Liza, Griffith, Alexandra E., Wall, Sarah M., Biswas, Amlan, Werner, Lael, Nunberg, Moran, Kammermeier, Jochen, Goettel, Jeremy A., Anand, Rajsavi, Chen, Hannah, Weiss, Batia, Jian Li, Loizides, Anthony, Baruch Yerushalmi, TadahiroYanagi, Beier, Rita, Conklin, Laurie S., Ebens, Christen L., Santos, Fernanda G. M. S.

Publikováno v: Inflammatory Bowel Diseases; Nov2017, Vol. 23 Issue 11, p1950-1961, 12p