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Items: 4

1.
Novel mutation in the MED23 gene for intellectual disability: A case report and literature review
Feyzollah Hashemi‐Gorji, Majid Fardaei, Seyed Mohammad Bagher Tabei, Mohammad Miryounesi
Clin Case Rep. 2019 Feb; 7(2): 331–335. Published online 2019 Jan 9. doi: 10.1002/ccr3.1942
PMCID:
PMC6389469
AbstractArticlePDF–204K
2.
Crystal structure of human Mediator subunit MED23
Didier Monté, Bernard Clantin, Frédérique Dewitte, Zoé Lens, Prakash Rucktooa, Els Pardon, Jan Steyaert, Alexis Verger, Vincent Villeret
Nat Commun. 2018; 9: 3389. Published online 2018 Aug 23. doi: 10.1038/s41467-018-05967-y
PMCID:
PMC6107663
AbstractArticlePDF–4.1M
3.
A 7-Gene Signature Depicts the Biochemical Profile of Early Prefibrotic Myelofibrosis
Vibe Skov, Mark Burton, Mads Thomassen, Thomas Stauffer Larsen, Caroline H. Riley, Ann Brinch Madelung, Lasse Kjær, Henrik Bondo, Inger Stamp, Mats Ehinger, Rasmus Dahl-Sørensen, Nana Brochmann, Karsten Nielsen, Jürgen Thiele, Morten K. Jensen, Ole Weis Bjerrum, Torben A. Kruse, Hans Carl Hasselbalch
PLoS One. 2016; 11(8): e0161570. Published online 2016 Aug 31. doi: 10.1371/journal.pone.0161570
PMCID:
PMC5007012
AbstractArticlePDF–720K
4.
Thyroid hormone receptor-binding protein, an LXXLL motif-containing protein, functions as a general coactivator
Lan Ko, Guemalli R. Cardona, William W. Chin
Proc Natl Acad Sci U S A. 2000 May 23; 97(11): 6212–6217. doi: 10.1073/pnas.97.11.6212
PMCID:
PMC18584
AbstractArticlePDF–512K

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