Dawson JE - Search Results

1

Clinical presentation and molecular basis of congenital antithrombin deficiency in children: a cohort study.

Kumar R, Chan AK, Dawson JE, Forman-Kay JD, Kahr WH, Williams S. Kumar R, et al. Among authors: dawson je. Br J Haematol. 2014 Jul;166(1):130-9. doi: 10.1111/bjh.12842. Epub 2014 Mar 29. Br J Haematol. 2014. PMID: 24684277 Free article.

2

Allosteric coupling between the intracellular coupling helix 4 and regulatory sites of the first nucleotide-binding domain of CFTR.

Dawson JE, Farber PJ, Forman-Kay JD. Dawson JE, et al. PLoS One. 2013 Sep 18;8(9):e74347. doi: 10.1371/journal.pone.0074347. eCollection 2013. PLoS One. 2013. PMID: 24058550 Free PMC article.

3

c.1058C>T variant in the SERPINC1 gene is pathogenic for antithrombin deficiency.

Kumar R, Dawson JE, Chan AK, Forman-Kay JD, Kahr WH, Williams S. Kumar R, et al. Among authors: dawson je. Br J Haematol. 2015 Jul;170(1):123-5. doi: 10.1111/bjh.13261. Epub 2014 Dec 19. Br J Haematol. 2015. PMID: 25522812 Free article. No abstract available.

4

Molecular structural analysis of a novel and de-novo mutation in the SERPINC1 gene associated with type 1 antithrombin deficiency.

Wang TF, Dawson JE, Forman-Kay JD, Kahr WHA, Williams S, Chan AK, Kumar R. Wang TF, et al. Among authors: dawson je. Br J Haematol. 2017 May;177(4):654-656. doi: 10.1111/bjh.14090. Epub 2016 Apr 21. Br J Haematol. 2017. PMID: 27098850 Free article. No abstract available.

5

Direct Binding of the Corrector VX-809 to Human CFTR NBD1: Evidence of an Allosteric Coupling between the Binding Site and the NBD1:CL4 Interface.

Hudson RP, Dawson JE, Chong PA, Yang Z, Millen L, Thomas PJ, Brouillette CG, Forman-Kay JD. Hudson RP, et al. Among authors: dawson je. Mol Pharmacol. 2017 Aug;92(2):124-135. doi: 10.1124/mol.117.108373. Epub 2017 May 25. Mol Pharmacol. 2017. PMID: 28546419

6

Stabilization of a nucleotide-binding domain of the cystic fibrosis transmembrane conductance regulator yields insight into disease-causing mutations.

Vernon RM, Chong PA, Lin H, Yang Z, Zhou Q, Aleksandrov AA, Dawson JE, Riordan JR, Brouillette CG, Thibodeau PH, Forman-Kay JD. Vernon RM, et al. Among authors: dawson je. J Biol Chem. 2017 Aug 25;292(34):14147-14164. doi: 10.1074/jbc.M116.772335. Epub 2017 Jun 27. J Biol Chem. 2017. PMID: 28655774 Free PMC article.

7

Fibrinogen Columbus II: A novel c.1075G>T mutation in the FGG gene causing hypodysfibrinogenemia and thrombosis in an adolescent male.

Kumar R, Dawson J, Varga E, Canini JT, Monda KL, Dunn AL. Kumar R, et al. Pediatr Blood Cancer. 2019 Sep;66(9):e27832. doi: 10.1002/pbc.27832. Epub 2019 May 27. Pediatr Blood Cancer. 2019. PMID: 31131962

8

Non-cooperative 4E-BP2 folding with exchange between eIF4E-binding and binding-incompatible states tunes cap-dependent translation inhibition.

Dawson JE, Bah A, Zhang Z, Vernon RM, Lin H, Chong PA, Vanama M, Sonenberg N, Gradinaru CC, Forman-Kay JD. Dawson JE, et al. Nat Commun. 2020 Jun 19;11(1):3146. doi: 10.1038/s41467-020-16783-8. Nat Commun. 2020. PMID: 32561718 Free PMC article.

9

Fibrinogen Columbus III: A novel c.963del frameshift mutation in the FGG gene resulting in hypofibrinogenemia with a bleeding phenotype.

Abdelghani E, Dawson J, Zajo K, Hallam M, Dunn A, Kumar R. Abdelghani E, et al. Pediatr Blood Cancer. 2021 Mar;68(3):e28713. doi: 10.1002/pbc.28713. Epub 2020 Oct 15. Pediatr Blood Cancer. 2021. PMID: 33058516 No abstract available.

10

Multisite phosphorylation and binding alter conformational dynamics of the 4E-BP2 protein.

Smyth S, Zhang Z, Bah A, Tsangaris TE, Dawson J, Forman-Kay JD, Gradinaru CC. Smyth S, et al. Biophys J. 2022 Aug 16;121(16):3049-3060. doi: 10.1016/j.bpj.2022.07.015. Epub 2022 Jul 15. Biophys J. 2022. PMID: 35841142 Free PMC article.

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