Wright NT - Search Results

1

The phenotypic spectrum of PTCD3 deficiency.

Lace B, Faqeih E, Kaya N, Krumina Z, Mayr JA, Micule I, Wright NT, Achleitner MT, AlQudairy H, Pajusalu S, Stavusis J, Zayakin P, Inashkina I. Lace B, et al. Among authors: wright nt. JIMD Rep. 2024 May 27;65(5):297-304. doi: 10.1002/jmd2.12424. eCollection 2024 Sep. JIMD Rep. 2024. PMID: 39544688 Free PMC article.

2

I told you to stop: obscurin's role in epithelial cell migration.

Shultz KD, Al Anbari YF, Wright NT. Shultz KD, et al. Among authors: wright nt. Biochem Soc Trans. 2024 Aug 28;52(4):1947-1956. doi: 10.1042/BST20240564. Biochem Soc Trans. 2024. PMID: 39051125 Review.

3

Compound heterozygous variants in MYBPC1 lead to severe distal arthrogryposis type-1 manifestations.

Iyer A, Lauerova B, Mariano J, Haberlová J, Lassuthova P, Zidkova J, Wright NT, Kontrogianni-Konstantopoulos A. Iyer A, et al. Among authors: wright nt. Gene. 2024 Jun 5;910:148339. doi: 10.1016/j.gene.2024.148339. Epub 2024 Mar 2. Gene. 2024. PMID: 38438057

4

Prevention of Protease-Induced Degradation of Desmoplakin via Small Molecule Binding.

Romov IM, Nowzari RA, Page CP, Benes MR, Borzok MA, Wright NT. Romov IM, et al. Among authors: wright nt. J Pers Med. 2024 Jan 31;14(2):163. doi: 10.3390/jpm14020163. J Pers Med. 2024. PMID: 38392596 Free PMC article.

5

A Perspective on Developing Modeling and Image Analysis Tools to Investigate Mechanosensing Proteins.

Ouderkirk S, Sedley A, Ong M, Shifflet MR, Harkrider QC, Wright NT, Miller CJ. Ouderkirk S, et al. Among authors: wright nt. Integr Comp Biol. 2023 Dec 29;63(6):1532-1542. doi: 10.1093/icb/icad107. Integr Comp Biol. 2023. PMID: 37558388 Free PMC article.

6

Calpain Regulation and Dysregulation-Its Effects on the Intercalated Disk.

Yoder MW, Wright NT, Borzok MA. Yoder MW, et al. Among authors: wright nt. Int J Mol Sci. 2023 Jul 21;24(14):11726. doi: 10.3390/ijms241411726. Int J Mol Sci. 2023. PMID: 37511485 Free PMC article. Review.

7

The N-terminus of obscurin is flexible in solution.

Mauriello GE, Moncure GE, Nowzari RA, Miller CJ, Wright NT. Mauriello GE, et al. Among authors: wright nt. Proteins. 2023 Apr;91(4):485-496. doi: 10.1002/prot.26442. Epub 2022 Nov 4. Proteins. 2023. PMID: 36306263

8

Case Report: Two Families With HPDL Related Neurodegeneration.

Micule I, Lace B, Wright NT, Chrestian N, Strautmanis J, Diriks M, Stavusis J, Kidere D, Kleina E, Zdanovica A, Laflamme N, Rioux N, Setty ST, Pajusalu S, Droit A, Lek M, Rivest S, Inashkina I. Micule I, et al. Among authors: wright nt. Front Genet. 2022 Feb 9;13:780764. doi: 10.3389/fgene.2022.780764. eCollection 2022. Front Genet. 2022. PMID: 35222531 Free PMC article.

9

Somatic uniparental disomy mitigates the most damaging EFL1 allele combination in Shwachman-Diamond syndrome.

Lee S, Shin CH, Lee J, Jeong SD, Hong CR, Kim JD, Kim AR, Park B, Son SJ, Kokhan O, Yoo T, Ko JS, Sohn YB, Kim OH, Ko JM, Cho TJ, Wright NT, Seong JK, Jin SW, Kang HJ, Kim HH, Choi M. Lee S, et al. Among authors: wright nt. Blood. 2021 Nov 25;138(21):2117-2128. doi: 10.1182/blood.2021010913. Blood. 2021. PMID: 34115847 Free article.

10

Creating a 'Molecular Band-Aid'; Blocking an Exposed Protease Target Site in Desmoplakin.

Hoover CA, Ott KL, Manring HR, Dew T, Borzok MA, Wright NT. Hoover CA, et al. Among authors: wright nt. J Pers Med. 2021 May 12;11(5):401. doi: 10.3390/jpm11050401. J Pers Med. 2021. PMID: 34065787 Free PMC article.

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