PMC Links for Nucleotide (Select 1519246137) - PMC

Select item 59964551.

Emerging roles of TRIO and F-actin-binding protein in human diseases

Sungjin Park, Hyunji Lee, Minhee Kim, Jisoo Park, Seon-Hwan Kim, Jongsun Park

Cell Commun Signal. 2018; 16: 29. Published online 2018 Jun 11. doi: 10.1186/s12964-018-0237-y

PMCID:: PMC5996455

Select item 58977102.

Localization and functional consequences of a direct interaction between TRIOBP-1 and hERG proteins in the heart

David K. Jones, Ashley C. Johnson, Elon C. Roti Roti, Fang Liu, Rebecca Uelmen, Rebecca A. Ayers, Istvan Baczko, David J. Tester, Michael J. Ackerman, Matthew C. Trudeau, Gail A. Robertson

J Cell Sci. 2018 Mar 15; 131(6): jcs206730. doi: 10.1242/jcs.206730

PMCID:: PMC5897710

Abstract Article

Select item 57121753.

Whole exome sequencing identifies TRIOBP pathogenic variants as a cause of post-lingual bilateral moderate-to-severe sensorineural hearing loss

Agnieszka Pollak, Urszula Lechowicz, Victor Abel Murcia Pieńkowski, Piotr Stawiński, Joanna Kosińska, Henryk Skarżyński, Monika Ołdak, Rafał Płoski

BMC Med Genet. 2017; 18: 142. Published online 2017 Dec 2. doi: 10.1186/s12881-017-0499-z

PMCID:: PMC5712175

Abstract Article PDF–731K

Select item 54654844.

An unpredicted aggregation-critical region of the actin-polymerizing protein TRIOBP-1/Tara, determined by elucidation of its domain structure

Nicholas J. Bradshaw, Antony S. K. Yerabham, Rita Marreiros, Tao Zhang, Luitgard Nagel-Steger, Carsten Korth

J Biol Chem. 2017 Jun 9; 292(23): 9583–9598. Published online 2017 Apr 24. doi: 10.1074/jbc.M116.767939

PMCID:: PMC5465484

Abstract Article PDF–4.1M

Select item 65394815.

Molecular Signature of Prospero Homeobox 1 (PROX1) in Follicular Thyroid Carcinoma Cells

Magdalena Rudzińska, Małgorzata Grzanka, Anna Stachurska, Michał Mikula, Katarzyna Paczkowska, Tomasz Stępień, Agnieszka Paziewska, Jerzy Ostrowski, Barbara Czarnocka

Int J Mol Sci. 2019 May; 20(9): 2212. Published online 2019 May 5. doi: 10.3390/ijms20092212

PMCID:: PMC6539481

Abstract Article PDF–7.3M

Select item 50726256.

A Large Genome-Wide Association Study of Age-Related Hearing Impairment Using Electronic Health Records

Thomas J. Hoffmann, Bronya J. Keats, Noriko Yoshikawa, Catherine Schaefer, Neil Risch, Lawrence R. Lustig

PLoS Genet. 2016 Oct; 12(10): e1006371. Published online 2016 Oct 20. doi: 10.1371/journal.pgen.1006371

PMCID:: PMC5072625

Abstract Article PDF–3.7M

Select item 45814127.

Screening of genetic alterations related to non-syndromic hearing loss using MassARRAY iPLEX® technology

Maria Carolina CCosta CMelo Svidnicki, Sueli Matilde Silva-Costa, Priscila Zonzini Ramos, Nathalia Zocal Pereira dos Santos, Fábio Tadeu Arrojo Martins, Arthur Menino Castilho, Edi Lúcia Sartorato

BMC Med Genet. 2015; 16: 85. Published online 2015 Sep 23. doi: 10.1186/s12881-015-0232-8

PMCID:: PMC4581412

Abstract Article PDF–759K

Select item 36362078.

Prevalence of p.V37I Variant of GJB2 in Mild or Moderate Hearing Loss in a Pediatric Population and the Interpretation of Its Pathogenicity

So Young Kim, Gibeom Park, Kyu-Hee Han, Ahreum Kim, Ja-Won Koo, Sun O. Chang, Seung Ha Oh, Woong-Yang Park, Byung Yoon Choi

PLoS One. 2013; 8(4): e61592. Published online 2013 Apr 25. doi: 10.1371/journal.pone.0061592

PMCID:: PMC3636207

Abstract Article PDF–737K

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