Shotelersuk V - Search Results

1

TIGIT Monoallelic Nonsense Variant in Patient with Severe COVID-19 Infection, Thailand.

Sodsai P, Ittiwut C, Ruenjaiman V, Ittiwut R, Jantarabenjakul W, Suphapeetiporn K, Shotelersuk V, Hirankarn N. Sodsai P, et al. Among authors: shotelersuk v. Emerg Infect Dis. 2022 Nov;28(11):2350-2352. doi: 10.3201/eid2811.220914. Epub 2022 Oct 3. Emerg Infect Dis. 2022. PMID: 36191906 Free PMC article.

2

PTEN c.511C>T nonsense mutation in a BRRS family disrupts a potential exonic splicing enhancer and causes exon skipping.

Suphapeetiporn K, Kongkam P, Tantivatana J, Sinthuwiwat T, Tongkobpetch S, Shotelersuk V. Suphapeetiporn K, et al. Among authors: shotelersuk v. Jpn J Clin Oncol. 2006 Dec;36(12):814-21. doi: 10.1093/jjco/hyl107. Epub 2006 Oct 16. Jpn J Clin Oncol. 2006. PMID: 17043057

3

Nonsense mutations of the CYBB gene in two Thai families with X-linked chronic granulomatous disease.

Vilaiphan P, Chatchatee P, Ngamphaiboon J, Tongkobpetch S, Suphapeetiporn K, Shotelersuk V. Vilaiphan P, et al. Among authors: shotelersuk v. Asian Pac J Allergy Immunol. 2007 Dec;25(4):243-7. Asian Pac J Allergy Immunol. 2007. PMID: 18402298 Free article.

4

Functional characterization of vasopressin receptor 2 mutations causing partial and complete congenital nephrogenic diabetes insipidus in Thai families.

Sahakitrungruang T, Tee MK, Rattanachartnarong N, Shotelersuk V, Suphapeetiporn K, Miller WL. Sahakitrungruang T, et al. Among authors: shotelersuk v. Horm Res Paediatr. 2010;73(5):349-54. doi: 10.1159/000308167. Epub 2010 Apr 14. Horm Res Paediatr. 2010. PMID: 20389105

5

HLA-B* 1502 screening: time to clinical practice.

Locharernkul C, Shotelersuk V, Hirankarn N. Locharernkul C, et al. Among authors: shotelersuk v. Epilepsia. 2010 May;51(5):936-8. doi: 10.1111/j.1528-1167.2010.02549.x. Epilepsia. 2010. PMID: 20536533 Free article. No abstract available.

6

Two siblings with a novel nonsense mutation, p.R50X, in the vitamin D receptor gene.

Supornsilchai V, Hiranras Y, Wacharasindhu S, Mahayosnond A, Suphapeetiporn K, Shotelersuk V. Supornsilchai V, et al. Among authors: shotelersuk v. Endocrine. 2011 Aug;40(1):62-6. doi: 10.1007/s12020-011-9450-9. Epub 2011 Mar 18. Endocrine. 2011. PMID: 21424181

7

Pharmacogenetic screening of carbamazepine-induced severe cutaneous allergic reactions.

Locharernkul C, Shotelersuk V, Hirankarn N. Locharernkul C, et al. Among authors: shotelersuk v. J Clin Neurosci. 2011 Oct;18(10):1289-94. doi: 10.1016/j.jocn.2010.12.054. Epub 2011 Jul 28. J Clin Neurosci. 2011. PMID: 21802305 Review.

8

Two novel CTNS mutations in cystinosis patients in Thailand.

Yeetong P, Tongkobpetch S, Kingwatanakul P, Deekajorndech T, Bernardini IM, Suphapeetiporn K, Gahl WA, Shotelersuk V. Yeetong P, et al. Among authors: shotelersuk v. Gene. 2012 May 15;499(2):323-5. doi: 10.1016/j.gene.2012.03.047. Epub 2012 Mar 16. Gene. 2012. PMID: 22450360 Free PMC article.

9

DcR3 mutations in patients with juvenile-onset systemic lupus erythematosus lead to enhanced lymphocyte proliferation.

Chokdeemeeboon C, Ammarinthnukrowh P, Tongkobpetch S, Srichomtong C, Deekajorndech T, Rianthavorn P, Kingwattanakul P, Avihingsanon Y, Wright HL, Akkahat P, Hoven VP, Mekboonsonglarp W, Edwards SW, Hirankarn N, Suphapeetiporn K, Shotelersuk V. Chokdeemeeboon C, et al. Among authors: shotelersuk v. J Rheumatol. 2013 Aug;40(8):1316-26. doi: 10.3899/jrheum.121285. Epub 2013 Jun 1. J Rheumatol. 2013. PMID: 23729807

10

FOXE1 mutations in Thai patients with oral clefts.

Srichomthong C, Ittiwut R, Siriwan P, Suphapeetiporn K, Shotelersuk V. Srichomthong C, et al. Among authors: shotelersuk v. Genet Res (Camb). 2013 Oct;95(5):133-7. doi: 10.1017/S0016672313000177. Epub 2013 Nov 20. Genet Res (Camb). 2013. PMID: 24252547

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