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Items: 23

1.

Clinical and functional studies of two novel variants in the LPL gene in subjects with severe hypertriglyceridemia.

Plengpanich W, Kiateprungvej A, Charoen S, Khovidhunkit W.

Clin Chim Acta. 2018 Dec;487:22-27. doi: 10.1016/j.cca.2018.08.041. Epub 2018 Sep 1.

PMID:
30179614
2.

Rare and common variants in LPL and APOA5 in Thai subjects with severe hypertriglyceridemia: A resequencing approach.

Khovidhunkit W, Charoen S, Kiateprungvej A, Chartyingcharoen P, Muanpetch S, Plengpanich W.

J Clin Lipidol. 2016 May-Jun;10(3):505-511.e1. doi: 10.1016/j.jacl.2015.11.007. Epub 2015 Nov 17.

PMID:
27206937
3.

Apolipoprotein A-V is not a major determinant of triglyceride levels during human sepsis.

Ngaosuwan K, Houngngam N, Limpisook P, Plengpanich W, Khovidhunkit W.

J Crit Care. 2015 Aug;30(4):727-31. doi: 10.1016/j.jcrc.2015.03.026. Epub 2015 Apr 8.

PMID:
25896654
4.

ABCG1 is involved in vitamin E efflux.

Olivier M, BottG R, Frisdal E, Nowick M, Plengpanich W, Desmarchelier C, Roi S, Quinn CM, Gelissen I, Jessup W, Van Eck M, Guérin M, Le Goff W, Reboul E.

Biochim Biophys Acta. 2014 Dec;1841(12):1741-51.

PMID:
25462452
5.

Adipocyte ATP-binding cassette G1 promotes triglyceride storage, fat mass growth, and human obesity.

Frisdal E, Le Lay S, Hooton H, Poupel L, Olivier M, Alili R, Plengpanich W, Villard EF, Gilibert S, Lhomme M, Superville A, Miftah-Alkhair L, Chapman MJ, Dallinga-Thie GM, Venteclef N, Poitou C, Tordjman J, Lesnik P, Kontush A, Huby T, Dugail I, Clement K, Guerin M, Le Goff W.

Diabetes. 2015 Mar;64(3):840-55. doi: 10.2337/db14-0245. Epub 2014 Sep 23.

6.

Multimerization of glycosylphosphatidylinositol-anchored high density lipoprotein-binding protein 1 (GPIHBP1) and familial chylomicronemia from a serine-to-cysteine substitution in GPIHBP1 Ly6 domain.

Plengpanich W, Young SG, Khovidhunkit W, Bensadoun A, Karnman H, Ploug M, Gårdsvoll H, Leung CS, Adeyo O, Larsson M, Muanpetch S, Charoen S, Fong LG, Niramitmahapanya S, Beigneux AP.

J Biol Chem. 2014 Jul 11;289(28):19491-9. doi: 10.1074/jbc.M114.558528. Epub 2014 May 20.

7.

Improved plasma cholesterol efflux capacity from human macrophages in patients with hyperalphalipoproteinemia.

El Khoury P, Plengpanich W, Frisdal E, Le Goff W, Khovidhunkit W, Guerin M.

Atherosclerosis. 2014 May;234(1):193-9. doi: 10.1016/j.atherosclerosis.2014.02.032. Epub 2014 Mar 12.

PMID:
24674903
8.

Up-regulation of the ATP-binding cassette transporter A1 inhibits hepatitis C virus infection.

Bocchetta S, Maillard P, Yamamoto M, Gondeau C, Douam F, Lebreton S, Lagaye S, Pol S, Helle F, Plengpanich W, Guérin M, Bourgine M, Michel ML, Lavillette D, Roingeard P, le Goff W, Budkowska A.

PLoS One. 2014 Mar 19;9(3):e92140. doi: 10.1371/journal.pone.0092140. eCollection 2014.

9.

Functional characterization of novel variants in the CETP promoter and the LIPC gene in subjects with hyperalphalipoproteinemia.

Plengpanich W, Tongkobpetch S, Shotelersuk V, Le Goff W, Khovidhunkit W.

Clin Chim Acta. 2013 Feb 1;416:92-5. doi: 10.1016/j.cca.2012.11.024. Epub 2012 Dec 5.

PMID:
23219720
10.

Resequencing CETP, LIPC and LIPG genes in Thai subjects with hyperalphalipoproteinemia.

Khovidhunkit W, Chartyingcharoen P, Siriwong S, Limumpornpetch P, Plengpanich W.

Am J Cardiol. 2012 Jul 1;110(1):62-6. doi: 10.1016/j.amjcard.2012.02.052. Epub 2012 Mar 29.

PMID:
22464213
11.

Retinol-binding protein 4 is not associated with insulin resistance in pregnancy.

Khovidhunkit W, Pruksakorn P, Plengpanich W, Tharavanij T.

Metabolism. 2012 Jan;61(1):65-9. doi: 10.1016/j.metabol.2011.05.019. Epub 2011 Jul 7.

PMID:
21741059
12.

CETP deficiency due to a novel mutation in the CETP gene promoter and its effect on cholesterol efflux and selective uptake into hepatocytes.

Plengpanich W, Le Goff W, Poolsuk S, Julia Z, Guerin M, Khovidhunkit W.

Atherosclerosis. 2011 Jun;216(2):370-3. doi: 10.1016/j.atherosclerosis.2011.01.051. Epub 2011 Feb 26.

PMID:
21354572
13.

Concurrent bilateral pheochromocytoma and thoracic paraganglioma during pregnancy.

Snabboon T, Plengpanich W, Houngngam N, Buranasupkajorn P, Plengvidhya N, Sereepapong W, Sunthornyothin S, Shotelersuk V.

Endocrine. 2010 Apr;37(2):261-4. doi: 10.1007/s12020-009-9292-x. Epub 2010 Jan 5.

PMID:
20960261
14.

Two novel mutations and functional analyses of the CETP and LIPC genes underlying severe hyperalphalipoproteinemia.

Plengpanich W, Siriwong S, Khovidhunkit W.

Metabolism. 2009 Aug;58(8):1178-84. doi: 10.1016/j.metabol.2009.03.020. Epub 2009 Jun 18.

PMID:
19428034
15.

Bilateral pheochromocytoma during the postpartum period.

Wattanachanya L, Bunworasate U, Plengpanich W, Houngngam N, Buranasupkajorn P, Sunthornyothin S, Shotelersuk V, Snabboon T.

Arch Gynecol Obstet. 2009 Dec;280(6):1055-8. doi: 10.1007/s00404-009-1057-5. Epub 2009 Apr 2.

PMID:
19340440
16.

Normal reference range of serum insulin-like growth factor (IGF)-I in healthy Thai adults.

Plengpanich W, Mangkala J, Buranasukajorn P, Boonruang K, Sunthornyothin S, Suwanwalaikorn S, Khovidhunkit W, Sridama V, Snabboon T.

J Med Assoc Thai. 2008 Nov;91(11):1681-4.

PMID:
19127789
17.

Two common and three novel PDS mutations in Thai patients with Pendred syndrome.

Snabboon T, Plengpanich W, Saengpanich S, Sirisalipoch S, Keelawat S, Sunthornyothin S, Khovidhunkit W, Suwanwalaikorn S, Sridama V, Shotelersuk V.

J Endocrinol Invest. 2007 Dec;30(11):907-13.

PMID:
18250610
18.

A novel SPINK1 gene mutation, c.206C>T, in a Thai patient with chronic alcoholic pancreatitis.

Rerknimitr R, Shotelersuk V, Buranasupkajorn P, Plengpanich W, Snabboon T.

JOP. 2008 Jan 8;9(1):33-6.

19.

A novel germline mutation, IVS4+1G>A, of the POU1F1 gene underlying combined pituitary hormone deficiency.

Snabboon T, Plengpanich W, Buranasupkajorn P, Khwanjaipanich R, Vasinanukorn P, Suwanwalaikorn S, Khovidhunkit W, Shotelersuk V.

Horm Res. 2008;69(1):60-4. Epub 2007 Dec 4.

PMID:
18059085
20.

Effects of human apolipoprotein A-I on endotoxin-induced leukocyte adhesion on endothelial cells in vivo and on the growth of Escherichia coli in vitro.

Thaveeratitham P, Plengpanich W, Naen-Udorn W, Patumraj S, Khovidhunkit W.

J Endotoxin Res. 2007;13(1):58-64.

PMID:
17621547
21.

A SPINK1 gene mutation in a Thai patient with fibrocalculous pancreatic diabetes.

Snabboon T, Plengpanich W, Sridama V, Sunthornyothin S, Suwanwalaikorn S, Khovidhunkit W.

Southeast Asian J Trop Med Public Health. 2006 May;37(3):559-62.

PMID:
17120980
22.

A germline mutation in a Thai family with familial multiple endocrine neoplasia type 1.

Snabboon T, Plengpanich W, Shotelersuk V, Sirisalipoch S, Nonthasoot B, Sirichindakul B, Wisedopas N, Suwanwalaikorn S.

J Med Assoc Thai. 2005 Feb;88(2):191-5.

PMID:
15962670
23.

A novel germline mutation, 1793delG, of the MEN1 gene underlying multiple endocrine neoplasia type 1.

Snabboon T, Plengpanich W, Siriwong S, Wisedopas N, Suwanwalaikorn S, Khovidhunkit W, Shotelersuk V.

Jpn J Clin Oncol. 2005 May;35(5):280-2. Epub 2005 May 13.

PMID:
15894711

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