Takol Chareonsirisuthigul
Overview
Explore the profile of Takol Chareonsirisuthigul including associated specialties, affiliations and a list of published articles.
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29
Citations
222
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Recent Articles
1.
Rattanapan Y, Nongwa K, Supanpong C, Satsadeedat C, Sai-Ong T, Kooltheat N, et al.
J Clin Med Res
. 2024 Dec;
16(11):536-546.
PMID: 39635336
Background: This study is designed to investigate the differential microRNA (miRNA) expression profiles in individuals with and without type 2 diabetes mellitus (T2DM). The focus is on miRNAs that play...
2.
Thangrua N, Siriboonpiputtana T, Rerkamnuaychoke B, Chareonsirisuthigul T, Korkiatsakul V, Pongphitcha P, et al.
Int J Lab Hematol
. 2024 Oct;
47(1):130-139.
PMID: 39357526
Introduction: Ph-like ALL has gene expression profile similar to Ph-positive ALL but without the BCR::ABL1 fusion. The disease presents higher rates of severe clinical features and is associated with unfavorable...
3.
Onsod P, Jaranasaksakul W, Chareonsirisuthigul T, Parinayok R, Rerkamnuaychoke B, Areesirisuk P
Eur J Obstet Gynecol Reprod Biol
. 2024 May;
298:31-34.
PMID: 38705011
Objective: This study evaluated the BACs-on-Beads™ (BoBs) efficiency assay in detecting chromosomal anomalies in products of conception (POC) specimens associated with anembryonic pregnancy (AP) among Thai pregnant women. Method: Retrospective...
4.
Rujirachaivej P, Siriboonpiputtana T, Luangwattananun P, Yuti P, Wutti-In Y, Choomee K, et al.
Clin Exp Med
. 2024 Apr;
24(1):90.
PMID: 38683232
Multiple myeloma (MM) is an incurable hematologic malignancy characterized by the rapid proliferation of malignant plasma cells within the bone marrow. Standard therapies often fail due to patient resistance. The...
5.
Prapasrat C, Onsod P, Korkiatsakul V, Rerkamnuaychoke B, Wattanasirichaigoon D, Chareonsirisuthigul T
J Pediatr Genet
. 2024 Jan;
12(4):273-279.
PMID: 38162164
Prader-Willi syndrome (PWS) is a genetic disorder caused by the expression disruption of genes on the paternally inherited allele of chromosome 15q11.2-q13. Apart from clinical diagnostic criteria, PWS is confirmed...
6.
Rattanapan Y, Narkpetch S, Chareonsirisuthigul T
Biomed Res Int
. 2023 Oct;
2023:5598590.
PMID: 37829050
Background: Packed red blood cells (PRBCs) can be preserved for 42 days, and stored PRBCs have slow, dangerous changes over time during storage. miRNA is approximately 22 nucleotides long, a...
7.
Parinayok R, Areesirisuk P, Chareonsirisuthigul T, Buchachat W, Rerkamnuaychoke B
Cytogenet Genome Res
. 2023 Mar;
162(7):345-353.
PMID: 36858029
Abortion is a common pregnancy complication. Fetuses with several types of chromosomal abnormalities are aborted during the first trimester, while others have a better chance of surviving. This research aims...
8.
Rattanapan Y, Charong N, Narkpetch S, Chareonsirisuthigul T
Hematol Transfus Cell Ther
. 2022 Oct;
45(4):449-455.
PMID: 36241527
Introduction: The para-Bombay phenotype, or H-deficient secretor, results from different mutations of the FUT1, with or without the FUT2 mutation. Consequently, there is an absent or weak expression of the...
9.
Rojanaporn D, Chitphuk S, Iemwimangsa N, Chareonsirisuthigul T, Saengwimol D, Aroonroch R, et al.
Transl Vis Sci Technol
. 2022 Sep;
11(9):30.
PMID: 36173648
Purpose: The study aimed to generate a stepwise method to reduce the workload of full-scale RB1 sequencing for germline mutation screening in retinoblastoma (RB) patients. The implication of germline mutation...
10.
Trachoo O, Yingchoncharoen T, Ngernsritrakul T, Iemwimangsa N, Panthan B, Klumsathian S, et al.
PLoS One
. 2022 Sep;
17(9):e0267770.
PMID: 36166435
Hypertrophic cardiomyopathy (HCM) and dilated cardiomyopathy (DCM) are the most common referrals in the Inherited Cardiovascular Condition (ICC) Genetics Service. Several issues must be discussed with patients and their families...