Search Results - "MUTIRANGURA, A"

Refine Results
  1. 1

    TRH site-specific methylation in oral and oropharyngeal squamous cell carcinoma by Puttipanyalears, C, Arayataweegool, A, Chalertpet, K, Rattanachayoto, P, Mahattanasakul, P, Tangjaturonsasme, N, Kerekhanjanarong, V, Mutirangura, A, Kitkumthorn, N

    Published in BMC cancer (06-08-2018)
    “…The incidence of oral squamous cell carcinoma (OSCC) continues to increase each year. Clinical examination and biopsy usually detect OSCC at an advanced stage…”
    Get full text
    Journal Article
  2. 2

    Investigation of PTEN promoter methylation in ameloblastoma by Lapthanasupkul, P, Klongnoi, B, Mutirangura, A, Kitkumthorn, N

    “…Phosphatase and tensin homolog (PTEN) acts as a tumor suppressor gene. Inactivation of PTEN has been reported in various types of cancers. PTEN promoter…”
    Get full text
    Journal Article
  3. 3

    LINE-1 methylation difference between ameloblastoma and keratocystic odontogenic tumor by Kitkumthorn, N, Mutirangura, A

    Published in Oral diseases (01-04-2010)
    “…Oral Diseases (2010) 16, 286–291 Objective:  Global hypomethylation is a common epigenetic event in cancer. Keratocystic odontogenic tumor (KCOT) and…”
    Get full text
    Journal Article
  4. 4

    Detection of global hypermethylation in well-differentiated thyroid neoplasms by immunohistochemical (5-methylcytidine) analysis by Keelawat, S., Thorner, P. S., Shuangshoti, S., Bychkov, A., Kitkumthorn, N., Rattanatanyong, P., Boonyayothin, W., Poumsuk, U., Ruangvejvorachai, P., Mutirangura, A.

    Published in Journal of endocrinological investigation (01-07-2015)
    “…Purpose While global hypomethylation of DNA has been found in several malignancies, studies on thyroid tumours have shown controversial results using different…”
    Get full text
    Journal Article
  5. 5

    Epstein-Barr Virus Infection-Associated Smooth-Muscle Tumors in Patients with AIDS by Suankratay, Chusana, Shuangshoti, Shanop, Mutirangura, Apiwat, Prasanthai, Vichit, Lerdlum, Sukalya, Shuangshoti, Somruetai, Pintong, Jarupan, Wilde, Henry

    Published in Clinical infectious diseases (15-05-2005)
    “…Background The aim of our study is to describe the unusual clinical manifestations of smooth-muscle tumors (SMTs) in patients with acquired immunodeficiency…”
    Get full text
    Journal Article
  6. 6

    Association of P53 codon 72 polymorphism and ameloblastoma by Kitkumthorn, N, Yanatatsaneejit, P, Rabalert, J, Dhammawipark, C, Mutirangura, A

    Published in Oral diseases (01-10-2010)
    “…Oral Diseases (2010) 16, 631–635 Objective:  To test the hypothesis that P53 codon 72 polymorphism was associated with an increased risk of developing…”
    Get full text
    Journal Article
  7. 7

    Serum/plasma viral DNA: mechanisms and diagnostic applications to nasopharyngeal and cervical carcinoma by Mutirangura, A

    Published in Annals of the New York Academy of Sciences (01-09-2001)
    “…Following reports describing circulating tumor DNA, serum/plasma viral nucleic acid has shown its potential as a new diagnostic target in cancer. In the…”
    Get full text
    Journal Article
  8. 8
  9. 9

    Southeast Asian origins of five Hill Tribe populations and correlation of genetic to linguistic relationships inferred with genome-wide SNP data by Listman, J.B., Malison, R.T., Sanichwankul, K., Ittiwut, C., Mutirangura, A., Gelernter, J.

    Published in American journal of physical anthropology (01-02-2011)
    “…In Thailand, the term Hill Tribe is used to describe populations whose members traditionally practice slash and burn agriculture and reside in the mountains…”
    Get full text
    Journal Article
  10. 10

    Stage specificity of Plasmodium falciparum telomerase and its inhibition by berberine by Sriwilaijareon, N, Petmitr, S, Mutirangura, A, Ponglikitmongkol, M, Wilairat, P

    Published in Parasitology international (01-03-2002)
    “…Telomerase activity in synchronized Plasmodium falciparum during its erythrocytic cycle was examined using the TRAP assay. Telomerase activity was detected at…”
    Get full text
    Journal Article
  11. 11

    Epstein-Barr viral DNA in serum of patients with nasopharyngeal carcinoma by MUTIRANGURA, A, PORNTHANAKASEM, W, THEAMBOONLERS, A, SRIURANPONG, V, LERTSANGUANSINCHI, P, YENRUDI, S, VORAVUD, N, SUPIYAPHUN, P, POOVORAWAN, Y

    Published in Clinical cancer research (01-03-1998)
    “…This study evaluated Epstein-Barr virus (EBV) DNA in sera of 42 patients with nasopharyngeal carcinoma (NPC) and 82 healthy individuals who had been infected…”
    Get full text
    Journal Article
  12. 12

    High frequency of mutation of epidermal growth factor receptor in lung adenocarcinoma in Thailand by Sriuranpong, V., Chantranuwat, C., Huapai, N., Chalermchai, T., Leungtaweeboon, K., Lertsanguansinchai, P., Voravud, N., Mutirangura, A.

    Published in Cancer letters (08-08-2006)
    “…Recent reports have suggested influences of racial difference on the frequency of mutation of EGFR in lung cancer. We therefore sought to characterize the…”
    Get full text
    Journal Article
  13. 13
  14. 14

    LINE-1 hypomethylation level as a potential prognostic factor for epithelial ovarian cancer by Pattamadilok, J, Huapai, N, Rattanatanyong, P, Vasurattana, A, Triratanachat, S, Tresukosol, D, Mutirangura, A

    “…A genome-wide hypomethylation is a common and crucial event in cancer. This study was to evaluate common epithelial ovarian cancer (EOC) if long interspersed…”
    Get more information
    Journal Article
  15. 15

    Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patients by CHRISTIAN, S. L, ROBINSON, W. P, HUANG, B, MUTIRANGURA, A, LINE, M. R, NAKAO, M, SURTI, U, CHAKRAVARTI, A, LEDBETTER, D. H

    Published in American journal of human genetics (01-07-1995)
    “…Prader-Willi syndrome (PWS) and Angelman syndrome (AS) are distinct mental retardation syndromes caused by paternal and maternal deficiencies, respectively, in…”
    Get full text
    Journal Article
  16. 16

    Molecular characterisation of four cases of intrachromosomal triplication of chromosome 15q11-q14 by Ungaro, Paola, Christian, Susan L, Fantes, Judy A, Mutirangura, Apiwat, Black, Susan, Reynolds, James, Malcolm, Sue, Dobyns, William B, Ledbetter, David H

    Published in Journal of medical genetics (01-01-2001)
    “…CONTEXT Chromosomal abnormalities that involve the proximal region of chromosome 15q occur relatively frequently in the human population. However, interstitial…”
    Get full text
    Journal Article
  17. 17

    Genomic alterations in nasopharyngeal carcinoma: loss of heterozygosity and Epstein-Barr virus infection by MUTIRANGURA, A, TANUNYUTTHAWONGESE, C, PORNTHANAKASEM, W, KEREKHANJANARONG, V, SRIURANPONG, V, YENRUDI, S, SUPLYAPHUN, P, VORAVUD, N

    Published in British journal of cancer (01-09-1997)
    “…Nasopharyngeal carcinoma is a subset of head and neck squamous cell cancers with unique endemic distribution and aetiological co-factors. Epstein-Barr virus…”
    Get full text
    Journal Article
  18. 18

    Telomerase activity and human papillomavirus in malignant, premalignant and benign cervical lesions by MUTIRANGURA, A, SRIURANPONG, V, TERMRUNGGRAUNGLERT, W, TRESUKOSOL, D, LERTSAGUANSINCHAI, P, VORAVUD, N, NIRUTHISARD, S

    Published in British journal of cancer (01-10-1998)
    “…The purpose of this study was to define a correlation between telomerase activity and human papillomavirus (HPV) in normal control tissue and in benign,…”
    Get full text
    Journal Article
  19. 19

    Role of human papillomavirus DNA testing in management of women with atypical squamous cells of undetermined significance by Kiatpongsan, S, Niruthisard, S, Mutirangura, A, Trivijitsilp, P, Vasuratna, A, Chaithongwongwatthana, S, Lertkhachonsuk, R

    “…To find the sensitivity, specificity, and positive and negative predictive values of the high-risk group human papillomavirus (HPV) DNA testing as a triage…”
    Get more information
    Journal Article
  20. 20

    Nondisjunction of chromosome 15 : origin and recombination by ROBINSON, W. P, BERNASCONI, F, MUTIRANGURA, A, LEDBETTER, D. H, LANGLOIS, S, MALCOLM, S, MORRIS, M. A, SCHINZEL, A. A

    Published in American journal of human genetics (01-09-1993)
    “…Thirty-two cases of uniparental disomy (UPD), ascertained from Prader-Willi syndrome patients (N = 27) and Angelman syndrome patients (N = 5), are used to…”
    Get full text
    Journal Article