Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Teerapat Seeratanachot"'
Autor:
Narutchala Suwannakhon, Tanapat Pangeson, Teerapat Seeratanachot, Khwanruedee Mahingsa, Arunee Pingyod, Wanwipa Bumrungpakdee, Torpong Sanguansermsri
Publikováno v:
Hematology Reports, Vol 11, Iss 3 (2019)
We propose using a modified amplification refractory mutation system real-time polymerase chain reaction (ARMS RTPCR) technique to exclude the invasive prenatal diagnosis for a non-paternally inherited beta thalassemia mutation in couples atrisk for
Externí odkaz:
https://doaj.org/article/463bcc8535774717a2d3c21ee1e278ba
Autor:
Narutchala Suwannakhon, Khajohnsilp Pongsawatkul, Teerapat Seeratanachot, Khwanruedee Mahingsa, Arunee Pingyod, Wanwipa Bumrungpakdee, Torpong Sanguansermsri
Publikováno v:
Hematology Reports, Vol 10, Iss 2 (2018)
We propose antenatal blood tests using high-resolution DNA melting (HRM) analysis for beta thalassemia mutation detection after hemoglobin A2 estimation as a modified strategy for the identification of beta thalassemia at-risk couples. Antenatal bloo
Externí odkaz:
https://doaj.org/article/54ae9324c0a3489892c347f49618aeb0
Autor:
Narutchala Suwannakhon, Khajohnsilp Pongsawatkul, Teerapat Seeratanachot, Wirawan Rasri, Khwanruedee Mahingsa, Arunee Pingyod, Wanwipa Bumrungpakdee, Torpong Sanguansermsri
Publikováno v:
Thalassemia Reports, Vol 7, Iss 1 (2017)
We propose a fast-track strategy [direct blood DNA analysis using a quantitative real-time polymerase chain reaction (PCR) technique] for the early risk detection and prenatal diagnosis of α(0)-thalassemia (SEA and Thai deletion). Blood DNA samples
Externí odkaz:
https://doaj.org/article/a313a911cbba4d07800a5ba17384051d
Autor:
Khwanruedee Mahingsa, Torpong Sanguansermsri, Teerapat Seeratanachot, Arunee Pingyod, Khajohnsilp Pongsawatkul, Narutchala Suwannakhon, Wanwipa Bumrungpakdee
Publikováno v:
Hematology Reports; Volume 10; Issue 2; Pages: 7530
Hematology Reports
Hematology Reports, Vol 10, Iss 2 (2018)
Hematology Reports
Hematology Reports, Vol 10, Iss 2 (2018)
We propose antenatal blood tests using high-resolution DNA melting (HRM) analysis for beta thalassemia mutation detection after hemoglobin A2 estimation as a modified strategy for the identification of beta thalassemia at-risk couples. Antenatal bloo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45f93716514c798ef1e51bea0aef0029
Publikováno v:
Hemoglobin. 39:270-273
We assessed whether urinary DNA sediment was a feasible sample type for the molecular diagnosis of α-thalassemia (α-thal) mutations. Urine samples (5–10 mL) were collected from 218 male and female volunteers. The cells were centrifuged, and DNA w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f75fedda9c69824d51486a33afbe3fa5
https://doi.org/10.3109/03630269.2015.1040887
https://doi.org/10.3109/03630269.2015.1040887
Autor:
Khwanruedee Mahingsa, Wirawan Rasri, Teerapat Seeratanachot, Arunee Pingyod, Narutchala Suwannakhon, Wanwipa Bumrungpakdee, Khajohnsilp Pongsawatkul, Torpong Sanguansermsri
Publikováno v:
Thalassemia Reports, Vol 7, Iss 1 (2017)
Thalassemia Reports; Volume 7; Issue 1; Pages: 6620
Thalassemia Reports; Volume 7; Issue 1; Pages: 6620
We propose a fast-track strategy [direct blood DNA analysis using a quantitative real-time polymerase chain reaction (PCR) technique] for the early risk detection and prenatal diagnosis of α(0)-thalassemia (SEA and Thai deletion). Blood DNA samples
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e5e91c2efcffabb3b493e93f27c44b7
http://www.pagepressjournals.org/index.php/thal/article/view/6620
http://www.pagepressjournals.org/index.php/thal/article/view/6620
Autor:
Phanchana Sanguansermsri, Narutchala Suwanakhon, Tanapat Pangeson, Teerapat Seeratanachot, Torpong Sanguansermsri, Worasak Kaewkong, Khwanruedee Mahingsa, Metawee Srikummool
Publikováno v:
Genetics & Epigenetics
Genetics and Epigenetics, Vol 9 (2017)
Genetics and Epigenetics, Vol 9 (2017)
In the wild-type allele, DNA methylation levels of 10 consecutive CpG sites adjacent to the upstream 5′-breakpoint of α-thalassemia Southeast Asian (SEA) deletion are not different between placenta and leukocytes. However, no previous study has re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c97f1286c982c88ab2ef4496b6934d3
https://pubmed.ncbi.nlm.nih.gov/29162979
https://pubmed.ncbi.nlm.nih.gov/29162979
Publikováno v:
Hemoglobin. 37:574-583
We used quantitative real-time polymerase chain reaction (qPCR) and high resolution melting (HRM) analyses for the detection of the common α-thalassemia (α-thal) genotypes in 40 northern Thai Hb H (β4) patients. The α(0)-thal [- -(SEA) (Southeast
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1fc5db0d363449b5a2e32768e515dbe
https://doi.org/10.3109/03630269.2013.828228
https://doi.org/10.3109/03630269.2013.828228
Autor:
Narutchala, Suwannakhon, Teerapat, Seeratanachot, Khwanruedee, Mahingsa, Torpong, Sanguansermsri
Publikováno v:
Hemoglobin. 39(4)
We assessed whether urinary DNA sediment was a feasible sample type for the molecular diagnosis of α-thalassemia (α-thal) mutations. Urine samples (5-10 mL) were collected from 218 male and female volunteers. The cells were centrifuged, and DNA was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::85fef805ad0dc9ceb37b16a89b264be5
https://pubmed.ncbi.nlm.nih.gov/26016898
https://pubmed.ncbi.nlm.nih.gov/26016898
Publikováno v:
Southeast Asian Journal of Tropical Medicine & Public Health; Jan2015, Vol. 46 Issue 1, p110-110, 1p