Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Sa-nga Pootrakul"'
Publikováno v:
Hemoglobin. 1:781-798
A healthy Thai male was found to have an abnormal hemoglobin moving faster than Hb A in starch-gel electrophoresis, in addition to the normal hemoglobin constituents. The abnormal hemoglobin constituted 28% of the whole hemoglobin. The subject was as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b3ddca3cf4ca9c04fd594a79d6983cba
https://doi.org/10.3109/03630267709003907
https://doi.org/10.3109/03630267709003907
Publikováno v:
Human Genetics. 29:121-126
In the Far East two types of alpha-thalassemia genes, namely alpha-thalassemia, (alpha-thal1), and alpha-thalassemia2 (alpha-thal2) exist. Definite diagnosis of the alpha-thal1 and alpha-thal2 traits is very difficult because their hematological find
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2210f36beeb34bbb7fc7ce3b16c36c3
https://doi.org/10.1007/bf00430348
https://doi.org/10.1007/bf00430348
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Protein Structure. 405:161-166
Four heterozygotes for a fast α-chain variant in a Thai family were detected on starch gel electrophoresis during a survey study on iron deficiency anaemia in a rural area not far from Bangkok. They were healthy and had normal haematological profile
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::102b62545ce463387ebd3206915bccec
https://doi.org/10.1016/0005-2795(75)90326-8
https://doi.org/10.1016/0005-2795(75)90326-8
Autor:
J. Paul, Sa-nga Pootrakul, Robert Williamson, Sergio Ottolenghi, Wong Hock Boon, Pritchard J, David J. Weatherall, J. B. Clegg, W G Lanyon
Publikováno v:
Nature. 251:389-392
Two independent groups show that the absence of all or part of the globin α-chain gene is the origin of the homozygous α thalassaemia.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d96afd8e17cb899664d9278d90ce5cff
https://doi.org/10.1038/251389a0
https://doi.org/10.1038/251389a0
Autor:
James F. Reynolds, Vanna Muang‐sup, John M. Optiz, Suthat Fucharoen, Sa-nga Pootrakul, Prawase Wasi
Publikováno v:
American journal of medical genetics. 29(1)
We describe hematologic data from 18 newborn infants including follow-up data. Of these, ten were the offspring of patients with beta-thal/Hb E disease and the remainder were infants who were found to have a decrease in red cell osmotic fragility dur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1bab0158762a4c4cd450340c2d23724e
https://pubmed.ncbi.nlm.nih.gov/2449818
https://pubmed.ncbi.nlm.nih.gov/2449818
Publikováno v:
Human Genetics. 23
A 28-year-old, healthy male of chinese ancestry with normal hematologic findings was found to have an abnormal hemoglobin moving more slowly than hemoglobin F in starch gel electrophoresis. The relative amounts of the abnormal component, hemoglobin A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a1d794b07d61fa21374f58b4a360f843
https://doi.org/10.1007/bf00285105
https://doi.org/10.1007/bf00285105
Publikováno v:
Biochemical and biophysical research communications. 64(2)
Thirteen adult and one newborn heterozygotes, and three homozygotes for hemoglobin Constant Spring were examined for globin chain synthesis. Reticulocytes from venous blood were incorporated with [3H]-leucine in an incubation mixture for 3 hours. Glo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2215b6a2c14a4f3ea184ae849708917
https://pubmed.ncbi.nlm.nih.gov/1147948
https://pubmed.ncbi.nlm.nih.gov/1147948
Publikováno v:
Nature. 223(5201)
HAEMOGLOBIN H disease is usually a mild to moderate, sometimes severe, thalassaemic disease, characterized by the presence of haemoglobin (Hb) H in addition to Hb A, and intraerythrocytic inclusion bodies1–3. Hb H is usually not detectable in eithe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1deaf50e25c061e5a6a57fb55cd8ab0
https://pubmed.ncbi.nlm.nih.gov/5792424
https://pubmed.ncbi.nlm.nih.gov/5792424