The Molecular Basis of β-Thalassemia

Por Thein, Swee Lay
Publicado em 2013

Anemia in the elderly: clinical implications and new therapeutic concepts

Por Stauder, Reinhard, Thein, Swee Lay
Publicado em 2014

The 12.6 kb-deletion in the β-globin gene cluster is the known Thai/Vietnamese (δβ)(0)-thalassemia commonly found in Southeast Asia

Por Chalaow, Nipon, Thein, Swee Lay, Viprakasit, Vip
Publicado em 2013

Selection of housekeeping genes for gene expression studies in human reticulocytes using real-time PCR

Por Silver, Nicholas, Best, Steve, Jiang, Jie, Thein, Swee Lay
Publicado em 2006

Control of fetal hemoglobin: new insights emerging from genomics and clinical implications

Por Thein, Swee Lay, Menzel, Stephan, Lathrop, Mark, Garner, Chad
Publicado em 2009

The effect of Duffy antigen receptor for chemokines on severity in sickle cell disease

Por Drasar, Emma R., Menzel, Stephan, Fulford, Tony, Thein, Swee Lay
Publicado em 2013

Experimental Generation of SNP Haplotype Signatures in Patients with Sickle Cell Anaemia

Por Menzel, Stephan, Qin, Jian, Vasavda, Nisha, Thein, Swee Lay, Ramakrishnan, Ramesh
Publicado em 2010

Evidence of Genetic Interaction between the β-Globin Complex and Chromosome 8q in the Expression of Fetal Hemoglobin

Por Garner, Chad P., Tatu, Thanusak, Best, Steve, Creary, Lisa, Thein, Swee Lay
Publicado em 2002

Genome annotation of a 1.5 Mb region of human chromosome 6q23 encompassing a quantitative trait locus for fetal hemoglobin expression in adults

Por Close, James, Game, Laurence, Clark, Barnaby, Bergounioux, Jean, Gerovassili, Ageliki, Thein, Swee Lay
Publicado em 2004

Association between hemolysis and albuminuria in adults with sickle cell anemia

Por Day, Thomas G., Drasar, Emma R., Fulford, Tony, Sharpe, Claire C., Thein, Swee Lay
Publicado em 2012

Adult patients with Eisenmenger syndrome report flying safely on commercial airlines

Por Broberg, Craig S, Uebing, Anselm, Cuomo, Linda, Thein, Swee Lay, Papadopoulos, Michael G, Gatzoulis, Michael A
Publicado em 2007

Genetic variants at HbF‐modifier loci moderate anemia and leukocytosis in sickle cell disease in Tanzania

Por Mtatiro, Siana Nkya, Makani, Julie, Mmbando, Bruno, Thein, Swee Lay, Menzel, Stephan, Cox, Sharon E.
Publicado no Am J Hematol (2014)

The clinical significance of K-Cl cotransport activity in red cells of patients with HbSC disease

Por Rees, David C., Thein, Swee Lay, Osei, Anna, Drasar, Emma, Tewari, Sanjay, Hannemann, Anke, Gibson, John S
Publicado no Haematologica (2015)

Genetic Regulation of Fetal Haemoglobin in Inherited Bone Marrow Failure Syndromes

Por Alter, Blanche P, Rosenberg, Philip S, Day, Thomas, Menzel, Stephan, Giri, Neelam, Savage, Sharon A, Thein, Swee Lay
Publicado em 2013

Interim assessment of liver damage in patients with sickle cell disease using new non-invasive techniques

Por Drasar, Emma, Fitzpatrick, Emer, Gardner, Kate, Awogbade, Moji, Dhawan, Anil, Bomford, Adrian, Suddle, Abid, Thein, Swee Lay
Publicado no Br J Haematol (2016)

Response of iron overload to deferasirox in rare transfusion-dependent anaemias: equivalent effects on serum ferritin and labile plasma iron for haemolytic or production anaemias

Por Porter, John B, Lin, Kai-Hsin, Beris, Photis, Forni, Gian Luca, Taher, Ali, Habr, Dany, Domokos, Gabor, Roubert, Bernard, Thein, Swee Lay
Publicado em 2011

Genetic Variation on Chromosome 6 Influences F Cell Levels in Healthy Individuals of African Descent and HbF Levels in Sickle Cell Patients

Por Creary, Lisa E., Ulug, Pinar, Menzel, Stephan, McKenzie, Colin A., Hanchard, Neil A., Taylor, Veronica, Farrall, Martin, Forrester, Terrence E., Thein, Swee Lay
Publicado em 2009

Extracranial internal carotid arterial disease in children with sickle cell anemia

Por Deane, Colin R., Goss, David, Bartram, Jack, Pohl, Keith R.E., Height, Susan E., Sibtain, Naomi, Jarosz, Jozef, Thein, Swee Lay, Rees, David C.
Publicado em 2010

Reversible binding of hemoglobin to band 3 constitutes the molecular switch that mediates O(2) regulation of erythrocyte properties

Por Chu, Haiyan, McKenna, Mary M., Krump, Nathan A., Zheng, Suilan, Mendelsohn, Laurel, Thein, Swee Lay, Garrett, Lisa J., Bodine, David M., Low, Philip S.
Publicado no Blood (2016)

A randomized Phase I/II Trial of HQK-1001, an oral fetal globin gene inducer, in β–thalassaemia intermedia and HbE/β–thalassaemia

Por Fucharoen, Suthat, Inati, Adlette, Siritanaratku, Noppadol, Thein, Swee Lay, Wargin, William C., Koussa, Suzanne, Taher, Ali, Chaneim, Nattawara, Boosalis, Michael, Berenson, Ronald, Perrine, Susan P.
Publicado em 2013