Results 181 to 190 of about 965,280 (210)

Letter to the Editor Based on Article "Analysis of Genotype-Phenotype Correlation in Patients With α-Thalassemia From Fujian Province, Southeastern China". [PDF]

J Clin Lab Anal
Arash M.
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G-quadruplex stabilizer CX-5461 effectively combines with radiotherapy to target α-thalassemia/mental retardation X-linked-deficient malignant glioma. [PDF]

Neuro Oncol
Dharmaiah S, Malgulwar PB, Johnson WE, Chen BA, Sharin V, Whitfield BT, Alvarez C, Tadimeti V, Farooqi AS, Huse JT.   +9 more
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Pseudogaucher cells in a patient with α-thalassemia minor and S-hemoglobin carrier. [PDF]

Hematol Transfus Cell Ther
Roldán Galiacho V, Moreno Gamiz M, García-Ruiz JC.   +2 more
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Routine antenatal molecular testing for α-thalassemia at a tertiary referral hospital in China: ten years of experience. [PDF]

Front Genet
Li D, Liang L, Meng D, He S.
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Support Vector Machine-Based Formula for Detecting Suspected α Thalassemia Carriers: A Path toward Universal Screening. [PDF]

Int J Mol Sci
Lachover-Roth I, Peretz S, Zoabi H, Harel E, Livshits L, Filon D, Levin C, Koren A.   +7 more
europepmc   +1 more source

Ancestry of the major long-range regulatory site of the α-globin genes in the Portuguese population with the common 3.7 kb α-thalassemia deletion. [PDF]

Mol Biol Rep
Pena R, Lopes P, Gaspar G, Miranda A, Faustino P.   +4 more
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Case Report: Acute hepatitis A virus infection presenting with direct antiglobulin test-negative autoimmune hemolytic anemia and α-thalassemia trait. [PDF]

F1000Res
Debbabi H, Chakroun E, Hassine H, Kchir H, Cherif D, Yacoub H, Maamouri N.   +6 more
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Use of HSC-targeted LNP to generate a mouse model of lethal α-thalassemia and treatment via lentiviral gene therapy.

Blood
Chappell ME, Breda L, Tricoli L, Guerra A, Jarocha D, Castruccio Castracani C, Papp TE, Tanaka N, Hamilton N, Triebwasser MP, Ghiaccio V, Fedorky MT, Gollomp KL, Bochenek V, Roche AM, Everett JK, Cook EJ, Bushman FD, Teawtrakul N, Glentis S, Kattamis A, Mui BL, Tam YK, Weissman D, Abdulmalik O, Parhiz H, Rivella S.   +26 more
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Rapid and simultaneous detection of β- thalassemia point mutations by reverse hybridization strip assay among Egyptian patients

Journal of Biochemistry, Microbiology and Biotechnology, 2016
Thalassemia is a wide range hereditary disease with high incidence in Egypt along with the high frequency of consanguineous marriages. Investigation the heterogeneity, molecular basis, and natural history are the most effective methods to deal with the thalassemia to develop effective method for management and prevention including the prenatal ...
Osama Shalaan, Moustafa Sakr, Ahmed Daif, Khalil Elhalfawy   +3 more
openaire   +1 more source