Results 191 to 200 of about 42,097 (242)

A Rare Case of Acute Hemolysis After Rasburicase Infusion. [PDF]

J Adv Pract Oncol
Broadway-Duren JB, Gardiner TP.
europepmc   +1 more source

PR inhibition stimulates G6PD expression to enhance malignancy in luminal breast cancer. [PDF]

Cell Death Dis
Jeong JW, Lee J, Bae SJ, Cha YJ, Fang S, Lee HK, Ahn SG.   +6 more
europepmc   +1 more source

IL21-STAT3 controls the pentose phosphate pathway to support metabolic reprogramming and tumor progression in chronic lymphocytic leukemia. [PDF]

Hemasphere
Del Prete R, Tusha V, Simon-Molas H, Gazziero VA, Nardi F, Drago R, Bartolini G, Licastro D, Malchiodi M, Mariottini C, Marotta G, Caravagna G, Bruscoli S, Eldering E, Gozzetti A, Bocchia M, Kabanova A.   +16 more
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Incorporating G6PD genotyping to identify patients with G6PD deficiency

Pharmacogenetics and Genomics, 2021
Glucose-6-phosphate-dehydrogenase (G6PD) deficiency is a common X-linked enzyme disorder associated with hemolytic anemia after exposure to fava beans or certain medications. Activity testing is the gold standard for detecting G6PD deficiency; however, this test is affected by various hematologic parameters.
Sarah A, Morris, Kristine R, Crews, Randall T, Hayden, Clifford M, Takemoto, Wenjian, Yang, Donald K, Baker, Ulrich, Broeckel, Mary V, Relling, Cyrine E, Haidar   +8 more
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Definition of the Mutations of G6PD Wayne, G6PD Viangchan, G6PD Jammu, and G6PD ‘Lejeune’

Acta Haematologica, 1991
We report the nucleotide (nt) substitutions of four unrelated glucose-6-phosphate dehydrogenase (G6PD)-deficient males. Only the mutation of G6PD Wayne was unique. It was a nt 769 C----G substitution causing a deduced substitution of glycine for arginine at amino acid 257.
E, Beutler, B, Westwood, W, Kuhl
openaire   +2 more sources

G6PD deficiency

JAAPA, 2019
ABSTRACT Although glucose-6-phosphate dehydrogenase (G6PD) deficiency is less known in Western countries than in the Middle East and Africa, global migration and immigration are bringing ethnic groups with the highest incidence of this inherited genetic disorder into the US healthcare system.
Susan J, Harcke, Denise, Rizzolo, H Theodore, Harcke   +2 more
openaire   +3 more sources

Three new G6PD variants, G6PD Adana, G6PD Samanda?, and G6PD Balcali in �ukurova, Turkey

Human Genetics, 1987
Glucose-6-phosphate dehydrogenase (G6PD) enzyme from cases known to be completely or mildly deficient were analyzed. The enzymes were purified from blood samples by utilizing DEAE-52 cellulose pH 7.0 column chromatography and ammonium sulphate precipitation.
Aksoy K., Yüregir G.T., Dikmen N., Ünlükurt I.   +3 more
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G6PD Murcia, G6PD Ube and G6PD Orissa: Report of three G6PD mutations unusual for Italian population

Clinical Biochemistry, 2010
No ...
Minucci, Angelo, Antenucci, Mirca, Giardina, Bruno, Zuppi, Cecilia, Capoluongo, Ettore Domenico   +4 more
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Characterization of a New G6PD Variant: G6PD Titusville

The American Journal of the Medical Sciences, 1989
We describe a new glucose-6-phosphate dehydrogenase mutant, G-6-PD Titusville. The propositus is a 7-month-old black male infant with a transient hemolytic episode. The mutant enzyme is characterized by abnormal electrophoretic mobility, thermolability, Km for NADP, abnormal deamino NADP use and a decreased sensitivity to inhibition by NADPH.
M, Csepreghy, M K, Hall, R L, Berkow, S, Jackson, J T, Prchal   +4 more
openaire   +2 more sources