Laurette Morlé
Université Claude Bernard Lyon 1(FR)Centre National de la Recherche Scientifique(FR)Inserm(FR)Institut NeuroMyoGène(FR)
Publications by Year
Research Areas
Erythrocyte Function and Pathophysiology, Blood properties and coagulation, Hemoglobinopathies and Related Disorders, Blood groups and transfusion, Caveolin-1 and cellular processes
Most-Cited Works
- Severe hereditary spherocytosis and distal renal tubular acidosis associated with the total absence of band 3.(2000)
- → Transcriptional control of genes involved in ciliogenesis: a first step in making cilia(2010)166 cited
- → RFX3 governs growth and beating efficiency of motile cilia in mouse and controls the expression of genes involved in human ciliopathies(2009)125 cited
- → Low expression allele alpha LELY of red cell spectrin is associated with mutations in exon 40 (alpha V/41 polymorphism) and intron 45 and with partial skipping of exon 46.(1993)106 cited
- → The Ciliogenic Transcription Factor RFX3 Regulates Early Midline Distribution of Guidepost Neurons Required for Corpus Callosum Development(2012)80 cited
- → RFX2 Is a Major Transcriptional Regulator of Spermiogenesis(2015)80 cited
- Hereditary spherocytosis: from clinical to molecular defects.(1998)