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Cell Death Discovery (1)
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Showing 1–4 of 4 results

Advanced filters: Author: Christian A Scerri Clear advanced filters

Linkage disequilibrium narrows locus for venous malformation with glomus cells (VMGLOM) to a single 1.48 Mbp YAC

Alexandre Irrthum
Pascal Brouillard
Miikka Vikkula
Research12 Jan 2001
European Journal of Human Genetics

Volume: 9, P: 34-38
Genome-wide association study identifies 48 common genetic variants associated with handedness

A genome-wide association study of 1.7 million individuals identified 41 genetic variants associated with left-handedness and 7 associated with ambidexterity. The genetic correlation between the traits was low, thereby implying different aetiologies.

Gabriel Cuellar-Partida
Joyce Y. Tung
Sarah E. Medland
Research28 Sept 2020
Nature Human Behaviour

Volume: 5, P: 59-70
Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin

Sjaak Philipsen and colleagues report that haploinsufficiency for KLF1 causes hereditary persistence of fetal hemoglobin in a large Maltese family. They further show that KLF1 is a key activator of BCL11A, which suppresses the expression of fetal hemoglobin.

Joseph Borg
Petros Papadopoulos
Sjaak Philipsen
Research01 Aug 2010
Nature Genetics

Volume: 42, P: 801-805
Parthenolide prevents resistance of MDA-MB231 cells to doxorubicin and mitoxantrone: the role of Nrf2

Daniela Carlisi
Anna De Blasio
Giovanni Tesoriere
ResearchOpen Access04 Dec 2017
Cell Death Discovery

Volume: 3, P: 1-12