A Novel Mutation in Isoform 3 of the Plasma Membrane Ca2+Pump Impairs Cellular Ca2+Homeostasis in a Patient with Cerebellar Ataxia and Laminin Subunit 1α Mutations

Mutations in LAMA1 Cause Cerebellar Dysplasia and Cysts with and without Retinal Dystrophy

(2014) Kimberly A. Aldinger et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Neuronal calcium signaling: function and dysfunction

(2014) Marisa Brini et al.   CELLULAR AND MOLECULAR LIFE SCIENCES

The Plasma Membrane Calcium Pump: New Ways to Look at an Old Enzyme

(2014) Raffaele Lopreiato et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Loss of β2-laminin alters calcium sensitivity and voltage-gated calcium channel maturation of neurotransmission at the neuromuscular junction

(2014) Kirat K. Chand et al.   JOURNAL OF PHYSIOLOGY-LONDON

Mesenchymal glioma stem cells are maintained by activated glycolytic metabolism involving aldehyde dehydrogenase 1A3

(2013) P. Mao et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Mutation of plasma membrane Ca2+ ATPase isoform 3 in a family with X-linked congenital cerebellar ataxia impairs Ca2+ homeostasis

(2012) G. Zanni et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Functional role of laminin α1 chain during cerebellum development

(2012) Celine Heng et al.   Cell Adhesion & Migration

The Novel PMCA2 Pump MutationTommyImpairs Cytosolic Calcium Clearance in Hair Cells and Links to Deafness in Mice

(2010) Mario Bortolozzi et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Reduced expression of the Ca2+transporter protein PMCA2 slows Ca2+dynamics in mouse cerebellar Purkinje neurones and alters the precision of motor coordination

(2010) Ruth M. Empson et al.   JOURNAL OF PHYSIOLOGY-LONDON

Calcium Pumps in Health and Disease

(2009) Marisa Brini et al.   PHYSIOLOGICAL REVIEWS