J. Purroy

Molecular genetics of calcium sensing in bone cells.

N. Spurr, J. Purroy, 2002, Human molecular genetics.

Aberrant δPKC activation in the spinal cord of Wobbler mouse: a model of motor neuron disease

W. Bradley, M. Perez-Pinzon, I. Kirkinezos, 2005, Neurobiology of Disease.

Molecular genetics of cystinuria: identification of four new mutations and seven polymorphisms, and evidence for genetic heterogeneity.

M. Gallucci, P. Gasparini, I. Dianzani, 1995, American journal of human genetics.

The amino acid transporter asc-1 is not involved in cystinuria.

G. Borsani, M. Manzoni, M. Palacín, 2004, Kidney international.

Non-type I cystinuria caused by mutations in SLC7A9, encoding a subunit (bo,+AT) of rBAT

X. Estivill, D. Torrents, G. Borsani, 1999, Nature Genetics.

Detection of two novel large deletions in SLC3A1 by semi‐quantitative fluorescent multiplex PCR

P. Gasparini, M. Palacín, J. Jaeken, 2000, Human mutation.

Cystinuria type I: identification of eight new mutations in SLC3A1.

M. Gallucci, P. Gasparini, G. Rizzoni, 2001, Kidney international.

The molecular basis of cystinuria: the role of the rBAT gene

X. Estivill, D. Torrents, P. Gasparini, 1996, Amino Acids.

Imaging Brain Inflammation with [11C]PK11195 by PET and Induction of the Peripheral-Type Benzodiazepine Receptor after Transient Focal Ischemia in Rats

Jordi Llop, Deborah Pareto, Santiago Rojas, 2007, Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism.

In vivo imaging of induction of heat-shock protein-70 gene expression with fluorescence reflectance imaging and intravital confocal microscopy following brain ischaemia in reporter mice

Anna M. Planas, Carles Justicia, Franck Couillaud, 2013, European Journal of Nuclear Medicine and Molecular Imaging.