T. Litjens

发表

Chromosomal localization of ARSB, the gene for human N-acetylgalactosamine-4-sulphatase

C. P. Morris, D. Callen, J. Hopwood, 1989, Human Genetics.

Transthyretin interacts with the lysosome-associated membrane protein (LAMP-1) in circulation.

P. Meikle, G. Hodge, L. Karageorgos, 2004, The Biochemical journal.

STORE‐OPERATED Ca2+ CHANNELS AND MICRODOMAINS OF Ca2+ IN LIVER CELLS

G. Barritt, E. Aromataris, J. Castro, 2009, Clinical and experimental pharmacology & physiology.

Long-term clinical progress in bone marrow transplanted mucopolysaccharidosis type I patients with a defined genotype

C. P. Morris, H. Scott, D. Brooks, 1993, Journal of Inherited Metabolic Disease.

Two site-directed mutations abrogate enzyme activity but have different effects on the conformation and cellular content of the N-acetylgalactosamine 4-sulphatase protein.

C. P. Morris, D. Brooks, J. Hopwood, 1995, The Biochemical journal.

Identification, expression, and biochemical characterization of N-acetylgalactosamine-4-sulfatase mutations and relationship with clinical phenotype in MPS-VI patients.

D. Brooks, J. Hopwood, T. Litjens, 1996, American journal of human genetics.

Mutation (AG,,,) Results in a Severe

C. P. Morris, K. Figura, J. Hopwood, 1992 .

An N‐acetylgalactosamine‐4‐sulfatase mutation (ΔG238) results in a severe Maroteaux‐Lamy phenotype

C. P. Morris, C. Peters, K. von Figura, 1992, Human mutation.

Arachidonic acid inhibits the store-operated Ca2+ current in rat liver cells.

G. Barritt, G. Rychkov, T. Litjens, 2005, The Biochemical journal.

Identification of mutations in the alpha-L-iduronidase gene (IDUA) that cause Hurler and Scheie syndromes.

C. P. Morris, H. Scott, D. Brooks, 1993, American journal of human genetics.

Feline Mucopolysaccharidosis Type VI

J. Hopwood, T. Litjens, D. Anson, 1996, The Journal of Biological Chemistry.

The predominant role of IP₃ type 1 receptors in activation of store-operated Ca²+ entry in liver cells.

G. Barritt, J. Castro, G. Rychkov, 2011, Biochimica et biophysica acta.

entry in liver cells

J. Castro, G. Rychkov, T. Litjens, 2011 .

Phospholipase C-gamma1 is required for the activation of store-operated Ca2+ channels in liver cells.

G. Barritt, E. Aromataris, J. Castro, 2007, The Biochemical journal.

Properties of Orai1 mediated store‐operated current depend on the expression levels of STIM1 and Orai1 proteins

G. Barritt, Linlin Ma, G. Rychkov, 2009, The Journal of physiology.

A common mutation for mucopolysaccharidosis type I associated with a severe Hurler syndrome phenotype

C. P. Morris, H. Scott, J. Hopwood, 1992, Human mutation.

Mucopolysaccharidosis type VI: Structural and clinical implications of mutations in N‐acetylgalactosamine‐4‐sulfatase

J. Hopwood, T. Litjens, Tom Litjens, 2001, Human mutation.

Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome): a Y210C mutation causes either altered protein handling or altered protein function of N-acetylgalactosamine 4-sulfatase at multiple points in the vacuolar network.

D. Brooks, J. Hopwood, T. Litjens, 2002, Biochemistry.

Multiple polymorphisms within the alpha-L-iduronidase gene (IDUA): implications for a role in modification of MPS-I disease phenotype.

C. P. Morris, H. Scott, J. Hopwood, 1993, Human molecular genetics.

α‐L‐iduronidase mutations (Q70X and P533R) associate with a severe Hurler phenotype

H. Scott, D. Brooks, J. Hopwood, 1992 .

Human N-acetylgalactosamine-4-sulphatase: protein maturation and isolation of genomic clones.

C. P. Morris, J. Hopwood, T. Litjens, 1991, Biochemistry international.

ATP and vasopressin activate a single type of store-operated Ca2+ channel, identified by patch-clamp recording, in rat hepatocytes.

G. Barritt, G. Rychkov, T. Litjens, 2005, Cell calcium.

Fast Ca2+‐dependent inactivation of the store‐operated Ca2+ current (ISOC) in liver cells: a role for calmodulin

G. Barritt, M. L. Harland, G. Rychkov, 2004, The Journal of physiology.