U. Lahtinen

发表

Loss of lysosomal association of cystatin B proteins representing progressive myoclonus epilepsy, EPM1, mutations

D. Lindhout, E. Weber, A. Lehesjoki, 2005, European Journal of Human Genetics.

Functional biology of the neuronal ceroid lipofuscinoses (NCL) proteins.

T. Braulke, U. Lahtinen, S. Hofmann, 2006, Biochimica et biophysica acta.

Involvement of caveolin‐2 in caveolar biogenesis in MDCK cells

Kai Simons, Paul Verkade, Robert G Parton, 2003, FEBS letters.

Oligomerization and interacellular localization of the glycoprotein receptor ERGIC-53 is independent of disulfide bonds.

R. Pettersson, U. Lahtinen, E. Neve, 2005, Journal of molecular biology.

Mass spectrometric analysis reveals changes in phospholipid, neutral sphingolipid and sulfatide molecular species in progressive epilepsy with mental retardation, EPMR, brain: a case study

M. Hermansson, P. Somerharju, A. Lehesjoki, 2005, Journal of neurochemistry.

Localization of the small GTP-binding protein rab1p to early compartments of the secretory pathway.

B. Goud, U. Lahtinen, J. Saraste, 1995, Journal of cell science.

The novel neuronal ceroid lipofuscinosis gene MFSD8 encodes a putative lysosomal transporter.

Xiao-qing Liu, A. Paterson, H. Lohi, 2007, American journal of human genetics.

Galactolipid deficiency in the early pathogenesis of neuronal ceroid lipofuscinosis model Cln8mnd: implications to delayed myelination and oligodendrocyte maturation

J. Cooper, M. Hermansson, P. Somerharju, 2012, Neuropathology and applied neurobiology.

TRIM37 defective in mulibrey nanism is a novel RING finger ubiquitin E3 ligase.

J. Kallijärvi, J. Palvimo, A. Lehesjoki, 2005, Experimental cell research.

Low density lipoprotein receptor‐related protein 5 (LRP5) mutations and osteoporosis, impaired glucose metabolism and hypercholesterolaemia

O. Mäkitie, W. Cole, T. Kivelä, 2010, Clinical endocrinology.

Molecular Cloning and Expression of a 58-kDa cis-Golgi and Intermediate Compartment Protein (*)

U. Hellman, C. Wernstedt, R. Pettersson, 1996, The Journal of Biological Chemistry.

Cystatin-B is expressed by neural stem cells and by differentiated neurons and astrocytes.

D. Lindholm, L. Korhonen, A. Lehesjoki, 2003, Biochemical and biophysical research communications.

Mapping of structural determinants for the oligomerization of p58, a lectin-like protein of the intermediate compartment and cis-Golgi.

R. Pettersson, U. Lahtinen, K. Svensson, 2001, European journal of biochemistry.

Characterization of a 58 kDa cis-Golgi protein in pancreatic exocrine cells.

B. Dahllöf, U. Lahtinen, J. Saraste, 1992, Journal of cell science.

Expression, purification, refolding and crystallization of the carbohydrate-recognition domain of p58/ERGIC-53, an animal C-type lectin involved in export of glycoproteins from the endoplasmic reticulum.

G. Schneider, Y. Lindqvist, R. Pettersson, 2002, Acta crystallographica. Section D, Biological crystallography.

Loss of lysosomal association of cystatin B proteins representing progressive myoclonus epilepsy, EPM1, mutations

D. Lindhout, E. Weber, A. Lehesjoki, 2005, European Journal of Human Genetics.

Galactolipid deficiency in the early pathogenesis of neuronal ceroid lipofuscinosis model Cln8mnd: implications to delayed myelination and oligodendrocyte maturation

P. Somerharju, T. Laitinen, U. Lahtinen, 2012, Neuropathology and applied neurobiology.