J. Viitala

发表

Enrichment of high mannose-type glycans in nervous tissue glycoproteins in neuronal ceroid-lipofuscinosis

J. Palo, C. Maury, T. Krusius, 1986, Journal of the Neurological Sciences.

The red cell surface revisited

J. Järnefelt, J. Viitala, 1985 .

Molecular cloning of cDNAs encoding lamp A, a human lysosomal membrane glycoprotein with apparent Mr approximately equal to 120,000.

M. Fukuda, S. Carlsson, P. Siebert, 1988, Proceedings of the National Academy of Sciences of the United States of America.

Glycosylation pattern of kappa light chains in massive cutaneous hyalinosis

C. Maury, A. Teppo, J. Järnefelt, 1987, Glycoconjugate Journal.

High-mannose structure of apolipoprotein-B from low-density lipoproteins of human plasma.

H. Rauvala, J. Parkkinen, M. Vauhkonen, 1985, European journal of biochemistry.

Cloning of cDNAs encoding human lysosomal membrane glycoproteins, h-lamp-1 and h-lamp-2. Comparison of their deduced amino acid sequences.

J. Matteson, S. Carlsson, M. Fukuda, 1988, The Journal of biological chemistry.

Specific cell-surface labeling of polyglycosyl chains in human erythrocytes and HL-60 cells using endo-beta-galactosidase and galactosyltransferase.

J. Finne, J. Viitala, 1984, European journal of biochemistry.

Blood-group A and B determinants are located in different polyglycosyl peptides isolated from human erythrocytes of blood-group AB.

C. Gahmberg, J. Finne, T. Krusius, 1981, European journal of biochemistry.

Blood group A and H determinants in polyglycosyl peptides of A1 and A2 erythrocytes.

J. Finne, T. Krusius, J. Viitala, 2005, European journal of biochemistry.

Blood group A and B glycosyltransferases synthesize A and B determinants on different acceptor polyglycosyl peptidesin vitro

J. Viitala, 1985, Glycoconjugate Journal.

A new congenital dyserythropoietic anaemia

T. Ruutu, J. Viitala, J. Ohisalo, 1988, British journal of haematology.

Preparation of high molecular weight glycopeptides and oligosaccharides (erythroglycan) from human erythrocytes.

R. Laine, J. Rush, J. Järnefelt, 1982, Methods in enzymology.

Does perinatal hypocarbia play a role in the pathogenesis of cerebral palsy?

L. Wendt, T. Salokorpi, J. Viitala, 1999, Acta paediatrica.

Confirmation of the chromosomal localization of human lamp genes and their exclusion as candidate genes for Salla disease

L. Peltonen, J. Schleutker, L. Haataja, 1991, Human Genetics.