J. Heikkinen

发表

Structure and expression of the human lysyl hydroxylase gene (PLOD): introns 9 and 16 contain Alu sequences at the sites of recombination in Ehlers-Danlos syndrome type VI patients.

K. Kivirikko, T. Hautala, R. Myllylä, 1994, Genomics.

Mutational analysis of the lysyl hydroxylase 1 gene (PLOD) in six unrelated patients with Ehlers‐Danlos syndrome type VI: Prenatal exclusion of this disorder in one family

L. Walker, H. Yeowell, J. Heikkinen, 2000 .

The third activity for lysyl hydroxylase 3: galactosylation of hydroxylysyl residues in collagens in vitro.

Chunguang Wang, R. Myllylä, Maija Risteli, 2002, Matrix biology : journal of the International Society for Matrix Biology.

Alu-Alu recombination results in a duplication of seven exons in the lysyl hydroxylase gene in a patient with the type VI variant of Ehlers-Danlos syndrome.

K. Kivirikko, T. Hautala, R. Myllylä, 1994, American journal of human genetics.

Duplication of seven exons in the lysyl hydroxylase gene is associated with longer forms of a repetitive sequence within the gene and is a common cause for the type VI variant of Ehlers-Danlos syndrome.

K. Kivirikko, T. Krieg, B. Steinmann, 1997, American journal of human genetics.

Lysyl Hydroxylase 3 Is a Multifunctional Protein Possessing Collagen Glucosyltransferase Activity*

Chunguang Wang, R. Myllylä, Maarit Rossi, 2000, The Journal of Biological Chemistry.

Expanding the lysyl hydroxylase toolbox: New insights into the localization and activities of lysyl hydroxylase 3 (LH3)

Chunguang Wang, A. Juffer, R. Myllylä, 2007, Journal of cellular physiology.

Lysyl hydroxylase 3 (LH3) modifies proteins in the extracellular space, a novel mechanism for matrix remodeling

R. Sormunen, Chunguang Wang, Miia H. Vapola, 2006, Journal of cellular physiology.

Identification of Amino Acids Important for the Catalytic Activity of the Collagen Glucosyltransferase Associated with the Multifunctional Lysyl Hydroxylase 3 (LH3)*

Chunguang Wang, R. Myllylä, Maija Risteli, 2002, The Journal of Biological Chemistry.

Dimerization of human lysyl hydroxylase 3 (LH3) is mediated by the amino acids 541-547.

Paula Alavesa, A. Juffer, R. Myllylä, 2011, Matrix biology : journal of the International Society for Matrix Biology.

A large duplication in the gene for lysyl hydroxylase accounts for the type VI variant of Ehlers-Danlos syndrome in two siblings.

K. Kivirikko, T. Hautala, R. Myllylä, 1993, Genomics.

Minoxidil specifically decreases the expression of lysine hydroxylase in cultured human skin fibroblasts.

K. Kivirikko, T. Hautala, R. Myllylä, 1992, The Biochemical journal.

Lysyl hydroxylase, a collagen processing enzyme, exemplifies a novel class of luminally-oriented peripheral membrane proteins in the endoplasmic reticulum.

S. Kellokumpu, R. Sormunen, R. Myllylä, 1994, The Journal of biological chemistry.

Mutational analysis of the lysyl hydroxylase 1 gene (PLOD) in six unrelated patients with Ehlers-Danlos syndrome type VI: prenatal exclusion of this disorder in one family.

H. Yeowell, J. Heikkinen, L. Walker, 2000, Human Mutation.