H. Kangas

In vitro expression analysis shows that the secretory form of gelsolin is the sole source of amyloid in gelsolin-related amyloidosis.

T. Paunio, L. Peltonen, A. Jalanko, 1996, Human molecular genetics.

The monopartite nuclear localization signal of autoimmune regulator mediates its nuclear import and interaction with multiple importin α molecules

H. Kangas, I. Ulmanen, T. Ilmarinen, 2006, The FEBS journal.

APECED‐causing mutations in AIRE reveal the functional domains of the protein

M. Vihinen, J. Ollila, J. Palvimo, 2004, Human mutation.

Toward understanding the pathogenic mechanisms in gelsolin-related amyloidosis: in vitro expression reveals an abnormal gelsolin fragment.

T. Paunio, L. Peltonen, J. Palo, 1994, Human molecular genetics.

Functional analysis of SAND mutations in AIRE supports dominant inheritance of the G228W mutation

M. Halonen, H. Kangas, I. Ulmanen, 2005, Human mutation.

Role of proprotein convertases in the pathogenic processing of the amyloidosis-associated form of secretory gelsolin

T. Paunio, N. Seidah, H. Kangas, 2002, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Cells of the Neuronal Lineage Play a Major Role in the Generation of Amyloid Precursor Fragments in Gelsolin-related Amyloidosis*

T. Paunio, L. Peltonen, J. Mallet, 1998, The Journal of Biological Chemistry.

The autoimmune regulator: a key toward understanding the molecular pathogenesis of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy.

M. Pelto-huikko, M. Halonen, H. Kangas, 2001, The Keio journal of medicine.

Functional consequences of amyloidosis mutation for gelsolin polypeptide‐ analysis of gelsolin‐actin interaction and gelsolin processing in gelsolin knock‐out fibroblasts

T. Paunio, L. Peltonen, D. Kwiatkowski, 1999, FEBS letters.

Tissue distribution and levels of gelsolin mRNA in normal individuals and patients with gelsolin‐related amyloidosis

T. Paunio, L. Peltonen, A. Syvänen, 1997, FEBS letters.

Functional interaction of AIRE with PIAS1 in transcriptional regulation.

J. Seeler, J. Saharinen, J. Palvimo, 2008, Molecular immunology.

Identification of the circulating amyloid precursor and other gelsolin metabolites in patients with G654A mutation in the gelsolin gene (Finnish familial amyloidosis): pathogenetic and diagnostic implications.

K. Sletten, N. Totty, C. Maury, 1997, Laboratory investigation; a journal of technical methods and pathology.

Gelsolin‐related familial amyloidosis, Finnish type, in a Portuguese family: Clinical and neurophysiological studies

T. Paunio, M. de Carvalho, M. Saraiva, 2003, Muscle & nerve.