Works by Kangas, Salla M

Results: 13

Structural analysis of the complex between calmodulin and full-length myelin basic protein, an intrinsically disordered molecule.

Published in:

Amino Acids, 2010, v. 39, n. 1, p. 59, doi. 10.1007/s00726-009-0364-2

By:

Majava, Viivi;
Chaozhan Wang;
Myllykoski, Matti;
Kangas, Salla M.;
Sung Ung Kang;
Hayashi, Nobuhiro;
Baumgärtel, Peter;
Heape, Anthony M.;
Lubec, Gert;
Kursula, Petri

Publication type:

Article

A novel pathogenic SLC12A5 missense variant in epilepsy of infancy with migrating focal seizures causes impaired KCC2 chloride extrusion.

Published in:

Frontiers in Molecular Neuroscience, 2024, p. 1, doi. 10.3389/fnmol.2024.1372662

By:

Järvelä, Viivi;
Hamze, Mira;
Komulainen-Ebrahim, Jonna;
Rahikkala, Elisa;
Piispala, Johanna;
Kallio, Mika;
Kangas, Salla M.;
Nickl, Tereza;
Huttula, Marko;
Hinttala, Reetta;
Uusimaa, Johanna;
Medina, Igor;
Immonen, Esa-Ville

Publication type:

Article

Brain MRI findings in paediatric genetic disorders associated with white matter abnormalities.

Published in:

Developmental Medicine & Child Neurology, 2025, v. 67, n. 2, p. 186, doi. 10.1111/dmcn.16036

By:

Oikarainen, Jaakko H.;
Knuutinen, Oula A.;
Kangas, Salla M.;
Rahikkala, Elisa J.;
Pokka, Tytti M.‐L.;
Moilanen, Jukka S.;
Hinttala, Reetta M.;
Vieira, Päivi M.;
Uusimaa, Johanna M.;
Suo‐Palosaari, Maria H.

Publication type:

Article

Epidemiological, clinical, and genetic characteristics of paediatric genetic white matter disorders in Northern Finland.

Published in:

Developmental Medicine & Child Neurology, 2021, v. 63, n. 9, p. 1066, doi. 10.1111/dmcn.14884

By:

Knuutinen, Oula A;
Oikarainen, Jaakko H;
Suo‐Palosaari, Maria H;
Kangas, Salla M;
Rahikkala, Elisa J;
Pokka, Tytti M‐L;
Moilanen, Jukka S;
Hinttala, Reetta M L;
Vieira, Päivi M;
Uusimaa, Johanna M

Publication type:

Article

Hyperkinetic Movement Disorder Caused by the Recurrent c.892C>T NACC1 Variant.

Published in:

Movement Disorders Clinical Practice, 2024, v. 11, n. 6, p. 708, doi. 10.1002/mdc3.14051

By:

Komulainen‐Ebrahim, Jonna;
Kangas, Salla M.;
López‐Martín, Estrella;
Feyma, Timothy;
Scaglia, Fernando;
Martínez‐Delgado, Beatriz;
Kuismin, Outi;
Suo‐Palosaari, Maria;
Carr, Lucinda;
Hinttala, Reetta;
Kurian, Manju A.;
Uusimaa, Johanna

Publication type:

Article

Infantile onset encephalomyopathy, retinopathy, optic atrophy, and mitochondrial DNA depletion associated with a novel pathogenic DHX16 variant.

Published in:

Clinical Genetics, 2023, v. 104, n. 6, p. 686, doi. 10.1111/cge.14416

By:

Hautakangas, Milla‐Riikka;
Widgren, Paula;
Korpelainen, Paavo;
Kangas, Salla M.;
Komulainen, Tuomas;
Vieira, Päivi;
Rahikkala, Elisa;
Pylkäs, Katri;
Tuominen, Hannu;
Kokkonen, Hannaleena;
Miinalainen, Ilkka;
Nadaf, Javad;
Majewski, Jacek;
Hinttala, Reetta;
Uusimaa, Johanna

Publication type:

Article

Homozygous TAF1C variants are associated with a novel childhood‐onset neurological phenotype.

Published in:

Clinical Genetics, 2020, v. 98, n. 5, p. 493, doi. 10.1111/cge.13827

By:

Knuutinen, Oula;
Pyle, Angela;
Suo‐Palosaari, Maria;
Duff, Jennifer;
Froukh, Tawfiq;
Lehesjoki, Anna‐Elina;
Kangas, Salla M.;
Cassidy, James;
Maraqa, Latifa;
Keski‐Filppula, Riikka;
Kokkonen, Hannaleena;
Uusimaa, Johanna;
Horvath, Rita;
Vieira, Päivi

Publication type:

Article

An approach to comprehensive genome and proteome expression analyses in Schwann cells and neurons during peripheral nerve myelin formation.

Published in:

Journal of Neurochemistry, 2016, v. 138, n. 6, p. 830, doi. 10.1111/jnc.13722

By:

Kangas, Salla M.;
Ohlmeier, Steffen;
Sormunen, Raija;
Jouhilahti, Eeva‐Mari;
Peltonen, Sirkku;
Peltonen, Juha;
Heape, Anthony M.

Publication type:

Article

The N-terminal domain of the myelin enzyme 2′,3′-cyclic nucleotide 3′-phosphodiesterase: direct molecular interaction with the calcium sensor calmodulin.

Published in:

Journal of Neurochemistry, 2012, v. 123, n. 4, p. 515, doi. 10.1111/jnc.12000

By:

Myllykoski, Matti;
Itoh, Kouichi;
Kangas, Salla M.;
Heape, Anthony M.;
Kang, Sung-Ung;
Lubec, Gert;
Kursula, Inari;
Kursula, Petri

Publication type:

Article

Variant in NHLRC2 leads to increased hnRNP C2 in developing neurons and the hippocampus of a mouse model of FINCA disease.

Published in:

Molecular Medicine, 2020, v. 26, n. 1, p. 1, doi. 10.1186/s10020-020-00245-4

By:

Hiltunen, Anniina E.;
Kangas, Salla M.;
Ohlmeier, Steffen;
Pietilä, Ilkka;
Hiltunen, Jori;
Tanila, Heikki;
McKerlie, Colin;
Govindan, Subashika;
Tuominen, Hannu;
Kaarteenaho, Riitta;
Hallman, Mikko;
Uusimaa, Johanna;
Hinttala, Reetta

Publication type:

Article

Analysis of human brain tissue derived from DBS surgery.

Published in:

Translational Neurodegeneration, 2022, v. 11, n. 1, p. 1, doi. 10.1186/s40035-022-00297-y

By:

Kangas, Salla M.;
Teppo, Jaakko;
Lahtinen, Maija J.;
Suoranta, Anu;
Ghimire, Bishwa;
Mattila, Pirkko;
Uusimaa, Johanna;
Varjosalo, Markku;
Katisko, Jani;
Hinttala, Reetta

Publication type:

Article

Modeling Rare Human Disorders in Mice: The Finnish Disease Heritage.

Published in:

Cells (2073-4409), 2021, v. 10, n. 11, p. 3158, doi. 10.3390/cells10113158

By:

Zárybnický, Tomáš;
Heikkinen, Anne;
Kangas, Salla M.;
Karikoski, Marika;
Martínez-Nieto, Guillermo Antonio;
Salo, Miia H.;
Uusimaa, Johanna;
Vuolteenaho, Reetta;
Hinttala, Reetta;
Sipilä, Petra;
Kuure, Satu

Publication type:

Article

Myeloid-related protein 8/14 in plasma and serum in patients with new-onset juvenile idiopathic arthritis in real-world setting in a single center.

Published in:

Pediatric Rheumatology, 2022, v. 20, n. 1, p. 1, doi. 10.1186/s12969-022-00701-x

By:

Keskitalo, Paula L.;
Kangas, Salla M.;
Sard, Sirja;
Pokka, Tytti;
Glumoff, Virpi;
Kulmala, Petri;
Vähäsalo, Paula

Publication type:

Article