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Erratum to: Variants in TNIP1, a regulator of the NF-kB pathway, found in two patients with neural tube defects.
Published in:
2016
By:
- La Carpia, Francesca;
- Rendeli, Claudia;
- Molinario, Clelia;
- Milillo, Annamaria;
- Farroni, Chiara;
- Cannelli, Natalia;
- Ausili, Emanuele;
- Paolucci, Valentina;
- Neri, Giovanni;
- Romagnoli, Costantino;
- Sangiorgi, Eugenio;
- Gurrieri, Fiorella
Publication type:
Erratum
Variants in TNIP1, a regulator of the NF-kB pathway, found in two patients with neural tube defects.
Published in:
Child's Nervous System, 2016, v. 32, n. 6, p. 1061, doi. 10.1007/s00381-016-3087-1
By:
- Francesca, La;
- Claudia, Rendeli;
- Molinario, Clelia;
- Annamaria, Milillo;
- Chiara, Farroni;
- Natalia, Cannelli;
- Emanuele, Ausili;
- Valentina, Paolucci;
- Giovanni, Neri;
- Costantino, Romagnoli;
- Eugenio, Sangiorgi;
- Fiorella, Gurrieri
Publication type:
Article
A SPRY2 mutation leading to MAPK/ERK pathway inhibition is associated with an autosomal dominant form of IgA nephropathy.
Published in:
European Journal of Human Genetics, 2015, v. 23, n. 12, p. 1673, doi. 10.1038/ejhg.2015.52
By:
- Milillo, Annamaria;
- La Carpia, Francesca;
- Costanzi, Stefano;
- D'Urbano, Vanessa;
- Martini, Maurizio;
- Lanuti, Paola;
- Vischini, Gisella;
- Larocca, Luigi M;
- Marchisio, Marco;
- Miscia, Sebastiano;
- Amoroso, Antonio;
- Gurrieri, Fiorella;
- Sangiorgi, Eugenio
Publication type:
Article
Defective activation of the MAPK/ERK pathway, leading to PARP1 and DNMT1 dysregulation, is a common defect in IgA nephropathy and Henoch-Schönlein purpura.
Published in:
Journal of Nephrology (JNonline), 2018, v. 31, n. 5, p. 731, doi. 10.1007/s40620-018-0482-6
By:
- Milillo, Annamaria;
- Molinario, Clelia;
- Costanzi, Stefano;
- Vischini, Gisella;
- La Carpia, Francesca;
- La Greca, Francesco;
- Rigante, Donato;
- Gambaro, Giovanni;
- Gurrieri, Fiorella;
- Sangiorgi, Eugenio
Publication type:
Article

Found: 4

Erratum to: Variants in TNIP1, a regulator of the NF-kB pathway, found in two patients with neural tube defects.

Variants in TNIP1, a regulator of the NF-kB pathway, found in two patients with neural tube defects.

A SPRY2 mutation leading to MAPK/ERK pathway inhibition is associated with an autosomal dominant form of IgA nephropathy.

Defective activation of the MAPK/ERK pathway, leading to PARP1 and DNMT1 dysregulation, is a common defect in IgA nephropathy and Henoch-Schönlein purpura.