• 411 Citations
  • 13 h-Index
1987 …2017
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Fingerprint Dive into the research topics where Gianfranco Biolcati is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 8 Similar Profiles
Porphyria Cutanea Tarda Medicine & Life Sciences
Benign Familial Pemphigus Medicine & Life Sciences
Erythropoietic Protoporphyria Medicine & Life Sciences
Acute Intermittent Porphyria Medicine & Life Sciences
Mutation Medicine & Life Sciences
Genes Medicine & Life Sciences
Hydroxymethylbilane Synthase Medicine & Life Sciences
Porphyrias Medicine & Life Sciences

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Research Output 1987 2017

  • 411 Citations
  • 13 h-Index
  • 45 Article
6 Citations (Scopus)

Disturbed iron metabolism in erythropoietic protoporphyria and association of GDF15 and gender with disease severity

Barman-Aksoezen, J., Girelli, D., Aurizi, C., Schneider-Yin, X., Campostrini, N., Barbieri, L., Minder, E. I. & Biolcati, G., May 2017, In : Journal of Inherited Metabolic Disease. 40, 3, p. 433-441

Research output: Contribution to journalArticle

Erythropoietic Protoporphyria
Iron
Ferrochelatase
Heme
Anemia
3 Citations (Scopus)

Glutathione S-transferase ϴ-subunit as a phenotypic suppressor of pmr1Δ strain, the Kluyveromyces lactis model for Hailey-Hailey disease

Ficociello, G., Zanni, E., Cialfi, S., Aurizi, C., Biolcati, G., Palleschi, C., Talora, C. & Uccelletti, D., Nov 1 2016, In : Biochimica et Biophysica Acta - Molecular Cell Research. 1863, 11, p. 2650-2657 8 p.

Research output: Contribution to journalArticle

Benign Familial Pemphigus
Kluyveromyces
Glutathione Transferase
Yeasts
Acantholysis
4 Citations (Scopus)

The loss of ATP2C1 impairs the DNA damage response and induces altered skin homeostasis: Consequences for epidermal biology in Hailey-Hailey disease

Cialfi, S., Le Pera, L., De Blasio, C., Mariano, G., Palermo, R., Zonfrilli, A., Uccelletti, D., Palleschi, C., Biolcati, G., Barbieri, L., Screpanti, I. & Talora, C., Aug 16 2016, In : Scientific Reports. 6, 31567.

Research output: Contribution to journalArticle

Benign Familial Pemphigus
Keratinocytes
DNA Damage
Homeostasis
Oxidative Stress
28 Citations (Scopus)

Twelve novel HGD gene variants identified in 99 alkaptonuria patients: Focus on 'black bone disease' in Italy

Nemethova, M., Radvanszky, J., Kadasi, L., Ascher, D. B., Pires, D. E. V., Blundell, T. L., Porfirio, B., Mannoni, A., Santucci, A., Milucci, L., Sestini, S., Biolcati, G., Sorge, F., Aurizi, C., Aquaron, R., Alsbou, M., Lourenço, C. M., Ramadevi, K., Ranganath, L. R., Gallagher, J. A. & 14 others, Van Kan, C., Hall, A. K., Olsson, B., Sireau, N., Ayoob, H., Timmis, O. G., Le Quan Sang, K. H., Genovese, F., Imrich, R., Rovensky, J., Srinivasaraghavan, R., Bharadwaj, S. K., Spiegel, R. & Zatkova, A., Jan 1 2016, In : European Journal of Human Genetics. 24, 1, p. 66-72 7 p.

Research output: Contribution to journalArticle

Homogentisate 1,2-Dioxygenase
Alkaptonuria
Bone Diseases
Italy
Protein Subunits