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Titolo:
Molecular basis of inherited spastic paraplegias
Autore:
Casari, G; Rugarli, E;
Indirizzi:
Hosp San Raffaele, Dibit, SCRI, Human Mol Genet Unit, I-20132 Milan, ItalyHosp San Raffaele Milan Italy I-20132 l Genet Unit, I-20132 Milan, Italy TIGEM, I-80131 Naples, Italy TIGEM Naples Italy I-80131TIGEM, I-80131 Naples, Italy
Titolo Testata:
CURRENT OPINION IN GENETICS & DEVELOPMENT
fascicolo: 3, volume: 11, anno: 2001,
pagine: 336 - 342
SICI:
0959-437X(200106)11:3<336:MBOISP>2.0.ZU;2-N
Fonte:
ISI
Lingua:
ENG
Soggetto:
PELIZAEUS-MERZBACHER-DISEASE; ATP-DEPENDENT DEGRADATION; PROTEOLIPID PROTEIN GENE; CHAPERONE-LIKE ACTIVITY; CELL-ADHESION MOLECULE; X-LINKED HYDROCEPHALUS; L1 KNOCKOUT MICE; INNER MEMBRANE; NERVOUS-SYSTEM; CHROMOSOME 2P;
Tipo documento:
Review
Natura:
Periodico
Settore Disciplinare:
Life Sciences
Citazioni:
66
Recensione:
Indirizzi per estratti:
Indirizzo: Casari, G Hosp San Raffaele, Dibit, SCRI, Human Mol Genet Unit, Via Olgettina 58, I-20132 Milan, Italy Hosp San Raffaele Via Olgettina 58 Milan Italy I-20132 n, Italy
Citazione:
G. Casari e E. Rugarli, "Molecular basis of inherited spastic paraplegias", CUR OP GEN, 11(3), 2001, pp. 336-342

Abstract

Recently, paraplegin and spastin have been found to be mutated in two autosomal forms of hereditary spastic paraplegia. Both proteins harbour a common ATPase domain that expresses a chaperone function. Paraplegin is a nuclear-encoded mitochondrial metalloprotease, while the exact role and subcellular localisation of spastin are still unclear.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 21/09/20 alle ore 11:09:17