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Brunella Franco

Researcher at University of Naples Federico II

Publications -  165
Citations -  10886

Brunella Franco is an academic researcher from University of Naples Federico II. The author has contributed to research in topics: Gene & Cilium. The author has an hindex of 49, co-authored 143 publications receiving 8987 citations. Previous affiliations of Brunella Franco include National Research Council & Baylor College of Medicine.

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Journal ArticleDOI

Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)

Daniel J. Klionsky, +2983 more
- 08 Feb 2021 - 
TL;DR: In this article, the authors present a set of guidelines for investigators to select and interpret methods to examine autophagy and related processes, and for reviewers to provide realistic and reasonable critiques of reports that are focused on these processes.
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A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules.

Brunella Franco, +16 more
- 10 Oct 1991 - 
TL;DR: A gene has now been isolated from the critical region on Xp22.3 to which Kallmann's syndrome locus has been assigned: this gene escapes X inactivation, has a homologue on the Y chromosome, and shows an unusual pattern of conservation across species.
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Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2-domain encoding gene

Alison J. Coffey, +43 more
- 01 Oct 1998 - 
TL;DR: A gene, SH2D1A, is identified that is mutated in XLP patients and encodes a novel protein composed of a single SH2 domain that is expressed in many tissues involved in the immune system.
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Mutations of SURF-1 in Leigh Disease Associated with Cytochrome c Oxidase Deficiency

Valeria Tiranti, +17 more
- 01 Dec 1998 - 
TL;DR: Sequence analysis of SURF-1 revealed mutations in numerous DNA samples from LD(COX-) patients, indicating that this gene is responsible for the major complementation group in this important mitochondrial disorder.
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Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22

Nandita Quaderi, +16 more
- 01 Nov 1997 - 
TL;DR: A new gene on Xp22f MIDI (Midline 1), which is disrupted in an OS patient carrying an X-chromosome inversion and is also mutated in several OS families, suggests an important role for this gene in midline development.