Franco, Brunella

Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition) 1

Klionsky, D. J., Abdel-Aziz, A. K., Abdelfatah, S., Abdellatif, M., Abdoli, A., Abel, S., Abeliovich, H., Abildgaard, M. H., Abudu, Y. P., Acevedo-Arozena, A., et al. (2021) · Autophagy

Autophagy in Disease and TherapyCalcium signaling and nucleotide metabolism

Cited by 2,897

A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules

Franco, B., Guioli, S., Pragliola, A., Incerti, B., Bardoni, B., Tonlorenzi, R., Carrozzo, R., Maestrini, E., Pieretti, M., Taillon-Miller, P., et al. (1991) · Nature

Hypothalamic control of reproductive hormonesOlfactory and Sensory Function Studies

Cited by 846

Autophagy promotes primary ciliogenesis by removing OFD1 from centriolar satellites

Tang, Z., Lin, M. G., Stowe, T. R., Chen, S., Zhu, M., Stearns, T., Franco, B., & Zhong, Q. (2013) · Nature

Genetic and Kidney Cyst DiseasesAutophagy in Disease and Therapy

Cited by 414

Activation of Autophagy, Observed in Liver Tissues From Patients With Wilson Disease and From ATP7B-Deficient Animals, Protects Hepatocytes From Copper-Induced Apoptosis

Polishchuk, E. V., Merolla, A., Lichtmannegger, J., Romano, A., Indrieri, A., Ilyechova, E. Y., Concilli, M., De Cegli, R., Crispino, R., Mariniello, M., et al. (2019) · Gastroenterology

Trace Elements in HealthAutophagy in Disease and Therapy

Cited by 265

An organelle-specific protein landscape identifies novel diseases and molecular mechanisms

Boldt, K., van Reeuwijk, J., Lu, Q., Koutroumpas, K., Nguyen, T.-M. T., Texier, Y., van Beersum, S. E. C., Horn, N., Willer, J. R., Mans, D. A., et al. (2016) · Nature Communications

Genetic and Kidney Cyst DiseasesCystic Fibrosis Research Advances

Cited by 240

Fifteen years of research on oral-facial-digital syndromes: from 1 to 16 causal genes

Bruel, A.-L., Franco, B., Duffourd, Y., Thevenon, J., Jego, L., Lopez, E., Deleuze, J.-F., Doummar, D., Giles, R. H., Johnson, C. A., et al. (2017) · Journal of Medical Genetics

Genetic and Kidney Cyst DiseasesCystic Fibrosis Research Advances

Cited by 115

OFD1, the Gene Mutated in Oral-Facial-Digital Syndrome Type 1, Is Expressed in the Metanephros and in Human Embryonic Renal Mesenchymal Cells

Romio, L., Wright, V., Price, K., Winyard, P. J. D., Donnai, D., Porteous, M. E., Franco, B., Giorgio, G., Malcolm, S., Woolf, A. S., et al. (2003) · Journal of the American Society of Nephrology

Genetic and Kidney Cyst DiseasesGenomics and Rare Diseases

Cited by 103

Renal insufficiency, a frequent complication with age in oral‐facial‐digital syndrome type I

Saal, S., Faivre, L., Aral, B., Gigot, N., Toutain, A., Van Maldergem, L., Destree, A., Maystadt, I., Cosyns, J., Jouk, P., et al. (2010) · Clinical Genetics

Genetic and Kidney Cyst DiseasesGenomics and Rare Diseases

Cited by 36

Role of uL3 in the Crosstalk between Nucleolar Stress and Autophagy in Colon Cancer Cells

Pecoraro, A., Carotenuto, P., Franco, B., De Cegli, R., Russo, G., & Russo, A. (2020) · International Journal of Molecular Sciences

Autophagy in Disease and TherapyNuclear Structure and Function

Cited by 35

Mutation-independent therapies for retinal diseases: focus on gene-based approaches

Carrella, S., Indrieri, A., Franco, B., & Banfi, S. (2020) · Frontiers in Neuroscience

Retinal Development and DisordersRetinal Diseases and Treatments

Cited by 14