Researcher
Manuela Morleo
University of Campania "Luigi Vanvitelli"
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37 papers found
All papers authored by Manuela Morleo
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Qin Wang,
Allan Bayat ,
Mark R. Battig ,
Yijing Zhou,
Daniëlle G. M. Bosch,
Gijs van Haaften ,
Leslie Granger,
Andrea K. Petersen,
Luis A. Pérez-Jurado ,
Gemma Aznar-Laín,
Anushree Aneja,
Miroslava Hancarova,
Sarka Bendova,
Martin Schwarz
and 139 other authors
Spliceosome malfunction causes neurodevelopmental disorders with overlapping features
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Jair Tenorio-Castano ,
Cyril Mignot,
Alexandra Afenjar,
Pedro Arias,
Natalia Gallego-Zazo ,
Alejandro Parra ,
Lucia Miranda ,
Mario Cazalla,
Cristina Silván,
Delphine Heron,
Boris Keren,
Ioana Popa,
María Palomares ,
Emi Rikeros
and 22 other authors
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Rossella Venditti,
Evangelos Theodorou,
Lauren C. Briere,
Marion Rosello,
Alfonsina Tirozzi,
Roberta Tammaro,
Nour Al-Badri,
Frances A. High,
Jiahai Shi,
Elena Putti,
Luigi Ferrante,
Viviana Cetrangolo,
Annalaura Torella,
Melissa A. Walker
and 316 other authors
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Museer A. Lone ,
Winston Lee,
Laura Capolupo ,
Sylvia Ho ,
Adekemi M. Adeyemi,
Erica H. Gerkes,
Alexander Pa A. Stegmann ,
Estrella López-Martín,
Eva Bermejo-Sánchez ,
Beatriz Martínez-Delgado,
Christiane Zweier,
Cornelia Kraus,
Bernt Popp ,
Vincent Strehlow
and 72 other authors
CERT1 mutations perturb human development by disrupting sphingolipid homeostasis
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Cristina Peduto,
Rosa di Fraia,
Selvaggio Ld,
Lucia Digitale Selvaggio,
Francesca Allosso,
Giacomo Accardo,
Zanobio Mt,
Maria Teresa Zanobio,
Silvia Maitz,
Milena Mariani
and 4 other authors
Patients with DeSanto-Shinawi syndrome: Further extension of phenotype from Italy.
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Alessia Romano,
Anna Barbato,
Paola Quadrano,
Simona Brillante,
Mariagrazia Volpe,
Luigi Ferrante,
Roberta Tammaro,
Manuela Morleo ,
Rossella De Cegli,
Antonella Iuliano,
Marialuisa Testa,
Fabrizio Andreone,
Gennaro Ciliberto,
Eduardo Clery
and 10 other authors
Targeting the MITF/APAF-1 axis as salvage therapy for MAPK inhibitors in resistant melanoma
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,
Kari Mattison,
G. Tossing,
F. Mulroe,
C. Simmons,
Butler Km,
A. Schreiber,
A. Alsadah,
Neilson De,
K. Naess,
A. Wedell,
A. Wredenberg,
A. Sorlin,
E. McCann,
Burghel Gj
and 30 other authors
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,
Martina Schaettin,
Médéric Jeanne,
Veranika Panasenkava,
Anne-Sophie Denommé-Pichon ,
Boris Keren,
Cyril Mignot,
Martine Doco-Fenzy,
Lance Rodan,
Keri Ramsey,
Vinodh Narayanan,
Julie R. Jones,
Eloise J. Prijoles,
Wendy G. Mitchell,
Jillian R. Ozmore
and 33 other authors
SEMA6B variants cause intellectual disability and alter dendritic spine density and axon guidance
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,
Vincenzo Nigro,
Silvia Maitz,
Grazia M. S. Mancini,
Claudia Ruivenkamp,
Eun-Kyung Suk,
Tobias Bartolomaeus,
Andreas Merkenschlager
and 21 other authors
De novo variants in ATP2B1 lead to neurodevelopmental delay
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,
Bianca Fiorillo,
Federica Moraca,
Giuliana Giamundo,
Giovanni Scala,
Andrea Raffeiner,
Omar Torres‐Quesada,
Eduard Stefan
and 7 other authors
The TBC1D31/praja2 complex controls primary ciliogenesis through PKA‐directed OFD1 ubiquitylation
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,
Manuela Morleo ,
Simona Brillante,
Alessandro Weisz,
Brunella Franco,
Pietro Vajro
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Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1
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