M
Mouna Haidar
Researcher at Florey Institute of Neuroscience and Mental Health
Publications - 11
Citations - 500
Mouna Haidar is an academic researcher from Florey Institute of Neuroscience and Mental Health. The author has contributed to research in topics: Medicine & Hippocampal formation. The author has an hindex of 8, co-authored 11 publications receiving 324 citations. Previous affiliations of Mouna Haidar include University of Melbourne.
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Journal ArticleDOI
Synaptopathies: synaptic dysfunction in neurological disorders - A review from students to students
Katarzyna Lepeta,Mychael V. Lourenco,Barbara Schweitzer,Pamela V. Martino Adami,Priyanjalee Banerjee,Silvina Catuara-Solarz,Mario de la Fuente Revenga,Alain M. Guillem,Mouna Haidar,Omamuyovwi M. Ijomone,Bettina Nadorp,Lin Qi,Nirma D Perera,Louise K. Refsgaard,Kimberley M. Reid,Mariam Sabbar,Arghyadip Sahoo,Natascha Schaefer,Rebecca K. Sheean,Anna Suska,Rajkumar Verma,Cinzia Vicidomini,Dean J. Wright,Xingding Zhang,Constanze I. Seidenbecher +24 more
TL;DR: Basic concepts of synapse structure and function are discussed, and a critical view of how aberrant synapse physiology may contribute to neurodevelopmental disorders as well as neurodegenerative disorders are provided.
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A Novel Ultra-Stable, Monomeric Green Fluorescent Protein For Direct Volumetric Imaging of Whole Organs Using CLARITY
Daniel Scott,Daniel Scott,Natalie Gunn,Natalie Gunn,Kelvin J. Yong,Kelvin J. Yong,Verena C. Wimmer,Nicholas A. Veldhuis,Leesa M. Challis,Mouna Haidar,Steven Petrou,Ross A. D. Bathgate,Ross A. D. Bathgate,Michael D. W. Griffin +13 more
TL;DR: The crystal structure of a recently engineered ultra-stable GFP (usGFP) is solved and it is proposed that the two stabilising mutations, Q69L and N164Y, act to improve hydrophobic packing in the core of the protein and facilitate hydrogen bonding networks at the surface, respectively.
Journal ArticleDOI
Relaxin-3/RXFP3 networks: an emerging target for the treatment of depression and other neuropsychiatric diseases?
Craig M. Smith,Andrew W. Walker,Ihaia T. Hosken,Berenice E. Chua,Cary Zhang,Mouna Haidar,Andrew L. Gundlach +6 more
TL;DR: Relaxin-3 is an arousal transmitter which is highly responsive to environmental stimuli, particularly neurogenic stressors, and in turn modulates behavioral responses to these stressors and alters key neural processes, including hippocampal theta rhythm and associated learning and memory.
Journal ArticleDOI
Perturbed BMP signaling and denervation promote muscle wasting in cancer cachexia
Roberta Sartori,Roberta Sartori,Adam Hagg,Adam Hagg,Adam Hagg,Sandra Zampieri,Andrea Armani,Catherine E. Winbanks,Laís R. Viana,Laís R. Viana,Mouna Haidar,Kevin I. Watt,Kevin I. Watt,Hongwei Qian,Hongwei Qian,Camilla Pezzini,Pardis Zanganeh,Bradley J. Turner,Anna Larsson,Gianpietro Zanchettin,Elisa Sefora Pierobon,Lucia Moletta,Michele Valmasoni,Alberto Ponzoni,Shady Attar,Gianfranco Da Dalt,Cosimo Sperti,Monika Kustermann,Rachel E. Thomson,Rachel E. Thomson,Lars Larsson,Lars Larsson,Kate L Loveland,Kate L Loveland,Paola Costelli,Aram Megighian,Stefano Merigliano,Fabio Penna,Paul Gregorevic,Marco Sandri +39 more
TL;DR: In this paper, diminished bone morphogenetic protein (BMP) signaling is observed early in the onset of skeletal muscle wasting associated with cancer cachexia in mouse models and in patients with cancer.
Journal ArticleDOI
Central injection of relaxin-3 receptor (RXFP3) antagonist peptides reduces motivated food seeking and consumption in C57BL/6J mice
Craig M. Smith,Craig M. Smith,Berenice E. Chua,Cary Zhang,Cary Zhang,Andrew W. Walker,Andrew W. Walker,Mouna Haidar,Mouna Haidar,David Hawkes,Fazel Shabanpoor,Mohammad Akhter Hossain,Mohammad Akhter Hossain,John D. Wade,John D. Wade,K. Johan Rosengren,Andrew L. Gundlach,Andrew L. Gundlach +17 more
TL;DR: Existing anatomical and functional evidence suggests the highly-conserved neuropeptide, relaxin-3, which signals via its cognate Gi/o-protein coupled receptor, RXFP3, contributes to behavioural arousal and feeding behaviour in rodents, and in light of the established biological and translational importance of other arousal systems, relax in-3/RXFP3 networks warrant further experimental investigation.