Volume 39, Issue 4, 2025

 

Original Research Articles

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Gut microbial metabolites link dietary history to appetite regulation

Emma C. Spillman, Andrew K. Shepherd, Meihua C. Kuang, In-Hwan Jang, Won-Jae Lee & Jing W. Wang

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Analysis of whole genome sequence data shows association of Alzheimer’s disease with rare coding variants in ABCA7, PSEN1, SORL1 and TREM2

David Curtis, Shujaani Joseph & the Alzheimer’s Disease Neuroimaging Initiative

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Simultaneous recording of spikes and calcium signals in odor-evoked responses of Drosophila antennal neurons

Yiyi Xiao, Shiuan-Tze Wu, Yinan Xuan, Scott A. Rifkin & Chih-Ying Su

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Conservation and diversification of mating behavior patterns among three sibling species in the Drosophila subobscura species subgroup

Kenta Tomihara, Ryoya Tanaka, Francisco Rodríguez-Trelles & Daisuke Yamamoto

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A cell-autonomous role for the vitamin B6 metabolism gene PNPO in Drosophila GABAergic neurons

Wenqin Fu, Saul Landaverde, Xiaoxi Zhuang & Atulya Iyengar

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Serum LncRNA XIST and miR-133b as non-invasive biomarkers for diagnosis and progression of Parkinson’s disease

Weihua Rao & Yanqiong Qin

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Review Article

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Genetic convergence in brain aging and neurodegeneration: from cellular mechanisms to therapeutic targets

Polu Picheswara Rao & Shubham Mishra

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Volume 39, Issue 2-3, 2025

 

Original Research Articles

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A novel role of Arp2/3 complex in the forgetting behavior of Caenorhabditis elegans to Pseudomonas aeruginosa PA14

Xin Zhao, Xinyu Li, Hua Bai, Xiaoying Liu, Yaqi Deng, Yu Duan, Qi Wang & Wei Zou

 

The ataxin-2 protein is required in kenyon cells for RNP-granule assembly and appetitive long-term memory formation

Camilla Roselli, Jens Hillebrand, Jenifer Kaldun, Vernon Leander Monteiro, Thomas Hurd, Simon G. Sprecher, Tamara Boto & Mani Ramaswami

 

Brief Reports

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Congenital mirror movements in a family: Outcomes associated with DCC mutations

Arife Derda Yücel Şen, Kursat Bora Carman, Çağrı Doğan, Mustafa Şen & Coşkun Yarar

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Impact of gene-gene interactions in Progressive Supranuclear Palsy: new genetic perspectives in the Asian-Indian population

Saikat Dey, Monojit Debnath, Ramchandra Yelamanchi, Nitish Kamble, Vikram V. Holla, Rohan R. Mahale, Pramod Kumar Pal & Ravi Yadav

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Original Research Article

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Analysis of 470,000 exome-sequenced UK biobank participants identifies genes containing rare variants which confer dementia risk

Lily Gibbons & David Curtis

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Volume 39, Issue 1, 2025

 

Commentaries

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Venerose: a nuptial gift with implications

Deepanshu N. D. Singh & Matthias Soller

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Two tales of therapeutic innovations for Leigh syndrome spectrum

Wei-Sheng Lin

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Original Research Articles

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Vitamin D receptor FokI polymorphism as a risk factor for painful diabetic neuropathy in type 2 diabetes mellitus patients

Aurelia Vania, Dewa Putu Gde Purwa Samatra, I Made Oka Adnyana, Made Ratna Saraswati, Agus Eka Darwinata & I Putu Eka Widyadharma

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The novel T107I Inherited prion disease can present as a clinical and biomarker mimic of familial Alzheimer’s disease

Leah Holm-Mercer, Thomas Coysh, Tze How Mok, Peter Rudge, Zita Reisz, Claire Troakes, Safa Al-Sarraj, Tracy Campbell, Laszlo L.P. Hosszu, Jan Bieschke, Fuquan Zhang, Jonathan D.F. Wadsworth, Colin Smith, Jenna Jenkinson, Timothy Rittman, Sebastian Brandner, Zane Jaunmuktane, John Collinge & Simon Mead

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Drosophila WDFY3/Bchs overexpression impairs neural function

Marek B. Körner, Akhil Velluva, Linnaeus Bundalian, Knut Krohn, Kathleen Schön, Isabell Schumann, Jessica Kromp, Andreas S. Thum, Antje Garten, Julia Hentschel, Rami Abou Jamra, Achmed Mrestani, Nicole Scholz, Tobias Langenhan & Diana Le Duc​