BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Rickman OJ, Baple EL, Crosby AH. Lipid metabolic pathways converge in motor neuron degenerative diseases. Brain 2020;143:1073-87. [PMID: 31848577 DOI: 10.1093/brain/awz382] [Cited by in Crossref: 12] [Cited by in F6Publishing: 12] [Article Influence: 6.0] [Reference Citation Analysis]
Number Citing Articles
1 Saputra L, Kumar KR. Challenges and Controversies in the Genetic Diagnosis of Hereditary Spastic Paraplegia. Curr Neurol Neurosci Rep 2021;21:15. [PMID: 33646413 DOI: 10.1007/s11910-021-01099-x] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
2 Wei Q, Luo WJ, Yu H, Wang PS, Dong HL, Li HF, Wu ZY. A novel PCYT2 mutation identified in a Chinese consanguineous family with hereditary spastic paraplegia. J Genet Genomics 2021:S1673-8527(21)00192-2. [PMID: 34384721 DOI: 10.1016/j.jgg.2021.06.008] [Reference Citation Analysis]
3 Varma VR, Büşra Lüleci H, Oommen AM, Varma S, Blackshear CT, Griswold ME, An Y, Roberts JA, O'Brien R, Pletnikova O, Troncoso JC, Bennett DA, Çakır T, Legido-Quigley C, Thambisetty M. Abnormal brain cholesterol homeostasis in Alzheimer's disease-a targeted metabolomic and transcriptomic study. NPJ Aging Mech Dis 2021;7:11. [PMID: 34075056 DOI: 10.1038/s41514-021-00064-9] [Reference Citation Analysis]
4 Kankel MW, Sen A, Lu L, Theodorou M, Dimlich DN, McCampbell A, Henderson CE, Shneider NA, Artavanis-Tsakonas S. Amyotrophic Lateral Sclerosis Modifiers in Drosophila Reveal the Phospholipase D Pathway as a Potential Therapeutic Target. Genetics 2020;215:747-66. [PMID: 32345615 DOI: 10.1534/genetics.119.302985] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 4.0] [Reference Citation Analysis]
5 Mackay-Sim A. Hereditary Spastic Paraplegia: From Genes, Cells and Networks to Novel Pathways for Drug Discovery. Brain Sci 2021;11:403. [PMID: 33810178 DOI: 10.3390/brainsci11030403] [Reference Citation Analysis]
6 Edgar JA, Molyneux RJ, Colegate SM. 1,2-Dehydropyrrolizidine Alkaloids: Their Potential as a Dietary Cause of Sporadic Motor Neuron Diseases. Chem Res Toxicol 2022. [PMID: 35238548 DOI: 10.1021/acs.chemrestox.1c00384] [Reference Citation Analysis]
7 Leonardis L, Skrjanec Pusenjak M, Maver A, Jaklic H, Ozura Brecko A, Koritnik B, Peterlin B, Writzl K. Axonal Polyneuropathy in 2 Brothers With a Homozygous Missense Variant in the First Catalytic Domain of PCYT2. Neurol Genet 2022;8:e658. [PMID: 35243002 DOI: 10.1212/NXG.0000000000000658] [Reference Citation Analysis]
8 Saneto RP, Perez FA. Mitochondria-Associated Membrane Scaffolding with Endoplasmic Reticulum: A Dynamic Pathway of Developmental Disease. Front Mol Biosci 2022;9:908721. [DOI: 10.3389/fmolb.2022.908721] [Reference Citation Analysis]
9 Magnuson JT, Caceres L, Sy N, Ji C, Tanabe P, Gan J, Lydy MJ, Schlenk D. The Use of Non-targeted Lipidomics and Histopathology to Characterize the Neurotoxicity of Bifenthrin to Juvenile Rainbow Trout (Oncorhynchus mykiss). Environ Sci Technol 2022. [PMID: 35876619 DOI: 10.1021/acs.est.2c01542] [Reference Citation Analysis]
10 Kaiyrzhanov R, Wortmann S, Reid T, Dehghani M, Vahidi Mehrjardi MY, Alhaddad B, Wagner M, Deschauer M, Cordts I, Fernandez-Murray JP, Treffer V, Metanat Z, Pitman A, Houlden H, Meitinger T, Carroll C, McMaster CR, Maroofian R. Defective phosphatidylethanolamine biosynthesis leads to a broad ataxia-spasticity spectrum. Brain 2021;144:e30. [PMID: 33454747 DOI: 10.1093/brain/awaa442] [Reference Citation Analysis]
11 Gunay A, Shin HH, Gozutok O, Gautam M, Ozdinler PH. Importance of lipids for upper motor neuron health and disease. Semin Cell Dev Biol 2021;112:92-104. [PMID: 33323321 DOI: 10.1016/j.semcdb.2020.11.004] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
12 Verdura E, Rodríguez-Palmero A, Vélez-Santamaria V, Planas-Serra L, de la Calle I, Raspall-Chaure M, Roubertie A, Benkirane M, Saettini F, Pavinato L, Mandrile G, O'Leary M, O'Heir E, Barredo E, Chacón A, Michaud V, Goizet C, Ruiz M, Schlüter A, Rouvet I, Sala-Coromina J, Fossati C, Iascone M, Canonico F, Marcé-Grau A, de Souza P, Adams DR, Casasnovas C, Rehm HL, Mefford HC, González Gutierrez-Solana L, Brusco A, Koenig M, Macaya A, Pujol A. Biallelic PI4KA variants cause a novel neurodevelopmental syndrome with hypomyelinating leukodystrophy. Brain 2021;144:2659-69. [PMID: 34415322 DOI: 10.1093/brain/awab124] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
13 Melentev PA, Ryabova EV, Surina NV, Zhmujdina DR, Komissarov AE, Ivanova EA, Boltneva NP, Makhaeva GF, Sliusarenko MI, Yatsenko AS, Mohylyak II, Matiytsiv NP, Shcherbata HR, Sarantseva SV. Loss of swiss cheese in Neurons Contributes to Neurodegeneration with Mitochondria Abnormalities, Reactive Oxygen Species Acceleration and Accumulation of Lipid Droplets in Drosophila Brain. Int J Mol Sci 2021;22:8275. [PMID: 34361042 DOI: 10.3390/ijms22158275] [Reference Citation Analysis]
14 De Winter J, Beijer D, De Ridder W, Synofzik M, Zuchner SL, Van Damme P, Spileers W, Baets J; PREPARE consortium. PCYT2 mutations disrupting etherlipid biosynthesis: phenotypes converging on the CDP-ethanolamine pathway. Brain 2021;144:e17. [PMID: 33230519 DOI: 10.1093/brain/awaa389] [Reference Citation Analysis]
15 Vélez-Santamaría V, Verdura E, Macmurdo C, Planas-Serra L, Schlüter A, Casas J, Martínez JJ, Casasnovas C, Si Y, Thompson SS, Maroofian R, Pujol A. Expanding the clinical and genetic spectrum of PCYT2-related disorders. Brain 2020;143:e76. [PMID: 32889549 DOI: 10.1093/brain/awaa229] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 4.0] [Reference Citation Analysis]
16 Sree S, Parkkinen I, Their A, Airavaara M, Jokitalo E. Morphological Heterogeneity of the Endoplasmic Reticulum within Neurons and Its Implications in Neurodegeneration. Cells 2021;10:970. [PMID: 33919188 DOI: 10.3390/cells10050970] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
17 Fernández-Beltrán LC, Godoy-Corchuelo JM, Losa-Fontangordo M, Williams D, Matias-Guiu J, Corrochano S. A Transcriptomic Meta-Analysis Shows Lipid Metabolism Dysregulation as an Early Pathological Mechanism in the Spinal Cord of SOD1 Mice. Int J Mol Sci 2021;22:9553. [PMID: 34502460 DOI: 10.3390/ijms22179553] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
18 Zhao J, Zhang H, Fan X, Yu X, Huai J. Lipid Dyshomeostasis and Inherited Cerebellar Ataxia. Mol Neurobiol 2022. [PMID: 35420383 DOI: 10.1007/s12035-022-02826-2] [Reference Citation Analysis]