These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
206 related articles for article (PubMed ID: 37491316)
1. Synapse-Specific Defects in Synaptic Transmission in the Cerebellum of W246G Mutant ELOVL4 Rats-a Model of Human SCA34. Nagaraja RY; Stiles MA; Sherry DM; Agbaga MP; Ahmad M J Neurosci; 2023 Aug; 43(33):5963-5974. PubMed ID: 37491316 [TBL] [Abstract][Full Text] [Related]
2. W246G Mutant ELOVL4 Impairs Synaptic Plasticity in Parallel and Climbing Fibers and Causes Motor Defects in a Rat Model of SCA34. Nagaraja RY; Sherry DM; Fessler JL; Stiles MA; Li F; Multani K; Orock A; Ahmad M; Brush RS; Anderson RE; Agbaga MP; Deák F Mol Neurobiol; 2021 Oct; 58(10):4921-4943. PubMed ID: 34227061 [TBL] [Abstract][Full Text] [Related]
3. The Spinocerebellar Ataxia 34-Causing W246G ELOVL4 Mutation Does Not Alter Cerebellar Neuron Populations in a Rat Model. Fessler JL; Stiles MA; Agbaga MP; Ahmad M; Sherry DM Cerebellum; 2024 Oct; 23(5):2082-2094. PubMed ID: 38850484 [TBL] [Abstract][Full Text] [Related]
4. The Elovl4 Spinocerebellar Ataxia-34 Mutation 736T>G (p.W246G) Impairs Retinal Function in the Absence of Photoreceptor Degeneration. Agbaga MP; Stiles MA; Brush RS; Sullivan MT; Machalinski A; Jones KL; Anderson RE; Sherry DM Mol Neurobiol; 2020 Nov; 57(11):4735-4753. PubMed ID: 32780351 [TBL] [Abstract][Full Text] [Related]
5. ELOVL4 Mutations That Cause Spinocerebellar Ataxia-34 Differentially Alter Very Long Chain Fatty Acid Biosynthesis. Gyening YK; Chauhan NK; Tytanic M; Ea V; Brush RS; Agbaga MP J Lipid Res; 2023 Jan; 64(1):100317. PubMed ID: 36464075 [TBL] [Abstract][Full Text] [Related]
6. A novel ELOVL4 variant, L168S, causes early childhood-onset Spinocerebellar ataxia-34 and retinal dysfunction: a case report. Gyening YK; Boris K; Cyril M; Brush RS; Nassogne MC; Agbaga MP Acta Neuropathol Commun; 2023 Aug; 11(1):131. PubMed ID: 37568198 [TBL] [Abstract][Full Text] [Related]
7. Homozygous Expression of Mutant ELOVL4 Leads to Seizures and Death in a Novel Animal Model of Very Long-Chain Fatty Acid Deficiency. Hopiavuori BR; Deák F; Wilkerson JL; Brush RS; Rocha-Hopiavuori NA; Hopiavuori AR; Ozan KG; Sullivan MT; Wren JD; Georgescu C; Szweda L; Awasthi V; Towner R; Sherry DM; Anderson RE; Agbaga MP Mol Neurobiol; 2018 Feb; 55(2):1795-1813. PubMed ID: 29168048 [TBL] [Abstract][Full Text] [Related]
8. A Novel Mutation in ELOVL4 Leading to Spinocerebellar Ataxia (SCA) With the Hot Cross Bun Sign but Lacking Erythrokeratodermia: A Broadened Spectrum of SCA34. Ozaki K; Doi H; Mitsui J; Sato N; Iikuni Y; Majima T; Yamane K; Irioka T; Ishiura H; Doi K; Morishita S; Higashi M; Sekiguchi T; Koyama K; Ueda N; Miura Y; Miyatake S; Matsumoto N; Yokota T; Tanaka F; Tsuji S; Mizusawa H; Ishikawa K JAMA Neurol; 2015 Jul; 72(7):797-805. PubMed ID: 26010696 [TBL] [Abstract][Full Text] [Related]
9. Novel Cellular Functions of Very Long Chain-Fatty Acids: Insight From ELOVL4 Mutations. Deák F; Anderson RE; Fessler JL; Sherry DM Front Cell Neurosci; 2019; 13():428. PubMed ID: 31616255 [TBL] [Abstract][Full Text] [Related]
10. Potential Clinical Benefit of Very Long Chain Fatty Acid Supplementation in Spinocerebellar Ataxia Type 34. Gazulla J; Berciano J Cerebellum; 2024 Oct; 23(5):2193-2196. PubMed ID: 38771545 [TBL] [Abstract][Full Text] [Related]
11. Cannabinoid receptor modulation of synapses received by cerebellar Purkinje cells. Takahashi KA; Linden DJ J Neurophysiol; 2000 Mar; 83(3):1167-80. PubMed ID: 10712447 [TBL] [Abstract][Full Text] [Related]
12. Neuropathology of SCA34 showing widespread oligodendroglial pathology with vacuolar white matter degeneration: a case study. Ozaki K; Irioka T; Uchihara T; Yamada A; Nakamura A; Majima T; Igarashi S; Shintaku H; Yakeishi M; Tsuura Y; Okazaki Y; Ishikawa K; Yokota T Acta Neuropathol Commun; 2021 Oct; 9(1):172. PubMed ID: 34689836 [TBL] [Abstract][Full Text] [Related]
13. ELOVL4: Very long-chain fatty acids serve an eclectic role in mammalian health and function. Hopiavuori BR; Anderson RE; Agbaga MP Prog Retin Eye Res; 2019 Mar; 69():137-158. PubMed ID: 30982505 [TBL] [Abstract][Full Text] [Related]
14. α2δ-2 Protein Controls Structure and Function at the Cerebellar Climbing Fiber Synapse. Beeson KA; Beeson R; Westbrook GL; Schnell E J Neurosci; 2020 Mar; 40(12):2403-2415. PubMed ID: 32086258 [TBL] [Abstract][Full Text] [Related]
15. Incomplete Elongation of Ultra-long-chain Polyunsaturated Acyl-CoAs by the Fatty Acid Elongase ELOVL4 in Spinocerebellar Ataxia Type 34. Tamura Y; Sassa T; Nishizawa T; Kihara A Mol Cell Biol; 2023 Feb; 43(2):1-17. PubMed ID: 36748939 [TBL] [Abstract][Full Text] [Related]
16. Impact of the leaner P/Q-type Ca2+ channel mutation on excitatory synaptic transmission in cerebellar Purkinje cells. Liu S; Friel DD J Physiol; 2008 Sep; 586(18):4501-15. PubMed ID: 18669535 [TBL] [Abstract][Full Text] [Related]
17. Very long chain fatty acid-containing lipids: a decade of novel insights from the study of ELOVL4. Yeboah GK; Lobanova ES; Brush RS; Agbaga MP J Lipid Res; 2021; 62():100030. PubMed ID: 33556440 [TBL] [Abstract][Full Text] [Related]
18. Bidirectional alterations in cerebellar synaptic transmission of tottering and rolling Ca2+ channel mutant mice. Matsushita K; Wakamori M; Rhyu IJ; Arii T; Oda S; Mori Y; Imoto K J Neurosci; 2002 Jun; 22(11):4388-98. PubMed ID: 12040045 [TBL] [Abstract][Full Text] [Related]
19. Alcohol impairs long-term depression at the cerebellar parallel fiber-Purkinje cell synapse. Belmeguenai A; Botta P; Weber JT; Carta M; De Ruiter M; De Zeeuw CI; Valenzuela CF; Hansel C J Neurophysiol; 2008 Dec; 100(6):3167-74. PubMed ID: 18922952 [TBL] [Abstract][Full Text] [Related]
20. Mutant PKCγ in spinocerebellar ataxia type 14 disrupts synapse elimination and long-term depression in Purkinje cells in vivo. Shuvaev AN; Horiuchi H; Seki T; Goenawan H; Irie T; Iizuka A; Sakai N; Hirai H J Neurosci; 2011 Oct; 31(40):14324-34. PubMed ID: 21976518 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]