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Search life-sciences literature (45,100,050 articles, preprints and more)

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Selective Enhancement of REM Sleep in Male Rats through Activation of Melatonin MT₁ Receptors Located in the Locus Ceruleus Norepinephrine Neurons.
López-Canul M, He Q, Sasson T, Ettaoussi M, Gregorio D, Ochoa-Sanchez R, Catoire H, Posa L, Rouleau G, Beaulieu JM, Comai S, Gobbi G
J Neurosci, 44(29):e0914232024, 17 Jul 2024
Cited by: 1 article | PMID: 38744530 | PMCID: PMC11255427
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Autism-associated CHD8 controls reactive gliosis and neuroinflammation via remodeling chromatin in astrocytes.
Megagiannis P, Mei Y, Yan RE, Yuan L, Wilde JJ, Eckersberg H, Suresh R, Tan X, Chen H, Farmer WT, Cha K, Le PU, Catoire H, Rochefort D, Kwan T, Yee BA, Dion P, Krishnaswamy A, Cloutier JF, [...] Zhou Y
Cell Rep, 43(8):114637, 17 Aug 2024
Cited by: 0 articles | PMID: 39154337
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Spinal cord extracts of amyotrophic lateral sclerosis spread TDP-43 pathology in cerebral organoids.
Tamaki Y, Ross JP, Alipour P, Castonguay CÉ, Li B, Catoire H, Rochefort D, Urushitani M, Takahashi R, Sonnen JA, Stifani S, Dion PA, Rouleau GA
PLoS Genet, 19(2):e1010606, 06 Feb 2023
Cited by: 17 articles | PMID: 36745687 | PMCID: PMC9934440
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Spinal cord extracts of amyotrophic lateral sclerosis spread TDP-43 pathology in cerebral organoids
Tamaki Y, Ross JP, Alipour P, Catoire H, Rochefort D, Urushitani M, Takahashi R, Sonnen JA, Stifani S, Dion PA, Rouleau GA
bioRxiv, 05 May 2022
Cited by: 0 articles | PPR: PPR489455
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Transcriptome-wide association study reveals increased neuronal FLT3 expression is associated with Tourette's syndrome.
Liao C, Vuokila V, Catoire H, Akçimen F, Ross JP, Bourassa CV, Dion PA, Meijer IA, Rouleau GA
Commun Biol, 5(1):289, 30 Mar 2022
Cited by: 4 articles | PMID: 35354918 | PMCID: PMC8967882
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Association of Essential Tremor With Novel Risk Loci: A Genome-Wide Association Study and Meta-analysis.
Liao C, Castonguay CE, Heilbron K, Vuokila V, Medeiros M, Houle G, Akçimen F, Ross JP, Catoire H, Diez-Fairen M, Kang J, Mueller SH, Girard SL, Hopfner F, Lorenz D, Clark LN, Soto-Beasley AI, Klebe S, Hallett M, [...] 23andMe Research Team
JAMA Neurol, 79(2):185-193, 01 Feb 2022
Cited by: 11 articles | PMID: 34982113 | PMCID: PMC8728658
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Assessing the NOTCH2NLC GGC expansion in European patients with essential tremor.
Liao C, Akçimen F, Diez-Fairen M, Houle G, Ross JP, Schmilovich Z, Spiegelman D, Vuokila V, Catoire H, Meijer IA, Pastor P, Rajput A, Dion PA, Rouleau GA
Brain, 143(11):e89, 01 Dec 2020
Cited by: 5 articles | PMID: 33146671
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Transcriptomic Changes Resulting From STK32B Overexpression Identify Pathways Potentially Relevant to Essential Tremor.
Liao C, Sarayloo F, Vuokila V, Rochefort D, Akçimen F, Diamond S, Houle G, Laporte AD, Spiegelman D, He Q, Catoire H, Dion PA, Rouleau GA
Front Genet, 11:813, 31 Jul 2020
Cited by: 8 articles | PMID: 32849812 | PMCID: PMC7413243
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Genome-wide association study identifies genetic factors that modify age at onset in Machado-Joseph disease.
Akçimen F, Martins S, Liao C, Bourassa CV, Catoire H, Nicholson GA, Riess O, Raposo M, França MC, Vasconcelos J, Lima M, Lopes-Cendes I, Saraiva-Pereira ML, Jardim LB, Sequeiros J, Dion PA, Rouleau GA
Aging (Albany NY), 12(6):4742-4756, 23 Mar 2020
Cited by: 4 articles | PMID: 32205469 | PMCID: PMC7138549
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Increased expression of genetically-regulatedFLT3implicated in Tourette’s Syndrome
Liao C, Vuokila V, Catoire H, Akçimen F, Ross JP, Bourassa CV, Dion PA, Meijer IA, Rouleau GA
bioRxiv, 21 Oct 2019
Cited by: 0 articles | PPR: PPR99276
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Mineral absorption is an enriched pathway in a brain region of restless legs syndrome patients with reduced MEIS1 expression.
Sarayloo F, Dionne-Laporte A, Catoire H, Rochefort D, Houle G, Ross JP, Akçimen F, Barros Oliveira R, Turecki G, Dion PA, Rouleau GA
PLoS One, 14(11):e0225186, 14 Nov 2019
Cited by: 7 articles | PMID: 31725784 | PMCID: PMC6855629
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Genome-wide association study identifies genetic factors that modify age at onset in Machado-Joseph disease
Akçimen F, Martins S, Liao C, Bourassa CV, Catoire H, Nicholson GA, Riess O, Raposo M, França MC, Vasconcelos J, Lima M, Lopes-Cendes I, Saraiva-Pereira ML, Jardim LB, Sequeiros J, Dion PA, Rouleau GA
bioRxiv, 08 Nov 2019
Cited by: 0 articles | PPR: PPR101355
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Somatic expansion of the C9orf72 hexanucleotide repeat does not occur in ALS spinal cord tissues.
Ross JP, Leblond CS, Catoire H, Volkening K, Strong M, Zinman L, Robertson J, Dion PA, Rouleau GA
Neurol Genet, 5(2):e317, 19 Mar 2019
Cited by: 6 articles | PMID: 31041398 | PMCID: PMC6454309
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Transcriptomic changes resulting fromSTK32Boverexpression identifies pathways potentially relevant to essential tremor
Liao C, Sarayloo F, Rochefort D, Akçimen F, Diamond GS, Laporte AD, Spiegelman D, He Q, Catoire H, Dion PA, Rouleau GA
bioRxiv, 18 Feb 2019
Cited by: 0 articles | PPR: PPR70833
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Reassessing GWAS findings for the shared genetic basis of insomnia and restless legs syndrome.
El Gewely M, Welman M, Xiong L, Yin S, Catoire H, Rouleau G, Montplaisir JY, Desautels A, Warby SC
Sleep, 41(11), 01 Nov 2018
Cited by: 11 articles | PMID: 30215811
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A direct interaction between two Restless Legs Syndrome predisposing genes: MEIS1 and SKOR1.
Catoire H, Sarayloo F, Mourabit Amari K, Apuzzo S, Grant A, Rochefort D, Xiong L, Montplaisir J, Earley CJ, Turecki G, Dion PA, Rouleau GA
Sci Rep, 8(1):12173, 15 Aug 2018
Cited by: 14 articles | PMID: 30111810 | PMCID: PMC6093889
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Exome sequencing identifies FUS mutations as a cause of essential tremor.
Merner ND, Girard SL, Catoire H, Bourassa CV, Belzil VV, Rivière JB, Hince P, Levert A, Dionne-Laporte A, Spiegelman D, Noreau A, Diab S, Szuto A, Fournier H, Raelson J, Belouchi M, Panisset M, Cossette P, Dupré N, [...] Rouleau GA
Am J Hum Genet, 91(2):313-319, 02 Aug 2012
Cited by: 116 articles | PMID: 22863194 | PMCID: PMC3415547
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Restless legs syndrome-associated MEIS1 risk variant influences iron homeostasis.
Catoire H, Dion PA, Xiong L, Amari M, Gaudet R, Girard SL, Noreau A, Gaspar C, Turecki G, Montplaisir JY, Parker JA, Rouleau GA
Ann Neurol, 70(1):170-175, 27 Jun 2011
Cited by: 54 articles | PMID: 21710629
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Cross-talk between canonical Wnt signaling and the sirtuin-FoxO longevity pathway to protect against muscular pathology induced by mutant PABPN1 expression in C. elegans.
Pasco MY, Catoire H, Parker JA, Brais B, Rouleau GA, Néri C
Neurobiol Dis, 38(3):425-433, 19 Mar 2010
Cited by: 10 articles | PMID: 20227501
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MEIS1 intronic risk haplotype associated with restless legs syndrome affects its mRNA and protein expression levels.
Xiong L, Catoire H, Dion P, Gaspar C, Lafrenière RG, Girard SL, Levchenko A, Rivière JB, Fiori L, St-Onge J, Bachand I, Thibodeau P, Allen R, Earley C, Turecki G, Montplaisir J, Rouleau GA
Hum Mol Genet, 18(6):1065-1074, 06 Jan 2009
Cited by: 58 articles | PMID: 19126776 | PMCID: PMC2722232
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Sirtuin inhibition protects from the polyalanine muscular dystrophy protein PABPN1.
Catoire H, Pasco MY, Abu-Baker A, Holbert S, Tourette C, Brais B, Rouleau GA, Parker JA, Néri C
Hum Mol Genet, 17(14):2108-2117, 07 Apr 2008
Cited by: 41 articles | PMID: 18397876
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Resveratrol rescues mutant polyglutamine cytotoxicity in nematode and mammalian neurons.
Parker JA, Arango M, Abderrahmane S, Lambert E, Tourette C, Catoire H, Néri C
Nat Genet, 37(4):349-350, 27 Mar 2005
Cited by: 313 articles | PMID: 15793589
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[Resveratrol rescues mutant polyglutamine cytotoxicity in nematode and mammalian neurons].
Parker AJ, Arango M, Abderrahmane S, Lambert E, Tourette C, Catoire H, Néri C
Med Sci (Paris), 21(5):556-557, 01 May 2005
Cited by: 10 articles | PMID: 15885210
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1-23 of 23 results

Search life-sciences literature (45,100,050 articles, preprints and more)

Search results

Selective Enhancement of REM Sleep in Male Rats through Activation of Melatonin MT₁ Receptors Located in the Locus Ceruleus Norepinephrine Neurons.

Autism-associated CHD8 controls reactive gliosis and neuroinflammation via remodeling chromatin in astrocytes.

Spinal cord extracts of amyotrophic lateral sclerosis spread TDP-43 pathology in cerebral organoids.

Spinal cord extracts of amyotrophic lateral sclerosis spread TDP-43 pathology in cerebral organoids

Transcriptome-wide association study reveals increased neuronal FLT3 expression is associated with Tourette's syndrome.

Association of Essential Tremor With Novel Risk Loci: A Genome-Wide Association Study and Meta-analysis.

Assessing the NOTCH2NLC GGC expansion in European patients with essential tremor.

Transcriptomic Changes Resulting From STK32B Overexpression Identify Pathways Potentially Relevant to Essential Tremor.

Genome-wide association study identifies genetic factors that modify age at onset in Machado-Joseph disease.

Increased expression of genetically-regulatedFLT3implicated in Tourette’s Syndrome

Mineral absorption is an enriched pathway in a brain region of restless legs syndrome patients with reduced MEIS1 expression.

Genome-wide association study identifies genetic factors that modify age at onset in Machado-Joseph disease

Somatic expansion of the C9orf72 hexanucleotide repeat does not occur in ALS spinal cord tissues.

Transcriptomic changes resulting fromSTK32Boverexpression identifies pathways potentially relevant to essential tremor

Reassessing GWAS findings for the shared genetic basis of insomnia and restless legs syndrome.

A direct interaction between two Restless Legs Syndrome predisposing genes: MEIS1 and SKOR1.

Exome sequencing identifies FUS mutations as a cause of essential tremor.

Restless legs syndrome-associated MEIS1 risk variant influences iron homeostasis.

Cross-talk between canonical Wnt signaling and the sirtuin-FoxO longevity pathway to protect against muscular pathology induced by mutant PABPN1 expression in C. elegans.

MEIS1 intronic risk haplotype associated with restless legs syndrome affects its mRNA and protein expression levels.

Sirtuin inhibition protects from the polyalanine muscular dystrophy protein PABPN1.

Resveratrol rescues mutant polyglutamine cytotoxicity in nematode and mammalian neurons.

[Resveratrol rescues mutant polyglutamine cytotoxicity in nematode and mammalian neurons].

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