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Search life-sciences literature (45,104,145 articles, preprints and more)

Suggested authors matching "AUTH:Holt I" with an ORCID

ian holt
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Dysregulated FOXO1 activity drives skeletal muscle intrinsic dysfunction in amyotrophic lateral sclerosis.
Zufiría M, Pikatza-Menoio O, Garciandia-Arcelus M, Bengoetxea X, Jiménez A, Elicegui A, Levchuk M, Arnold-García O, Ondaro J, Iruzubieta P, Rodríguez-Gómez L, Fernández-Pelayo U, Muñoz-Oreja M, Aiastui A, García-Verdugo JM, Herranz-Pérez V, Zulaica M, Poza JJ, Ruiz-Onandi R, [...] Alonso-Martín S
Acta Neuropathol, 148(1):43, 16 Sep 2024
Cited by: 0 articles | PMID: 39283487 | PMCID: PMC11405449
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Deep learning-driven neuromorphogenesis screenings identify repurposable drugs for mitochondrial disease
Menacho C, Okawa S, Álvarez-Merz I, Wittich A, Muñoz-Oreja M, Lisowski P, Pentimalli TM, Rybak-Wolf A, Inak G, Zakin S, Thevandavakkam M, Petersilie L, Zaliani A, Mlody B, Seibt A, Donnelly J, Woleben K, Fernandez-Checa J, Herebian D, [...] Prigione A
bioRxiv, 12 Jul 2024
Cited by: 0 articles | PPR: PPR880171
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Dysregulated FOXO1 activity drives skeletal muscle intrinsic dysfunction in amyotrophic lateral sclerosis
Zufiría M, Pikatza-Menoio O, Garciandia-Arcelus M, Bengoetxea X, Jiménez A, Elicegui A, Levchuk M, Arnold-García O, Iruzubieta P, Ondaro J, Fernández-Pelayo U, Muñoz-Oreja M, Aiastui A, García-Verdugo JM, Herranz-Pérez V, Zulaica M, Poza JJ, Ruiz-Onandi R, Fernández-Torrón R, [...] Alonso-Martín S
medRxiv, 17 Jul 2024
Cited by: 0 articles | PPR: PPR883013
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Elevated cholesterol in ATAD3 mutants is a compensatory mechanism that leads to membrane cholesterol aggregation.
Muñoz-Oreja M, Sandoval A, Bruland O, Perez-Rodriguez D, Fernandez-Pelayo U, de Arbina AL, Villar-Fernandez M, Hernández-Eguiazu H, Hernández I, Park Y, Goicoechea L, Pascual-Frías N, Garcia-Ruiz C, Fernandez-Checa J, Martí-Carrera I, Gil-Bea FJ, Hasan MT, Gegg ME, Bredrup C, [...] Holt IJ
Brain, 147(5):1899-1913, 01 May 2024
Cited by: 0 articles | PMID: 38242545 | PMCID: PMC11068212
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Proteomic characterization of human LMNA-related congenital muscular dystrophy muscle cells.
Storey EC, Holt I, Brown S, Synowsky S, Shirran S, Fuller HR
Neuromuscul Disord, 38:26-41, 15 Mar 2024
Cited by: 0 articles | PMID: 38554696
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Mitochondrial DNA competition: starving out the mutant genome.
Spinazzola A, Perez-Rodriguez D, Ježek J, Holt IJ
Trends Pharmacol Sci, 45(3):225-242, 23 Feb 2024
Cited by: 1 article | PMID: 38402076
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Energy scarcity and impaired mitochondrial translation induce perinuclear stress granule clustering
Fernandez-Pelayo U, Muñoz-Oreja M, Villar-Fernandez M, de Arbina AL, Aiestaran-Zelaia I, Sánchez-Guisado MJ, Pantic B, Elicegui A, Zufiria M, Iruzubieta P, Sagartzazu-Aizpurua M, Aizpurua JM, Gegg M, Alonso-Martin S, Ruiz-Cabello J, Gil-Bea F, Spinazzola A, de Munain AL, Holt IJ
bioRxiv, 04 Feb 2024
Cited by: 0 articles | PPR: PPR800755
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Metabolic Malfunction Mars Muscle Mitochondria.
Primiano G, Holt I
Neurol Genet, 10(1):e200126, 22 Jan 2024
Cited by: 0 articles | PMID: 38716325 | PMCID: PMC11073863
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Lipid Dysregulation Unveil the Intricate Interplay of Lysosomal and Mitochondrial Changes in Frontotemporal Dementia with GRN Haploinsufficiency
Ondaro J, Zúñiga-Elizari JL, Zufiría M, Garciandia-Arcelus M, Zulaica M, Lafarga M, Riancho J, Holt IJ, López de Munaín A, Moreno F, Gil-Bea FJ, Gereñu G
bioRxiv, 22 Jan 2024
Cited by: 0 articles | PPR: PPR791065
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Recombinant lysyl oxidase effects on embryonic tendon cell phenotype and behavior.
Nguyen PK, Hall K, Holt I, Kuo CK
J Orthop Res, 41(10):2175-2185, 10 Jul 2023
Cited by: 0 articles | PMID: 37365857 | PMCID: PMC11487497
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Establishing in vivo and ex vivo chick embryo models to investigate fetal tendon healing.
Nguyen PK, Hart C, Hall K, Holt I, Kuo CK
Sci Rep, 13(1):9600, 13 Jun 2023
Cited by: 0 articles | PMID: 37311784 | PMCID: PMC10264358
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The Proteome Signatures of Fibroblasts from Patients with Severe, Intermediate and Mild Spinal Muscular Atrophy Show Limited Overlap.
Brown SJ, Kline RA, Synowsky SA, Shirran SL, Holt I, Sillence KA, Claus P, Wirth B, Wishart TM, Fuller HR
Cells, 11(17):2624, 23 Aug 2022
Cited by: 4 articles | PMID: 36078032 | PMCID: PMC9454632
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Tendon mechanical properties are enhanced via recombinant lysyl oxidase treatment.
Nguyen PK, Jana A, Huang C, Grafton A, Holt I, Giacomelli M, Kuo CK
Front Bioeng Biotechnol, 10:945639, 05 Aug 2022
Cited by: 7 articles | PMID: 35992359 | PMCID: PMC9389157
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2 deoxy-D-glucose augments the mitochondrial respiratory chain in heart.
Aiestaran-Zelaia I, Sánchez-Guisado MJ, Villar-Fernandez M, Azkargorta M, Fadon-Padilla L, Fernandez-Pelayo U, Perez-Rodriguez D, Ramos-Cabrer P, Spinazzola A, Elortza F, Ruíz-Cabello J, Holt IJ
Sci Rep, 12(1):6890, 27 Apr 2022
Cited by: 6 articles | PMID: 35478201 | PMCID: PMC9044724
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Defects of Nutrient Signaling and Autophagy in Neurodegeneration.
Ondaro J, Hernandez-Eguiazu H, Garciandia-Arcelus M, Loera-Valencia R, Rodriguez-Gómez L, Jiménez-Zúñiga A, Goikolea J, Rodriguez-Rodriguez P, Ruiz-Martinez J, Moreno F, Lopez de Munain A, Holt IJ, Gil-Bea FJ, Gereñu G
Front Cell Dev Biol, 10:836196, 28 Mar 2022
Cited by: 3 articles | PMID: 35419363 | PMCID: PMC8996160
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R-Loops and Mitochondrial DNA Metabolism.
Holt IJ
Methods Mol Biol, 2528:173-202, 01 Jan 2022
Cited by: 5 articles | PMID: 35704192
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2-Deoxy-D-glucose couples mitochondrial DNA replication with mitochondrial fitness and promotes the selection of wild-type over mutant mitochondrial DNA.
Pantic B, Ives D, Mennuni M, Perez-Rodriguez D, Fernandez-Pelayo U, Lopez de Arbina A, Muñoz-Oreja M, Villar-Fernandez M, Dang TJ, Vergani L, Johnston IG, Pitceathly RDS, McFarland R, Hanna MG, Taylor RW, Holt IJ, Spinazzola A
Nat Commun, 12(1):6997, 06 Dec 2021
Cited by: 8 articles | PMID: 34873176 | PMCID: PMC8648849
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Role of Bradykinin Type 2 Receptors in Human Sweat Secretion: Translational Evidence Does Not Support a Functional Relationship.
Wilson TE, Narra S, Metzler-Wilson K, Schneider A, Bullens KA, Holt IS
Skin Pharmacol Physiol, 34(3):162-166, 01 Apr 2021
Cited by: 1 article | PMID: 33794540 | PMCID: PMC10246487
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Uniparental isodisomy of chromosome 2 causing MRPL44-related multisystem mitochondrial disease.
Horga A, Manole A, Mitchell AL, Bugiardini E, Hargreaves IP, Mowafi W, Bettencourt C, Blakely EL, He L, Polke JM, Woodward CE, Dalla Rosa I, Shah S, Pittman AM, Quinlivan R, Reilly MM, Taylor RW, Holt IJ, Hanna MG, [...] Houlden H
Mol Biol Rep, 48(3):2093-2104, 19 Mar 2021
Cited by: 4 articles | PMID: 33742325
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Role of bradykinin type 2 receptors in human sweat secretion: translational evidence does not support a functional relationship
Wilson TE, Narra S, Metzler-Wilson K, Schneider A, Bullens KA, Holt IS
bioRxiv, 02 Dec 2020
Cited by: 0 articles | PPR: PPR248171
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An interaction of heart disease-associated proteins POPDC1/2 with XIRP1 in transverse tubules and intercalated discs.
Holt I, Fuller HR, Schindler RFR, Shirran SL, Brand T, Morris GE
BMC Mol Cell Biol, 21(1):88, 01 Dec 2020
Cited by: 6 articles | PMID: 33261556 | PMCID: PMC7709239
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Muscle cell differentiation and development pathway defects in Emery-Dreifuss muscular dystrophy.
Storey EC, Holt I, Morris GE, Fuller HR
Neuromuscul Disord, 30(6):443-456, 11 May 2020
Cited by: 5 articles | PMID: 32522500
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Recurrent De Novo NAHR Reciprocal Duplications in the ATAD3 Gene Cluster Cause a Neurogenetic Trait with Perturbed Cholesterol and Mitochondrial Metabolism.
Gunning AC, Strucinska K, Muñoz Oreja M, Parrish A, Caswell R, Stals KL, Durigon R, Durlacher-Betzer K, Cunningham MH, Grochowski CM, Baptista J, Tysoe C, Baple E, Lahiri N, Homfray T, Scurr I, Armstrong C, Dean J, Fernandez Pelayo U, [...] Ellard S
Am J Hum Genet, 106(2):272-279, 30 Jan 2020
Cited by: 19 articles | PMID: 32004445 | PMCID: PMC7010973
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Reply to: "Mitochondrial Parkinsonism due to SPG7/Paraplegin variants with secondary mtDNA depletion".
De la Casa-Fages B, Fernández-Eulate G, Gamez J, Barahona-Hernando R, Morís G, García-Barcina M, Infante J, Zulaica M, Fernández-Pelayo U, Muñoz-Oreja M, Urtasun M, Olaskoaga A, Zelaya V, Jericó I, Saez-Villaverde R, Catalina I, Sola E, Martínez-Sáez E, Pujol A, [...] López de Munaín A
Mov Disord, 34(12):1932-1933, 01 Dec 2019
Cited by: 0 articles | PMID: 31845766
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Lamin A/C dysregulation contributes to cardiac pathology in a mouse model of severe spinal muscular atrophy.
Šoltić D, Shorrock HK, Allardyce H, Wilson EL, Holt I, Synowsky SA, Shirran SL, Parson SH, Gillingwater TH, Fuller HR
Hum Mol Genet, 28(21):3515-3527, 01 Nov 2019
Cited by: 8 articles | PMID: 31397869 | PMCID: PMC6927462
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Search life-sciences literature (45,104,145 articles, preprints and more)

Suggested authors matching "AUTH:Holt I" with an ORCID

Search results

Dysregulated FOXO1 activity drives skeletal muscle intrinsic dysfunction in amyotrophic lateral sclerosis.

Deep learning-driven neuromorphogenesis screenings identify repurposable drugs for mitochondrial disease

Dysregulated FOXO1 activity drives skeletal muscle intrinsic dysfunction in amyotrophic lateral sclerosis

Elevated cholesterol in ATAD3 mutants is a compensatory mechanism that leads to membrane cholesterol aggregation.

Proteomic characterization of human LMNA-related congenital muscular dystrophy muscle cells.

Mitochondrial DNA competition: starving out the mutant genome.

Energy scarcity and impaired mitochondrial translation induce perinuclear stress granule clustering

Metabolic Malfunction Mars Muscle Mitochondria.

Lipid Dysregulation Unveil the Intricate Interplay of Lysosomal and Mitochondrial Changes in Frontotemporal Dementia with GRN Haploinsufficiency

Recombinant lysyl oxidase effects on embryonic tendon cell phenotype and behavior.

Establishing in vivo and ex vivo chick embryo models to investigate fetal tendon healing.

The Proteome Signatures of Fibroblasts from Patients with Severe, Intermediate and Mild Spinal Muscular Atrophy Show Limited Overlap.

Tendon mechanical properties are enhanced via recombinant lysyl oxidase treatment.

2 deoxy-D-glucose augments the mitochondrial respiratory chain in heart.

Defects of Nutrient Signaling and Autophagy in Neurodegeneration.

R-Loops and Mitochondrial DNA Metabolism.

2-Deoxy-D-glucose couples mitochondrial DNA replication with mitochondrial fitness and promotes the selection of wild-type over mutant mitochondrial DNA.

Role of Bradykinin Type 2 Receptors in Human Sweat Secretion: Translational Evidence Does Not Support a Functional Relationship.

Uniparental isodisomy of chromosome 2 causing MRPL44-related multisystem mitochondrial disease.

Role of bradykinin type 2 receptors in human sweat secretion: translational evidence does not support a functional relationship

An interaction of heart disease-associated proteins POPDC1/2 with XIRP1 in transverse tubules and intercalated discs.

Muscle cell differentiation and development pathway defects in Emery-Dreifuss muscular dystrophy.

Recurrent De Novo NAHR Reciprocal Duplications in the ATAD3 Gene Cluster Cause a Neurogenetic Trait with Perturbed Cholesterol and Mitochondrial Metabolism.

Reply to: "Mitochondrial Parkinsonism due to SPG7/Paraplegin variants with secondary mtDNA depletion".

Lamin A/C dysregulation contributes to cardiac pathology in a mouse model of severe spinal muscular atrophy.

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