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Juliana Heidler
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RTN4IP1 is essential for the final stages of mitochondrial complex I assembly and coenzyme Q biosynthesis
Oláhová M, Guerra RM, Collier JJ, Heidler J, Thompson K, White CR, Castañeda-Tamez P, Cabrera-Orefice A, Lightowlers RN, Chrzanowska-Lightowlers ZMA, Wittig I, Pagliarini DJ, Taylor RW
bioRxiv, 05 Sep 2024
Cited by: 0 articles | PPR: PPR906300
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Hyperbaric oxygen treatment reveals spatiotemporal OXPHOS plasticity in the porcine heart.
Heidler J, Cabrera-Orefice A, Wittig I, Heyne E, Tomczak JN, Petersen B, Henze D, Pohjoismäki JLO, Szibor M
PNAS Nexus, 3(6):pgae210, 30 May 2024
Cited by: 0 articles | PMID: 38881840 | PMCID: PMC11179111
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Impaired complex I repair causes recessive Leber's hereditary optic neuropathy.
Stenton SL, Sheremet NL, Catarino CB, Andreeva NA, Assouline Z, Barboni P, Barel O, Berutti R, Bychkov I, Caporali L, Capristo M, Carbonelli M, Cascavilla ML, Charbel Issa P, Freisinger P, Gerber S, Ghezzi D, Graf E, Heidler J, [...] Prokisch H
J Clin Invest, 131(6):138267, 01 Mar 2021
Cited by: 71 articles | PMID: 33465056 | PMCID: PMC7954600
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Prodromal sensory neuropathy in Pink1^-/- SNCA^A53T double mutant Parkinson mice.
Valek L, Tran B, Wilken-Schmitz A, Trautmann S, Heidler J, Schmid T, Brüne B, Thomas D, Deller T, Geisslinger G, Auburger G, Tegeder I
Neuropathol Appl Neurobiol, 47(7):1060-1079, 28 May 2021
Cited by: 8 articles | PMID: 33974284
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Genetic deletion of Nox4 enhances cancerogen-induced formation of solid tumors.
Helfinger V, Freiherr von Gall F, Henke N, Kunze MM, Schmid T, Rezende F, Heidler J, Wittig I, Radeke HH, Marschall V, Anderson K, Shah AM, Fulda S, Brüne B, Brandes RP, Schröder K
Proc Natl Acad Sci U S A, 118(11):e2020152118, 01 Mar 2021
Cited by: 14 articles | PMID: 33836590 | PMCID: PMC7980388
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Bi-allelic pathogenic variants in NDUFC2 cause early-onset Leigh syndrome and stalled biogenesis of complex I.
Alahmad A, Nasca A, Heidler J, Thompson K, Oláhová M, Legati A, Lamantea E, Meisterknecht J, Spagnolo M, He L, Alameer S, Hakami F, Almehdar A, Ardissone A, Alston CL, McFarland R, Wittig I, Ghezzi D, Taylor RW
EMBO Mol Med, 12(11):e12619, 24 Sep 2020
Cited by: 13 articles | PMID: 32969598 | PMCID: PMC7645371
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Mitochondrial Complexome Profiling.
Giese H, Meisterknecht J, Heidler J, Wittig I
Methods Mol Biol, 2192:269-285, 01 Jan 2021
Cited by: 8 articles | PMID: 33230779
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Platelet-derived calpain cleaves the endothelial protease-activated receptor 1 to induce vascular inflammation in diabetes.
Kyselova A, Elgheznawy A, Wittig I, Heidler J, Mann AW, Ruf W, Fleming I, Randriamboavonjy V
Basic Res Cardiol, 115(6):75, 01 Dec 2020
Cited by: 8 articles | PMID: 33258989 | PMCID: PMC7716944
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Mapping the Endothelial Cell S-Sulfhydrome Highlights the Crucial Role of Integrin Sulfhydration in Vascular Function.
Bibli SI, Hu J, Looso M, Weigert A, Ratiu C, Wittig J, Drekolia MK, Tombor L, Randriamboavonjy V, Leisegang MS, Goymann P, Delgado Lagos F, Fisslthaler B, Zukunft S, Kyselova A, Justo AFO, Heidler J, Tsilimigras D, Brandes RP, [...] Fleming I
Circulation, 143(9):935-948, 14 Dec 2020
Cited by: 37 articles | PMID: 33307764
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Redox Regulation of PPARγ in Polarized Macrophages.
Trümper V, Wittig I, Heidler J, Richter F, Brüne B, von Knethen A
PPAR Res, 2020:8253831, 01 Jul 2020
Cited by: 10 articles | PMID: 32695149 | PMCID: PMC7350077
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A salvage pathway maintains highly functional respiratory complex I.
Szczepanowska K, Senft K, Heidler J, Herholz M, Kukat A, Höhne MN, Hofsetz E, Becker C, Kaspar S, Giese H, Zwicker K, Guerrero-Castillo S, Baumann L, Kauppila J, Rumyantseva A, Müller S, Frese CK, Brandt U, Riemer J, [...] Trifunovic A
Nat Commun, 11(1):1643, 02 Apr 2020
Cited by: 53 articles | PMID: 32242014 | PMCID: PMC7118099
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Loss of mitochondrial ClpP, Lonp1, and Tfam triggers transcriptional induction of Rnf213, a susceptibility factor for moyamoya disease.
Key J, Maletzko A, Kohli A, Gispert S, Torres-Odio S, Wittig I, Heidler J, Bárcena C, López-Otín C, Lei Y, West AP, Münch C, Auburger G
Neurogenetics, 21(3):187-203, 28 Apr 2020
Cited by: 12 articles | PMID: 32342250 | PMCID: PMC7283203
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Pathogenic Bi-allelic Mutations in NDUFAF8 Cause Leigh Syndrome with an Isolated Complex I Deficiency.
Alston CL, Veling MT, Heidler J, Taylor LS, Alaimo JT, Sung AY, He L, Hopton S, Broomfield A, Pavaine J, Diaz J, Leon E, Wolf P, McFarland R, Prokisch H, Wortmann SB, Bonnen PE, Wittig I, Pagliarini DJ, Taylor RW
Am J Hum Genet, 106(1):92-101, 19 Dec 2019
Cited by: 27 articles | PMID: 31866046 | PMCID: PMC7042492
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Early prodromal sensory neuropathy in Pink1-SNCA double mutant Parkinson mice
Valek L, Tran B, Wilken-Schmitz A, Trautmann S, Heidler J, Schmid T, Brüne B, Thomas D, Deller T, Geisslinger G, Auburger G, Tegeder I
Research Square, 31 Mar 2020
Cited by: 0 articles | PPR: PPR134320
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Cyp2c44 regulates prostaglandin synthesis, lymphangiogenesis, and metastasis in a mouse model of breast cancer.
Kesavan R, Frömel T, Zukunft S, Laban H, Geyer A, Naeem Z, Heidler J, Wittig I, Elwakeel E, Brüne B, Weigert A, Popp R, Fleming I
Proc Natl Acad Sci U S A, 117(11):5923-5930, 02 Mar 2020
Cited by: 5 articles | PMID: 32123095 | PMCID: PMC7084120
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Respiratory chain signalling is essential for adaptive remodelling following cardiac ischaemia.
Szibor M, Schreckenberg R, Gizatullina Z, Dufour E, Wiesnet M, Dhandapani PK, Debska-Vielhaber G, Heidler J, Wittig I, Nyman TA, Gärtner U, Hall AR, Pell V, Viscomi C, Krieg T, Murphy MP, Braun T, Gellerich FN, Schlüter KD, Jacobs HT
J Cell Mol Med, 24(6):3534-3548, 10 Feb 2020
Cited by: 9 articles | PMID: 32040259 | PMCID: PMC7131948
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Doping free transfer of graphene using aqueous ammonia flow.
Hassanpour Amiri M, Heidler J, Hasnain A, Anwar S, Lu H, Müllen K, Asadi K
RSC Adv, 10(2):1127-1131, 06 Jan 2020
Cited by: 2 articles | PMID: 35494438 | PMCID: PMC9047975
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Bioenergetic consequences from xenotopic expression of a tunicate AOX in mouse mitochondria: Switch from RET and ROS to FET.
Szibor M, Gainutdinov T, Fernandez-Vizarra E, Dufour E, Gizatullina Z, Debska-Vielhaber G, Heidler J, Wittig I, Viscomi C, Gellerich F, Moore AL
Biochim Biophys Acta Bioenerg, 1861(2):148137, 09 Dec 2019
Cited by: 28 articles | PMID: 31825809
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Global Proteome of LonP1^+/- Mouse Embryonal Fibroblasts Reveals Impact on Respiratory Chain, but No Interdependence between Eral1 and Mitoribosomes.
Key J, Kohli A, Bárcena C, López-Otín C, Heidler J, Wittig I, Auburger G
Int J Mol Sci, 20(18):E4523, 12 Sep 2019
Cited by: 12 articles | PMID: 31547314 | PMCID: PMC6770551
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Nitric oxide maintains endothelial redox homeostasis through PKM2 inhibition.
Siragusa M, Thöle J, Bibli SI, Luck B, Loot AE, de Silva K, Wittig I, Heidler J, Stingl H, Randriamboavonjy V, Kohlstedt K, Brüne B, Weigert A, Fisslthaler B, Fleming I
EMBO J, 38(17):e100938, 22 Jul 2019
Cited by: 26 articles | PMID: 31328803 | PMCID: PMC6717893
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Myeloid-Specific Deletion of the AMPKα2 Subunit Alters Monocyte Protein Expression and Atherogenesis.
Fisslthaler B, Zippel N, Abdel Malik R, Delgado Lagos F, Zukunft S, Thoele J, Siuda D, Soehnlein O, Wittig I, Heidler J, Weigert A, Fleming I
Int J Mol Sci, 20(12):E3005, 19 Jun 2019
Cited by: 9 articles | PMID: 31248224 | PMCID: PMC6627871
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Global proteome of LonP1^+/- mouse embryonal fibroblasts reveals impact on respiratory chain, but no interdependence between Eral1 and mitoribosomes
Key J, Kohli A, Bárcena C, López-Otín C, Heidler J, Wittig I, Auburger G
Preprints.org, 10 Jul 2019
Cited by: 0 articles | PPR: PPR85340
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Design guidelines for an electron diffractometer for structural chemistry and structural biology.
Heidler J, Pantelic R, Wennmacher JTC, Zaubitzer C, Fecteau-Lefebvre A, Goldie KN, Müller E, Holstein JJ, van Genderen E, De Carlo S, Gruene T
Acta Crystallogr D Struct Biol, 75(pt 5):458-466, 08 Apr 2019
Cited by: 6 articles | PMID: 31063148 | PMCID: PMC6503764
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TLR2-Dependent Reversible Oxidation of Connexin 43 at Cys260 Modifies Electrical Coupling After Experimental Myocardial Ischemia/Reperfusion.
Raimann FJ, Dröse S, Bonke E, Schneider L, Tybl E, Wittig I, Heidler J, Heide H, Josipovic I, Leisegang M, Brandes RP, Roeper J, Zacharowski K, Mersmann J
J Cardiovasc Transl Res, 12(5):478-487, 08 Apr 2019
Cited by: 2 articles | PMID: 30963423
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Bi-allelic Mutations in NDUFA6 Establish Its Role in Early-Onset Isolated Mitochondrial Complex I Deficiency.
Alston CL, Heidler J, Dibley MG, Kremer LS, Taylor LS, Fratter C, French CE, Glasgow RIC, Feichtinger RG, Delon I, Pagnamenta AT, Dolling H, Lemonde H, Aiton N, Bjørnstad A, Henneke L, Gärtner J, Thiele H, Tauchmannova K, [...] Taylor RW
Am J Hum Genet, 103(4):592-601, 20 Sep 2018
Cited by: 24 articles | PMID: 30245030 | PMCID: PMC6174280
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Search life-sciences literature (45,103,589 articles, preprints and more)

Suggested authors matching "AUTH:Heidler J" with an ORCID

Search results

RTN4IP1 is essential for the final stages of mitochondrial complex I assembly and coenzyme Q biosynthesis

Hyperbaric oxygen treatment reveals spatiotemporal OXPHOS plasticity in the porcine heart.

Impaired complex I repair causes recessive Leber's hereditary optic neuropathy.

Prodromal sensory neuropathy in Pink1^-/- SNCA^A53T double mutant Parkinson mice.

Genetic deletion of Nox4 enhances cancerogen-induced formation of solid tumors.

Bi-allelic pathogenic variants in NDUFC2 cause early-onset Leigh syndrome and stalled biogenesis of complex I.

Mitochondrial Complexome Profiling.

Platelet-derived calpain cleaves the endothelial protease-activated receptor 1 to induce vascular inflammation in diabetes.

Mapping the Endothelial Cell S-Sulfhydrome Highlights the Crucial Role of Integrin Sulfhydration in Vascular Function.

Redox Regulation of PPARγ in Polarized Macrophages.

A salvage pathway maintains highly functional respiratory complex I.

Loss of mitochondrial ClpP, Lonp1, and Tfam triggers transcriptional induction of Rnf213, a susceptibility factor for moyamoya disease.

Pathogenic Bi-allelic Mutations in NDUFAF8 Cause Leigh Syndrome with an Isolated Complex I Deficiency.

Early prodromal sensory neuropathy in Pink1-SNCA double mutant Parkinson mice

Cyp2c44 regulates prostaglandin synthesis, lymphangiogenesis, and metastasis in a mouse model of breast cancer.

Respiratory chain signalling is essential for adaptive remodelling following cardiac ischaemia.

Doping free transfer of graphene using aqueous ammonia flow.

Bioenergetic consequences from xenotopic expression of a tunicate AOX in mouse mitochondria: Switch from RET and ROS to FET.

Global Proteome of LonP1^+/- Mouse Embryonal Fibroblasts Reveals Impact on Respiratory Chain, but No Interdependence between Eral1 and Mitoribosomes.

Nitric oxide maintains endothelial redox homeostasis through PKM2 inhibition.

Myeloid-Specific Deletion of the AMPKα2 Subunit Alters Monocyte Protein Expression and Atherogenesis.

Global proteome of LonP1^+/- mouse embryonal fibroblasts reveals impact on respiratory chain, but no interdependence between Eral1 and mitoribosomes

Design guidelines for an electron diffractometer for structural chemistry and structural biology.

TLR2-Dependent Reversible Oxidation of Connexin 43 at Cys260 Modifies Electrical Coupling After Experimental Myocardial Ischemia/Reperfusion.

Bi-allelic Mutations in NDUFA6 Establish Its Role in Early-Onset Isolated Mitochondrial Complex I Deficiency.

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