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

Ingrid Hausser
UniversitätsKlinikum Heidelberg
4
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54
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Exploring Structural and Molecular Features of Sciatic Nerve Lesions in Diabetic Neuropathy: Unveiling Pathogenic Pathways and Targets.
Schwarz D, Marois ML, Sturm V, Peters AS, Longuespée R, Helm D, Schneider M, Eichmüller B, Hidmark AS, Fischer M, Kender Z, Schwab C, Hausser I, Weis J, Dihlmann S, Böckler D, Bendszus M, Heiland S, Herzig S, [...] Fleming T
Diabetes, db240493, 17 Oct 2024
Cited by: 0 articles | PMID: 39418320
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Skin fragility and wound management in Ehlers- Danlos Syndrome: a report by the Ehlers Danlos Syndrome society skin working group.
Angwin C, Doolan BJ, Hausser I, Labine B, Lavallee M, Mackay D, Pope FM, Seneviratne SL, Winship I, Burrows NP
Clin Exp Dermatol, llae201, 20 May 2024
Cited by: 1 article | PMID: 38767179
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Autosomal Dominant Lamellar Ichthyosis Due to a Missense Variant in the Gene NKPD1.
Komlosi K, Glocker C, Hsu-Rehder HH, Alter S, Kopp J, Hotz A, Zimmer AD, Hausser I, Sandhoff R, Oji V, Fischer J
J Invest Dermatol, S0022-202X(24)00303-8, 18 Apr 2024
Cited by: 1 article | PMID: 38642798
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Impaired Detoxification of Trans, Trans-2,4-Decadienal, an Oxidation Product from Omega-6 Fatty Acids, Alters Insulin Signaling, Gluconeogenesis and Promotes Microvascular Disease.
Qian X, Klatt S, Bennewitz K, Wohlfart DP, Lou B, Meng Y, Buettner M, Poschet G, Morgenstern J, Fleming T, Sticht C, Hausser I, Fleming I, Szendroedi J, Nawroth PP, Kroll J
Adv Sci (Weinh), 11(4):e2302325, 07 Dec 2023
Cited by: 3 articles | PMID: 38059818 | PMCID: PMC10811472
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Epidermal or Dermal Collagen VII Is Sufficient for Skin Integrity: Insights to Anchoring Fibril Homeostasis.
Conradt G, Hausser I, Nyström A
J Invest Dermatol, 144(6):1301-1310.e7, 24 Nov 2023
Cited by: 2 articles | PMID: 38007090
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Extracutaneous features and complications of the Ehlers-Danlos syndromes: A systematic review.
Doolan BJ, Lavallee ME, Hausser I, Schubart JR, Michael Pope F, Seneviratne SL, Winship IM, Burrows NP
Front Med (Lausanne), 10:1053466, 23 Jan 2023
Cited by: 7 articles | PMID: 36756177 | PMCID: PMC9899794
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Dermatologic manifestations and diagnostic assessments of the Ehlers-Danlos syndromes: A clinical review.
Doolan BJ, Lavallee M, Hausser I, Pope FM, Seneviratne SL, Winship IM, Burrows NP
J Am Acad Dermatol, 89(3):551-559, 08 Feb 2023
Cited by: 1 article | PMID: 36764582
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Loss of glyoxalase 2 alters the glucose metabolism in zebrafish.
Tabler CT, Lodd E, Bennewitz K, Middel CS, Erben V, Ott H, Poth T, Fleming T, Morgenstern J, Hausser I, Sticht C, Poschet G, Szendroedi J, Nawroth PP, Kroll J
Redox Biol, 59:102576, 14 Dec 2022
Cited by: 4 articles | PMID: 36535130 | PMCID: PMC9792892
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Comparative Morphological, Metabolic and Transcriptome Analyses in elmo1 ^-/- , elmo2 ^-/- , and elmo3 ^-/- Zebrafish Mutants Identified a Functional Non-Redundancy of the Elmo Proteins.
Boger M, Bennewitz K, Wohlfart DP, Hausser I, Sticht C, Poschet G, Kroll J
Front Cell Dev Biol, 10:918529, 08 Jul 2022
Cited by: 0 articles | PMID: 35874819 | PMCID: PMC9304559
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Cell tropism and viral clearance during SARS-CoV-2 lung infection.
Schwab C, Domke LM, Rose F, Hausser I, Schirmacher P, Longerich T
Pathol Res Pract, 236:154000, 30 Jun 2022
Cited by: 2 articles | PMID: 35797854 | PMCID: PMC9245394
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Multiple Arterial Dissections and Connective Tissue Abnormalities.
Erhart P, Körfer D, Dihlmann S, Qiao JL, Hausser I, Ringleb P, Männer J, Dikow N, Schaaf CP, Grond-Ginsbach C, Böckler D
J Clin Med, 11(12):3264, 07 Jun 2022
Cited by: 4 articles | PMID: 35743335 | PMCID: PMC9224905
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The role of cutaneous manifestations in the diagnosis of the Ehlers-Danlos syndromes.
Stembridge N, Doolan BJ, Lavallee ME, Hausser I, Pope FM, Seneviratne SL, Winship IM, Burrows NP
Skin Health Dis, 3(1):e140, 15 Jul 2022
Cited by: 2 articles | PMID: 36751332 | PMCID: PMC9892481
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pdx1 Knockout Leads to a Diabetic Nephropathy- Like Phenotype in Zebrafish and Identifies Phosphatidylethanolamine as Metabolite Promoting Early Diabetic Kidney Damage.
Wiggenhauser LM, Metzger L, Bennewitz K, Soleymani S, Boger M, Tabler CT, Hausser I, Sticht C, Wohlfart P, Volk N, Heidenreich E, Buettner M, Hammes HP, Kroll J
Diabetes, 71(5):1073-1080, 01 May 2022
Cited by: 12 articles | PMID: 35100334
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Accumulation of acetaldehyde in aldh2.1^-/- zebrafish causes increased retinal angiogenesis and impaired glucose metabolism.
Wohlfart DP, Lou B, Middel CS, Morgenstern J, Fleming T, Sticht C, Hausser I, Hell R, Hammes HP, Szendrödi J, Nawroth PP, Kroll J
Redox Biol, 50:102249, 26 Jan 2022
Cited by: 6 articles | PMID: 35114580 | PMCID: PMC8818574
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Author Correction: Mutations in PYCR1 cause cutis laxa with progeroid features.
Reversade B, Escande-Beillard N, Dimopoulou A, Fischer B, Chng SC, Li Y, Shboul M, Tham PY, Kayserili H, Al-Gazali L, Shahwan M, Brancati F, Lee H, O'Connor BD, Kegler MS, Merriman B, Nelson SF, Masri A, Alkazaleh F, [...] Kornak U
Nat Genet, 54(2):213, 01 Feb 2022
Cited by: 0 articles | PMID: 35064218
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Fatal Neonatal DOLK-CDG as a Rare Form of Syndromic Ichthyosis.
Komlosi K, Claris O, Collardeau-Frachon S, Kopp J, Hausser I, Mazereeuw-Hautier J, Jonca N, Zimmer AD, Sanlaville D, Fischer J
Front Genet, 12:719624, 08 Dec 2021
Cited by: 4 articles | PMID: 34956305 | PMCID: PMC8693085
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Quality of life and clinical characteristics of self-improving congenital ichthyosis within the disease spectrum of autosomal-recessive congenital ichthyosis.
Hake L, Süßmuth K, Komlosi K, Kopp J, Drerup C, Metze D, Traupe H, Hausser I, Eckl KM, Hennies HC, Fischer J, Oji V
J Eur Acad Dermatol Venereol, 36(4):582-591, 13 Jan 2022
Cited by: 1 article | PMID: 34908195
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Methylglyoxal Induces Endothelial Dysfunction via Stunning-like Phenotype
Fleming T, von Nettelbladt B, Morgenstern J, Campos M, Le Marois M, Bartosova M, Hausser I, Schwab C, Fischer A, Nawroth PP, Szendroedi J, Herzig S
bioRxiv, 19 Nov 2021
Cited by: 0 articles | PPR: PPR422657
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Vitamin D Status in Distinct Types of Ichthyosis: Importance of Genetic Type and Severity of Scaling.
Kim MR, Oji V, Valentin F, Traupe H, Nofer JR, Hausser I, Hennies HC, Eckl K, Wudy SA, Sánchez-Guijo A, Kerschke L, Fischer J, Süßmuth K
Acta Derm Venereol, 101(9):adv00546, 15 Sep 2021
Cited by: 1 article | PMID: 34396419 | PMCID: PMC9425607
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Caffey disease is associated with distinct arginine to cysteine substitutions in the proα1(I) chain of type I procollagen.
Dhooge T, Syx D, Hermanns-Lê T, Hausser I, Mortier G, Zonana J, Symoens S, Byers PH, Malfait F
Genet Med, 23(12):2378-2385, 16 Jul 2021
Cited by: 0 articles | PMID: 34272483
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Mouse models for dominant dystrophic epidermolysis bullosa carrying common human point mutations recapitulate the human disease.
Smith BRC, Nyström A, Nowell CJ, Hausser I, Gretzmeier C, Robertson SJ, Varigos GA, Has C, Kern JS, Pang KC
Dis Model Mech, 14(6):dmm048082, 04 Jun 2021
Cited by: 2 articles | PMID: 34085701 | PMCID: PMC8214732
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Reduced Acrolein Detoxification in akr1a1a Zebrafish Mutants Causes Impaired Insulin Receptor Signaling and Microvascular Alterations.
Qi H, Schmöhl F, Li X, Qian X, Tabler CT, Bennewitz K, Sticht C, Morgenstern J, Fleming T, Volk N, Hausser I, Heidenreich E, Hell R, Nawroth PP, Kroll J
Adv Sci (Weinh), 8(18):e2101281, 18 Jul 2021
Cited by: 8 articles | PMID: 34278746 | PMCID: PMC8456208
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Prohibitin, STAT3 and SH2D4A physically and functionally interact in tumor cell mitochondria.
Ploeger C, Huth T, Sugiyanto RN, Pusch S, Goeppert B, Singer S, Tabti R, Hausser I, Schirmacher P, Désaubry L, Roessler S
Cell Death Dis, 11(11):1023, 30 Nov 2020
Cited by: 13 articles | PMID: 33257655 | PMCID: PMC7705682
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Regulation of Gluconeogenesis by Aldo-keto-reductase 1a1b in Zebrafish.
Li X, Schmöhl F, Qi H, Bennewitz K, Tabler CT, Poschet G, Hell R, Volk N, Poth T, Hausser I, Morgenstern J, Fleming T, Nawroth PP, Kroll J
iScience, 23(12):101763, 03 Nov 2020
Cited by: 6 articles | PMID: 33251496 | PMCID: PMC7683270
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Mutations in ATP6V1E1 or ATP6V1A Cause Autosomal-Recessive Cutis Laxa.
Van Damme T, Gardeitchik T, Mohamed M, Guerrero-Castillo S, Freisinger P, Guillemyn B, Kariminejad A, Dalloyaux D, van Kraaij S, Lefeber DJ, Syx D, Steyaert W, De Rycke R, Hoischen A, Kamsteeg EJ, Wong SY, van Scherpenzeel M, Jamali P, Brandt U, [...] Wevers RA
Am J Hum Genet, 107(2):374, 01 Aug 2020
Cited by: 5 articles | PMID: 32763190 | PMCID: PMC7413885
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Search life-sciences literature (45,100,050 articles, preprints and more)

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

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Exploring Structural and Molecular Features of Sciatic Nerve Lesions in Diabetic Neuropathy: Unveiling Pathogenic Pathways and Targets.

Skin fragility and wound management in Ehlers- Danlos Syndrome: a report by the Ehlers Danlos Syndrome society skin working group.

Autosomal Dominant Lamellar Ichthyosis Due to a Missense Variant in the Gene NKPD1.

Impaired Detoxification of Trans, Trans-2,4-Decadienal, an Oxidation Product from Omega-6 Fatty Acids, Alters Insulin Signaling, Gluconeogenesis and Promotes Microvascular Disease.

Epidermal or Dermal Collagen VII Is Sufficient for Skin Integrity: Insights to Anchoring Fibril Homeostasis.

Extracutaneous features and complications of the Ehlers-Danlos syndromes: A systematic review.

Dermatologic manifestations and diagnostic assessments of the Ehlers-Danlos syndromes: A clinical review.

Loss of glyoxalase 2 alters the glucose metabolism in zebrafish.

Comparative Morphological, Metabolic and Transcriptome Analyses in elmo1 ^-/- , elmo2 ^-/- , and elmo3 ^-/- Zebrafish Mutants Identified a Functional Non-Redundancy of the Elmo Proteins.

Cell tropism and viral clearance during SARS-CoV-2 lung infection.

Multiple Arterial Dissections and Connective Tissue Abnormalities.

The role of cutaneous manifestations in the diagnosis of the Ehlers-Danlos syndromes.

pdx1 Knockout Leads to a Diabetic Nephropathy- Like Phenotype in Zebrafish and Identifies Phosphatidylethanolamine as Metabolite Promoting Early Diabetic Kidney Damage.

Accumulation of acetaldehyde in aldh2.1^-/- zebrafish causes increased retinal angiogenesis and impaired glucose metabolism.

Author Correction: Mutations in PYCR1 cause cutis laxa with progeroid features.

Fatal Neonatal DOLK-CDG as a Rare Form of Syndromic Ichthyosis.

Quality of life and clinical characteristics of self-improving congenital ichthyosis within the disease spectrum of autosomal-recessive congenital ichthyosis.

Methylglyoxal Induces Endothelial Dysfunction via Stunning-like Phenotype

Vitamin D Status in Distinct Types of Ichthyosis: Importance of Genetic Type and Severity of Scaling.

Caffey disease is associated with distinct arginine to cysteine substitutions in the proα1(I) chain of type I procollagen.

Mouse models for dominant dystrophic epidermolysis bullosa carrying common human point mutations recapitulate the human disease.

Reduced Acrolein Detoxification in akr1a1a Zebrafish Mutants Causes Impaired Insulin Receptor Signaling and Microvascular Alterations.

Prohibitin, STAT3 and SH2D4A physically and functionally interact in tumor cell mitochondria.

Regulation of Gluconeogenesis by Aldo-keto-reductase 1a1b in Zebrafish.

Mutations in ATP6V1E1 or ATP6V1A Cause Autosomal-Recessive Cutis Laxa.

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