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NLRP3 is activated in Alzheimer's disease and contributes to pathology in APP/PS1 mice.
Nature. 2013 Jan 31;493(7434):674-8. doi: 10.1038/nature11729. Epub 2012 Dec 19.
Nature. 2013.
PMID: 23254930
Free PMC article.
Nitric oxide decreases the enzymatic activity of insulin degrading enzyme in APP/PS1 mice.
Kummer MP, Hülsmann C, Hermes M, Axt D, Heneka MT.
Kummer MP, et al. Among authors: axt d.
J Neuroimmune Pharmacol. 2012 Mar;7(1):165-72. doi: 10.1007/s11481-011-9339-7. Epub 2012 Jan 8.
J Neuroimmune Pharmacol. 2012.
PMID: 22227962
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Mrp14 deficiency ameliorates amyloid β burden by increasing microglial phagocytosis and modulation of amyloid precursor protein processing.
Kummer MP, Vogl T, Axt D, Griep A, Vieira-Saecker A, Jessen F, Gelpi E, Roth J, Heneka MT.
Kummer MP, et al. Among authors: axt d.
J Neurosci. 2012 Dec 5;32(49):17824-9. doi: 10.1523/JNEUROSCI.1504-12.2012.
J Neurosci. 2012.
PMID: 23223301
Free PMC article.
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Pan-PPAR modulation effectively protects APP/PS1 mice from amyloid deposition and cognitive deficits.
Kummer MP, Schwarzenberger R, Sayah-Jeanne S, Dubernet M, Walczak R, Hum DW, Schwartz S, Axt D, Heneka MT.
Kummer MP, et al. Among authors: axt d.
Mol Neurobiol. 2015 Apr;51(2):661-71. doi: 10.1007/s12035-014-8743-4. Epub 2014 May 17.
Mol Neurobiol. 2015.
PMID: 24838579
Free PMC article.
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PPARγ/RXRα-induced and CD36-mediated microglial amyloid-β phagocytosis results in cognitive improvement in amyloid precursor protein/presenilin 1 mice.
Yamanaka M, Ishikawa T, Griep A, Axt D, Kummer MP, Heneka MT.
Yamanaka M, et al. Among authors: axt d.
J Neurosci. 2012 Nov 28;32(48):17321-31. doi: 10.1523/JNEUROSCI.1569-12.2012.
J Neurosci. 2012.
PMID: 23197723
Free PMC article.
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Four hypotrichosis families with mutations in the gene LSS presenting with and without neurodevelopmental phenotypes.
Cesarato N, Wehner M, Ghughunishvili M, Schmidt A, Axt D, Thiele H, Lentze MJ, Has C, Geyer M, Basmanav FB, Betz RC.
Cesarato N, et al. Among authors: axt d.
Am J Med Genet A. 2021 Dec;185(12):3900-3904. doi: 10.1002/ajmg.a.62438. Epub 2021 Jul 27.
Am J Med Genet A. 2021.
PMID: 34318586
No abstract available.
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Assessment of the Genetic Spectrum of Uncombable Hair Syndrome in a Cohort of 107 Individuals.
Basmanav FB, Cesarato N, Kumar S, Borisov O, Kokordelis P, Ralser DJ, Wehner M, Axt D, Xiong X, Thiele H, Dolgin V, Gossmann Y, Fricker N, Dewenter MK, Weller K, Suri M, Reichenbach H, Oji V, Addor MC, Ramirez K, Stewart H, Garcia Bartels N, Weibel L, Wagner N, George S, Kilic A, Tantcheva-Poor I, Stewart A, Dikow N, Blaumeiser B, Medvecz M, Blume-Peytavi U, Farrant P, Grimalt R, Bertok S, Bradley L, Eskin-Schwartz M, Birk OS, Bygum A, Simon M, Krawitz P, Fischer C, Hamm H, Fritz G, Betz RC.
Basmanav FB, et al. Among authors: axt d.
JAMA Dermatol. 2022 Nov 1;158(11):1245-1253. doi: 10.1001/jamadermatol.2022.2319.
JAMA Dermatol. 2022.
PMID: 36044230
Free PMC article.
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[Elevated CEA values after cystectomy for bladder cancer and intestinal urinary diversion not evidence of tumor recurrence].
Klippel KF, Axt D, Schärfe T, Preiss J, Alves de Oliveira CR.
Klippel KF, et al. Among authors: axt d.
Onkologie. 1983 Jun;6(3):126, 127-31.
Onkologie. 1983.
PMID: 6350964
German.
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