Weis J - Search Results

1

Impact of Hypermannosylation on the Structure and Functionality of the ER and the Golgi Complex.

Franzka P, Schüler SC, Kentache T, Storm R, Bock A, Katona I, Weis J, Buder K, Kaether C, Hübner CA. Franzka P, et al. Among authors: weis j. Biomedicines. 2023 Jan 6;11(1):146. doi: 10.3390/biomedicines11010146. Biomedicines. 2023. PMID: 36672654 Free PMC article.

2

Small-fiber neuropathy in patients with ALS.

Weis J, Katona I, Müller-Newen G, Sommer C, Necula G, Hendrich C, Ludolph AC, Sperfeld AD. Weis J, et al. Neurology. 2011 Jun 7;76(23):2024-9. doi: 10.1212/WNL.0b013e31821e553a. Neurology. 2011. PMID: 21646630

3

Altered localization, abnormal modification and loss of function of Sigma receptor-1 in amyotrophic lateral sclerosis.

Prause J, Goswami A, Katona I, Roos A, Schnizler M, Bushuven E, Dreier A, Buchkremer S, Johann S, Beyer C, Deschauer M, Troost D, Weis J. Prause J, et al. Among authors: weis j. Hum Mol Genet. 2013 Apr 15;22(8):1581-600. doi: 10.1093/hmg/ddt008. Epub 2013 Jan 11. Hum Mol Genet. 2013. PMID: 23314020

4

A de novo gain-of-function mutation in SCN11A causes loss of pain perception.

Leipold E, Liebmann L, Korenke GC, Heinrich T, Giesselmann S, Baets J, Ebbinghaus M, Goral RO, Stödberg T, Hennings JC, Bergmann M, Altmüller J, Thiele H, Wetzel A, Nürnberg P, Timmerman V, De Jonghe P, Blum R, Schaible HG, Weis J, Heinemann SH, Hübner CA, Kurth I. Leipold E, et al. Among authors: weis j. Nat Genet. 2013 Nov;45(11):1399-404. doi: 10.1038/ng.2767. Epub 2013 Sep 15. Nat Genet. 2013. PMID: 24036948

5

Glycogenosome accumulation in the arrector pili muscle in Pompe disease.

Katona I, Weis J, Hanisch F. Katona I, et al. Among authors: weis j. Orphanet J Rare Dis. 2014 Feb 5;9:17. doi: 10.1186/1750-1172-9-17. Orphanet J Rare Dis. 2014. PMID: 24495340 Free PMC article.

6

Spinal cord organotypic slice cultures for the study of regenerating motor axon interactions with 3D scaffolds.

Gerardo-Nava J, Hodde D, Katona I, Bozkurt A, Grehl T, Steinbusch HW, Weis J, Brook GA. Gerardo-Nava J, et al. Among authors: weis j. Biomaterials. 2014 May;35(14):4288-96. doi: 10.1016/j.biomaterials.2014.02.007. Epub 2014 Feb 22. Biomaterials. 2014. PMID: 24565523

7

Loss of function of the ALS protein SigR1 leads to ER pathology associated with defective autophagy and lipid raft disturbances.

Vollrath JT, Sechi A, Dreser A, Katona I, Wiemuth D, Vervoorts J, Dohmen M, Chandrasekar A, Prause J, Brauers E, Jesse CM, Weis J, Goswami A. Vollrath JT, et al. Among authors: weis j. Cell Death Dis. 2014 Jun 12;5(6):e1290. doi: 10.1038/cddis.2014.243. Cell Death Dis. 2014. PMID: 24922074 Free PMC article.

8

Accumulation of STIM1 is associated with the degenerative muscle fibre phenotype in ALS and other neurogenic atrophies.

Goswami A, Jesse CM, Chandrasekar A, Bushuven E, Vollrath JT, Dreser A, Katona I, Beyer C, Johann S, Feller AC, Grond M, Wagner S, Nikolin S, Troost D, Weis J. Goswami A, et al. Among authors: weis j. Neuropathol Appl Neurobiol. 2015 Apr;41(3):304-18. doi: 10.1111/nan.12164. Neuropathol Appl Neurobiol. 2015. PMID: 24957221

9

Regulation of endoplasmic reticulum turnover by selective autophagy.

Khaminets A, Heinrich T, Mari M, Grumati P, Huebner AK, Akutsu M, Liebmann L, Stolz A, Nietzsche S, Koch N, Mauthe M, Katona I, Qualmann B, Weis J, Reggiori F, Kurth I, Hübner CA, Dikic I. Khaminets A, et al. Among authors: weis j. Nature. 2015 Jun 18;522(7556):354-8. doi: 10.1038/nature14498. Epub 2015 Jun 3. Nature. 2015. PMID: 26040720

10

Cold-aggravated pain in humans caused by a hyperactive NaV1.9 channel mutant.

Leipold E, Hanson-Kahn A, Frick M, Gong P, Bernstein JA, Voigt M, Katona I, Oliver Goral R, Altmüller J, Nürnberg P, Weis J, Hübner CA, Heinemann SH, Kurth I. Leipold E, et al. Among authors: weis j. Nat Commun. 2015 Dec 8;6:10049. doi: 10.1038/ncomms10049. Nat Commun. 2015. PMID: 26645915 Free PMC article.

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