Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2022 | 1 |
2023 | 4 |
2024 | 2 |
Search Results
5 results
Results by year
Filters applied: . Clear all
It looks like you are searching for an author.
Results are currently sorted by Best Match. To see the newest results first,
change the sort order to Most Recent.
Page 1
B-complex vitamins for patients with TANGO2-deficiency disorder.
J Inherit Metab Dis. 2023 Mar;46(2):161-162. doi: 10.1002/jimd.12585. Epub 2022 Dec 30.
J Inherit Metab Dis. 2023.
PMID: 36550018
Free PMC article.
No abstract available.
BAG3 regulates the specificity of the recognition of specific MAPT species by NBR1 and SQSTM1.
Lin H, Sandkuhler S, Dunlea C, Rodwell-Bullock J, King DH, Johnson GVW.
Lin H, et al. Among authors: sandkuhler s.
Autophagy. 2024 Mar;20(3):577-589. doi: 10.1080/15548627.2023.2276622. Epub 2023 Nov 8.
Autophagy. 2024.
PMID: 37899687
Item in Clipboard
BAG3 regulates the specificity of the recognition of specific MAPT species by NBR1 and SQSTM1.
Lin H, Sandkuhler S, Dunlea C, King DH, Johnson GVW.
Lin H, et al. Among authors: sandkuhler s.
bioRxiv [Preprint]. 2023 Feb 9:2023.02.08.527546. doi: 10.1101/2023.02.08.527546.
bioRxiv. 2023.
PMID: 36798173
Free PMC article.
Updated.
Preprint.
Item in Clipboard
Haem's relevance genuine? Re-visiting the roles of TANGO2 homologues including HRG-9 and HRG-10 in C. elegans.
Sandkuhler SE, Youngs KS, Owlett L, Bandora MB, Naaz A, Kim ES, Wang L, Wojtovich AP, Gupta VA, Sacher M, Mackenzie SJ.
Sandkuhler SE, et al.
bioRxiv [Preprint]. 2023 Dec 4:2023.11.29.569072. doi: 10.1101/2023.11.29.569072.
bioRxiv. 2023.
PMID: 38106020
Free PMC article.
Preprint.
Item in Clipboard
Multicenter appraisal of comorbid TANGO2 deficiency disorder in patients with 22q11.2 deletion syndrome.
Owlett LD, Zapanta B, Sandkuhler SE, Ames EG, Hickey SE, Mackenzie SJ, Meisner JK.
Owlett LD, et al. Among authors: sandkuhler se.
Am J Med Genet A. 2024 Jun 3:e63778. doi: 10.1002/ajmg.a.63778. Online ahead of print.
Am J Med Genet A. 2024.
PMID: 38829177
Item in Clipboard
Cite
Cite