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Year | Number of Results |
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2014 | 1 |
2017 | 1 |
2018 | 1 |
2020 | 1 |
2024 | 0 |
PubMed (GeneRIF) for id: 209692
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CMT2Q-causing mutation in the Dhtkd1 gene lead to sensory defects, mitochondrial accumulation and altered metabolism in a knock-in mouse model.
Acta Neuropathol Commun. 2020 Mar 13;8(1):32. doi: 10.1186/s40478-020-00901-0.
Acta Neuropathol Commun. 2020.
PMID: 32169121
Free PMC article.
DHTKD1 Deficiency Causes Charcot-Marie-Tooth Disease in Mice.
Xu WY, Zhu H, Shen Y, Wan YH, Tu XD, Wu WT, Tang L, Zhang HX, Lu SY, Jin XL, Fei J, Wang ZG.
Xu WY, et al.
Mol Cell Biol. 2018 Jun 14;38(13):e00085-18. doi: 10.1128/MCB.00085-18. Print 2018 Jul 1.
Mol Cell Biol. 2018.
PMID: 29661920
Free PMC article.
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Elevated glutaric acid levels in Dhtkd1-/Gcdh- double knockout mice challenge our current understanding of lysine metabolism.
Biagosch C, Ediga RD, Hensler SV, Faerberboeck M, Kuehn R, Wurst W, Meitinger T, Kölker S, Sauer S, Prokisch H.
Biagosch C, et al.
Biochim Biophys Acta Mol Basis Dis. 2017 Sep;1863(9):2220-2228. doi: 10.1016/j.bbadis.2017.05.018. Epub 2017 May 22.
Biochim Biophys Acta Mol Basis Dis. 2017.
PMID: 28545977
Free article.
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Multilayered genetic and omics dissection of mitochondrial activity in a mouse reference population.
Wu Y, Williams EG, Dubuis S, Mottis A, Jovaisaite V, Houten SM, Argmann CA, Faridi P, Wolski W, Kutalik Z, Zamboni N, Auwerx J, Aebersold R.
Wu Y, et al.
Cell. 2014 Sep 11;158(6):1415-1430. doi: 10.1016/j.cell.2014.07.039.
Cell. 2014.
PMID: 25215496
Free PMC article.
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