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Correction: A transgenic mice model of retinopathy of cblG‑type inherited disorder of one‑carbon metabolism highlights epigenome‑wide alterations related to cone photoreceptor cells development and retinal metabolism.
Clin Epigenetics. 2024 Feb 8;16(1):23. doi: 10.1186/s13148-024-01636-8.
Clin Epigenetics. 2024.
PMID: 38331911
Free PMC article.
No abstract available.
Multiomic analysis in fibroblasts of patients with inborn errors of cobalamin metabolism reveals concordance with clinical and metabolic variability.
Wiedemann A, Oussalah A, Guéant Rodriguez RM, Jeannesson E, Mertens M, Rotaru I, Alberto JM, Baspinar O, Rashka C, Hassan Z, Siblini Y, Matmat K, Jeandel M, Chery C, Robert A, Chevreux G, Lignières L, Camadro JM, Feillet F, Coelho D, Guéant JL.
Wiedemann A, et al. Among authors: matmat k.
EBioMedicine. 2024 Jan;99:104911. doi: 10.1016/j.ebiom.2023.104911. Epub 2024 Jan 1.
EBioMedicine. 2024.
PMID: 38168585
Free PMC article.
Item in Clipboard
A transgenic mice model of retinopathy of cblG-type inherited disorder of one-carbon metabolism highlights epigenome-wide alterations related to cone photoreceptor cells development and retinal metabolism.
Matmat K, Conart JB, Graindorge PH, El Kouche S, Hassan Z, Siblini Y, Umoret R, Safar R, Baspinar O, Robert A, Alberto JM, Oussalah A, Coelho D, Guéant JL, Guéant-Rodriguez RM.
Matmat K, et al.
Clin Epigenetics. 2023 Oct 5;15(1):158. doi: 10.1186/s13148-023-01567-w.
Clin Epigenetics. 2023.
PMID: 37798757
Free PMC article.
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Cognitive Impairment Is Associated with AMPAR Glutamatergic Dysfunction in a Mouse Model of Neuronal Methionine Synthase Deficiency.
Hassan Z, Coelho D, Bossenmeyer-Pourié C, Matmat K, Arnold C, Savladori A, Alberto JM, Umoret R, Guéant JL, Pourié G.
Hassan Z, et al. Among authors: matmat k.
Cells. 2023 Apr 27;12(9):1267. doi: 10.3390/cells12091267.
Cells. 2023.
PMID: 37174668
Free PMC article.
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Ocular manifestations in patients with inborn errors of intracellular cobalamin metabolism: a systematic review.
Matmat K, Guéant-Rodriguez RM, Oussalah A, Wiedemann-Fodé A, Dionisi-Vici C, Coelho D, Guéant JL, Conart JB.
Matmat K, et al.
Hum Genet. 2022 Jul;141(7):1239-1251. doi: 10.1007/s00439-021-02350-8. Epub 2021 Oct 15.
Hum Genet. 2022.
PMID: 34652574
Review.
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