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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2003 1
2004 1
2006 2
2007 2
2010 1
2014 1
2015 2
2017 1
2021 1
2022 1
2023 1
2024 0

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12 results

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Page 1
Plant Secondary Metabolites with an Overview of Populus.
Movahedi A, Almasi Zadeh Yaghuti A, Wei H, Rutland P, Sun W, Mousavi M, Li D, Zhuge Q. Movahedi A, et al. Among authors: rutland p. Int J Mol Sci. 2021 Jun 26;22(13):6890. doi: 10.3390/ijms22136890. Int J Mol Sci. 2021. PMID: 34206964 Free PMC article. Review.
Anatomy, histology, development and functions of Ossa cordis: A review.
Best A, Egerbacher M, Swaine S, Pérez W, Alibhai A, Rutland P, Kubale V, El-Gendy SAA, Alsafy MAM, Baiker K, Sturrock CJ, Rutland CS. Best A, et al. Among authors: rutland p. Anat Histol Embryol. 2022 Nov;51(6):683-695. doi: 10.1111/ahe.12861. Epub 2022 Sep 8. Anat Histol Embryol. 2022. PMID: 36073246 Free PMC article. Review.
Kantaputra mesomelic dysplasia: a second reported family.
Shears DJ, Offiah A, Rutland P, Sirimanna T, Bitner-Glindzicz M, Hall C. Shears DJ, et al. Among authors: rutland p. Am J Med Genet A. 2004 Jul 1;128A(1):6-11. doi: 10.1002/ajmg.a.20640. Am J Med Genet A. 2004. PMID: 15211647
FOXRED1, encoding an FAD-dependent oxidoreductase complex-I-specific molecular chaperone, is mutated in infantile-onset mitochondrial encephalopathy.
Fassone E, Duncan AJ, Taanman JW, Pagnamenta AT, Sadowski MI, Holand T, Qasim W, Rutland P, Calvo SE, Mootha VK, Bitner-Glindzicz M, Rahman S. Fassone E, et al. Among authors: rutland p. Hum Mol Genet. 2015 Jul 15;24(14):4183. doi: 10.1093/hmg/ddv164. Epub 2015 May 28. Hum Mol Genet. 2015. PMID: 26022995 Free PMC article. No abstract available.
Fraser syndrome and mouse blebbed phenotype caused by mutations in FRAS1/Fras1 encoding a putative extracellular matrix protein.
McGregor L, Makela V, Darling SM, Vrontou S, Chalepakis G, Roberts C, Smart N, Rutland P, Prescott N, Hopkins J, Bentley E, Shaw A, Roberts E, Mueller R, Jadeja S, Philip N, Nelson J, Francannet C, Perez-Aytes A, Megarbane A, Kerr B, Wainwright B, Woolf AS, Winter RM, Scambler PJ. McGregor L, et al. Among authors: rutland p. Nat Genet. 2003 Jun;34(2):203-8. doi: 10.1038/ng1142. Nat Genet. 2003. PMID: 12766769
FOXRED1, encoding an FAD-dependent oxidoreductase complex-I-specific molecular chaperone, is mutated in infantile-onset mitochondrial encephalopathy.
Fassone E, Duncan AJ, Taanman JW, Pagnamenta AT, Sadowski MI, Holand T, Qasim W, Rutland P, Calvo SE, Mootha VK, Bitner-Glindzicz M, Rahman S. Fassone E, et al. Among authors: rutland p. Hum Mol Genet. 2010 Dec 15;19(24):4837-47. doi: 10.1093/hmg/ddq414. Epub 2010 Sep 21. Hum Mol Genet. 2010. PMID: 20858599 Free PMC article.
12 results