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Year Number of Results
2003 1
2004 1
2006 2
2007 2
2010 1
2014 1
2015 2
2017 1
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12 results

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Page 1
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.
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.
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.
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.
A novel homeobox mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome associated with brain, ocular, and dental phenotypes.
Idrees F, Bloch-Zupan A, Free SL, Vaideanu D, Thompson PJ, Ashley P, Brice G, Rutland P, Bitner-Glindzicz M, Khaw PT, Fraser S, Sisodiya SM, Sowden JC. Idrees F, et al. Among authors: rutland p. Am J Med Genet B Neuropsychiatr Genet. 2006 Mar 5;141B(2):184-91. doi: 10.1002/ajmg.b.30237. Am J Med Genet B Neuropsychiatr Genet. 2006. PMID: 16389592
12 results