Anatomy Bibliography

1. Bakker, E. ; Breuning, M. H. ; Ginjaar, H. B. ; Helderman-van den Enden, A. T. J. M. ; Tibben, A. ; van den Bergen, J. C. ; Vershuuren, J. J. G. M. “Duchenne/Becker muscular dystrophy in the family: have potential carriers been tested at a molecular level? ” Journal of Clinical Genetics. Vol. 79 Issue 3, p236-242, 2011. 2. Chandramohan, Arthi; Lakshmi, Bremadesam Raman; Murugan, Sakthivel. “Use of multiplex ligation-dependent probe amplification (MLPA) for Duchenne musculardystrophy (DMD) gene mutation analysis” Indian Journal of Medical Research. Vol.

132 Issue 3, p303-311, 2010. 3. Bachrach, Estanislao; Bennett, Richard R. ; Guyon, Jeffrey; Kunkel, Louis M. ; Steffen, Leta. “Diagnosis and cell-based therapy for Duchenne muscular dystrophy in humans, mice, and zebrafish” Journal of Human Genetics. Vol. 51 Issue 5, p397- 406, 2006. 4. Awano, Hiroyuki; Matsuo, Masafumi; Nishio, Hisahide; Okizuka, Yo; Takeshima, Yasuhiro; Yagi, Mariko; Yamauchi, Yumiko; Zhang, Zhujun. “Mutation spectrum of the dystrophin gene in 442 Duchenne/Becker muscular dystrophy cases from one Japanese referral center” Journal of Human Genetics.

Vol. 55 Issue 6, p379-388, 2010 5. Clark, Mary-Jo; Jih-Yuan Chen. “Family Resources and Parental Health in Families of Children With Duchenne MuscularDystrophy” Journal of Nursing Research. Vol. 18 Issue 4, p239-248, 2010. 6. Azeddoug, Houssine; Bellayou, Hanane; Hamzi, Khalil; Karkouri, Mehdil; Nadifi, Sellama; Rafai, Mohamed Abdou; Slassi, Ilham. “Duchenne and Becker Muscular Dystrophy: Contribution of a Molecular and Immunohistochemical Analysis in Diagnosis in Morocco” Journal of Biomedicine & Biotechnology.

Regular Issue, p1-5, 2009. 7. Bouchet, Celine; Campbell, Kevin P. ; Clarke, Nigel F. ; Chouery, Eliane; Endo, Tamao; Gray, Francoise; Guicheney, Pascale; Manya, Hiroshi; Maugenre, Svetlana; Megarbane, Andre; Peat, Rachel A. ; Urtizberea, J. Andoni; Vandebrouck, Aurelie; Vuillaumier-Barrot, Sandrine; Willer, Tobias. “Congenital muscular dystrophy type 1D (MDC1D) due to a large intragenic insertion/deletion, involving intron 10 of the LARGE gene” European Journal of Human Genetics. Vol. 19 Issue 4, p452-457, 2011. 8.

Angelini, Corrado; Aurino, Stefania; Cacciottolo, Mafalda; Caserta, Imma Rosaria; Fanin, Marina; Minetti, Carlo; Nigro, Vincenzo; Numitone, Gelsomina; Piluso, Giulio; Politano, Luisa; Ricci, Enzo. “Congenital muscular dystrophy type 1D (MDC1D) due to a large intragenic insertion/deletion, involving intron 10 of the LARGE gene” European Journal of Human Genetics. Vol. 19 Issue 9, p974-980, 2011. 9. Kanagawa, Motoi; Toda, Tatsushi. “The genetic and molecular basis of muscular dystrophy: roles of cell–matrix linkage in the pathogenesis” Journal of Human Genetics. Vol.

51 Issue 11, p915-926, 2006. 10. Allen, David G. ; Gervasio, Othon L. ; Whitehead, Nicholas P. ; Yeung, Ella W. “Calcium and the damage pathways in muscular dystrophy” Canadian Journal of Physiology & Pharmacology. Vol. 88 Issue 2, p83-91, 2010. 11. Davidson, Z. E. ; Truby, H. “A review of nutrition in Duchenne muscular dystrophy” Journal of Human Nutrition & Dietetics. Vol. 22 Issue 5, p383-393, 2009. 12. Bower, Matthew; Brown, Charlotte A. ; Ellis, Juliet A. ; Felice, Kevin; Mendell, Jerry R. ; Meriggioli, Matthew N. ; Scharner, Juergen; Tarnopolsky, Mark; Zammit, Peter S.

“Novel and recurrent EMD mutations in patients with Emery Dreifuss muscular dystrophy, identify exon 2 as a mutation hot spot” Journal of Human Genetics. Vol. 56 Issue 8, p589-594, 2011 13. Punnoose, Ann R. “Muscular Dystrophy” Journal of the American Medical Association. Vol. 306 Issue 22, p2526-2526, 2011 14. Aoyama, Chieko; Goto, Kanako; Hayashi, Yukiko K. ; Ikeda, Kazutaka; Kale, Gulsev; Karahashi, Minako; Koksal, Burcu; Koumura, Tomoko; Kurihara, Mana; Mitsuhashi, Hiroaki; Mitsuhashi, Satomi; Noguchi, Satoru; Nonaka, Ikuya; Ohkuma, Aya; Quinlivan, Ros; Sewry, Caroline; Sher, Roger B.

; Sugimoto, Hiroyuki; Taguchi, Ryo; Talim, Beril. “A Congenital Muscular Dystrophy with Mitochondrial Structural Abnormalities Caused by Defective De Novo Phosphatidylcholine Biosynthesis” American Journal of Human Genetics. Vol. 88 Issue 6, p845-851, 2011. 15. Awano, Hiroyuki; Itoh, Kyoko; Kumagai, Toshiyuki; Maruyama, Koichi; Matsuo, Masafumi; Okizuka, Yo; Takeshima, Yasuhiro; Yagi, Mariko; Zhang, Zhujun. “Low incidence of limb-girdle muscular dystrophy type 2C revealed by a mutation study in Japanese patients clinically diagnosed with DMD” BMC Medical Genetics. Vol. 11, p49-54, 2010.

For the assignment this week, I chose the topic of Medication Errors to find three reputable sources to cite the information on with an annotated bibliography. The sources I chose from the ProQuest database because I think they have a …

Genes are precise sequences of passes that code instruction on how to synthesis proteins. Mostly genes get a lot of attention but it’s the proteins in them that carry out most life functions and frame most of cellular structures. Genetic …

Know general characteristics of signal-transducing receptors: Bind to a ligand (drug or endogenous molecule) Participate in a signaling cascade Distinguish from non-receptor-mediated drug action Graded or Dose-Response effects (vs. all-or-none) Understand “occupational theory” of drug action Molecular basis (ligand-receptor interaction) …

In certain geographically isolated or ethnic populations, particular mutations are found with increased frequency relative to other populations. A common explanation for this is that the population is descended from a relatively small group of individuals, at least one of …

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