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Items: 1 to 20 of 114

1.

Research from the bedside to the lab bench & back.

White RA, Silvey M, Logsdon DP.

Mo Med. 2012 May-Jun;109(3):195-8.

PMID:
22860286
2.

Mammalian animal models for Duchenne muscular dystrophy.

Willmann R, Possekel S, Dubach-Powell J, Meier T, Ruegg MA.

Neuromuscul Disord. 2009 Apr;19(4):241-9. doi: 10.1016/j.nmd.2008.11.015. Epub 2009 Feb 12. Review.

PMID:
19217290
3.

Shrinking genes for therapy.

Bonetta L.

Nat Med. 2002 Mar;8(3):222. No abstract available.

PMID:
11875490
4.

Animal models of hereditary hematologic disease.

Bannerman RM.

Birth Defects Orig Artic Ser. 1974;10(10):278-85. No abstract available.

PMID:
4462638
5.

Animal models for genetic neuromuscular diseases.

Vainzof M, Ayub-Guerrieri D, Onofre PC, Martins PC, Lopes VF, Zilberztajn D, Maia LS, Sell K, Yamamoto LU.

J Mol Neurosci. 2008 Mar;34(3):241-8. doi: 10.1007/s12031-007-9023-9. Epub 2008 Jan 18. Review.

PMID:
18202836
6.

Will models of naturally occurring disease in animals reduce the bench-to-bedside gap in biomedical research?

Manuel B.

Zhonghua Wei Zhong Bing Ji Jiu Yi Xue. 2013 Jan;25(1):5-7. doi: 10.3760/cma.j.issn.2095-4352.2013.01.003. Chinese, English. No abstract available.

7.

The marmoset monkey: a multi-purpose preclinical and translational model of human biology and disease.

't Hart BA, Abbott DH, Nakamura K, Fuchs E.

Drug Discov Today. 2012 Nov;17(21-22):1160-5. doi: 10.1016/j.drudis.2012.06.009. Epub 2012 Jun 21.

PMID:
22728226
8.

Transgenic pigs as models for translational biomedical research.

Aigner B, Renner S, Kessler B, Klymiuk N, Kurome M, W√ľnsch A, Wolf E.

J Mol Med (Berl). 2010 Jul;88(7):653-64. doi: 10.1007/s00109-010-0610-9. Epub 2010 Mar 26. Review.

PMID:
20339830
9.

A translational approach for limb vascular delivery of the micro-dystrophin gene without high volume or high pressure for treatment of Duchenne muscular dystrophy.

Rodino-Klapac LR, Janssen PM, Montgomery CL, Coley BD, Chicoine LG, Clark KR, Mendell JR.

J Transl Med. 2007 Sep 24;5:45.

10.

Blood-brain barrier alterations in MDX mouse, an animal model of the Duchenne muscular dystrophy.

Nico B, Roncali L, Mangieri D, Ribatti D.

Curr Neurovasc Res. 2005 Jan;2(1):47-54. Review. Erratum in: Curr Neurovasc Res. 2005 Apr;2(2):185.

PMID:
16181099
11.
12.

Mutation in erythroid specific transcription factor KLF1 causes Hereditary Spherocytosis in the Nan hemolytic anemia mouse model.

Heruth DP, Hawkins T, Logsdon DP, Gibson MI, Sokolovsky IV, Nsumu NN, Major SL, Fegley B, Woods GM, Lewing KB, Neville KA, Cornetta K, Peterson KR, White RA.

Genomics. 2010 Nov;96(5):303-7. doi: 10.1016/j.ygeno.2010.07.009. Epub 2010 Aug 5.

13.

[Study on the gene knockout model mice of Duchenne muscular dystrophy].

Chen S, Zhang C, Liu X, Gao L, Zhang W, Huang W, Lu X, Wang Z.

Sichuan Da Xue Xue Bao Yi Xue Ban. 2003 Apr;34(2):210-3. Chinese.

PMID:
12947691
14.

Animal models for translational research on shoulder pathologies: from bench to bedside.

Longo UG, Forriol F, Campi S, Maffulli N, Denaro V.

Sports Med Arthrosc. 2011 Sep;19(3):184-93. doi: 10.1097/JSA.0b013e318205470e. Review.

PMID:
21822100
15.

Hereditary spherocytosis: a review of the clinical and molecular aspects of the disease.

Hassoun H, Palek J.

Blood Rev. 1996 Sep;10(3):129-47. Review.

PMID:
8932827
16.

Of mice and men: more neurobiology in dementia.

Codita A, Winblad B, Mohammed AH.

Curr Opin Psychiatry. 2006 Nov;19(6):555-63. Review.

PMID:
17012931
17.

Use of genetically modified rat models for translational medicine.

Cozzi J, Fraichard A, Thiam K.

Drug Discov Today. 2008 Jun;13(11-12):488-94. doi: 10.1016/j.drudis.2008.03.021. Epub 2008 May 15. Review.

PMID:
18549974
18.

Collaborative translational research leading to multicenter clinical trials in Duchenne muscular dystrophy: the Cooperative International Neuromuscular Research Group (CINRG).

Escolar DM, Henricson EK, Pasquali L, Gorni K, Hoffman EP.

Neuromuscul Disord. 2002 Oct;12 Suppl 1:S147-154. Review.

PMID:
12206809
19.
20.

Cardiac dysfunction and pathology in the dystrophin and utrophin-deficient mouse during development of dilated cardiomyopathy.

Chun JL, O'Brien R, Berry SE.

Neuromuscul Disord. 2012 Apr;22(4):368-79. doi: 10.1016/j.nmd.2011.07.003. Epub 2012 Jan 21.

PMID:
22266080

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