NDRI: Publications

You are currently filtering by: 2013 Rare Disease

Rare Disease • 2013 • American Thoracic Society Journals 187(1): A2031.

Src Kinase Activation Promotes Epithelial-Mesenchymal Transition In Lymphangioleimymatosis

Tyryshkin A, Eissa N

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Rare Disease • 2013 • PLoS Genetics 9(12):e1003866. PMID: 24367268.

Detection of slipped-DNAs at the trinucleotide repeats of the myotonic dystrophy type I disease locus in patient tissues.

Axford MM, Wang YH, Nakamori M, Zannis-Hadjopoulos M, Thornton CA, Pearson CE

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Rare Disease • 2013 • Nature 501(7467): 380-384. PMID: 24025767.

Usp16 contributes to somatic stem-cell defects in Down's syndrome.

Adorno M, Sikandar S, Mitra SS, Kuo A, Nicolis Di Robilant B, Haro-Acosta V, Ouadah Y, Quarta M, Rodriguez J, Qian D, Reddy VM, Cheshier S, Garner CC, Clarke MF

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Rare Disease • 2013 • American Journal of Respiratory Cell and Molecular Biology 49(5): 704-709. PMID: 23947572.

Statins in lymphangioleiomyomatosis. Simvastatin and atorvastatin induce differential effects on tuberous sclerosis complex 2-null cell growth and signaling.

Atochina-Vasserman EN, Goncharov DA, Volgina AV, Milavec M, James ML, Krymskaya VP

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Rare Disease • 2013 • Journal of Histochemistry Cytochemistry 61(8): 580-590. PMID: 23609227.

Lymphatic endothelial differentiation in pulmonary lymphangioleiomyomatosis cells.

Davis JM, Hyjek E, Husain AN, Shen L, Jones J, Schuger LA

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Rare Disease • 2013 • Human Molecular Genetics 22(20): 4127-4135. PMID: 23740943.

Method for widespread microRNA-155 inhibition prolongs survival in ALS-model mice.

Koval ED, Shaner C, Zhang P, du Maine X, Fischer K, Tay J, Chau BN, Wu GF, Miller TM

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Publications

You are currently filtering by: 2013 Rare Disease

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