Mutations in FAM20C Are Associated with Lethal Osteosclerotic Bone Dysplasia (Raine Syndrome), Highlighting a Crucial Molecule in Bone Development von Simpson, M.A., Hsu, R., Keir, L.S., Hao, J., Sivapalan, G., Ernst, L.M., Zackai, E.H., Al-Gazali, L.I., Hulskamp, G., Kingston, H.M., Prescott, T.E., Ion, A., Patton, M.A., Murday, V., George, A., Crosby, A.H.

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The natural history of Noonan syndrome: a long-term follow-up study von Shaw, A C, Kalidas, K, Crosby, A H, Jeffery, S, Patton, M A

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Mutations in FAM20C also identified in non-lethal osteosclerotic bone dysplasia von Simpson, MA, Scheuerle, A, Hurst, J, Patton, MA, Stewart, H, Crosby, AH

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TRPV4 mutations and cytotoxic hypercalcemia in axonal Charcot-Marie-Tooth neuropathies von KLEIN, C. J, SHI, Y, SIDDIQUE, T, DENG, H.-X, DYCK, P. J, FECTO, F, DONAGHY, M, NICHOLSON, G, MCENTAGART, M. E, CROSBY, A. H, WU, Y, LOU, H, MCEVOY, K. M

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Diagnostic strategies in CADASIL von MARKUS, H. S, MARTIN, R. J, SIMPSON, M. A, DONG, Y. B, ALI, N, CROSBY, A. H, POWELL, J. F

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Correction: Castanea sativa (European Chestnut) Leaf Extracts Rich in Ursene and Oleanene Derivatives Block Staphylococcus aureus Virulence and Pathogenesis without Detectable Resi... von Quave, C L, Lyles, J T, Kavanaugh, J S, Nelson, K, Parlet, C P, Crosby, H A, Heilmann, K P, Horswill, A R

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Evidence for equilibrium iron isotope fractionation by nitrate-reducing iron(II)-oxidizing bacteria von Kappler, A., Johnson, C.M., Crosby, H.A., Beard, B.L., Newman, D.K.

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Homozygous mutation of MYBPC3 associated with severe infantile hypertrophic cardiomyopathy at high frequency among the Amish von Zahka, K, Kalidas, K, Simpson, M A, Cross, H, Keller, B B, Galambos, C, Gurtz, K, Patton, M A, Crosby, A H

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A novel locus for an autosomal recessive hereditary spastic paraplegia (SPG35) maps to 16q21-q23 von DICK, K. J, AL-MJENI, Hons R, BASKIR, W, KOUL, R, SIMPSON, M. A, PATTON, M. A, RAEBURN, S, CROSBY, A. H

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Homozygous Mutation of Desmocollin-2 in Arrhythmogenic Right Ventricular Cardiomyopathy with Mild Palmoplantar Keratoderma and Woolly Hair von Simpson, M.A., Mansour, S., Ahnood, D., Kalidas, K., Patton, M.A., McKenna, W.J., Behr, E.R., Crosby, A.H.

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The Silver Syndrome Variant of Hereditary Spastic Paraplegia Maps to Chromosome 11q12-q14, with Evidence for Genetic Heterogeneity within This Subtype von Patel, H., Hart, P.E., Warner, T.T., Houlston, R.S., Patton, M.A., Jeffery, S., Crosby, A.H.

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Expression of the stem cell factor receptor c‐kit in normal and diseased pediatric liver: Identification of a human hepatic progenitor cell? von Baumann, Ulrich, Crosby, Heather A., Ramani, Pramila, Kelly, Deirdre A., Strain, Alastair J.

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Immunolocalization of putative human liver progenitor cells in livers from patients with end-stage primary biliary cirrhosis and sclerosing cholangitis using the monoclonal antibod... von Crosby, HA, Hubscher, S, Fabris, L, Joplin, R, Sell, S, Kelly, D, Strain, AJ

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Hepatic stem cells von STRAIN, A J, CROSBY, H A

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A clinical and genetic study of SPG5A linked autosomal recessive hereditary spastic paraplegia von WILKINSON, P. A, CROSBY, A. H, TURNER, C, PATEL, H, WOOD, N. W, SCHAPIRA, A. H, WARNER, T. T

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Characterization and Isolation of Ductular Cells Coexpressing Neural Cell Adhesion Molecule and Bcl-2 from Primary Cholangiopathies and Ductal Plate Malformations von Fabris, Luca, Strazzabosco, Mario, Crosby, Heather A., Ballardini, Giorgio, Hubscher, Stefan G., Kelly, Deirdre A., Neuberger, James M., Strain, Alastair J., Joplin, Ruth

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Mutations in PTPN11 , encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome von Tartaglia, Marco, Mehler, Ernest L, Goldberg, Rosalie, Zampino, Giuseppe, Brunner, Han G, Kremer, Hannie, van der Burgt, Ineke, Crosby, Andrew H, Ion, Andra, Jeffery, Steve, Kalidas, Kamini, Patton, Michael A, Kucherlapati, Raju S, Gelb, Bruce D

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A large family with hereditary spastic paraparesis due to a frame shift mutation of the spastin (SPG4) gene: association with multiple sclerosis in two affected siblings and epilep... von Mead, S H, Proukakis, C, Wood, N, Crosby, A H, Plant, G T, Warner, T T

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SPG3A mutation screening in English families with early onset autosomal dominant hereditary spastic paraplegia von Wilkinson, P.A., Hart, P.E., Patel, H., Warner, T.T., Crosby, A.H.

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A human mitochondrial poly(A) polymerase mutation reveals the complexities of post-transcriptional mitochondrial gene expression von Wilson, William C, Hornig-Do, Hue-Tran, Bruni, Francesco, Chang, Jeong Ho, Jourdain, Alexis A, Martinou, Jean-Claude, Falkenberg, Maria, Spåhr, Henrik, Larsson, Nils-Göran, Lewis, Richard J, Hewitt, Lorraine, Baslé, Arnaud, Cross, Harold E, Tong, Liang, Lebel, Robert R, Crosby, Andrew H, Chrzanowska-Lightowlers, Zofia M A, Lightowlers, Robert N

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