Reduced synthesis of basement membrane heparan sulfate proteoglycan in streptozotocin-induced diabetic mice von Rohrbach, D H, Wagner, C W, Star, V L, Martin, G R, Brown, K S, Yoon, J W

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Reduced aminergic synthesis in the hypothalamus of the infertile, genetically diabetic (C57BL/ksJ-db/db) male mouse von KING, T. S, ROHRBACH, D. H

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Characterization of a Novel Glycoprotein Isolated from the Basement Membrane Matrix of the Engelbreth-Holm-Swarm Tumor von Robinson, L K, Murrah, V A, Moyer, M P, Rohrbach, D H

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Gene mapping of human ocular connective tissue proteins. Assignment of the structural gene for corneal type I procollagen to human chromosome 7 in human corneal stroma-mouse fibrob... von Church, R L, SundarRaj, N, Rohrbach, D H

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Loss of the Basement Membrane Matrix Molecule, Bamin, in Diphenylamine-Treated Mice von Rohrbach, David H., Robinson, Leann K., Murrah, Valerie A.

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STRUCTURE OF BASEMENT MEMBRANE IN NORMAL AND DIABETIC TISSUE von Rohrbach, David H., Martin, George R.

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Role of laminin in the attachment of PAM 212 (epithelial) cells to basement membrane collagen von Terranova, Victor P., Rohrbach, David H., Martin, George R.

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The adhesive glycoprotein laminin is an agglutinin von Kennedy, Dorothy W., Rohrbach, David H., Martin, George R., Momoi, Takashi, Yamada, Kenneth M.

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Interaction between the neural crest and extracellular matrix proteins in craniofacial skeletogenesis von Mina, M, Kollar, E J, Bishop, J A, Rohrbach, D H

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Localization of the human fibronectin (FN) gene on chromosome 8 by a specific enzyme immunoassay von Rennard, S I, Church, R L, Rohrbach, D H, Shupp, D E, Abe, S, Hewitt, A T, Murray, J C, Martin, G R

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REDUCED HYPOTHALAMIC SEROTONIN SYNTHESIS AND SERUM LUTEINIZING HORMONE LEVELS IN STREPTOZOTOCIN-DIABETIC MALE RATS von KING, THOMAS S., ROHRBACH, DAVID H., MILLER, ALEXANDER L., MORGAN, WILLIAM W.

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In vitro production of basement membrane collagen by a clonal line of mouse lens epithelial cells von Rohrbach, David H., Russell, Paul, Church, Robert L.

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Longitudinal elastic properties and porosity of cortical bone tissue vary with age in human proximal femur von Malo, M.K.H, Rohrbach, D, Isaksson, H, Töyräs, J, Jurvelin, J.S, Tamminen, I.S, Kröger, H, Raum, K

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The Effector Domain of MARCKS Is a Nuclear Localization Signal that Regulates Cellular PIP2 Levels and Nuclear PIP2 Localization von Rohrbach, Timothy D, Shah, Nishi, Jackson, William P, Feeney, Erin V, Scanlon, Samantha, Gish, Robert, Khodadadi, Ryan, Hyde, Stephen O, Hicks, Patricia H, Anderson, Joshua C, Jarboe, John S, Willey, Christopher D

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ZNF469 frequently mutated in the brittle cornea syndrome (BCS) is a single exon gene possibly regulating the expression of several extracellular matrix components von Rohrbach, Marianne, Spencer, Helen L., Porter, Louise F., Burkitt-Wright, Emma M.M., Bürer, Céline, Janecke, Andreas, Bakshi, Madhura, Sillence, David, Al-Hussain, Hailah, Baumgartner, Matthias, Steinmann, Beat, Black, Graeme C.M., Manson, Forbes D.C., Giunta, Cecilia

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Regulation of Drosophila oviduct muscle contractility by octopamine von Deshpande, Sonali A., Rohrbach, Ethan W., Asuncion, James D., Harrigan, Jenna, Eamani, Aditya, Schlingmann, Ellery H., Suto, Daniel J., Lee, Pei-Tseng, Schweizer, Felix E., Bellen, Hugo J., Krantz, David E.

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Sustainable soil management options for Malawi: can smallholder farmers grow more legumes? von Snapp, S.S., Rohrbach, D.D., Simtowe, F., Freeman, H.A.

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Mutations in PRDM5 in Brittle Cornea Syndrome Identify a Pathway Regulating Extracellular Matrix Development and Maintenance von BURKITT WRIGHT, Emma M. M, SPENCER, Helen L, MADDEN, Colm, DODDS, Annabel, CHANDLER, Kate E, BANKA, Siddharth, AU, Leon, CLAYTON-SMITH, Jill, KHAN, Naz, BIESECKER, Leslie G, WILSON, Meredith, ROHRBACH, Marianne, DALY, Sarah B, COLOMBI, Marina, GIUNTA, Cecilia, BLACK, Graeme C. M, MANSON, Forbes D. C, ZEEF, Leo A. H, URQUHART, Jill, ZOPPI, Nicoletta, BONSHEK, Richard, TOSOUNIDIS, Ioannis, MOHAN, Meyyammai

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Delocalized, asynchronous, closed-loop discovery of organic laser emitters von Strieth-Kalthoff, Felix, Hao, Han, Rathore, Vandana, Derasp, Joshua, Gaudin, Théophile, Angello, Nicholas H, Seifrid, Martin, Trushina, Ekaterina, Guy, Mason, Liu, Junliang, Tang, Xun, Mamada, Masashi, Wang, Wesley, Tsagaantsooj, Tuul, Lavigne, Cyrille, Pollice, Robert, Wu, Tony C, Hotta, Kazuhiro, Bodo, Leticia, Li, Shangyu, Haddadnia, Mohammad, Wołos, Agnieszka, Roszak, Rafał, Ser, Cher Tian, Bozal-Ginesta, Carlota, Hickman, Riley J, Vestfrid, Jenya, Aguilar-Granda, Andrés, Klimareva, Elena L, Sigerson, Ralph C, Hou, Wenduan, Gahler, Daniel, Lach, Slawomir, Warzybok, Adrian, Borodin, Oleg, Rohrbach, Simon, Sanchez-Lengeling, Benjamin, Adachi, Chihaya, Grzybowski, Bartosz A, Cronin, Leroy, Hein, Jason E, Burke, Martin D, Aspuru-Guzik, Alán

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Mutations in FKBP14 Cause a Variant of Ehlers-Danlos Syndrome with Progressive Kyphoscoliosis, Myopathy, and Hearing Loss von Baumann, Matthias, Giunta, Cecilia, Krabichler, Birgit, Rüschendorf, Franz, Zoppi, Nicoletta, Colombi, Marina, Bittner, Reginald E., Quijano-Roy, Susana, Muntoni, Francesco, Cirak, Sebahattin, Schreiber, Gudrun, Zou, Yaqun, Hu, Ying, Romero, Norma Beatriz, Carlier, Robert Yves, Amberger, Albert, Deutschmann, Andrea, Straub, Volker, Rohrbach, Marianne, Steinmann, Beat, Rostásy, Kevin, Karall, Daniela, Bönnemann, Carsten G., Zschocke, Johannes, Fauth, Christine

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