Adamts10 inactivation in mice leads to persistence of ocular microfibrils subsequent to reduced fibrillin-2 cleavage von Wang, Lauren W., Kutz, Wendy E., Mead, Timothy J., Beene, Lauren C., Singh, Shweta, Jenkins, Michael W., Reinhardt, Dieter P., Apte, Suneel S.

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Secreted metalloproteases ADAMTS9 and ADAMTS20 have a non-canonical role in ciliary vesicle growth during ciliogenesis von Nandadasa, Sumeda, Kraft, Caroline M., Wang, Lauren W., O’Donnell, Anna, Patel, Rushabh, Gee, Heon Yung, Grobe, Kay, Cox, Timothy C., Hildebrandt, Friedhelm, Apte, Suneel S.

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Chronic stress and adiposity in youth-parent dyads: An actor-partner interdependence analysis von Jiang, Tao, Lam, Phoebe H, Brody, Elizabeth J, Germer, Sarah O, Wang, Lauren E, Miller, Gregory E, Chen, Edith

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Mutations in the TGFβ Binding-Protein-Like Domain 5 of FBN1 Are Responsible for Acromicric and Geleophysic Dysplasias von Le Goff, Carine, Mahaut, Clémentine, Wang, Lauren W., Allali, Slimane, Abhyankar, Avinash, Jensen, Sacha, Zylberberg, Louise, Collod-Beroud, Gwenaelle, Bonnet, Damien, Alanay, Yasemin, Brady, Angela F., Cordier, Marie-Pierre, Devriendt, Koen, Genevieve, David, Kiper, Pelin Özlem Simsek, Kitoh, Hiroshi, Krakow, Deborah, Lynch, Sally Ann, Le Merrer, Martine, Mégarbane, André, Mortier, Geert, Odent, Sylvie, Polak, Michel, Rohrbach, Marianne, Sillence, David, Stolte-Dijkstra, Irene, Superti-Furga, Andrea, Rimoin, David L., Topouchian, Vicken, Unger, Sheila, Zabel, Bernhard, Bole-Feysot, Christine, Nitschke, Patrick, Handford, Penny, Casanova, Jean-Laurent, Boileau, Catherine, Apte, Suneel S., Munnich, Arnold, Cormier-Daire, Valérie

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Cerebral hemodynamic response to caffeine: effect of dietary caffeine consumption von Peng, Shin‐Lei, Chu, Lok Wang Lauren, Su, Feng‐Yi

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A disintegrin-like and metalloproteinase domain with thrombospondin type 1 motif 9 (ADAMTS9) regulates fibronectin fibrillogenesis and turnover von Wang, Lauren W., Nandadasa, Sumeda, Annis, Douglas S., Dubail, Joanne, Mosher, Deane F., Willard, Belinda B., Apte, Suneel S.

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Proteolysis of fibrillin-2 microfibrils is essential for normal skeletal development von Mead, Timothy J, Martin, Daniel R, Wang, Lauren W, Cain, Stuart A, Gulec, Cagri, Cahill, Elisabeth, Mauch, Joseph, Reinhardt, Dieter, Lo, Cecilia, Baldock, Clair, Apte, Suneel S

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Adamtsl2 deletion results in bronchial fibrillin microfibril accumulation and bronchial epithelial dysplasia--a novel mouse model providing insights into geleophysic dysplasia von Hubmacher, Dirk, Wang, Lauren W, Mecham, Robert P, Reinhardt, Dieter P, Apte, Suneel S

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Hedgehog pathway inhibition in chondrosarcoma using the smoothened inhibitor IPI-926 directly inhibits sarcoma cell growth von Campbell, Veronica T, Nadesan, Puviindran, Ali, S Amanda, Wang, Chang Ye Yale, Whetstone, Heather, Poon, Raymond, Wei, Qingxia, Keilty, John, Proctor, Jennifer, Wang, Lauren W, Apte, Suneel S, McGovern, Karen, Alman, Benjamin A, Wunder, Jay S

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Time-resolved Analysis of the Matrix Metalloproteinase 10 Substrate Degradome von Schlage, Pascal, Egli, Fabian E., Nanni, Paolo, Wang, Lauren W., Kizhakkedathu, Jayachandran N., Apte, Suneel S., Keller, Ulrich auf dem

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ADAMTSL4, a secreted glycoprotein widely distributed in the eye, binds fibrillin-1 microfibrils and accelerates microfibril biogenesis von Gabriel, Luis A R, Wang, Lauren W, Bader, Hannah, Ho, Jason C, Majors, Alana K, Hollyfield, Joe G, Traboulsi, Elias I, Apte, Suneel S

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Post-translational Modification of Thrombospondin Type-1 Repeats in ADAMTS-like 1/Punctin-1 by C-Mannosylation of Tryptophan von Wang, Lauren W., Leonhard-Melief, Christina, Haltiwanger, Robert S., Apte, Suneel S.

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Nonselective assembly of fibrillin 1 and fibrillin 2 in the rodent ocular zonule and in cultured cells: implications for Marfan syndrome von Beene, Lauren C, Wang, Lauren W, Hubmacher, Dirk, Keene, Douglas R, Reinhardt, Dieter P, Annis, Douglas S, Mosher, Deane F, Mecham, Robert P, Traboulsi, Elias I, Apte, Suneel S

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Impaired ADAMTS9 secretion: A potential mechanism for eye defects in Peters Plus Syndrome von Dubail, Johanne, Vasudevan, Deepika, Wang, Lauren W., Earp, Sarah E., Jenkins, Michael W., Haltiwanger, Robert S., Apte, Suneel S.

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ADAMTS10 Protein Interacts with Fibrillin-1 and Promotes Its Deposition in Extracellular Matrix of Cultured Fibroblasts von Kutz, Wendy E., Wang, Lauren W., Bader, Hannah L., Majors, Alana K., Iwata, Kazushi, Traboulsi, Elias I., Sakai, Lynn Y., Keene, Douglas R., Apte, Suneel S.

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ADAMTSL2 mutations in geleophysic dysplasia demonstrate a role for ADAMTS-like proteins in TGF-β bioavailability regulation von Cormier-Daire, Valérie, Le Goff, Carine, Wang, Lauren W, Ge, Gaoxiang, Bauer, Florence, Krakow, Deborah, Perrot, Claire, Flori, Elisabeth, Prost-Squarcioni, Catherine, Bonnet, Damien, Munnich, Arnold, Apte, Suneel S, Greenspan, Daniel S, Le Merrer, Martine, Dagoneau, Nathalie, Crow, Yanick J, Morice-Picard, Fanny

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A disintegrin-like and metalloprotease domain containing thrombospondin type 1 motif-like 5 (ADAMTSL5) is a novel fibrillin-1-, fibrillin-2-, and heparin-binding member of the ADAM... von Bader, Hannah L., Wang, Lauren W., Ho, Jason C., Tran, Thu, Holden, Paul, Fitzgerald, Jamie, Atit, Radhika P., Reinhardt, Dieter P., Apte, Suneel S.

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Freeman Center for intellectual and developmental disabilities: Patient-centered interdisciplinary care von Smith, Joshua, Hand, Brittany N., Johnson, Emily, Keeton, Corey, Wang, Lauren

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Identification and functional analysis of an ADAMTSL1 variant associated with a complex phenotype including congenital glaucoma, craniofacial, and other systemic features in a thre... von Hendee, Kathryn, Wang, Lauren Weiping, Reis, Linda M., Rice, Gregory M., Apte, Suneel S., Semina, Elena V.

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An ADAMTSL2 founder mutation causes Musladin-Lueke Syndrome, a heritable disorder of beagle dogs, featuring stiff skin and joint contractures von Bader, Hannah L, Ruhe, Alison L, Wang, Lauren W, Wong, Aaron K, Walsh, Kari F, Packer, Rebecca A, Mitelman, Jonathan, Robertson, Kathryn R, O'Brien, Dennis P, Broman, Karl W, Shelton, G Diane, Apte, Suneel S, Neff, Mark W

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