COL6A3 Protein Deficiency in Mice Leads to Muscle and Tendon Defects Similar to Human Collagen VI Congenital Muscular Dystrophy von Pan, Te-Cheng, Zhang, Rui-Zhu, Markova, Dessislava, Arita, Machiko, Zhang, Yejia, Bogdanovich, Sasha, Khurana, Tejvir S., Bönnemann, Carsten G., Birk, David E., Chu, Mon-Li

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Tumor-specific expression and alternative splicing of the COL6A3 gene in pancreatic cancer von Arafat, Hwyda, MD, PhD, Lazar, Melissa, MD, Salem, Khalifa, MD, Chipitsyna, Galina, PhD, Gong, Qiaoke, MD, Pan, Te-Cheng, PhD, Zhang, Rui-Zhu, MD, Yeo, Charles J., MD, Chu, Mon-Li, PhD

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Muscle Interstitial Fibroblasts Are the Main Source of Collagen VI Synthesis in Skeletal Muscle: Implications for Congenital Muscular Dystrophy Types Ullrich and Bethlem von Zou, Yaqun, Zhang, Rui-Zhu, Sabatelli, Patrizia, Chu, Mon-Li, Bönnemann, Carsten G

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Clinical Significance of Serum COL6A3 in Pancreatic Ductal Adenocarcinoma von Kang, Christopher Y., Wang, Jonathan, Axell-House, Dierdre, Soni, Pranay, Chu, Mon-Li, Chipitsyna, Galina, Sarosiek, Konrad, Sendecki, Jocelyn, Hyslop, Terry, Al-Zoubi, Mazhar, Yeo, Charles J., Arafat, Hwyda A.

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Compound heterozygous mutations in fibulin-4 causing neonatal lethal pulmonary artery occlusion, aortic aneurysm, arachnodactyly, and mild cutis laxa von Dasouki, Majed, Markova, Dessislava, Garola, Robert, Sasaki, Takako, Charbonneau, Noe L., Sakai, Lynn Y., Chu, Mon-Li

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Loss of fibulin-4 results in abnormal collagen fibril assembly in bone, caused by impaired lysyl oxidase processing and collagen cross-linking von Sasaki, Takako, Stoop, Reinout, Sakai, Takao, Hess, Andreas, Deutzmann, Rainer, Schlötzer-Schrehardt, Ursula, Chu, Mon-Li, von der Mark, Klaus

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Fibulin-2 and Fibulin-5 Cooperatively Function to Form the Internal Elastic Lamina and Protect From Vascular Injury von Chapman, Shelby L, Sicot, F -X, Davis, Elaine C, Huang, Jianbin, Sasaki, Takako, Chu, Mon-Li, Yanagisawa, Hiromi

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Retinoic acid receptors are required for skeletal growth, matrix homeostasis and growth plate function in postnatal mouse von Williams, Julie A., Kondo, Naoki, Okabe, Takahiro, Takeshita, Nobuo, Pilchak, Diane M., Koyama, Eiki, Ochiai, Takanaga, Jensen, Deborah, Chu, Mon-Li, Kane, Maureen A., Napoli, Joseph L., Enomoto-Iwamoto, Motomi, Ghyselinck, Norbert, Chambon, Pierre, Pacifici, Maurizio, Iwamoto, Masahiro

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Forelimb contractures and abnormal tendon collagen fibrillogenesis in fibulin-4 null mice von Markova, Dessislava Z., Pan, Te-Cheng, Zhang, Rui-Zhu, Zhang, Guiyun, Sasaki, Takako, Arita, Machiko, Birk, David E., Chu, Mon-Li

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Fibulins: a versatile family of extracellular matrix proteins von Timpl, Rupert, Sasaki, Takako, Kostka, Günter, Chu, Mon-Li

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Loss of fibulin-2 protects against progressive ventricular dysfunction after myocardial infarction von Tsuda, Takeshi, Wu, Jing, Gao, Erhe, Joyce, Jennifer, Markova, Dessislava, Dong, Hailong, Liu, Ying, Zhang, Hangxiang, Zou, Yaqun, Gao, Feng, Miller, Thomas, Koch, Walter, Ma, Xingliang, Chu, Mon-Li

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Fibulin-2 is essential for angiotensin II-induced myocardial fibrosis mediated by transforming growth factor (TGF)-β von Khan, Shaukat A, Dong, Hailong, Joyce, Jennifer, Sasaki, Takako, Chu, Mon-Li, Tsuda, Takeshi

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Ullrich Scleroatonic Muscular Dystrophy is Caused by Recessive Mutations in Collagen Type VI von Vanegas, Olga Camacho, Bertini, Enrico, Zhang, Rui-Zhu, Petrini, Stefania, Minosse, Claudia, Sabatelli, Patrizia, Giusti, Betti, Chu, Mon-Li, Pepe, Guglielmina

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Fibulins in development and heritable disease von Chu, Mon-Li, Tsuda, Takeshi

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New Molecular Mechanism for Ullrich Congenital Muscular Dystrophy: A Heterozygous In-Frame Deletion in the COL6A1 Gene Causes a Severe Phenotype von Pan, Te-Cheng, Zhang, Rui-Zhu, Sudano, Dominick G., Marie, Suely K., Bönnemann, Carsten G., Chu, Mon-Li

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Genetic Heterogeneity of Cutis Laxa: A Heterozygous Tandem Duplication within the Fibulin-5 (FBLN5) Gene von Markova, Dessislava, Zou, Yaqun, Ringpfeil, Franziska, Sasaki, Takako, Kostka, Günter, Timpl, Rupert, Uitto, Jouni, Chu, Mon-Li

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Identification of Novel TGF-β/Smad Gene Targets in Dermal Fibroblasts using a Combined cDNA Microarray/Promoter Transactivation Approach von Verrecchia, Franck, Chu, Mon-Li, Mauviel, Alain

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Human adipose-derived stem cell transplantation as a potential therapy for collagen VI-related congenital muscular dystrophy von Alexeev, Vitali, Arita, Machiko, Donahue, Adele, Bonaldo, Paolo, Chu, Mon-Li, Igoucheva, Olga

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Fibulin-4 E57K Knock-in Mice Recapitulate Cutaneous, Vascular and Skeletal Defects of Recessive Cutis Laxa 1B with both Elastic Fiber and Collagen Fibril Abnormalities von Igoucheva, Olga, Alexeev, Vitali, Halabi, Carmen M., Adams, Sheila M., Stoilov, Ivan, Sasaki, Takako, Arita, Machiko, Donahue, Adele, Mecham, Robert P., Birk, David E., Chu, Mon-Li

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Reduced Fibulin-2 Contributes to Loss of Basement Membrane Integrity and Skin Blistering in Mice Lacking Integrin α3β1 in the Epidermis von Longmate, Whitney M., Monichan, Ruby, Chu, Mon-Li, Tsuda, Takeshi, Mahoney, My G., DiPersio, C.Michael

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