Insights on the Evolution of Prolyl 3-Hydroxylation Sites from Comparative Analysis of Chicken and Xenopus Fibrillar Collagens

por Hudson, David M., Weis, MaryAnn, Eyre, David R.
Publicado 2011

Evolutionary Origins of C-Terminal (GPP)n 3-Hydroxyproline Formation in Vertebrate Tendon Collagen

por Hudson, David M., Werther, Rachel, Weis, MaryAnn, Wu, Jiann-Jiu, Eyre, David R.
Publicado 2014

Age-related type I collagen modifications reveal tissue-defining differences between ligament and tendon

por Hudson, David M., Archer, Marilyn, Rai, Jyoti, Weis, MaryAnn, Fernandes, Russell J., Eyre, David R.
Publicado 2021

Asporin-deficient mice have tougher skin and altered skin glycosaminoglycan content and structure

por Maccarana, Marco, Svensson, René B., Knutsson, Anki, Giannopoulos, Antonis, Pelkonen, Mea, Weis, MaryAnn, Eyre, David, Warman, Matthew, Kalamajski, Sebastian
Publicado 2017

Abnormal Bone Collagen Cross‐Linking in Osteogenesis Imperfecta/Bruck Syndrome Caused by Compound Heterozygous PLOD2 Mutations

por Gistelinck, Charlotte, Weis, MaryAnn, Rai, Jyoti, Schwarze, Ulrike, Niyazov, Dmitriy, Song, Kit M, Byers, Peter H, Eyre, David R
Publicado 2021

3-D ultrastructure and collagen composition of healthy and overloaded human tendon: evidence of tenocyte and matrix buckling

por Pingel, Jessica, Lu, Yinhui, Starborg, Tobias, Fredberg, Ulrich, Langberg, Henning, Nedergaard, Anders, Weis, MaryAnn, Eyre, David, Kjaer, Michael, Kadler, Karl E
Publicado 2014

A Novel Mutation in LEPRE1 That Eliminates Only the KDEL ER- Retrieval Sequence Causes Non-Lethal Osteogenesis Imperfecta

por Takagi, Masaki, Ishii, Tomohiro, Barnes, Aileen M., Weis, MaryAnn, Amano, Naoko, Tanaka, Mamoru, Fukuzawa, Ryuji, Nishimura, Gen, Eyre, David R., Marini, Joan C., Hasegawa, Tomonobu
Publicado 2012

Generalized Connective Tissue Disease in Crtap-/- Mouse

por Baldridge, Dustin, Lennington, Jennifer, Weis, MaryAnn, Homan, Erica P., Jiang, Ming-Ming, Munivez, Elda, Keene, Douglas R., Hogue, William R., Pyott, Shawna, Byers, Peter H., Krakow, Deborah, Cohn, Daniel H., Eyre, David R., Lee, Brendan, Morello, Roy
Publicado 2010

Abnormal Type I Collagen Post-translational Modification and Crosslinking in a Cyclophilin B KO Mouse Model of Recessive Osteogenesis Imperfecta

por Cabral, Wayne A., Perdivara, Irina, Weis, MaryAnn, Terajima, Masahiko, Blissett, Angela R., Chang, Weizhong, Perosky, Joseph E., Makareeva, Elena N., Mertz, Edward L., Leikin, Sergey, Tomer, Kenneth B., Kozloff, Kenneth M., Eyre, David R., Yamauchi, Mitsuo, Marini, Joan C.
Publicado 2014

Sc65-Null Mice Provide Evidence for a Novel Endoplasmic Reticulum Complex Regulating Collagen Lysyl Hydroxylation

por Heard, Melissa E., Besio, Roberta, Weis, MaryAnn, Rai, Jyoti, Hudson, David M., Dimori, Milena, Zimmerman, Sarah M., Kamykowski, Jeffrey A., Hogue, William R., Swain, Frances L., Burdine, Marie S., Mackintosh, Samuel G., Tackett, Alan J., Suva, Larry J., Eyre, David R., Morello, Roy
Publicado 2016

Receptor Tyrosine Kinases Activate Canonical WNT/β-Catenin Signaling via MAP Kinase/LRP6 Pathway and Direct β-Catenin Phosphorylation

por Krejci, Pavel, Aklian, Anie, Kaucka, Marketa, Sevcikova, Eva, Prochazkova, Jirina, Masek, Jan Kukla, Mikolka, Pavol, Pospisilova, Tereza, Spoustova, Tereza, Weis, MaryAnn, Paznekas, William A., Wolf, Joshua H., Gutkind, J. Silvio, Wilcox, William R., Kozubik, Alois, Jabs, Ethylin Wang, Bryja, Vitezslav, Salazar, Lisa, Vesela, Iva, Balek, Lukas
Publicado 2012

Absence of the ER Cation Channel TMEM38B/TRIC-B Disrupts Intracellular Calcium Homeostasis and Dysregulates Collagen Synthesis in Recessive Osteogenesis Imperfecta

por Cabral, Wayne A., Ishikawa, Masaki, Garten, Matthias, Makareeva, Elena N., Sargent, Brandi M., Weis, MaryAnn, Barnes, Aileen M., Webb, Emma A., Shaw, Nicholas J., Ala-Kokko, Leena, Lacbawan, Felicitas L., Högler, Wolfgang, Leikin, Sergey, Blank, Paul S., Zimmerberg, Joshua, Eyre, David R., Yamada, Yoshihiko, Marini, Joan C.
Publicado 2016

MBTPS2 mutations cause defective regulated intramembrane proteolysis in X-linked osteogenesis imperfecta

por Lindert, Uschi, Cabral, Wayne A., Ausavarat, Surasawadee, Tongkobpetch, Siraprapa, Ludin, Katja, Barnes, Aileen M., Yeetong, Patra, Weis, Maryann, Krabichler, Birgit, Srichomthong, Chalurmpon, Makareeva, Elena N., Janecke, Andreas R., Leikin, Sergey, Röthlisberger, Benno, Rohrbach, Marianne, Kennerknecht, Ingo, Eyre, David R., Suphapeetiporn, Kanya, Giunta, Cecilia, Marini, Joan C., Shotelersuk, Vorasuk
Publicado 2016

Zebrafish type I collagen mutants faithfully recapitulate human type I collagenopathies

por Gistelinck, Charlotte, Kwon, Ronald Y., Malfait, Fransiska, Symoens, Sofie, Harris, Matthew P., Henke, Katrin, Hawkins, Michael B., Fisher, Shannon, Sips, Patrick, Guillemyn, Brecht, Bek, Jan Willem, Vermassen, Petra, De Saffel, Hanna, Witten, Paul Eckhard, Weis, MaryAnn, De Paepe, Anne, Eyre, David R., Willaert, Andy, Coucke, Paul J.
Publicado 2018

Dominant negative variants in KIF5B cause osteogenesis imperfecta via down regulation of mTOR signaling

por Marom, Ronit, Zhang, Bo, Washington, Megan E., Song, I-Wen, Burrage, Lindsay C., Rossi, Vittoria C., Berrier, Ava S., Lindsey, Anika, Lesinski, Jacob, Nonet, Michael L., Chen, Jian, Baldridge, Dustin, Silverman, Gary A., Sutton, V. Reid, Rosenfeld, Jill A., Tran, Alyssa A., Hicks, M. John, Murdock, David R., Dai, Hongzheng, Weis, MaryAnn, Jhangiani, Shalini N., Muzny, Donna M., Gibbs, Richard A., Caswell, Richard, Pottinger, Carrie, Cilliers, Deirdre, Stals, Karen, Eyre, David, Krakow, Deborah, Schedl, Tim, Pak, Stephen C., Lee, Brendan H.
Publicado 2023