Stem Cells and Cartilage Development: Complexities of a Simple Tissue

por Hollander, Anthony P, Dickinson, Sally C, Kafienah, Wael
Publicado 2010

The crystal structure of a bacterial Sufu-like protein defines a novel group of bacterial proteins that are similar to the N-terminal domain of human Sufu

por Das, Debanu, Finn, Robert D, Abdubek, Polat, Astakhova, Tamara, Axelrod, Herbert L, Bakolitsa, Constantina, Cai, Xiaohui, Carlton, Dennis, Chen, Connie, Chiu, Hsiu-Ju, Chiu, Michelle, Clayton, Thomas, Deller, Marc C, Duan, Lian, Ellrott, Kyle, Farr, Carol L, Feuerhelm, Julie, Grant, Joanna C, Grzechnik, Anna, Han, Gye Won, Jaroszewski, Lukasz, Jin, Kevin K, Klock, Heath E, Knuth, Mark W, Kozbial, Piotr, Sri Krishna, S, Kumar, Abhinav, Lam, Winnie W, Marciano, David, Miller, Mitchell D, Morse, Andrew T, Nigoghossian, Edward, Nopakun, Amanda, Okach, Linda, Puckett, Christina, Reyes, Ron, Tien, Henry J, Trame, Christine B, van den Bedem, Henry, Weekes, Dana, Wooten, Tiffany, Xu, Qingping, Yeh, Andrew, Zhou, Jiadong, Hodgson, Keith O, Wooley, John, Elsliger, Marc-André, Deacon, Ashley M, Godzik, Adam, Lesley, Scott A, Wilson, Ian A
Publicado 2010

Zinc deficiency activates S100A8 inflammation in the absence of COX-2 and promotes murine oral-esophageal tumor progression

por Wan, Shao-Gui, Taccioli, Cristian, Jiang, Yubao, Chen, Hongping, Smalley, Karl J, Huang, Kun, Liu, Xiu-Ping, Farber, John L, Croce, Carlo M, Fong, Louise Y Y
Publicado 2011

Mutational spectrum in congenital dyserythropoietic anemia type II: Identification of 19 novel variants in SEC23B gene

por Russo, Roberta, Esposito, Maria Rosaria, Asci, Roberta, Gambale, Antonella, Perrotta, Silverio, Ramenghi, Ugo, Forni, Gian Luca, Uygun, Vedat, Delaunay, Jean, Iolascon, Achille
Publicado 2010

A qualitative study of perceived social barriers to care for eating disorders: Perspectives from ethnically diverse health care consumers

por Becker, Anne E, Hadley Arrindell, Adrienne, Perloe, Alexandra, Fay, Kristen, Striegel-Moore, Ruth H
Publicado 2010

Accelerated Cardiac Magnetic Resonance Imaging in the Mouse Using an Eight-Channel Array at 9.4 Tesla

por Schneider, Jürgen E, Lanz, Titus, Barnes, Hannah, Stork, Lee-Anne, Bohl, Steffen, Lygate, Craig A, Ordidge, Roger J, Neubauer, Stefan
Publicado 2011

Plectin Deficiency Leads to Both Muscular Dystrophy and Pyloric Atresia in Epidermolysis Bullosa Simplex

por Natsuga, Ken, Nishie, Wataru, Shinkuma, Satoru, Arita, Ken, Nakamura, Hideki, Ohyama, Makiko, Osaka, Hitoshi, Kambara, Takeshi, Hirako, Yoshiaki, Shimizu, Hiroshi
Publicado 2010

A Rare Novel Deletion of the Tyrosine Hydroxylase Gene in Parkinson Disease

por Bademci, Güney, Edwards, Todd L, Torres, Andre L, Scott, William K, Züchner, Stephan, Martin, Eden R, Vance, Jeffery M, Wang, Liyong
Publicado 2010

Investigation of Maternal Effects, Maternal-Fetal Interactions and Parent-of-Origin Effects (Imprinting), Using Mothers and Their Offspring

por Ainsworth, Holly F, Unwin, Jennifer, Jamison, Deborah L, Cordell, Heather J
Publicado 2011

Developmental and Degenerative Features in a Complicated Spastic Paraplegia

por Manzini, M Chiara, Rajab, Anna, Maynard, Thomas M, Mochida, Ganeshwaran H, Tan, Wen-Hann, Nasir, Ramzi, Hill, R Sean, Gleason, Danielle, Al Saffar, Muna, Partlow, Jennifer N, Barry, Brenda J, Vernon, Mike, LaMantia, Anthony-Samuel, Walsh, Christopher A
Publicado 2010

Mutations and Deletions in PCDH19 Account for Various Familial or Isolated Epilepsies in Females

por Depienne, Christel, Trouillard, Oriane, Bouteiller, Delphine, Gourfinkel-An, Isabelle, Poirier, Karine, Rivier, François, Berquin, Patrick, Nabbout, Rima, Chaigne, Denys, Steschenko, Dominique, Gautier, Agnès, Hoffman-Zacharska, Dorota, Lannuzel, Annie, Lackmy-Port-Lis, Marilyn, Maurey, Hélène, Dusser, Anne, Bru, Marie, Gilbert-Dussardier, Brigitte, Roubertie, Agathe, Kaminska, Anna, Whalen, Sandra, Mignot, Cyril, Baulac, Stéphanie, Lesca, Gaetan, Arzimanoglou, Alexis, LeGuern, Eric
Publicado 2011

A Phase 1/2, Dose-Escalation Trial of Deferasirox for the Treatment of Iron Overload in HFE-Related Hereditary Hemochromatosis

por Phatak, Pradyumna, Brissot, Pierre, Wurster, Mark, Adams, Paul C, Bonkovsky, Herbert L, Gross, John, Malfertheiner, Peter, McLaren, Gordon D, Niederau, Claus, Piperno, Alberto, Powell, Lawrie W, Russo, Mark W, Stoelzel, Ulrich, Stremmel, Wolfgang, Griffel, Louis, Lynch, Nicola, Zhang, Yiyun, Pietrangelo, Antonello
Publicado 2010

Foot Pad Skin Biopsy in Mouse Models of Hereditary Neuropathy

por Dacci, Patrizia, Dina, Giorgia, Cerri, Federica, Previtali, Stefano Carlo, Lopez, Ignazio Diego, Lauria, Giuseppe, Feltri, Maria Laura, Bolino, Alessandra, Comi, Giancarlo, Wrabetz, Lawrence, Quattrini, Angelo
Publicado 2010

Evaluation of Germline BMP4 Mutation as a Cause of Colorectal Cancer

por Lubbe, Steven J, Pittman, Alan M, Matijssen, Cornelis, Twiss, Philip, Olver, Bianca, Lloyd, Amy, Qureshi, Mobshra, Brown, Nathan, Nye, Emma, Stamp, Gordon, Blagg, Julian, Houlston, Richard S
Publicado 2011

A Novel CRYGD Mutation (p.Trp43Arg) Causing Autosomal Dominant Congenital Cataract in a Chinese Family

por Wang, Binbin, Yu, Changhong, Xi, Yi-Bo, Cai, Hong-Chen, Wang, Jing, Zhou, Sirui, Zhou, Shiyi, Wu, Yi, Yan, Yong-Bin, Ma, Xu, Xie, Lixin
Publicado 2011

LQTS Gene LOVD Database

por Zhang, Tao, Moss, Arthur, Cong, Peikuan, Pan, Min, Chang, Bingxi, Zheng, Liangrong, Fang, Quan, Zareba, Wojciech, Robinson, Jennifer, Lin, Changsong, Li, Zhongxiang, Wei, Junfang, Zeng, Qiang, Qi, Ming
Publicado 2010

PRO-MINE: A Bioinformatics Repository and Analytical Tool for TARDBP Mutations

por Pinto, Sofia, Vlahoviček, Kristian, Buratti, Emanuele
Publicado 2011

Legius Syndrome in Fourteen Families

por Denayer, Ellen, Chmara, Magdalena, Brems, Hilde, Kievit, Anneke Maat, van Bever, Yolande, Van den Ouweland, Ans MW, Van Minkelen, Rick, de Goede-Bolder, Arja, Oostenbrink, Rianne, Lakeman, Phillis, Beert, Eline, Ishizaki, Takuma, Mori, Tomoaki, Keymolen, Kathelijn, Van den Ende, Jenneke, Mangold, Elisabeth, Peltonen, Sirkku, Brice, Glen, Rankin, Julia, Van Spaendonck-Zwarts, Karin Y, Yoshimura, Akihiko, Legius, Eric
Publicado 2011

The Prevalence and Assessment of ErbB2-Positive Breast Cancer in Asia: A Literature Survey

por Tan, Yew Oo, Han, Sehwan, Lu, Yen-Shen, Yip, Cheng-Har, Sunpaweravong, Patrapim, Jeong, Joon, Caguioa, Priscilla B, Aggarwal, Shyam, Yeoh, Ee Min, Moon, Hanlim
Publicado 2010

Selective ERK Activation Differentiates Mouse and Human Tolerogenic Dendritic Cells, Expands Antigen-Specific Regulatory T Cells, and Suppresses Experimental Inflammatory Arthritis

por Arce, Frederick, Breckpot, Karine, Stephenson, Holly, Karwacz, Katarzyna, Ehrenstein, Michael R, Collins, Mary, Escors, David
Publicado 2011