Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Tessa N, Campbell"'
Publikováno v:
McMaster University Medical Journal. 16:1-5
Kikuchi-Fujimoto disease is a rare, self-limited, histiocytic necrotizing lymphadenitis characterized by cervical lymphadenopathy and fever. An association has been made between the presence of this disease and systemic lupus erythematosus. We descri
Publikováno v:
Modern rheumatology case reports. 4(2)
Chronic non-bacterial osteomyelitis is a rare auto-inflammatory bone disease seen predominantly in the paediatric population. We describe a unique case of a 30-year-old female who presented with right-sided jaw pain and intermittent swelling over the
Autor:
Francis Y. M. Choy, Tessa N. Campbell
Publikováno v:
International Journal of Cell Biology, Vol 2011 (2011)
Gaucher disease is an inherited disorder caused by a deficiency in the lysosomal hydrolase glucocerebrosidase. There is a wide spectrum of clinical presentations, with the most common features being hepatosplenomegaly, skeletal disease, and cytopenia
Externí odkaz:
https://doaj.org/article/7e2d42bcf645453e9f1097a5cd3cf0f7
Autor:
Tessa N. Campbell, Francis Y.M. Choy
Publikováno v:
BioTechniques, Vol 30, Iss 1, Pp 32-34 (2001)
Externí odkaz:
https://doaj.org/article/16829fde9adb4b268ec92de13f177174
Publikováno v:
Biochemical and Biophysical Research Communications. 375:362-366
Eph receptor tyrosine kinases and their membrane-bound ligand ephrins form an essential cell communication system. Both ephrin classes have been shown to localize within cell surface lipid rafts, yet regulate different biological processes. In order
Autor:
Agnes Zay, Tessa N. Campbell, Francis Y.M. Choy, Patrick Ferreira, Nelson L.S. Tang, Weimin Zhang, HuiPing Shi
Publikováno v:
Blood Cells, Molecules, and Diseases. 38:287-293
Gaucher disease, the most prevalent lysosomal storage disease, results from an inherited deficiency in the enzyme glucocerebrosidase. Three clinical forms of Gaucher disease have been described: Type 1 non-neuronopathic, Type 2 acute neuronopathic, a
Gaucher disease is due to a deficiency in the lysosomal hydrolase glucocerebrosidase. The disease has been further subdivided into three phenotypes based upon clinical symptoms of neurological involvement: Type 1 (non-neuronopathic), Type 2 (acute ne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f206dbe2b33cae829119a8781d9e93d0
https://doi.org/10.1016/b978-0-12-407824-6.00007-0
https://doi.org/10.1016/b978-0-12-407824-6.00007-0
Autor:
Angela Marie Abbatecola, Koji Abe, Jose F. Abisambra, Aliya Ahmad, Hojjatollah Alaei, Kannayiram Alagiakrishnan, Gjumrakch Aliev, Ricardo Francisco Allegri, Osvaldo P. Almeida, Fernando J. Álvarez-Cervera, Nor Amalina Ahmad Alwi, David Ames, Amelia Jane Anderson-Mooney, José Paulo Andrade, Neus Anglés, R.A. Armstrong, Marco Assunção, Hebatallah Husseini Atteia, Marco Fidel Avila, Ming-Jong Bair, Mario Barbagallo, Pascale Barberger-Gateau, Michelangela Barbieri, George E. Barreto, José L. Bata-García, Monirun Begum, Francesco Bellia, Mario Belvedere, Louise E. Bennett, Monika Białecka, Michael Bird, Carlo Blundo, Virginia Boccardi, Irene Bolea, Domenico Bosco, Elske M. Brouwer-Brolsma, John C.M. Brust, Roberto Buffa, Kendra D. Bunner, Lena Burri, Ricardo Cabezas, María Alicia Camina, Tessa N. Campbell, Lourdes Rexach Cano, Huan-Lin Chen, Jianmin Chen, David Wing-Shing Cheung, Francis Y.M. Choy, J. Chua, Carmen Colica, Philippe Corcia, Suzanne Craft, Dario Cristiano, Michael D. Cusimano, Kate Dalton, Terry L. Davidson, Matteo De Bartolo, Andreza Fabro de Bem, Isac de Castro, Lisette C.P.G.M. de Groot, Sandra de la Cruz Marcos, Jade de Oliveira, Valeria del Balzo, Kentaro Deguchi, Shoko Deguchi, Richard Deth, Ligia J. Dominguez, Lorenzo M. Donini, Huseyin Doruk, Rainer Dziewas, Rafael Carles Díes, Ramon Santos El-Bachá, Sahar Elsayed El-Swefy, Laura Carreño Enciso, Caterina Ermio, Begoña M. Escribano, Ana María Estrada-Sánchez, Thorleif Etgen, Marcelo Farina, Antonietta Fava, Catherine Feart, Lei Feng, Laura Fernández-Fernández, Danilio Alvear Sampaio Ferreira, Milan Fiala, Renata Caruso Fialdini, Cheryl Fisher, Daniela Galimberti, James E. Galvin, Rebecca P. Gelber, Carmela Gerace, Panteleimon Giannakopoulos, Phillip F. Giannopoulos, Vijayasree V. Giridharan, Anna Maria Giusti, Janneth Gonzalez, José L. Góngora-Alfaro, Paul H. Gordon, Jeffrey S. Greiwe, Natalie A. Grima, Rubem Guedes, Susham Gupta, Erika Gyengesi, Sven Haller, Angela J. Hanson, Jenni Harvey, Ossama Morsi Hassan, Samuel T. Henderson, Karl Herrup, M.A. Hickey, Robert Hoerr, Xiaoli Hou, Chengyu Huang, Helmut M. Hügel, Sam-Long Hwang, Yoshio Ikeda, Kazuhiro Irie, Alexandria Jack, Neale Jackson, Richard L. Jackson, Brittany Jannise, Yugang Jiang, C.Shanthi Johnson, James S. Jolliff, Mariona Jové, Jonathan S. Kam, Scott E. Kanoski, Khurshid Khan, Takemi Kimura, Yasuko Kitagishi, Tetsuya Konishi, Gabor G. Kovacs, Debra Krause, Ee-Heok Kua, Tomoko Kurata, Mini Kurian, Timothy Kwok, Wai Ping Lam, Fabrizia Lattanzio, Catherine B. Lawrence, Tih-Shih Lee, Yuan-Kai Lee, Paula Leslie, Ping Chung Leung, Runping Li, Willmann Liang, Siong-Meng Lim, Fengwu Lin, I-Tsung Lin, Martin Loef, Karl-Olof Lovblad, Evelio Luque, Protásio Lemos da Luz, S.Lance Macaulay, Swati Madan, Walter Maetzler, R. Mahendran, Abu Bakar Abdul Majeed, Alastair G. Mander, Vasudevan Mani, Graham Manley, Danny Manor, Christine Margetts, Elisabetta Marini, J.Javier Martin-Fernandez, José Manuel Martínez-Martos, Irene Villegas Martínez, Beatriz de Mateo Silleras, Satoru Matsuda, Brian H. May, Alexander McGirr, Laurie M. McCormick, Jatin Mehta, Elena Mereu, Antonino Messina, Akari Minami, John Mirowsky, Eileen M. Moore, Eduardo Luiz Gasnhar Moreira, José Ramón Morelló, Takashi Mori, Gerald Münch, Kazuma Murakami, Joachim Mutter, Mehmet Ilkin Naharci, Frank Shigeo Nakao, Tze-Pin Ng, Julie Nigro, Toshiharu Ninomiya, Marcelo Nishiyama, Erum Nomani, Astrid C.J. Nooyens, Adriana Leico Oda, Hitoshi Okamura, Acary Souza Bulle Oliveira, Yuna Ono, Giuseppe Orsitto, Mio Ozawa, Véronique Pallet, Reinald Pamplona, Giuseppe Paolisso, Sergio Paradiso, Matthew P. Pase, Gaurav Patki, Olivier Piguet, Alessandro Pinto, Domenico Pirritano, Massimiliano Plastino, Eleonora Poggiogalle, M.Cristina Polidori, Renato Polimanti, Manuel Portero-Otin, Brian D. Power, Domenico Praticò, Rui Daniel S. Prediger, Victor R. Preedy, Mark A. Prendergast, Daniela Rae, Kalavathy Ramasamy, Muhammad Zaki Ramli, Bartolomé Ramirez, María Jesús Ramírez-Expósito, George V. Rebec, V.Prakash Reddy, María Paz Redondo del Río, Jordi Reguant, Parham Reisi, Ruth Remington, Monica Ricci, Enrico Rizzarelli, Stephen R. Robinson, Eugene Rogers, Francesca Rosini, Peter Roupas, Alessandra Rufa, María Julieta Russo, Ramesh Sahathevan, Samina Salim, Cristina Cleide dos Santos Salvioni, Camille H. Sample, Abel Santamaría, Maher Saqqur, Bruno Saragat, Julie Sauvant, Patrick Sauvant, Elio Scarpini, M.F.Z. Scelza, Richard J. Schwen, Rachel L. Self, José C.E. Serrano, Thomas B. Shea, Ping-Hsiao Shih, Takahiko Shimizu, Shinagawa Shunichiro, Zahra Siahmard, Jarosław Sławek, Christine Smoliner, Montse Solé, Delia Sprini, Rosanna Squitti, Karin Srulijes, Wilhelm Stahl, Patricia Stanich, Brian R. Stephens, Mingxue Sun, Junichi Takamatsu, Hong Chai Tang, Rajarajan A. Thandavarayan, Daniel Torrente, Terrence Town, Isaac Túnez, Lynn Ulatowski, Mercedes Unzeta, Tony Valente, Jolanda van Keizerswaard, Ondine van de Rest, Nikita L. van der Zwaluw, Graziella Vecchio, Judith Jimenez Veiga, Fidel Vila-Rodriguez, Harald Walach, Tobias Warnecke, David A.K. Watters, Wolfgang Weber, Rachel Weitzman, Lon R. White, Rainer Wirth, Chia-Hsien Wu, Kai Xiao, Charlie C.L. Xue, Gow-Chin Yen, David Tai-Wai Yew, Teruo Yokoi, Anthony L. Zhang, Lihong Zhang, Giancarlo Zito
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f8c14ebe7d7e10b6124e3def13c2328
https://doi.org/10.1016/b978-0-12-407824-6.00120-8
https://doi.org/10.1016/b978-0-12-407824-6.00120-8
Publikováno v:
Protein & Peptide Letters. 13:353-356
We examined the production and secretion of fusion constructs containing α-N-acetylglucosaminidase, the enzyme deficient in Sanfilippo B, and either wildtype TAT or modified TAT in cultured Spodoptera frugiperda cells. All constructs exhibited succe
Autor:
Janice E. A. Braun, Brandy Barren, Michael Natochin, Tessa N. Campbell, Shahid Hameed, Nikolai O. Artemyev, Linda C. Miller
Publikováno v:
Journal of Biological Chemistry. 280:30236-30241
Cysteine string protein (CSP) is an abundant regulated secretory vesicle protein that is composed of a string of cysteine residues, a linker domain, and an N-terminal J domain characteristic of the DnaJ/Hsp40 co-chaperone family. We have shown previo