50 Years of the steric-blocking mechanism in vertebrate skeletal muscle: a retrospective

por Parry, David A. D.
Publicado 2022

Structures of the ß-Keratin Filaments and Keratin Intermediate Filaments in the Epidermal Appendages of Birds and Reptiles (Sauropsids)

por Parry, David A.D.
Publicado 2021

An experimental model of contusion injury in humans

por Barnes, Matthew J., Lomiwes, Dominic, Parry, David A. D., Mackintosh, Stephen
Publicado 2022

Periplakin, a Novel Component of Cornified Envelopes and Desmosomes That Belongs to the Plakin Family and Forms Complexes with Envoplakin

por Ruhrberg, Christiana, Hajibagheri, M.A. Nasser, Parry, David A.D., Watt, Fiona M.
Publicado 1997

In Vitro Assembly and Structure of Trichocyte Keratin Intermediate Filaments: A Novel Role for Stabilization by Disulfide Bonding

por Wang, He, Parry, David A.D., Jones, Leslie N., Idler, William W., Marekov, Lyuben N., Steinert, Peter M.
Publicado 2000

Cingulin Contains Globular and Coiled-Coil Domains and Interacts with Zo-1, Zo-2, Zo-3, and Myosin

por Cordenonsi, Michelangelo, D'Atri, Fabio, Hammar, Eva, Parry, David A.D., Kendrick-Jones, John, Shore, David, Citi, Sandra
Publicado 1999

Microcephalic osteodysplastic primordial dwarfism type II is associated with global vascular disease

por Duker, Angela L., Kinderman, Dagmar, Jordan, Christy, Niiler, Tim, Baker-Smith, Carissa M., Thompson, Louise, Parry, David A., Carroll, Ricki S., Bober, Michael B.
Publicado 2021

Follicular regulatory T cells eliminate HIV-1-infected follicular helper T cells in an IL-2 concentration dependent manner

por Ollerton, Matthew T., Folkvord, Joy M., La Mantia, Andriana, Parry, David A., Meditz, Amie L., McCarter, Martin D., D’Aquila, Richard T., Connick, Elizabeth
Publicado 2022

Deletion of ameloblastin exon 6 is associated with amelogenesis imperfecta

por Poulter, James A., Murillo, Gina, Brookes, Steven J., Smith, Claire E. L., Parry, David A., Silva, Sandra, Kirkham, Jennifer, Inglehearn, Chris F., Mighell, Alan J.
Publicado 2014

Mutations in the Beta Propeller WDR72 Cause Autosomal-Recessive Hypomaturation Amelogenesis Imperfecta

por El-Sayed, Walid, Parry, David A., Shore, Roger C., Ahmed, Mushtaq, Jafri, Hussain, Rashid, Yasmin, Al-Bahlani, Suhaila, Al Harasi, Sharifa, Kirkham, Jennifer, Inglehearn, Chris F., Mighell, Alan J.
Publicado 2009

New consensus nomenclature for mammalian keratins

por Schweizer, Jürgen, Bowden, Paul E., Coulombe, Pierre A., Langbein, Lutz, Lane, E. Birgitte, Magin, Thomas M., Maltais, Lois, Omary, M. Bishr, Parry, David A.D., Rogers, Michael A., Wright, Mathew W.
Publicado 2006

Targeted genetic analysis in a large cohort of familial and sporadic cases of aneurysm or dissection of the thoracic aorta

por Weerakkody, Ruwan, Ross, David, Parry, David A., Ziganshin, Bulat, Vandrovcova, Jana, Gampawar, Piyush, Abdullah, Abdulshakur, Biggs, Jennifer, Dumfarth, Julia, Ibrahim, Yousef, Bicknell, Colin, Field, Mark, Elefteriades, John, Cheshire, Nick, Aitman, Tim
Publicado 2018

Loss of Integrin-Linked Kinase Sensitizes Breast Cancer to SRC Inhibitors

por Beetham, Henry, Griffith, Billie G.C., Murina, Olga, Loftus, Alexander E.P., Parry, David A., Temps, Carolin, Culley, Jayne, Muir, Morwenna, Unciti-Broceta, Asier, Sims, Andrew H., Byron, Adam, Brunton, Valerie G.
Publicado 2022

Cingulin and paracingulin tether myosins-2 to junctions to mechanoregulate the plasma membrane

por Rouaud, Florian, Huang, Wenmao, Flinois, Arielle, Jain, Kunalika, Vasileva, Ekaterina, Di Mattia, Thomas, Mauperin, Marine, Parry, David A.D., Dugina, Vera, Chaponnier, Christine, Méan, Isabelle, Montessuit, Sylvie, Mutero-Maeda, Annick, Yan, Jie, Citi, Sandra
Publicado 2023

Novel SIX6 mutations cause recessively inherited congenital cataract, microcornea, and corneal opacification with or without coloboma and microphthalmia

por Panagiotou, Evangelia S., Fernandez-Fuentes, Narcis, Farraj, Layal Abi, McKibbin, Martin, Elçioglu, Nursel H., Jafri, Hussain, Cerman, Eren, Parry, David A., Logan, Clare V., Johnson, Colin A., Inglehearn, Chris F., Toomes, Carmel, Ali, Manir
Publicado 2022

Regulation of flagellar motility by the conserved flagellar protein CG34110/Ccdc135/FAP50

por Yang, Yong, Cochran, Deborah A., Gargano, Mary D., King, Iryna, Samhat, Nayef K., Burger, Benjain P., Sabourin, Katherine R., Hou, Yuqing, Awata, Junya, Parry, David A.D., Marshall, Wallace F., Witman, George B., Lu, Xiangyi
Publicado 2011

Mutation Screening of Retinal Dystrophy Patients by Targeted Capture from Tagged Pooled DNAs and Next Generation Sequencing

por Watson, Christopher M., El-Asrag, Mohammed, Parry, David A., Morgan, Joanne E., Logan, Clare V., Carr, Ian M., Sheridan, Eamonn, Charlton, Ruth, Johnson, Colin A., Taylor, Graham, Toomes, Carmel, McKibbin, Martin, Inglehearn, Chris F., Ali, Manir
Publicado 2014

A homozygous STIM1 mutation impairs store-operated calcium entry and natural killer cell effector function without clinical immunodeficiency

por Parry, David A., Holmes, Tim D., Gamper, Nikita, El-Sayed, Walid, Hettiarachchi, Nishani T., Ahmed, Mushtaq, Cook, Graham P., Logan, Clare V., Johnson, Colin A., Joss, Shelagh, Peers, Chris, Prescott, Katrina, Savic, Sinisa, Inglehearn, Chris F., Mighell, Alan J.
Publicado 2016

Biallelic variants in DNA2 cause microcephalic primordial dwarfism

por Tarnauskaitė, Žygimantė, Bicknell, Louise S., Marsh, Joseph A., Murray, Jennie E., Parry, David A., Logan, Clare V., Bober, Michael B., de Silva, Deepthi C., Duker, Angela L., Sillence, David, Wise, Carol, Jackson, Andrew P., Murina, Olga, Reijns, Martin A. M.
Publicado 2019

Variability of systemic and oro-dental phenotype in two families with non-lethal Raine syndrome with FAM20C mutations

por Acevedo, Ana Carolina, Poulter, James A, Alves, Priscila Gomes, de Lima, Caroline Lourenço, Castro, Luiz Claudio, Yamaguti, Paulo Marcio, Paula, Lilian M, Parry, David A, Logan, Clare V, Smith, Claire E L, Johnson, Colin A, Inglehearn, Chris F, Mighell, Alan J
Publicado 2015