International Trade Norms in the Age of Covid-19 Nationalism on the Rise?

Por Albertoni, Nicolás, Wise, Carol
Publicado no Fudan J. Hum. Soc. Sci. (2020)

Reply to Boylan

Por Wise, Carol A., Garcia, Carlos A., Patel, Pragna I., Lupski, James R.
Publicado em 1994

Understanding Genetic Factors in Idiopathic Scoliosis, a Complex Disease of Childhood

Por Wise, Carol A, Gao, Xiaochong, Shoemaker, Scott, Gordon, Derek, Herring, John A
Publicado em 2008

Genomic analyses of patients with unexplained early onset scoliosis

Por Gao, Xiaochong, Gotway, Garrett, Rathjen, Karl, Johnston, Charles, Sparagana, Steven, Wise, Carol A.
Publicado no Spine Deform (2014)

TDT-HET: A new transmission disequilibrium test that incorporates locus heterogeneity into the analysis of family-based association data

Por Londono, Douglas, Buyske, Steven, Finch, Stephen J, Sharma, Swarkar, Wise, Carol A, Gordon, Derek
Publicado em 2012

ptk7 mutant zebrafish models of congenital and idiopathic scoliosis implicate dysregulated Wnt signalling in disease

Por Hayes, Madeline, Gao, Xiaochong, Yu, Lisa X, Paria, Nandina, Henkelman, R. Mark, Wise, Carol A., Ciruna, Brian
Publicado em 2014

Pyrin binds the PSTPIP1/CD2BP1 protein, defining familial Mediterranean fever and PAPA syndrome as disorders in the same pathway

Por Shoham, Nitza G., Centola, Michael, Mansfield, Elizabeth, Hull, Keith M., Wood, Geryl, Wise, Carol A., Kastner, Daniel L.
Publicado em 2003

Somatic gain-of-function mutations in PIK3CA in patients with macrodactyly

Por Rios, Jonathan J., Paria, Nandina, Burns, Dennis K., Israel, Bonnie A., Cornelia, Reuel, Wise, Carol A., Ezaki, Marybeth
Publicado em 2013

Novel homozygous variant in WISP3 in a family with unrecognized progressive pseudorheumatoid dysplasia

Por Patel, Chandreshkumar, Khanshour, Anas M., Wilkes, David, Rios, Jonathan J., Sheff, Kelly W., Nassi, Lorien, Wise, Carol A.
Publicado no Clin Case Rep (2020)

Evaluation of GPR50, hMel-1B, and ROR-Alpha Melatonin-Related Receptors and the Etiology of Adolescent Idiopathic Scoliosis

Por Shyy, William, Wang, Kai, Gurnett, Christina A., Dobbs, Matthew B., Miller, Nancy H., Wise, Carol, Sheffield, Val C., Morcuende, Jose A.
Publicado em 2010

TCOF1 gene encodes a putative nucleolar phosphoprotein that exhibits mutations in Treacher Collins Syndrome throughout its coding region

Por Wise, Carol A., Chiang, Lydia C., Paznekas, William A., Sharma, Mridula, Musy, Maurice M., Ashley, Jennifer A., Lovett, Michael, Jabs, Ethylin W.
Publicado em 1997

Asymmetric Lower-Limb Malformations in Individuals with Homeobox PITX1 Gene Mutation

Por Gurnett, Christina A., Alaee, Farhang, Kruse, Lisa M., Desruisseau, David M., Hecht, Jacqueline T., Wise, Carol A., Bowcock, Anne M., Dobbs, Matthew B.
Publicado em 2008

Altered Transmission of HOX and Apoptotic SNPs Identify a Potential Common Pathway for Clubfoot

Por Ester, Audrey R., Weymouth, Katelyn S., Burt, Amber, Wise, Carol, Scott, Allison, Gurnett, Christina A, Dobbs, Matthew B., Blanton, Susan H., Hecht, Jacqueline T.
Publicado em 2009

Common polymorphisms in human lysyl oxidase genes are not associated with the adolescent idiopathic scoliosis phenotype

Por McGregor, Tracy L, Gurnett, Christina A, Dobbs, Matthew B, Wise, Carol A, Morcuende, Jose A, Morgan, Thomas M, Menon, Ramkumar, Muglia, Louis J
Publicado em 2011

Clinical, Molecular, and Genetic Characteristics of PAPA Syndrome: A Review

Por Smith, Elisabeth J, Allantaz, Florence, Bennett, Lynda, Zhang, Dongping, Gao, Xiaochong, Wood, Geryl, Kastner, Daniel L, Punaro, Marilynn, Aksentijevich, Ivona, Pascual, Virginia, Wise, Carol A
Publicado em 2010

Whole Exome Screening Identifies Novel and Recurrent WISP3 Mutations Causing Progressive Pseudorheumatoid Dysplasia in Jammu and Kashmir-India

Por Rai, Ekta, Mahajan, Ankit, Kumar, Parvinder, Angural, Arshia, Dhar, Manoj K, Razdan, Sushil, Thangaraj, Kumarasamy, Wise, Carol A., Ikegawa, Shiro, Pandita, Kamal Kishore, Sharma, Swarkar
Publicado no Sci Rep (2016)

Blood leukocyte microarrays to diagnose systemic onset juvenile idiopathic arthritis and follow the response to IL-1 blockade

Por Allantaz, Florence, Chaussabel, Damien, Stichweh, Dorothee, Bennett, Lynda, Allman, Windy, Mejias, Asuncion, Ardura, Monica, Chung, Wendy, Wise, Carol, Palucka, Karolina, Ramilo, Octavio, Punaro, Marilynn, Banchereau, Jacques, Pascual, Virginia
Publicado em 2007

The cartilage matrisome in adolescent idiopathic scoliosis

Por Wise, Carol A., Sepich, Diane, Ushiki, Aki, Khanshour, Anas M., Kidane, Yared H., Makki, Nadja, Gurnett, Christina A., Gray, Ryan S., Rios, Jonathan J., Ahituv, Nadav, Solnica-Krezel, Lila
Publicado no Bone Res (2020)

Blood leukocyte microarrays to diagnose systemic onset juvenile idiopathic arthritis and follow the response to IL-1 blockade

Por Allantaz, Florence, Chaussabel, Damien, Stichweh, Dorothee, Bennett, Lynda, Allman, Windy, Mejias, Asuncion, Ardura, Monica, Chung, Wendy, Smith, Elisabeth, Wise, Carol, Palucka, Karolina, Ramilo, Octavio, Punaro, Marilynn, Banchereau, Jacques, Pascual, Virginia
Publicado em 2009

CHD7 Gene Polymorphisms Are Associated with Susceptibility to Idiopathic Scoliosis

Por Gao, Xiaochong, Gordon, Derek, Zhang, Dongping, Browne, Richard, Helms, Cynthia, Gillum, Joseph, Weber, Samuel, Devroy, Shonn, Swaney, Saralove, Dobbs, Matthew, Morcuende, Jose, Sheffield, Val, Lovett, Michael, Bowcock, Anne, Herring, John, Wise, Carol
Publicado em 2007