Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Kandice Swindle"'
Autor:
Cristina M. Justice, Kevin Bishop, Blake Carrington, Jim C. Mullikin, Kandice Swindle, Beth Marosy, Raman Sood, Nancy H. Miller, Alexander F. Wilson
Publikováno v:
G3: Genes, Genomes, Genetics, Vol 6, Iss 6, Pp 1707-1712 (2016)
Because of genetic heterogeneity present in idiopathic scoliosis, we previously defined clinical subsets (a priori) from a sample of families with idiopathic scoliosis to find genes involved with spinal curvature. Previous genome-wide linkage analysi
Externí odkaz:
https://doaj.org/article/f3f7ef86b11a46798e4452e6df4739fa
Autor:
Alex W. Poole, Kandice Swindle, Robin M. Baschal, Nancy H. Miller, Cambria I Wethey, Cristina M. Justice, Erin E. Baschal, Olivier Pourquié, Anoja Perera, Olivier Tassy
Publikováno v:
Spine Deformity. 3:288-296
Study Design A hypothesis-driven study was conducted in a familial cohort to determine the potential association between variants within the T-box 6 (TBX6) gene and familial idiopathic scoliosis (FIS). Objective To determine whether variants within e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5ec4d7485203ee72b0cb32f85331291c
https://doi.org/10.1016/j.jspd.2015.01.005
https://doi.org/10.1016/j.jspd.2015.01.005
Autor:
Matthew R.G. Taylor, Erin E. Baschal, Kenneth L. Jones, Matthew B. Dobbs, Gabe Haller, Christina A. Gurnett, Robin M. Baschal, Nelson L.S. Tang, Katherine Gowan, Cambria I Wethey, Kandice Swindle, Nancy H. Miller, David M. Alvarado
Publikováno v:
G3: Genes|Genomes|Genetics
Idiopathic scoliosis occurs in 3% of individuals and has an unknown etiology. The objective of this study was to identify rare variants that contribute to the etiology of idiopathic scoliosis by using exome sequencing in a multigenerational family wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::417eaa50ce7811e1dd3a5221559bfbf0
https://doi.org/10.1534/g3.114.015669
https://doi.org/10.1534/g3.114.015669
Autor:
Kevin Bishop, Jim C. Mullikin, Cristina M. Justice, Raman Sood, Kandice Swindle, Nancy H. Miller, Alexander F. Wilson, Beth A. Marosy, Blake Carrington
Publikováno v:
G3: Genes|Genomes|Genetics
G3: Genes, Genomes, Genetics, Vol 6, Iss 6, Pp 1707-1712 (2016)
G3: Genes, Genomes, Genetics, Vol 6, Iss 6, Pp 1707-1712 (2016)
Because of genetic heterogeneity present in idiopathic scoliosis, we previously defined clinical subsets (a priori) from a sample of families with idiopathic scoliosis to find genes involved with spinal curvature. Previous genome-wide linkage analysi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10d108b0214a9992f824efc6943a5192
https://pubmed.ncbi.nlm.nih.gov/27172222
https://pubmed.ncbi.nlm.nih.gov/27172222
Autor:
Erin E, Baschal, Kandice, Swindle, Cristina M, Justice, Robin M, Baschal, Anoja, Perera, Cambria I, Wethey, Alex, Poole, Olivier, Pourquié, Olivier, Tassy, Nancy H, Miller
Publikováno v:
Spine deformity. 3(4)
A hypothesis-driven study was conducted in a familial cohort to determine the potential association between variants within theTo determine if variants within exons of theIdiopathic Scoliosis (IS) is a structural curvature of the spine whose underlyi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fd2167188da4e8df2afd6d2d3aebbe17
https://pubmed.ncbi.nlm.nih.gov/26120555
https://pubmed.ncbi.nlm.nih.gov/26120555
Autor:
Nathalie Caron, Marc Grimaux, Armando D'Angelo, Annalisa Fattorini, Deborah J. Stearns-Kurosawa, Shinichiro Kurosawa, Barry Woodhams, Kandice Swindle, Patrizia Della Valle
Publikováno v:
Blood. 99:526-530
The endothelial protein C receptor (EPCR) facilitates protein C activation and plays a protective role in the response toEscherichia coli–mediated sepsis in primates. Previously, a soluble form of EPCR (sEPCR) in human plasma was characterized, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28995c0537f2f9df0273be34b5fd8f34
https://doi.org/10.1182/blood.v99.2.526
https://doi.org/10.1182/blood.v99.2.526
Autor:
Mera K. Tilley, Cristina M. Justice, Beth Marosy, Kandice Swindle, Nancy H. Miller, Alexander F. Wilson
Publikováno v:
Spine. 38(22)
STUDY DESIGN Model-independent linkage analysis and tests of association were performed for 22 single nucleotide polymorphisms in the CHD7 gene in 244 families of European descent with familial idiopathic scoliosis (FIS). OBJECTIVE To replicate an as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae00e1d8864b347e3f34e5f1c51a0220
https://pubmed.ncbi.nlm.nih.gov/23883829
https://pubmed.ncbi.nlm.nih.gov/23883829
Autor:
Kimberly F. Doheny, Yoonhee Kim, Cristina M. Justice, Elizabeth W. Pugh, Kandice Swindle, Beth Marosy, Nancy H. Miller, Alexander F. Wilson, Dana Behneman, Heejong Sung, Marie-Hélène Roy-Gagnon
Objective: Custom genotyping of markers in families with familial idiopathic scoliosis were used to fine-map candidate regions on chromosomes 9 and 16 in order to identify candidate genes that contribute to this disorder and prioritize them for next-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66da53d011ffc6434cdaa004f98ec86a
https://europepmc.org/articles/PMC4123546/
https://europepmc.org/articles/PMC4123546/
Autor:
R. de Groot, E. D. de Kleijn, Shinichiro Kurosawa, Jan A. Hazelzet, Kandice Swindle, C. E. Hack, D. J. Stearns-Kurosawa
Publikováno v:
Shock. 15:55-56
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7c90a62eff9d59c92fe3a01cdc37b162
https://doi.org/10.1097/00024382-200106001-00165
https://doi.org/10.1097/00024382-200106001-00165