Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

215 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Abnormal vertebral segmentation and the notch signaling pathway in man.
Turnpenny PD, Alman B, Cornier AS, Giampietro PF, Offiah A, Tassy O, Pourquié O, Kusumi K, Dunwoodie S. Turnpenny PD, et al. Among authors: pourquie o. Dev Dyn. 2007 Jun;236(6):1456-74. doi: 10.1002/dvdy.21182. Dev Dyn. 2007. PMID: 17497699 Free article. Review.
When body segmentation goes wrong.
Pourquié O, Kusumi K. Pourquié O, et al. Clin Genet. 2001 Dec;60(6):409-16. doi: 10.1034/j.1399-0004.2001.600602.x. Clin Genet. 2001. PMID: 11846732 Review.
Molecular diagnosis of vertebral segmentation disorders in humans.
Giampietro PF, Dunwoodie SL, Kusumi K, Pourquié O, Tassy O, Offiah AC, Cornier AS, Alman BA, Blank RD, Raggio CL, Glurich I, Turnpenny PD. Giampietro PF, et al. Among authors: pourquie o. Expert Opin Med Diagn. 2008 Oct;2(10):1107-21. doi: 10.1517/17530059.2.10.1107. Expert Opin Med Diagn. 2008. PMID: 23496422
Summary of the first inaugural joint meeting of the International Consortium for scoliosis genetics and the International Consortium for vertebral anomalies and scoliosis, March 16-18, 2017, Dallas, Texas.
Giampietro PF, Pourquie O, Raggio C, Ikegawa S, Turnpenny PD, Gray R, Dunwoodie SL, Gurnett CA, Alman B, Cheung K, Kusumi K, Hadley-Miller N, Wise CA. Giampietro PF, et al. Among authors: pourquie o. Am J Med Genet A. 2018 Jan;176(1):253-256. doi: 10.1002/ajmg.a.38550. Epub 2017 Nov 21. Am J Med Genet A. 2018. PMID: 29159998 Free PMC article.
Mutations in the MESP2 gene cause spondylothoracic dysostosis/Jarcho-Levin syndrome.
Cornier AS, Staehling-Hampton K, Delventhal KM, Saga Y, Caubet JF, Sasaki N, Ellard S, Young E, Ramirez N, Carlo SE, Torres J, Emans JB, Turnpenny PD, Pourquié O. Cornier AS, et al. Among authors: pourquie o. Am J Hum Genet. 2008 Jun;82(6):1334-41. doi: 10.1016/j.ajhg.2008.04.014. Epub 2008 May 15. Am J Hum Genet. 2008. PMID: 18485326 Free PMC article.
Evolutionary plasticity of segmentation clock networks.
Krol AJ, Roellig D, Dequéant ML, Tassy O, Glynn E, Hattem G, Mushegian A, Oates AC, Pourquié O. Krol AJ, et al. Among authors: pourquie o. Development. 2011 Jul;138(13):2783-92. doi: 10.1242/dev.063834. Development. 2011. PMID: 21652651 Free PMC article.
215 results