Dean WB - Search Results

1

A recessive form of the Ehlers-Danlos syndrome caused by tenascin-X deficiency.

Schalkwijk J, Zweers MC, Steijlen PM, Dean WB, Taylor G, van Vlijmen IM, van Haren B, Miller WL, Bristow J. Schalkwijk J, et al. Among authors: dean wb. N Engl J Med. 2001 Oct 18;345(16):1167-75. doi: 10.1056/NEJMoa002939. N Engl J Med. 2001. PMID: 11642233 Free article.

2

Elastic fiber abnormalities in hypermobility type Ehlers-Danlos syndrome patients with tenascin-X mutations.

Zweers MC, Dean WB, van Kuppevelt TH, Bristow J, Schalkwijk J. Zweers MC, et al. Among authors: dean wb. Clin Genet. 2005 Apr;67(4):330-4. doi: 10.1111/j.1399-0004.2005.00401.x. Clin Genet. 2005. PMID: 15733269

3

Tenascin-X deficiency mimics Ehlers-Danlos syndrome in mice through alteration of collagen deposition.

Mao JR, Taylor G, Dean WB, Wagner DR, Afzal V, Lotz JC, Rubin EM, Bristow J. Mao JR, et al. Among authors: dean wb. Nat Genet. 2002 Apr;30(4):421-5. doi: 10.1038/ng850. Epub 2002 Mar 4. Nat Genet. 2002. PMID: 11925569

4

Haploinsufficiency of TNXB is associated with hypermobility type of Ehlers-Danlos syndrome.

Zweers MC, Bristow J, Steijlen PM, Dean WB, Hamel BC, Otero M, Kucharekova M, Boezeman JB, Schalkwijk J. Zweers MC, et al. Among authors: dean wb. Am J Hum Genet. 2003 Jul;73(1):214-7. doi: 10.1086/376564. Am J Hum Genet. 2003. PMID: 12865992 Free PMC article. No abstract available.

5

Tenascin-C deficiency attenuates TGF-ß-mediated fibrosis following murine lung injury.

Carey WA, Taylor GD, Dean WB, Bristow JD. Carey WA, et al. Among authors: dean wb. Am J Physiol Lung Cell Mol Physiol. 2010 Dec;299(6):L785-93. doi: 10.1152/ajplung.00385.2009. Epub 2010 Sep 10. Am J Physiol Lung Cell Mol Physiol. 2010. PMID: 20833777 Free PMC article.

6

ARHGEF9 disruption in a female patient is associated with X linked mental retardation and sensory hyperarousal.

Marco EJ, Abidi FE, Bristow J, Dean WB, Cotter P, Jeremy RJ, Schwartz CE, Sherr EH. Marco EJ, et al. Among authors: dean wb. J Med Genet. 2008 Feb;45(2):100-5. doi: 10.1136/jmg.2007.052324. Epub 2007 Sep 24. J Med Genet. 2008. PMID: 17893116

7

ARHGEF9 disruption in a female patient is associated with X linked mental retardation and sensory hyperarousal.

Marco EJ, Abidi FE, Bristow J, Dean WB, Cotter P, Jeremy RJ, Schwartz CE, Sherr EH. Marco EJ, et al. Among authors: dean wb. BMJ Case Rep. 2009;2009:bcr06.2009.1999. doi: 10.1136/bcr.06.2009.1999. Epub 2009 Jul 2. BMJ Case Rep. 2009. PMID: 21731583 Free PMC article.

8

High-efficiency type II cell-enhanced green fluorescent protein expression facilitates cellular identification, tracking, and isolation.

Vanderbilt JN, Gonzalez RF, Allen L, Gillespie A, Leaffer D, Dean WB, Chapin C, Dobbs LG. Vanderbilt JN, et al. Among authors: dean wb. Am J Respir Cell Mol Biol. 2015 Jul;53(1):14-21. doi: 10.1165/rcmb.2014-0348MA. Am J Respir Cell Mol Biol. 2015. PMID: 25692334 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

8 results

Search Page

Filters