Russell LJ - Search Results

1

Cochleosaccular dysplasia associated with a connexin 26 mutation in keratitis-ichthyosis-deafness syndrome.

Griffith AJ, Yang Y, Pryor SP, Park HJ, Jabs EW, Nadol JB Jr, Russell LJ, Wasserman DI, Richard G, Adams JC, Merchant SN. Griffith AJ, et al. Among authors: russell lj. Laryngoscope. 2006 Aug;116(8):1404-8. doi: 10.1097/01.mlg.0000224549.75161.ca. Laryngoscope. 2006. PMID: 16885744 Free PMC article.

2

Auditory manifestations of Keratitis-Ichthyosis-Deafness (KID) syndrome.

Szymko-Bennett YM, Russell LJ, Bale SJ, Griffith AJ. Szymko-Bennett YM, et al. Among authors: russell lj. Laryngoscope. 2002 Feb;112(2):272-80. doi: 10.1097/00005537-200202000-00014. Laryngoscope. 2002. PMID: 11889383

3

Missense mutations in GJB2 encoding connexin-26 cause the ectodermal dysplasia keratitis-ichthyosis-deafness syndrome.

Richard G, Rouan F, Willoughby CE, Brown N, Chung P, Ryynänen M, Jabs EW, Bale SJ, DiGiovanna JJ, Uitto J, Russell L. Richard G, et al. Am J Hum Genet. 2002 May;70(5):1341-8. doi: 10.1086/339986. Epub 2002 Mar 22. Am J Hum Genet. 2002. PMID: 11912510 Free PMC article.

4

A de novo 2.1-Mb deletion of 13q12.11 in a child with developmental delay and minor dysmorphic features.

Der Kaloustian VM, Russell L, Aradhya S, Richard G, Rosenblatt B, Melançon S. Der Kaloustian VM, et al. Am J Med Genet A. 2011 Oct;155A(10):2538-42. doi: 10.1002/ajmg.a.34198. Am J Med Genet A. 2011. PMID: 22043489

5

Congenital recessive ichthyosis unlinked to loci for epidermal transglutaminases.

Bale SJ, Russell LJ, Lee ML, Compton JG, DiGiovanna JJ. Bale SJ, et al. Among authors: russell lj. J Invest Dermatol. 1996 Dec;107(6):808-11. doi: 10.1111/1523-1747.ep12330566. J Invest Dermatol. 1996. PMID: 8941665 Free article.

6

Linkage of autosomal recessive lamellar ichthyosis to chromosome 14q.

Russell LJ, DiGiovanna JJ, Hashem N, Compton JG, Bale SJ. Russell LJ, et al. Am J Hum Genet. 1994 Dec;55(6):1146-52. Am J Hum Genet. 1994. PMID: 7977373 Free PMC article.

7

Mutations in the gene for transglutaminase 1 in autosomal recessive lamellar ichthyosis.

Russell LJ, DiGiovanna JJ, Rogers GR, Steinert PM, Hashem N, Compton JG, Bale SJ. Russell LJ, et al. Nat Genet. 1995 Mar;9(3):279-83. doi: 10.1038/ng0395-279. Nat Genet. 1995. PMID: 7773290

8

Genetic heterogeneity in lamellar ichthyosis.

Bale SJ, Compton JG, Russell LJ, DiGiovanna JJ. Bale SJ, et al. Among authors: russell lj. J Invest Dermatol. 1996 Jul;107(1):140-1. doi: 10.1111/1523-1747.ep12298430. J Invest Dermatol. 1996. PMID: 8752853 Free article. No abstract available.

9

The potential role of environmentally associated DNA methylation in childhood acute lymphoblastic leukaemia subtypes.

Saville JR, Russell LJ, Padget K, Ghantous A, Nordlund J, McKay JA. Saville JR, et al. Among authors: russell lj. Int J Cancer. 2025 Jun 9. doi: 10.1002/ijc.35506. Online ahead of print. Int J Cancer. 2025. PMID: 40490854

10

Rectification of planar orientation angle switches behavior and replenishes contractile junctions.

Linvill K, Russell LJ, Vanderleest TE, Miao H, Xie Y, Blankenship JT, Loerke D. Linvill K, et al. Among authors: russell lj. J Cell Biol. 2025 Apr 3;224(4):e202309069. doi: 10.1083/jcb.202309069. Epub 2025 Jan 23. J Cell Biol. 2025. PMID: 39846952 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

90 results

Search Page

Filters