Brown N - Search Results

1

An integrated physical map of 8q22-q24: use in positional cloning and deletion analysis of Langer-Giedion syndrome.

Hilton MJ, Gutiérrez L, Zhang L, Moreno PA, Reddy M, Brown N, Tan Y, Hill A, Wells DE. Hilton MJ, et al. Among authors: brown n. Genomics. 2001 Jan 15;71(2):192-9. doi: 10.1006/geno.2000.6438. Genomics. 2001. PMID: 11161813

2

Chromosomal localization of the human and mouse hyaluronan synthase genes.

Spicer AP, Seldin MF, Olsen AS, Brown N, Wells DE, Doggett NA, Itano N, Kimata K, Inazawa J, McDonald JA. Spicer AP, et al. Among authors: brown n. Genomics. 1997 May 1;41(3):493-7. doi: 10.1006/geno.1997.4696. Genomics. 1997. PMID: 9169154

3

Identification of novel mutations in the human EXT1 tumor suppressor gene.

Wells DE, Hill A, Lin X, Ahn J, Brown N, Wagner MJ. Wells DE, et al. Among authors: brown n. Hum Genet. 1997 May;99(5):612-5. doi: 10.1007/s004390050415. Hum Genet. 1997. PMID: 9150727

4

Identification of the Xenopus laevis cDNA for EXT1: a phylogenetic perspective.

Hill AL, Brown N, Hill MS, Wells DE. Hill AL, et al. Among authors: brown n. DNA Seq. 2002 Apr;13(2):85-92. doi: 10.1080/10425170290029990. DNA Seq. 2002. PMID: 12180350

5

Genetic heterogeneity in erythrokeratodermia variabilis: novel mutations in the connexin gene GJB4 (Cx30.3) and genotype-phenotype correlations.

Richard G, Brown N, Rouan F, Van der Schroeff JG, Bijlsma E, Eichenfield LF, Sybert VP, Greer KE, Hogan P, Campanelli C, Compton JG, Bale SJ, DiGiovanna JJ, Uitto J. Richard G, et al. Among authors: brown n. J Invest Dermatol. 2003 Apr;120(4):601-9. doi: 10.1046/j.1523-1747.2003.12080.x. J Invest Dermatol. 2003. PMID: 12648223 Free article.

6

trans-dominant inhibition of connexin-43 by mutant connexin-26: implications for dominant connexin disorders affecting epidermal differentiation.

Rouan F, White TW, Brown N, Taylor AM, Lucke TW, Paul DL, Munro CS, Uitto J, Hodgins MB, Richard G. Rouan F, et al. Among authors: brown n. J Cell Sci. 2001 Jun;114(Pt 11):2105-13. doi: 10.1242/jcs.114.11.2105. J Cell Sci. 2001. PMID: 11493646

7

The spectrum of mutations in erythrokeratodermias--novel and de novo mutations in GJB3.

Richard G, Brown N, Smith LE, Terrinoni A, Melino G, Mackie RM, Bale SJ, Uitto J. Richard G, et al. Among authors: brown n. Hum Genet. 2000 Mar;106(3):321-9. doi: 10.1007/s004390051045. Hum Genet. 2000. PMID: 10798362

8

American Academy of Orthopaedic Surgeons Clinical Practice Guideline Summary Management of Osteoarthritis of the Hip.

Hannon CP, Delanois RE, Nandi S, Fillingham Y; Management of Osteoarthritis of the Hip Work Group; Staff of the American Academy of Orthopaedic Surgeons; Management of Osteoarthritis of the Hip Work Group and Staff of the American Academy of Orthopaedic Surgeons. Hannon CP, et al. J Am Acad Orthop Surg. 2024 May 22. doi: 10.5435/JAAOS-D-24-00420. Online ahead of print. J Am Acad Orthop Surg. 2024. PMID: 38781351

9

Broad proteomics analysis of seeding-induced aggregation of α-synuclein in M83 neurons reveals remodeling of proteostasis mechanisms that might contribute to Parkinson's disease pathogenesis.

Lumpkin CJ, Patel H, Potts GK, Chaurasia S, Gibilisco L, Srivastava GP, Lee JY, Brown NJ, Amarante P, Williams JD, Karran E, Townsend M, Woods D, Ravikumar B. Lumpkin CJ, et al. Among authors: brown nj. Mol Brain. 2024 May 22;17(1):26. doi: 10.1186/s13041-024-01099-1. Mol Brain. 2024. PMID: 38778381 Free PMC article.

10

'We did everything by phone': a qualitative study of mothers' experience of smartphone-aided screening of cerebral palsy in Kathmandu, Nepal.

Kukka AJ, Bhattarai P, Sundelin HEK, Gurung R, Brown NJW, Litorp H, Axelin A, Kc A. Kukka AJ, et al. Among authors: brown njw. BMC Pediatr. 2024 May 22;24(1):357. doi: 10.1186/s12887-024-04829-5. BMC Pediatr. 2024. PMID: 38778316 Free PMC article.

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