N F Box
Overview
Explore the profile of N F Box including associated specialties, affiliations and a list of published articles.
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Articles
15
Citations
609
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Recent Articles
11.
Box N, Wyeth J, Mayne C, OGorman L, Martin N, Sturm R
Mamm Genome
. 1998 Jan;
9(1):50-3.
PMID: 9434945
The complete 24,667 nucleotide sequence spanning the human TYRP1 gene has been determined from the inserts of two overlapping lambda clones. A LINE-1 repeat element is immediately adjacent to and...
12.
Manga P, Kromberg J, Box N, Sturm R, Jenkins T, Ramsay M
Am J Hum Genet
. 1997 Nov;
61(5):1095-101.
PMID: 9345097
Oculocutaneous albinism (OCA) is the most common autosomal recessive disorder among southern African Blacks. There are three forms that account for almost all OCA types in this region. Tyrosinase-positive OCA...
13.
Box N, Wyeth J, OGorman L, Martin N, Sturm R
Hum Mol Genet
. 1997 Sep;
6(11):1891-7.
PMID: 9302268
The association between MSHR coding region variation and hair colour in humans has been examined by genotyping 25 red haired and 62 non-red Caucasians, all of whom were 12 years...
14.
Sturm R, OSullivan B, Box N, Smith A, Smit S, Puttick E, et al.
Genomics
. 1995 Sep;
29(1):24-34.
PMID: 8530077
The structures of the human tyrosinase-related protein genes TYRP1 and TYRP2 have been determined and compared with that of the tyrosinase gene (TYR). The TYRP1 protein is encoded in 7...
15.