<p>The novel mutations are marked by an asterisk. A: Exon structure of the <i>TYR</i> gene showing the positional mutations; B: Tyrosinase protein showing the common central domain of tyrosinase showing positions of missense mutations.</p
Background: Tyrosinase (TYR) catalyzes the rate-limiting, first step in melanin production and its g...
Review on TYR (tyrosinase (oculocutaneous albinism IA)), with data on DNA, on the protein encoded, a...
It has recently been demonstrated that mutations in the gene for Bruton's tyrosine kinase (BTK) are ...
<p><a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0106656#pone.0106656-Stenso...
Tyrosinase gene (TYR) encodes a protein that regulates the production of the pigment melanin, a prim...
Item does not contain fulltextMutations in the Tyrosinase gene (TYR, 11q14-q21) cause oculocutaneous...
Mutations in the Tyrosinase gene (TYR, 11q14–q21) cause oculocutaneous albinism type 1 (OCA1). The 3...
Background and aims:Protein Kinases having significant effects on signal transduction as well as mos...
Misfolding and structural alteration in proteins lead to serious malfunctions and cause various dise...
Tyrosinemia is an autosomal recessive disorder. The complete molecular mechanism of these diseases h...
Tyrosinase (monophenol, dihydroxyphenylalanine: oxygen oxidoreductase, EC 1.14.18.1) is an essential...
A. Crystal structure of arrestin-3 (Protein Data Bank entry 3P2D [33]) with selected mutations indic...
Tyrosinase (Ec: 1.14.18.1) is a copper - containing enzyme which is distributed in all domains...
Background: Protein Kinases are a superfamily of proteins involved in crucial cellular processes suc...
<p>(A) Sanger sequencing chromatograms corresponding to confirmed JAK2/JAK3 variants. (B) Domain str...
Background: Tyrosinase (TYR) catalyzes the rate-limiting, first step in melanin production and its g...
Review on TYR (tyrosinase (oculocutaneous albinism IA)), with data on DNA, on the protein encoded, a...
It has recently been demonstrated that mutations in the gene for Bruton's tyrosine kinase (BTK) are ...
<p><a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0106656#pone.0106656-Stenso...
Tyrosinase gene (TYR) encodes a protein that regulates the production of the pigment melanin, a prim...
Item does not contain fulltextMutations in the Tyrosinase gene (TYR, 11q14-q21) cause oculocutaneous...
Mutations in the Tyrosinase gene (TYR, 11q14–q21) cause oculocutaneous albinism type 1 (OCA1). The 3...
Background and aims:Protein Kinases having significant effects on signal transduction as well as mos...
Misfolding and structural alteration in proteins lead to serious malfunctions and cause various dise...
Tyrosinemia is an autosomal recessive disorder. The complete molecular mechanism of these diseases h...
Tyrosinase (monophenol, dihydroxyphenylalanine: oxygen oxidoreductase, EC 1.14.18.1) is an essential...
A. Crystal structure of arrestin-3 (Protein Data Bank entry 3P2D [33]) with selected mutations indic...
Tyrosinase (Ec: 1.14.18.1) is a copper - containing enzyme which is distributed in all domains...
Background: Protein Kinases are a superfamily of proteins involved in crucial cellular processes suc...
<p>(A) Sanger sequencing chromatograms corresponding to confirmed JAK2/JAK3 variants. (B) Domain str...
Background: Tyrosinase (TYR) catalyzes the rate-limiting, first step in melanin production and its g...
Review on TYR (tyrosinase (oculocutaneous albinism IA)), with data on DNA, on the protein encoded, a...
It has recently been demonstrated that mutations in the gene for Bruton's tyrosine kinase (BTK) are ...
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