ライフサイエンスコーパス: dopachrome tautomerase

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1 on of an early zebrafish melanoblast marker, dopachrome tautomerase.

2 melanocytes, Tyr, Tyr-related protein 1, and dopachrome tautomerase accumulated in enlarged granules

3 also has been described recently to exhibit dopachrome tautomerase activity and to be structurally h

4 yphenylalanine oxidation drop rapidly, while DOPAchrome tautomerase activity increases and dihydroxyi

5 ne is the same as the catalytic site for the dopachrome tautomerase activity of MIF.

6 methyl ester (ISO-1), an inhibitor of MIF d-dopachrome tautomerase activity, reveals that ISO-1 bind

7 nd of the melanogenic enzymes tyrosinase and dopachrome tautomerase, all major players in melanogenes

8 cy of an enhancer required for expression of dopachrome tautomerase, an enzyme that functions in mela

9 igens gp100 and tyrosinase-related protein 2/dopachrome tautomerase and increased protection from a l

10 cell development and pigmentation, including dopachrome tautomerase and tyrosinase.

11 as tyrosinase, tyrosinase-related protein-1, dopachrome tautomerase, and Pmel17, are known, the funct

12 rophthalmia-associated transcription factor, dopachrome tautomerase, and tyrosinase promoters, leadin

13 be the protein encoded by the homologous, D-dopachrome tautomerase (D-DT) gene.

14 ation inhibitory factor (MIF), its homolog D-dopachrome tautomerase (D-DT), and their common receptor

15 y factor (MIF) and its functional homolog, d-dopachrome tautomerase (d-DT), have protumorigenic funct

16 rine MIF and its only known family member, D-dopachrome tautomerase (D-DT), promote the expression of

17 ew inflammatory activity for extracellular d-dopachrome tautomerase (D-DT), the recruitment of neutro

18 Tyrosinase and dopachrome tautomerase (DCT) activities were found exclu

19 DOPAchrome tautomerase (Dct) functions downstream of tyr

20 The melanin synthesis enzyme dopachrome tautomerase (DCT) is involved in intracellula

21 carrying a tyrosinase minigene driven by the dopachrome tautomerase (Dct) promoter region.

22 cell development in transgenic mice from the dopachrome tautomerase (Dct) promoter.

23 inase, tyrosinase-related protein-1 (Tyrp1), dopachrome tautomerase (Dct), and LAMP1 and 3 localizati

24 essing neural precursor cells (line Ntva) or dopachrome tautomerase (DCT)-expressing melanoblasts (li

25 yrosinase-related protein-1 (TYRP1/gp75) and dopachrome tautomerase (DCT/TYRP2) belong to a family of

26 Recent work by others has described D-dopachrome tautomerase (DDT) as a functional homologue o

27 D-dopachrome tautomerase (DDT) is an enzyme that lacks phy

28 The expression of the dopachrome tautomerase gene (Dct) and its protein produc

29 lite resident within an intron of the bovine dopachrome tautomerase gene.

30 s and for physiological investigations (e.g. dopachrome tautomerase in melanogenesis).

31 l-Dopachrome tautomerase (l-DCT), also called tyrosinase-r

32 osinase or on the mRNA levels of tyrosinase, dopachrome tautomerase, Pmel17, or MITF mRNA levels.

33 nder the regulation of a melanocyte-specific dopachrome tautomerase promoter.

34 enic line with Grm1 expression driven by the dopachrome tautomerase promoter.

35 (HO)2IndCOOH from dopachrome is catalyzed by dopachrome tautomerase, that the melanogenic protein tyr

36 yrosinase, melanocortin receptor (MC1R), and dopachrome tautomerase (TRP-2).

37 tyrosinase, tyrosinase-related protein-1 and dopachrome tautomerase/tyrosinase-related protein-2 and

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