Related references
Note: Only part of the references are listed.Protein Stability and Functional Characterization of Intra-Melanosomal Domain of Human Recombinant Tyrosinase-Related Protein 1
Monika B. Dolinska et al.
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2020)
Membrane-associated human tyrosinase is an enzymatically active monomeric glycoprotein
Nicole J. Kus et al.
PLOS ONE (2018)
The role of dynamic enzyme assemblies and substrate channelling in metabolic regulation
Lee J. Sweetlove et al.
NATURE COMMUNICATIONS (2018)
An Improved Method for Modeling Voltage-Gated Ion Channels at Atomic Accuracy Applied to Human Cav Channels
Wilnelly Martinez-Ortiz et al.
CELL REPORTS (2018)
Structure and Function of Human Tyrosinase and Tyrosinase-Related Proteins
Xuelei Lai et al.
CHEMISTRY-A EUROPEAN JOURNAL (2018)
The consequences of deglycosylation of recombinant intra-melanosomal domain of human tyrosinase
Monika B. Dolinska et al.
BIOLOGICAL CHEMISTRY (2018)
Pigmentation-Independent Susceptibility Loci for Actinic Keratosis Highlighted by Compound Heterozygosity Analysis
Kaiyin Zhong et al.
JOURNAL OF INVESTIGATIVE DERMATOLOGY (2017)
Interaction between G Protein-Coupled Receptor 143 and Tyrosinase: Implications for Understanding Ocular Albinism Type 1
Elisabetta De Filippo et al.
JOURNAL OF INVESTIGATIVE DERMATOLOGY (2017)
The importance of N-glycosylation on β3 integrin ligand binding and conformational regulation
Xiulei Cai et al.
SCIENTIFIC REPORTS (2017)
Structure of Human Tyrosinase Related Protein 1 Reveals a Binuclear Zinc Active Site Important for Melanogenesis
Xuelei Lai et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2017)
Identification of Susceptibility Loci for Cutaneous Squamous Cell Carcinoma
Maryam M. Asgari et al.
JOURNAL OF INVESTIGATIVE DERMATOLOGY (2016)
IRF4, MC1R and TYR genes are risk factors for actinic keratosis independent of skin color
Leonie C. Jacobs et al.
HUMAN MOLECULAR GENETICS (2015)
DNA Variations in Oculocutaneous Albinism: An Updated Mutation List and Current Outstanding Issues in Molecular Diagnostics
Dimitre R. Simeonov et al.
HUMAN MUTATION (2013)
Molecular and Functional Studies of Tyrosinase Variants Among Indian Oculocutaneous Albinism Type 1 Patients
Moumita Chaki et al.
JOURNAL OF INVESTIGATIVE DERMATOLOGY (2011)
A method and server for predicting damaging missense mutations
Ivan A. Adzhubei et al.
NATURE METHODS (2010)
Variant of TYR and Autoimmunity Susceptibility Loci in Generalized Vitiligo.
Ying Jin et al.
NEW ENGLAND JOURNAL OF MEDICINE (2010)
Genome-wide association studies of pigmentation and skin cancer: a review and meta-analysis
Meg R. Gerstenblith et al.
PIGMENT CELL & MELANOMA RESEARCH (2010)
The genetics of generalized vitiligo: autoimmune pathways and an inverse relationship with malignant melanoma
Richard A. Spritz
GENOME MEDICINE (2010)
New insights into Vogt-Koyanagi-Harada disease
Francisco Max Damico et al.
ARQUIVOS BRASILEIROS DE OFTALMOLOGIA (2009)
CC plus : a relational database of coiled-coil structures
Oliver D. Testa et al.
NUCLEIC ACIDS RESEARCH (2009)
Docking analysis of transient complexes:: Interaction of ferredoxin-NADP+ reductase with ferredoxin and flavodoxin
Milagros Medina et al.
PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS (2008)
Direct interaction of tyrosinase with Tyrp1 to form heterodimeric complexes in vivo
Takeshi Kobayashi et al.
JOURNAL OF CELL SCIENCE (2007)
Genetic determinants of hair, eye and skin pigmentation in Europeans
Patrick Sulem et al.
NATURE GENETICS (2007)
Improving CAPRI predictions:: Optimized desolvation for rigid-body docking
J Fernández-Recio et al.
PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS (2005)
Optimal docking area: A new method for predicting protein-protein interaction sites
J Fernandez-Recio et al.
PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS (2005)
Tyrosinase processing and intracellular trafficking is disrupted in mouse primary melanocytes carrying the underwhite (uw) mutation.: A model for oculocutaneous albinism (OCA) type 4
GE Costin et al.
JOURNAL OF CELL SCIENCE (2003)
ICM-DISCO docking by global energy optimization with fully flexible side-chains
J Fernández-Recio et al.
PROTEINS-STRUCTURE FUNCTION AND GENETICS (2003)
Skin pigmentation, biogeographical ancestry and admixture mapping
MD Shriver et al.
HUMAN GENETICS (2003)
Pink-eyed dilution protein controls the processing of tyrosinase
K Chen et al.
MOLECULAR BIOLOGY OF THE CELL (2002)
Mutations in the human orthologue of the mouse underwhite gene (uw) underlie a new form of oculocutaneous albinism, OCA4
JM Newton et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2001)
Oculocutaneous albinism types 1 and 3 are ER retention diseases: mutation of tyrosinase or Tyrp1 can affect the processing of both mutant and wild-type proteins
K Toyofuku et al.
FASEB JOURNAL (2001)
The molecular basis of oculocutaneous albinism type 1 (OCA1): sorting failure and degradation of mutant tyrosinases results in a lack of pigmentation
K Toyofuku et al.
BIOCHEMICAL JOURNAL (2001)
Mutational analysis of the modulation of tyrosinase by tyrosinase-related proteins 1 and 2 in vitro
P Manga et al.
PIGMENT CELL RESEARCH (2000)
Insect melanogenesis -: III.: Metabolon formation in the melanogenic pathway -: Regulation of phenoloxidase activity by endogenous dopachrome isomerase (decarboxylating) from Manduca sexta
M Sugumaran et al.
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS (2000)
Endoplasmic reticulum retention is a common defect associated with tyrosinase-negative albinism
R Halaban et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2000)
A common temperature-sensitive allelic form of human tyrosinase is retained in the endoplasmic reticulum at the nonpermissive temperature
JF Berson et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2000)
Estimating local backbone structural deviation in homology models
T Cardozo et al.
COMPUTERS & CHEMISTRY (2000)