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- MITF Gene Melanocyte Inducing Transcription Factor
- Malar Rash in Classical Homocystinuria Arushi Gahlot Saini, Hansashree Padmanabha, Savita Attri, Pratibha Singhi
- Waardenburg Syndrome
- Two Cases of Tyrosinemia Type Ii, and Its Rare Occurrence in Two Brothers
- Relative DOPA Deficiency in Lightly Pigmented Skin Contributes to UV-Independent Melanoma Susceptibility
- Prospective Study of the Phenotypic and Mutational Spectrum of Ocular Albinism and Oculocutaneous Albinism
- Amelanism in the Corn Snake Is Associated with the Insertion of An
- Featured Photo Multiple Color Abnormalities in a Wintering Mew Gull Jeff N
- Genome Mapping of a LYST Mutation in Corn Snakes Indicates That Vertebrate Chromatophore Vesicles Are Lysosome-Related Organelles
- PPCO Twist System
- Vitiligo Update Rebat M
- Inborn Errors of Amino Acid Metabolism
- Albinism: Epidemiology, Genetics, Cutaneous
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- The Tyrosinemia Type I
- Two Records of Amelanism in the Australian Skink Ctenotus Fallens (Storr, 1974)
- What Colour Is That Bird? the Causes and Recognition of Common Colour Aberrations in Birds
- Abnormal Plumage Survey: an Update
- Genetic Disorders of Pigmentation
- Oculocutaneous Albinism
- Increase in Melanin Formation and Promotion of Cytotoxicity in Cultured Melanoma Cells Caused by Phosphorylated Isomers of L-Dopa1
- Biology and Genetics of Oculocutaneous Albinism and Vitiligo – Common Pigmentation Disorders in Southern Africa
- More Than Skin Deep: Genetics, Clinical Manifestations, and Diagnosis of Albinism
- Tyrosinemia Type Iii: a Case Report of Siblings
- Waardenburg Syndrome
- Genomic Analysis and Assessment of Melanin Synthesis in Amorphotheca Resinae KUC3009
- Effect of Ions on Melanin Formation*,1
- Degradation of Tyrosinase by Melanosomal Ph Change and a New Mechanism of Whitening with Propylparaben
- Melanin Pigmentation in Mammalian Skin and Its Hormonal Regulation
- A Short Review of Pigmentation Disorders in Systemic Diseases Mohit Vijay Rojekar*,1,Swati D Sawant1 1Rajiv Gandhi Medical College, Thane, Maharashtra, India
- Synthesis of Melanin Biosynthesis of Catecholamines
- Sudden Eruption of Pigmentary Spots on Vitiligo Universalis Patient: Possible Misdiagnosis
- Role of Tyrosinase As the Determinant of Pigmentation in Cultured Human Melanocytes
- Waardenburg Syndrome
- Updates and New Medical Treatments for Vitiligo (Review)
- Waardenburg Syndrome: a Rare Genetic Disorder in Four Generations of a Family
- A Case of Homocystinuria: Anesthetic Implications Kewal Krishan Gupta, MD*, Sammer Sethi, MD**
- Current Management Options for Tyrosinemia
- Gekko 4 1 July 29
- Signaling Pathways in Melanogenesis
- Albinism in Life
- Albinism in Birds
- Genetic Basis of Melanin Pigmentation in Butterfly
- UP256 Inhibits Hyperpigmentation by Tyrosinase Expression/Dendrite Formation Via Rho-Dependent Signaling and by Primary Cilium Formation in Melanocytes
- TYR1) (Metabolic Condition: Amino Acid Disorder)
- Some Black-And-White Facts About the Faeroese White-Speckled Common Raven Corvus Corax Varius
- A Rare Case of Classic Homocystinuria with Hyperpigmentation
- Function-Blocking Autoantibodies to the Melanin-Concentrating Hormone Receptor in Vitiligo Patients
- Clinical and Morphological Features of Waardenburg Syndrome Type II
- Genetic Control of Melanin Metabolism Within the Melanin Unit
- Amelanistic Phenotypes in Western Palearctic Water Frogs from Poland (Anura: Ranidae: Rana)
- Phenylalanine & Tyrosine Metabolic Disorders