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Skin Pigmentation. Genetics, Geographic Variation & Disorders (Dermatology -- Laboratory & Clinical Research Series)
Smith, J.B. — Haworth, M.B.
1ª Edición Julio 2013
Inglés
Tapa dura
155 pags
442 gr
16 x 23 x null cm
ISBN 9781626184176
Editorial NOVA SCIENCE PUBLISHERS INC. U.S.
LIBRO IMPRESO
-5%
131,99 €125,39 €IVA incluido
126,91 €120,57 €IVA no incluido
Recíbelo en un plazo de
2 - 3 semanas
Description
In this book, the authors discuss the genetics, geographic variation and disorders associated with skin pigmentation. Topics include the melanocortin-1 receptor as a key melanoma risk determinant and a critical regulator of the UV DNA damage repair response; three major signalling pathways involved in the establishment of mammalian skin and hair coloration via the regulation of tyrosinase activity; multiple genes and diverse hierarchical pathways that affect human pigmentation; acquired skin pigmenation; the pro-opiomelanocortin (POMC) and melanocortin systems in the regulation of human skin pigmentation; and an overview on the melanocyte precursor migration from neural crest.
Table of Contents
Preface; The Melanocortin-1 Receptor: A Key Melanoma Risk Determinant & a Critical Regulator of the UV DNA Damage Repair Response; MC1R. EDNRB, & Kit Signaling in Pigment Regulation & Related Disorders; Multiple Genes & Diverse Hierarchical Pathways Affect Human Pigmentation; Acquired Skin Pigmentation; The Pro-Opiomelanocortin (POMC) & Melanocortin System in Regulation of Human Skin Pigmentation; Overview on the Melanocyte Precursor Migration from Neural Crest; Index.
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