MITF mutations associated with pigment deficiency syndromes and melanoma have different effects on protein function.
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The melanocyte lineage in development and diseaseBiallelic Mutations in MITF Cause Coloboma, Osteopetrosis, Microphthalmia, Macrocephaly, Albinism, and DeafnessMITF in melanoma: mechanisms behind its expression and activity.Efficient CRISPR/Cas9-mediated biallelic gene disruption and site-specific knockin after rapid selection of highly active sgRNAs in pigs.Microphthalmia-associated transcription factor in melanoma development and MAP-kinase pathway targeted therapy.CSE1L Links cAMP/PKA and Ras/ERK pathways and regulates the expressions and phosphorylations of ERK1/2, CREB, and MITF in melanoma cells.Prenatal diagnosis and genetic counseling for Waardenburg syndrome type I and II in Chinese families.Wnt signaling pathway involvement in genotypic and phenotypic variations in Waardenburg syndrome type 2 with MITF mutations.Cochlear morphology in the developing inner ear of the porcine model of spontaneous deafness.
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MITF mutations associated with pigment deficiency syndromes and melanoma have different effects on protein function.
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 20 June 2013
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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MITF mutations associated with ...... t effects on protein function.
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MITF mutations associated with ...... t effects on protein function.
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MITF mutations associated with ...... t effects on protein function.
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MITF mutations associated with ...... t effects on protein function.
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MITF mutations associated with ...... t effects on protein function.
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MITF mutations associated with ...... t effects on protein function.
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MITF mutations associated with ...... t effects on protein function.
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Alexander Schepsky
Christine Grill
Eiríkur Steingrímsson
Kristín Bergsteinsdóttir
Margrét H Ogmundsdóttir
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P304
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10.1093/HMG/DDT285
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2013-06-20T00:00:00Z