scholarly journals Regulatory mutations in TBX3 disrupt asymmetric hair pigmentation that underlies Dun camouflage color in horses

2015 ◽  
Vol 48 (2) ◽  
pp. 152-158 ◽  
Author(s):  
Freyja Imsland ◽  
Kelly McGowan ◽  
Carl-Johan Rubin ◽  
Corneliu Henegar ◽  
Elisabeth Sundström ◽  
...  
Keyword(s):  
Hair Pigmentation ◽  
Regulatory Mutations

Prediction of eye and hair pigmentation phenotypes using the HIrisPlex system in a Brazilian admixed population sample

2021 ◽  
Author(s):  
Thássia Mayra Telles Carratto ◽  
Letícia Marcorin ◽  
Guilherme do Valle-Silva ◽  
Maria Luiza Guimarães de Oliveira ◽  
Eduardo Antônio Donadi ◽  
...  
Keyword(s):  
Population Sample ◽  
Hair Pigmentation ◽  
Admixed Population

Hair Follicle Melanogenesis Reflected in Hair Pigmentation as a Developmental Factor in Alopecia Areata

2021 ◽  
pp. 1-3
Author(s):  
Margit Juhasz ◽  
Rosalynn R.Z. Conic ◽  
Natasha Atanaskova Mesinkovska
Keyword(s):  
Hair Follicle ◽  
Alopecia Areata ◽  
Large Scale ◽  
Medical Center ◽  
Control Group ◽  
Hair Color ◽  
Natural Hair ◽  
Hair Pigmentation ◽  
Developmental Factor ◽  
Record Review

The mechanism of alopecia areata (AA) is not well-elucidated, and hair follicle melanogenesis pathways are implicated as possible sources for autoantigens. After a retrospective medical record review at a single tertiary medical center, the hair color of 112 AA patients were identified and compared to a control group of 104 androgenetic alopecia patients. There were no statistically significant differences in the natural hair color prevalence between the 2 groups (<i>p</i> = 0.164), and hair color was not a predictor of the alopecia type. Our results suggest hair pigmentation, determined by the eumelanin-to-pheomelanin ratio, is not a positive risk factor for AA development. We hope that our study will encourage multiple large-scale, collaborative, retrospective medical reviews to determine if our results are reproducible in diverse patient populations.

scholarly journals Regulatory Mutations of mir-48, a C. elegans let-7 Family MicroRNA, Cause Developmental Timing Defects

2005 ◽  
Vol 9 (3) ◽  
pp. 415-422 ◽  
Author(s):  
Ming Li ◽  
Matthew W. Jones-Rhoades ◽  
Nelson C. Lau ◽  
David P. Bartel ◽  
Ann E. Rougvie
Keyword(s):  
Developmental Timing ◽  
C Elegans ◽  
Regulatory Mutations ◽  
Timing Defects

scholarly journals Evolution of the Drosophila larval trichome pattern through cis-regulatory mutations at an enhancer of a single gene

2008 ◽  
Vol 319 (2) ◽  
pp. 495
Author(s):  
Gregory K. Davis ◽  
Laura Sillers ◽  
Purak Parikh ◽  
Alistair McGregor ◽  
Virginie Orgogozo ◽  
...  
Keyword(s):  
Single Gene ◽  
Regulatory Mutations

Dinucleotide tag‐based parallel reporter gene assay method enables efficient identification of regulatory mutations

2021 ◽  
pp. 2100341
Author(s):  
Naixia Ren ◽  
Bo Li ◽  
Qingqing Liu ◽  
Lele Yang ◽  
Xiaodan Liu ◽  
...  
Keyword(s):  
Reporter Gene ◽  
Reporter Gene Assay ◽  
Assay Method ◽  
Gene Assay ◽  
Regulatory Mutations
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