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Taking Advantage of Phenotype Variability in a Local Animal Genetic Resource: Identification of Genomic Regions Associated with the Hairless Phenotype in Casertana Pigs

research Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs

16 citations , April 2018 in “Animal Genetics”

Researchers found two genes that may explain why some Casertana pigs don't have hair.

research Construction and Verification of Recombinant Follicle-specific Expression Vector

January 2011 in “Anhui nongye kexue”

The vector successfully directed specific gene expression in hair follicles.

research Heterozygous KRT32 variant is responsible for autosomal dominant loose anagen hair syndrome

May 2025

A KRT32 gene variant causes loose anagen hair syndrome.

research NAC1 directs CEP1-CEP3 peptidase expression and modulates root hair growth in Arabidopsis

1 citations , March 2023 in “bioRxiv (Cold Spring Harbor Laboratory)”

NAC1 controls certain enzymes that reduce root hair growth in Arabidopsis.

Loss-Of-Function Mutations of an Inhibitory Upstream ORF in the Human Hairless Transcript Cause Marie Unna Hereditary Hypotrichosis

research Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis

181 citations , January 2009 in “Nature Genetics”

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

research Progeny of Lgr5-expressing hair follicle stem cell contributes to papillomavirus-induced tumor development in epidermis

52 citations , September 2012 in “Oncogene”

research Multiple roles for activated LEF/TCF transcription complexes during hair follicle development and differentiation

990 citations , October 1999 in “Development”

Activated LEF/TCF complexes are crucial for hair development and cycling.

research Itpr3 Is Responsible for the Mouse Tufted (tf) Locus

6 citations , October 2012 in “Journal of Heredity”

The Itpr3 gene causes a specific hair pattern in mice.

research Localized Autosomal Recessive Hypotrichosis Due to a Frameshift Mutation in the Desmoglein 4 Gene Exhibits Extensive Phenotypic Variability within a Pakistani Family

25 citations , March 2007 in “The journal of investigative dermatology/Journal of investigative dermatology”

A specific gene mutation causes varying hair loss severity in a Pakistani family.

research Loss of Memo, a novel FGFR regulator, results in reduced lifespan

27 citations , September 2013 in “The FASEB Journal”

Losing Memo protein shortens lifespan and affects health.

research Clonal expansion from standing genetic variation underpins the evolution of an emerging plant pathogen in Australia

2 citations , December 2024

The plant pathogen in Australia evolves through existing genetic variation, not new genotypes.

research Identification and Expression of the Target Gene SLC24A2 of oar-miR-377 and Its Novel SNPs Effects on Wool Traits in Sheep

January 2024 in “Kafkas Universitesi Veteriner Fakultesi Dergisi”

A specific genetic variation affects wool quality in sheep.

research Sebaceous gland abnormalities in fatty acyl CoA reductase 2 (Far2) null mice result in primary cicatricial alopecia

14 citations , October 2018 in “PloS one”

Deleting the Far2 gene in mice causes sebaceous gland issues and patchy hair loss.

FGF7-Dependent Inhibition of Human Hair Growth by an Osteopontin-Derived Peptide: A Novel Solution for Hirsutism and Hypertrichosis

research 1371 FGF7-dependent inhibition of human hair growth byan osteopontin-derived peptide: A novel solution for hirsutism and hypertrichosis?

April 2018 in “Journal of Investigative Dermatology”

A new peptide, FOL-005, may help treat excessive hair growth by reducing a hair growth promoter, FGF7.

research The Feasibility and Utility of Hair Follicle Sampling To Measure FMRP and FMR1 mRNA in Children With or Without Fragile X Syndrome

December 2021 in “Research Square (Research Square)”

Hair follicle sampling is a feasible method to measure FMRP and FMR1 mRNA levels in children.

research Osteopontin Gene Polymorphisms rs1126616 C>T and rs1126772 A>G are Associated with Atopic Dermatitis in Polish Population

3 citations , October 2021 in “The Application of Clinical Genetics”

Certain gene changes in osteopontin are linked to higher risk of atopic dermatitis and asthma.

research CD98hc (SLC3A2) regulation of skin homeostasis wanes with age

35 citations , January 2013 in “The Journal of experimental medicine/The journal of experimental medicine”

CD98hc's role in skin health decreases with age.

The Feasibility and Utility of Hair Follicle Sampling to Measure FMRP and FMR1 mRNA in Children With or Without Fragile X Syndrome: A Pilot Study

research The feasibility and utility of hair follicle sampling to measure FMRP and FMR1 mRNA in children with or without fragile X syndrome: a pilot study

December 2022 in “Journal of neurodevelopmental disorders”

Hair follicle sampling is a practical method for measuring biomarkers in children with and without Fragile X syndrome.

research Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1

December 2022 in “American journal of medical genetics. Part A”

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

research Deregulated expression of E2F1 induces hyperplasia and cooperates with ras in skin tumor development

136 citations , March 1998 in “Oncogene”

Overexpression of E2F1 can lead to skin tumors and disrupt hair growth.

research Genome‐wide association study identifies variants associated with hair length in Brangus cattle

9 citations , June 2020 in “Animal genetics”

Scientists found genes linked to hair length in Brangus cattle that could help breed heat-tolerant cattle.

research Effect of lentivirus-mediated miR-182 targeting FGF9 on hallux valgus

4 citations , January 2021 in “International Journal of Medical Sciences”

miR-182 may help treat hallux valgus by targeting FGF9.

research Reclassification of Botryococcus braunii chemical races into separate species based on a comparative genomics analysis

8 citations , July 2024 in “PLoS ONE”

Botryococcus braunii's three chemical races should be reclassified as separate species.

research The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria

2 citations , September 2022

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

research Epithelial Integrity Is Maintained by a Matriptase-Dependent Proteolytic Pathway

137 citations , October 2009 in “The American journal of pathology”

Matriptase is crucial for keeping epithelial tissues healthy and functioning properly.

Genetic Diversity of Armillaria Species Symbiotic with Polyporus Umbellatus in China

research Genetic diversity of Armillaria spp. symbiotic with Polyporus umbellatus in China

2 citations , July 2015 in “Biochemical Systematics and Ecology”

Different types of Armillaria fungus have a high genetic variety when partnering with Polyporus umbellatus mushrooms in China.

research Building Models for Keratin Disorders

4 citations , April 2012 in “The journal of investigative dermatology/Journal of investigative dermatology”

Krt16-deficient mice help understand skin disorders like PC and FNEPPK.

Functional Mapping of the Mouse Hairless Gene Promoter Region

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