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Reshaped DNA Methylation Cooperating with Homoeolog-Divergent Expression Promotes Improved Root Traits in Synthesized Tetraploid Wheat

research Reshaped DNA methylation cooperating with homoeolog‐divergent expression promotes improved root traits in synthesized tetraploid wheat

February 2024 in “New phytologist”

DNA changes in tetraploid wheat improve root growth and nitrogen use.

research ANALYSIS OF CTLA 4 GENE +49A/G AND CT60 A/G POLYMORPHISMS IN ALOPECIA AREATA PATIENTS

August 2023 in “Sabuncuoglu Serefeddin Health Sciences”

CT60 polymorphism might increase the risk of Alopecia Areata.

TRPS1 Mutation Associated with Trichorhinophalangeal Syndrome Type 1 with 15 Supernumerary Teeth, Hypoplastic Mandibular Condyles with Slender Condylar Necks and Unique Hair Morphology

research TRPS1 mutation associated with trichorhinophalangeal syndrome type 1 with 15 supernumerary teeth, hypoplastic mandibular condyles with slender condylar necks and unique hair morphology

9 citations , April 2020 in “Journal of dermatology”

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

research Deletions in the KAP6-1 gene are associated with fiber traits in cashmere-producing goats

1 citations , February 2021 in “Animal biotechnology”

Certain changes in the KAP6-1 gene affect the thickness and length of cashmere goat fibers.

research Association between SQSTM1 dysregulation and risk in alopecia areata: a Mendelian randomization study

November 2025 in “Frontiers in Immunology”

SQSTM1 gene issues may increase the risk of alopecia areata.

research Raman spectroscopic analysis of L‐phenylalanine and hydrolyzed eggwhite protein penetration into keratin fibers

12 citations , June 2011 in “Journal of applied polymer science”

L-phenylalanine and hydrolyzed eggwhite protein deeply penetrate human hair.

research Serine Biosynthesis In Human Hair Follicles By The Phosphorylated Pathway: Follicular 3-Phosphoglycerate Dehydrogenase

6 citations , June 1976 in “Journal of Investigative Dermatology”

research Gsdma3 Mutation Causes Bulge Stem Cell Depletion and Alopecia Mediated by Skin Inflammation

54 citations , December 2011 in “American Journal Of Pathology”

A Gsdma3 mutation causes hair loss due to stem cell damage from skin inflammation.

research A case report of a novel homozygote mutation causing severe Leydig cell hypoplasia: insights in the coexistence of nonsense mutation and polymorphism in the same LHCGR gene locus

November 2012 in “Experimental and Clinical Endocrinology & Diabetes”

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

research Mutations in Homocysteine Metabolism Genes Increase Keratin N-Homocysteinylation and Damage in Mice

5 citations , September 2018 in “International journal of genomics”

Genetic mutations that disrupt homocysteine breakdown lead to increased damage in mouse hair keratin.

research Causal effects of glutamine and lipid-related metabolites on alopecia areata: A 2-sample Mendelian randomization study

December 2025 in “Medicine”

Glutamine may protect against alopecia areata, while certain cholesterol and glucose levels may increase risk.

research Genomic Organization and Amplification of the Human Keratin 15 and Keratin 19 Genes

12 citations , January 2000 in “Biochemical and Biophysical Research Communications”

The study mapped keratin 15 and 19 genes, aiding future genetic disorder research.

research Sequence, expression, and evolutionary conservation of a gene encoding a glycine/tyrosine-rich keratin-associated protein of hair.

76 citations , February 1993 in “Journal of Biological Chemistry”

KAP6 genes are conserved across species and active in hair follicles.

research Supplementary material from "Giant axonal neuropathy alters the structure of keratin intermediate filaments in human hair"

January 2017

Giant axonal neuropathy changes the structure of keratin in human hair, making it stiffer and stronger.

Multi-Ancestry Tandem Repeat Association Study of Hair Color Using Exome-Wide Sequencing

research Multi-ancestry tandem repeat association study of hair colour using exome-wide sequencing

February 2024 in “bioRxiv (Cold Spring Harbor Laboratory)”

Tandem repeats significantly influence hair color, especially darker shades, across different ancestries.

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 Variation in the ovine keratin-associated protein 15-1 gene affects wool yield

18 citations , September 2018 in “The Journal of Agricultural Science”

Genetic variation in the KRTAP15-1 gene affects wool yield in sheep.

research Author response: Structural basis of malodour precursor transport in the human axilla

1 citations , June 2018

The transporter protein SH1446 in Staphylococcus hominis is key to underarm odor production.

research The Fraser Complex Proteins (Frem1, Frem2, and Fras1) Can Form Anchoring Cords in the Absence of AMACO at the Dermal–Epidermal Junction of Mouse Skin

1 citations , April 2023 in “International journal of molecular sciences”

Certain skin proteins can form anchoring structures without the protein AMACO.

research Deletion of an Enhancer in FGF5 is Associated With Ectopic Expression in Goat Hair Follicles and the Cashmere Growth Phenotype

1 citations , October 2020 in “Research Square (Research Square)”

A genetic variant in goats is linked to cashmere growth.

research Read-Through for Nonsense Mutations in Type XVII Collagen‒Deficient Junctional Epidermolysis Bullosa

5 citations , April 2022 in “The journal of investigative dermatology/Journal of investigative dermatology”

A new therapy for a skin blistering condition has not been developed yet.

research Hereditary 1,25‐Dihydroxyvitamin D–Resistant Rickets Due to an Opal Mutation Causing Premature Termination of the Vitamin D Receptor

47 citations , February 1998 in “Journal of bone and mineral research”

A specific gene mutation causes vitamin D-resistant rickets and hair loss.

research A novel monilethrix mutation in coil 2A of KRT86 causing autosomal dominant monilethrix with incomplete penetrance

15 citations , June 2012 in “British Journal of Dermatology”

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

research Image 3_Associations between ionomic profile and metabolic abnormalities in a murine model of sodium sulfide induced alopecia areata.tif

May 2025 in “OPAL (Open@LaTrobe) (La Trobe University)”

Linoleic acid and magnesium are key in alopecia areata progression, and tofacitinib can help by affecting their pathway.

research A functional polymorphism in interleukin-1α (IL1A) gene is associated with risk of alopecia areata in Chinese populations

11 citations , March 2013 in “Gene”

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

research Bioinformatics analysis of EST segment from goat

1 citations , January 2008 in “China Journal of Bioinformatics”

Goat skin has more keratin genes, while the mammary gland has more immunity-related genes.

research The Influence of the MDR1 C3435T Polymorphism on Methotrexate Responsiveness in Rheumatoid Arthritis Patients

1 citations , July 2020 in “The Egyptian Journal of Hospital Medicine”

The MDR1 C3435T polymorphism does not significantly affect methotrexate response in rheumatoid arthritis patients.

research Independent DSG4 frameshift variants in cats with hair shaft dystrophy

December 2021 in “Molecular genetics and genomics”

Cats with abnormal hair had DSG4 gene changes causing hair problems.

research Mutations in the vitamin D receptor gene in four patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets

24 citations , November 2008 in “Arquivos Brasileiros de Endocrinologia & Metabologia”

Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

research Image 2_Associations between ionomic profile and metabolic abnormalities in a murine model of sodium sulfide induced alopecia areata.tif

May 2025 in “OPAL (Open@LaTrobe) (La Trobe University)”

Linoleic acid and magnesium are key in alopecia areata progression, and tofacitinib can help by affecting their pathway.

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