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Hair loss in Androgenetic alopecia (AGA) is due to altered cell sensitivity to hormones, not increased hormone levels. Hair growth periods shorten over time, causing hair to become thinner and shorter. This is linked to miscommunication between cell pathways in hair follicles. There's also a change in gene expression related to blood vessels and cell growth in balding hair follicles. The exact molecular causes of AGA are still unclear.

ATP-dependent chromatin-remodeling complexes are crucial for gene regulation, cell differentiation, and organ development in mammals.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

A gene variation is linked to hair thickness in Asians.

Skin and hair can regenerate after injury due to changes in gene activity, with potential links to how cancer spreads. Future research should focus on how new hair follicles form and the processes that trigger their creation.

sPLA2-X is crucial for normal hair growth and follicle health.

Changing light exposure can affect hair growth timing in goats, possibly due to a key gene, CSDC2.

Blocking the FGF5 gene in sheep leads to more fine wool and active hair follicles due to changes in certain cell signaling pathways.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

Alopecia areata involves persistent gene abnormalities and immune activity, even in regrown hair, suggesting a risk of relapse.

KAP9.2 and Hoxc13 genes are important for cashmere growth and vary in activity during different stages.

The near-naked hairless mutation causes hair loss but is not due to a mutation in the hairless gene itself.

Common gene patterns may cause skin autoimmune diseases.

Key genes can rewire networks, changing skin appendage types.

Injecting CHIR-99021 into goose embryos improves feather growth by changing gene activity and energy processes.

Scientists found 53 keratin genes in yaks that are important for hair growth and share similarities with those in other animals.

ELL is crucial for gene transcription related to skin cell growth.

The research found that the gene activity in mouse skin stem cells changes significantly as they age.

Hair loss in certain mice is linked to changes in keratin-related genes.

IRS-specific genes in Tan sheep hair follicles peak at birth and may affect wool crimp.

KRTAP6 genes affect wool quality in sheep.

PTEN was identified as a specific marker for the skin disease cutaneous lupus erythematosus, and it helps increase the expression of harmful type I interferons.

Scientists created a detailed map of gene activity in different parts of human hair follicles.

Atopic dermatitis shows a link between skin layers in inflammation, detectable with detailed gene analysis.

The peach gene pCTG134 helps control the interaction between auxin and ethylene hormones during fruit ripening.

Testosterone raises blood pressure by affecting kidney function and brain gene regulation over time.

R-spondin2 may help treat hair loss, gene differences could explain baldness, a peptide's regulation is linked to psoriasis, B-defensin gene copies may affect a skin condition's risk and severity, and potential markers and targets for alopecia areata were identified.

TRα and CRABPII genes change their activity levels during goat fetal skin development.

The study concluded that the arachidonic acid pathway and the protein KRT79 play a role in determining the fineness of cashmere.

Researchers made a detailed map of gene activity for different parts of human hair follicles to help create targeted hair disorder treatments.