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The study found that giant pandas have more melanin in black hair follicles than white, with gene expression differences that could affect hair color and skin health.

A gene network led by RSL4 is crucial for early root hair growth in response to cold in Arabidopsis thaliana.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

Gender affects hair and scalp characteristics, with differences in hormone responses, graying patterns, and trace metals.

The conclusion is that the nuclear lamina and LINC complex in skin cells respond to mechanical signals, affecting gene expression and cell differentiation, which is important for skin health and can impact skin diseases.

Understanding skin patterns can help us learn about skin diseases and their treatments.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

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

The tumor suppressor gene FLCN affects mitochondrial function and energy use in cells.

E211 G>A gene linked to lower risk of severe prostate cancer and hair loss.

A gene in Arabidopsis thaliana, AtPRPL1, affects root hair length but not cell wall composition.

Testing for CAG repeat polymorphism in the androgen receptor gene is not currently recommended for managing hypogonadism.

Proper control of β-catenin activity is crucial for development and preventing diseases like cancer.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

Different processes create patterns in skin and things like hair and feathers.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

The length of CAG repeats in the androgen receptor gene is linked to ovarian reserve but does not affect how the ovaries respond to stimulation.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

The gene Tfap2b is essential for creating a type of stem cell in zebrafish that can become different pigment cells.

Removing a specific gene in certain skin cells causes hair loss on the body by disrupting normal hair development.

The HoxC gene cluster and its enhancers are essential for developing hair and nails in mammals.

The gene Prss53 affects hair shape and bone development in rabbits.

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.

The article concludes that better understanding gene regulation related to seasonal changes can offer insights into the mechanisms of seasonal timing in mammals.

Feather growth and regeneration involve complex patterns, stem cells, and evolutionary insights.

Colchicine can inhibit hair growth by affecting cell activity and protein expression in hair follicles.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

Disrupting the FGF5 gene in rabbits leads to longer hair by extending the hair growth phase.

The research found that a complex gene network, controlled by microRNAs, is important for hair growth in cashmere goats.