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TBX5 gene influences feathered feet in Guangxi chickens by affecting cell growth and movement.

Genes related to keratin, skin cell differentiation, and immune functions are key in hedgehog skin and spine development.

SSAT is a key enzyme affecting cell growth and metabolism, with potential but risky use in disease treatment.

OXI1 kinase is essential for plant defense and root hair growth in Arabidopsis.

EDA2R is a key gene linked to ageing and diseases, and targeting it may help treat conditions like hair loss and chronic diseases.

SP1 promotes and KROX20 inhibits hair cell growth by affecting the CUX1 gene.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

The transcription factor Meis2 is essential for touch sensation and proper nerve development in touch receptors.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

CXCR2 in skin cells promotes tumor growth.

Mice without the Sept4/ARTS gene heal wounds better due to more stem cells that don't die easily.

A specific gene mutation causes complete hair loss without other health issues.

The KRTAP36-2 gene in sheep affects wool yield.

Syntaxin 9 helps in transporting and signaling of the EGF receptor in skin and stomach cells.

The fuzzy gene is crucial for controlling hair growth cycles.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

Sox2 controls hair color by affecting pigment production in hair follicles.

Certain genetic changes in the STX17 and KRT82 genes contribute to hair loss in alopecia areata.

CD2 might be a new treatment target for patchy alopecia areata.

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.

A new gene causes hairlessness and skin cysts in rats.

A new goat gene affects cashmere fiber thickness; certain variations can make the fibers coarser.

Axolotls regenerate their spinal cord through a signal that recruits cells, influenced by cell sensitivity and signal spread.

A mutation in the IKZF1 gene causes immune system overactivity, linked to autoimmune diseases like lupus.

Axolotl spinal cord regeneration may be controlled by a specific signal affecting cell sensitivity and diffusion.

The EDA pathway plays a key role in bone development by interacting with other signaling pathways.

The new model helps understand and develop treatments for genetic skin disorders like AEC.

Krox20 (Egr2) is important for the function of epithelial stem cells.

Arab APS1 patients have unique and recurrent AIRE gene mutations.