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The specific skin disease variant p.(Arg2000Trp) in plectin can cause a wide range of symptoms, which should be considered when diagnosing patients.

High glycine–tyrosine keratin-associated proteins help make hair strong and maintain its shape.

The N-K GM Series offers highly selective, eco-friendly medicines targeting harmful microbes, free for personal use.

Igf1r helps regulate hair growth cycles.

Genosomes are promising for safe and effective gene delivery in therapy.

AGD1's PH domain is essential for its role in root hair growth and polarity.

Lichen planus may be associated with a higher risk of metabolic syndrome.

BBS7 is essential for healthy gums by supporting cell movement and blood flow.

A new gene mutation is linked to monilethrix in the studied family.

Transgenic sheep cells with spider silk gene were successfully created for future sheep hair expression.

Dietary L-serine supplementation can reduce symptoms of HSAN1 by lowering harmful 1-deoxySL levels.

GPC1 is important for blood vessel growth in hair follicles and could help treat hair loss.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

CD61 is important for mouse tooth cell growth and works through Lgr5.

A new mutation, Glu402Lys, in hair keratin is linked to variable symptoms of monilethrix.

BBS7 is essential for healthy gums by supporting cell function and blood flow.

Mice with LSS deficiency showed hair loss and cataracts, similar to humans, and can help in understanding and treating this condition.

Gap junctions help control feather pattern formation by enabling cell communication.

Emulgels are effective for delivering skin medications and cosmetics due to their easy application and controlled release.

Loliolide can boost hair growth by activating specific cell pathways.

Meis2 is essential for touch sensation and nerve function in mice.

The research explains how a human enzyme binds and processes its substrate, which could relate to its role in biological functions and hair loss.

Ixekizumab may be an effective first treatment for a rare skin condition causing hair loss.

FGF9 controls which receptors it binds to through a process where two FGF9 molecules join, and changes in FGF9 can lead to incorrect receptor activation.

Deleting the MAD2L1 gene in mice led to rapid tumor growth despite chromosomal instability.

LPA3 signaling in the uterus is crucial for placental formation and fetal development.

Long non-coding RNAs play a key role in yak hair growth cycles.

CD18-deficient mice developed psoriasis-like skin disease, useful for studying inflammatory skin disorders.

A specific mutation in PA-PLA1α causes abnormal hair growth.

Entospletinib effectively prevents eye and skin GVHD in mice.