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Beta-trace protein may help diagnose and predict treatment response in certain nerve disorders.

A new gene, mrp4, is found in mice and may play a unique role in hair follicle development in tails and ears.

The study concluded that specific proteins are necessary to maintain the structure that holds epithelial cells tightly together.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

TRPV4 channel affects skin health and could be a target for treating skin disorders.

Tsc2-deficient stem cells can help understand and treat TSC-related tumors.

TRPV3 could be a target for treating pain, skin disorders, and hair problems, but more research is needed to create effective drugs.

The study found genetic differences related to hair development that may explain hair loss in a patient with Trichorhinophalangeal syndrome type I.

TRPV3 is important for skin health and could be a target for treating skin diseases.

CTIP2 may help in skin development and maintenance.

Frizzled 3 and Frizzled 6 together control the orientation of mouse hair follicles.

ODC expression in mouse skin and tumors is varied and can be inhibited by retinoic acid or cycloheximide.

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

HDAC4 and HDAC7 are crucial for Th17 cell development and could be targeted to treat inflammatory diseases.

Mutations in the KRT16 gene can cause skin and nail disorders.

Different ligands change the shape of the TRPV3 ion channel in unique ways.

Removing both Atr and Trp53 genes in adult mice causes severe tissue damage and death due to DNA damage.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.

KRT72 gene helps form hair.

Esrp1 is important for skin health by helping form and maintain the skin barrier.

CRABP2 helps increase the growth of cells important for hair growth by activating a specific growth pathway.

Sox13 is a marker for early hair follicle development but not essential for skin and hair growth.

CGRP-IR axons may help maintain and renew tissues.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

Ptprq has multiple forms that change during inner ear development.

Activating TRPV4 in skin cells helps regrow hair in mice, possibly offering a treatment for hair loss.

K6 gene expression can be controlled and manipulated in mice for studying skin disorders.