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The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

Keratins K4 and K13 form stable dimers in mature esophageal cells, aiding cell stability.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

New compounds may help treat heart disease by activating specific potassium channels.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Interleukin-1 increases keratin K6 production in skin cells.

Lgr6+ cells are important for tissue repair and could be a target for treating cancer and other diseases.

Radiation damages hair stem cells and changes keratin expression, with Krt5 as a potential marker for radiation effects.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

Kdm6b is crucial for skin cell differentiation.

Normal skin cell renewal doesn't need RAR signaling, but vitamin A-related skin thickening does.

A chromosomal change may cause ectodermal dysplasia and developmental issues in a child.

A new sheep gene, KRTAP36-1, may help breed sheep with better wool by reducing prickle factor.

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

CPK1 helps root hair growth in Arabidopsis by activating channels for calcium signaling.

Zfp157 is active in many mouse tissues during development and in specific adult cells.

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

The KDM1 gene helps Venus flytraps close by managing potassium ions.

K6/ODC transgenic mice are effective for quickly identifying cancer-causing chemicals.

Keratin 17 is crucial for normal hair growth by regulating hair cycle transitions with TNFα.

Type II keratins are uniquely phosphorylated during stress and mitosis, affecting their structure and function.

The Itpr3 gene causes a specific hair pattern in mice.

PKC ε increases hair follicle stem cell turnover and may raise skin cancer risk.

Two specific hair keratin genes are active during hair growth and decline as hair transitions to rest.