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An 8-year-old girl developed a rare skin condition in a linear pattern on one side of her body after a lung infection, which improved with treatment.

Hairless mice have longer hair follicles and abnormal structures during the catagen phase.

A new mouse gene, Keratin 17n, is mainly found in nail tissue and may explain why mice without Keratin 17 don't have nail issues.

MicroRNA-148a is crucial for maintaining healthy skin and hair growth by affecting stem cell functions.

MPZL3 is important for controlling the hair growth cycle in mice and humans.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

The gene for Clouston syndrome in a large Indian family is located in the 13q11-q12.1 region.

Acidic keratin genes are on CFA9 and basic keratin genes are on CFA27 in dogs.

Basonuclin may help control ribosomal RNA gene activity in skin cells.

The new sensor can detect a toxic chemical in water with high sensitivity and accuracy.

A new mutation in mice causes crooked whiskers and messy hair.

The method effectively images and correlates elements and metabolites in tissue samples at a micron scale.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

LA-ICP-MS can effectively track mercury exposure over time in hair.

Proper niche formation in Drosophila requires Slit-Robo signaling for cell migration.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

There's a growing resistance to the antibiotic mupirocin in children's skin infections caused by MRSA in New York.

Dynamic, light touch is sensed through a common mechanism involving Piezo2 channels in sensory axons.

A defective gene causes hair loss and taste insensitivity in BTBR mice.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Malassezia restricta may be linked to intestinal diseases like Crohn's and ulcerative colitis.

miR-144 affects hair growth by interacting with Lhx2.

Folliculotropic mycosis fungoides has unique molecular features and cell interactions that could guide targeted therapy.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

MPA increases cancer spread by boosting Eph A2 activity.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

The hairy ear mutation in mice is linked to changes in gene expression affecting hair growth.

Sebaceous glands help study fatty acid transporters and binding proteins.

Pachyonychia congenita is linked to a keratin gene on chromosome 17.

The L412F variant of TLR3 is linked to skin infections, more viral infections, and autoimmune issues.