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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.

A new method, iSiMPRe, effectively identifies key protein regions in cancer genes, highlighting potential drug targets.

MC-1R is present in skin cells and may help reduce inflammation.

Defective protein folding due to a mutation is key in ANE syndrome.

Two microRNAs affect hair follicle development in sheep by targeting specific genes.

A 3-year-old girl with skin mast cell buildup and congenital baldness improved with treatment, suggesting a rare link between these conditions.

Copper therapy improved health and enzyme activity in mice with copper deficiency.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

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

Different conditions affect how hair proteins assemble, and certain mutations can change their structure.

Super-enhancers control CD25 expression in specific cell types, affecting immune function.

Suppressing ODC activity reduces tumor growth in hair follicles.

Researchers found a gene mutation responsible for a rare hair loss condition.

A point mutation in the androgen receptor gene causes complete androgen insensitivity.

A painless cheek lump was misdiagnosed but found to be a rare, benign skin lesion called pilomatrixoma, treatable by surgery.

A JAK1 variant causes hair loss, skin issues, and thyroid disease, but treatment with a specific inhibitor can help.

Researchers found WNT10A to be a key gene in developing goat hair follicles.

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

A specific DNA sequence caused hair loss in male mice by activating immune cells and increasing a certain immune signal.

A rare case of trichothiodystrophy was found with autism, seizures, and mental retardation.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

Mouse touch-sensitive nerve cells adjust their connections based on competition with other similar cells.

Taohong Siwu Decoction may help treat hair loss by targeting multiple genes and pathways.

Exosomal miR-222-3p reduces melanin production in rabbits by targeting the SOX10 gene.

A specific gene mutation causes different hair defects in Indian monilethrix families.

Researchers found 15 new genetic links to skin traits in Japanese women.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

CaM7 and CNGC14 interaction controls root hair growth in Arabidopsis.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.