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Keloid skin disorder involves abnormal fibroblast activation and immune response, linked to a group of genes including FGF11.

Changes in certain RNA and protein levels may contribute to alopecia areata and could be treatment targets.

Alternating treatment with two drugs could help cells in a rapid aging disease.

Seven genes are highly expressed in both germ-line and hematopoietic stem cells.

FGF5s can block the effects of FGF5, which may help control hair growth in cashmere goats.

Gene expression in wool follicles changes with growth cycles, offering insights into wool and human hair growth.

lncRNAs play a key role in hair follicle development, affecting cashmere quality and yield.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

H19 may help cause PCOS by affecting CTGF levels, suggesting a new treatment target.

The research developed new fortilin protein constructs for potential heart disease treatments.

Resident memory T cells and necroptosis may drive fibrosis in eosinophilic fasciitis and morphea.

AGA progression involves increased lipid synthesis, electron transport, and hair follicle miniaturization.

Different types of fibroblasts exist in skin and understanding them can help improve wound healing and treat scars.

Researchers found a non-functional sheep keratin gene due to mutations.

Removing a specific gene in certain skin cells causes hair loss in mice by disrupting hair follicle development.

A genetic change in the FGF5 gene affects hair growth in cashmere goats.

Baricitinib and its combination with lonafarnib improve fat cell formation in certain genetic disorders.

Non-coding RNAs help control hair growth in cashmere goats.

The malignant pilomatricoma showed strong epithelial keratin expression, suggesting it may not calcify.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

OCT4B1 and SOX-2 levels are higher in Crohn's and ulcerative colitis patients, possibly aiding tissue repair.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

The early genes of a specific virus can cause abnormal skin cell growth and hair follicle changes.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

A specific hair protein variant increases the spread of breast cancer and is linked to worse survival rates.

A specific gene region can control targeted and responsive gene expression in mice, useful for skin disorder treatments.

Combining certain treatments, including FOL005, may improve healing of difficult wounds.

lncRNA MTC affects protein levels in goat skin cells, impacting hair growth.

The RNA AL136131.3 slows down hair growth and speeds up hair loss by affecting sugar breakdown in hair follicles.

rPanglaoDB helps study rare cell types by merging RNA data, confirming fibrocytes' role in healing.