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The SLICK1 allele in Holstein heifers affects hair and immune traits without altering prolactin signaling.

New mouse models of Pemphigus show severe symptoms and need better treatments.

The study created a mouse model that survives longer and shows fewer symptoms of pemphigus vulgaris.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

The Dfl mutation in mice causes poor sebaceous gland function and complete hair loss.

CaBP1 and 2 are important for maintaining the activity of calcium channels necessary for hearing in inner ear cells.

Mutations in the hairless gene cause a rare form of permanent hair loss.

BBS7 is essential for healthy gums by supporting cell function and blood flow.

Methylation in specific gene region causes finasteride resistance in some BPH patients.

AGC2-1 protein is essential for root hair growth in Arabidopsis.

Truncated LTBP-1 disrupts TGF-beta signaling, affecting hair growth.

CEP135 may predict cancer outcomes, and targeting PLK1 could help treat certain sarcomas.

CLE40 and CRN/CLV2 pathways have opposite effects on root growth in Arabidopsis.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

Increasing Smurf2 hinders hair follicle stem cell differentiation and wound healing.

Reactive lipids from aging cells change the extracellular matrix, affecting cell function and inflammation.

Lablab purpureus peptides may effectively kill cancer cells with fewer side effects.

Platelet-rich plasma can improve erectile function in older individuals by reducing prostate enlargement.

Autophagy helps delay aging in mouse glands, maintains fat balance, and controls scent production.

A mutation in mice causes hair loss and skin issues due to a defect in a gene affecting cell adhesion.

Activating PKCα in skin causes cell death and inflammation through different pathways.

Removing Ctip2 in skin cells causes skin inflammation similar to atopic dermatitis.

KRTAP2-3 could help predict cancer recurrence by identifying specific cancer cells.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

Mirex seems to promote a unique group of skin cells different from those affected by another tumor promoter, TPA.

RPGRIP1L helps skin cells stick together by blocking PKCβII, which can prevent skin blistering like in pemphigus.

A gene mutation in Lama3 is linked to a common type of hair loss.

CDP is crucial for lung and hair follicle cell development.

Mutations in the SNRPE gene cause hereditary hair loss.

Certain drugs change freshwater snail shells to a "banana" shape.