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Scientists found a new type of skin cell that could help with skin repair and these cells work better with a certain protein.

Different hair types in mammals are linked to variations in specific protein genes, with changes influenced by their living environments.

The study found a specific peptide that helps detect TGase 3 activity in skin and hair follicles.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

Not having the gene PLAAT3 leads to fat loss, high insulin resistance, and abnormal fat levels in the blood due to a disruption in fat cell development and function.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

PGD2 increases androgen receptor activity in hair cells, which could be targeted to treat hair loss.

Ruxolitinib may effectively treat APS-1 by reducing harmful immune responses.

The androgen receptor gene doesn't help identify women likely to have female pattern hair loss.

The research found genes that may protect certain scalp cells from hair loss.

CGRP may help protect hair follicles from immune system attacks, potentially slowing hair loss.

ASLNC168501 may help restore hair growth in androgenetic alopecia by improving hair follicle stem cell function.

The hexosamine pathway helps protect skin cells from stress and may improve skin and hair health.

Newly designed proteins can effectively degrade specific proteins in cells, offering a promising alternative for targeted protein degradation.

A protein called PLC2 is important for the growth and development of plant roots influenced by auxin.

Potential compounds may inhibit hair loss by targeting a non-androgen pathway.

A specific genetic mutation may increase male pattern baldness risk, especially in Europeans.

Seven new genetic risk areas for prostate cancer were found.

Finasteride helps female-pattern hair loss.

Certain interactions help prepare the androgen receptor for pairing and activation, which is important for its role in development and disease.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

Disrupting Acvr1b in mice causes severe hair loss and thicker skin.

The laser system helps study brain cell functions by precisely removing specific cells and observing changes.

Newly designed proteins can effectively degrade specific proteins in cells, offering a potential new therapy method.

The arrector pili muscle attaches to the extracellular matrix using α5β1 integrin and connects muscle cells using α1β1 integrin.