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ALRN-6924 may prevent hair loss caused by chemotherapy.

A mutation in the KRT25 gene causes woolly hair and hair loss.

Different keratins have unique expression patterns in mouse skin cells.

Skin cells and certain hair follicle areas produce hemoglobin, which may help protect against oxidative stress like UV damage.

CLE14 peptide promotes root hair growth in Arabidopsis.

Isoproterenol helps hair follicle stem cells turn into beating heart muscle cells.

AL136131.3 slows hair growth by affecting energy processes in hair loss.

Hair stem cells produce a protein called COL17A1 that plays a key role in their development and is linked to hair thinning and baldness.

Activated ras can protect kidney cells from a certain substance that causes cell death.

Two genes, ERBB4 and ROR1, may cause the unique pigmentation in Lanping black-boned sheep.

Altering the keratin 17 gene in mice hair follicles caused temporary hair issues, but changes were minimal and short-lived.

A single amino acid change in the vitamin D receptor can disrupt its function and lead to hair loss.

Skin organoids with NCSTN mutation show changes in hair follicle development and higher inflammation, key features of Hidradenitis Suppurativa.

The protein FLCN is involved in cellular cleanup and is regulated by ULK1.

Defects in certain proteins cause major heart abnormalities during early development.

A mutation in the FAM83G gene is linked to skin and hair abnormalities in two related individuals.

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

Dermatologists should consider congenital syndromes like TRPS in young adults with early hair loss.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

Rat hair follicle stem cells can be successfully cultured and may be useful for creating tissue-engineered hair, vessels, and skin.

BBS7 is crucial for maintaining periodontal health by supporting Shh signaling.

Removing alkaline phosphatase from human skin cells hinders the creation of new hair follicles.

Higher RBP4 levels are linked to severe alopecia areata, but genetic variant rs3758539 doesn't affect baricitinib response.

Overexpression of sPLA2-IIA in mouse skin reduces hair stem cells and increases cell differentiation through JNK/c-Jun pathway activation.

SP1 promotes and KROX20 inhibits hair cell growth by affecting the CUX1 gene.

PADI4 enzyme slows down cell growth in developing hair follicles.

New mutations in KRT83 and KRT86 are linked to the hair disorder monilethrix.