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LPA3 signaling in the uterus is crucial for placental formation and fetal development.

TRPS1 is crucial for bone, kidney, and hair follicle development.

uPA helps hair follicle cells grow.

ERULUS is crucial for root hair growth by controlling calcium levels.

Certain genetic markers on the Y-chromosome may influence prostate cancer risk in Iraqi males.

Keratin 14 is uniquely found in a specific group of placental cells.

Researchers found genes for cysteine-rich proteins that form the protective layer of hair in humans and sheep.

Suppressing the HGPS mutation may improve symptoms and suggest reversibility.

GSK-36 downregulation with UTMD improves plaque stability in atherosclerosis treatment.

Mutations at Val-889 and Arg-752 disrupt key interactions in androgen receptor dimerization.

A PKP1 gene mutation causes skin fragility and hair loss in Chesapeake Bay retriever puppies.

IGF2BP3 and other m6A-related genes are linked to keloid formation and could be potential treatment targets.

PAD3 plays a key role in hair and skin protein structure and may be linked to skin diseases.

Increased methylation of the Filip1l gene may contribute to aggressive skin cancer.

Uncombable hair is inherited dominantly with complete penetrance.

A new mutation in the STS gene causes X-linked ichthyosis, even in rare female cases.

Lymphoid-specific helicase (Lsh) is crucial for skin growth, change, and healing after injury.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

Ber‐EP4 marks cells related to the secondary hair germ in hair follicles.

Targeting protein S-palmitoylation could lead to new skin disease treatments.

Keratin-associated proteins are part of the developing hair fiber cuticle.

A certain gene variation can affect protein production and is linked to male pattern baldness.

A new type of hereditary hair loss in a Chinese family is linked to chromosome 2p25.1–2p23.2.

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

An 8-year-old boy developed a rare condition after a liver transplant, which improved after changing his medication.