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A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.

The MTR gene affects wool quality and production in Chinese Merino sheep.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

Mdm2 is crucial for controlling p53 to maintain healthy cells and prevent tumors.

Injecting α-MSH made mice's hair turn black.

Both SMS1 and SMS2 are crucial for normal hair growth and cycle in mice.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

HtrA2 activity is crucial for normal hair growth by regulating fat cell development.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

The gene Msx2 is crucial for hair follicle regeneration during wound healing.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

Monilethrix is linked to a gene cluster on chromosome 12.

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

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

A mutation in the MAP2 gene causes reduced hair follicle density, leading to hairlessness.

MOF controls skin development by regulating genes for mitochondria and cilia.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Ets2 gene is crucial for placental development in mice.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

Monilethrix severity varies and may be influenced by other genetic or environmental factors.

Specific keratin gene mutations can cause monilethrix.

A specific gene mutation causes different hair defects in Indian monilethrix families.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

Estrogen and MLL enzymes work together to regulate genes important for hair growth and leukemia.

Hedgehog signaling controls hair follicle development and can affect skin cancer growth.

The Gsdma3 gene is essential for normal hair development in mice.