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The new hair loss treatment combining nitric oxide and minoxidil in a special carrier is effective for hair regrowth.

Different people show different symptoms for genetic diseases because of how sensitive their bodies are to small changes in important factors.

The circadian clock plays a key role in hair growth and its disruption can affect hair regeneration.

Testosterone replacement therapy helps manage deficiency and has various methods, but requires careful monitoring to avoid side effects.

The Notch signaling pathway is important for hair follicle development and could help create treatments for hair disorders.

Melatonin increased the activity of a hair growth gene in Cashmere goats.

CDP is crucial for lung and hair follicle cell development.

Loss of Rap1 protein speeds up heart aging in mice.

The protein p53 directly reduces the production of Keratin 17, a skin and hair protein, in rats with radiation dermatitis.

The HR protein's role as a repressor is essential for controlling hair growth.

BMI1 is essential for preventing hair greying and maintaining hair color.

The Ovol2-Zeb1 circuit is crucial for skin healing and hair growth by guiding cell movement and growth.

BLMP-1 is important for regular molting and gene expression cycles in worms.

Jumonji genes are important for development and their mutations can cause abnormalities, especially in the heart and brain.

PRC1 is essential for proper skin development and stem cell formation by controlling gene activity.

BMP signaling is important for skin color, affecting melanin production, pigment spread, and cell movement.

Blocking a specific immune cell signal can trigger hair growth.

The research found that a specific skin cell type not only triggers hair growth but also controls hair color, and that aging can lead to hair loss and color changes.

Researchers found that the Leptin receptor is a consistent marker for hair follicle dermal cells, which may help future hair research.

Fgf20 is important for the development and regulation of the cells that form the base of hair follicles.

Estrogens significantly influence hair growth by interacting with receptors in hair follicles and may help regulate the hair growth cycle.

Notch/CSL signaling controls hair follicle differentiation through Wnt5a and FoxN1.

Mice without the Sp6 gene have problems developing several body parts, including hair, teeth, limbs, and lungs.

A mutation in the Adam10 gene causes freckle-like spots on Hairless mice.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

Certain bacteria can enhance skin regeneration.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

Mice without the vitamin D receptor have bone issues and other health problems, suggesting vitamin D is important for preventing various diseases in humans.

The vitamin D receptor is crucial for bone health and affects various body systems, with mutations potentially leading to disease.