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sPLA2-IIA increases growth in hair follicle stem cells and cancer cells, suggesting it could be targeted for hair growth and cancer treatment.

PADI4 enzyme slows down cell growth in developing hair follicles.

An 8-year-old girl developed a rare skin condition in a linear pattern on one side of her body after a lung infection, which improved with treatment.

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.

New genetic mutations causing hair loss were found in a Chinese family.

An infant with Hutchinson-Gilford Progeria Syndrome had successful surgery to fix breathing issues caused by a new genetic mutation.

Lysophosphatidic acid affects sensory neurons and may cause neuropathic pain and itch.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

New LSS gene variants help understand congenital hypotrichosis 14 better.

lncRNA2919 slows down rabbit hair growth by stopping cell growth and causing cell death.

The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.

The research suggests that SFRP2 and PTGDS proteins might be indicators of female pattern hair loss and could contribute to hair loss.

Removing PLCg1 from skin cells caused thicker oil glands and less hair in mice.

The document suggests a rare skin condition might be caused by a genetic phenomenon.

Prolactin may play a significant role in skin and hair health and could be a target for treating skin and hair disorders.

CTIP2 may help in skin development and maintenance.

A new genetic mutation linked to Hutchinson-Gilford progeria syndrome was found in China.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Several genes, including Hox-7A, Stra6, and Lim-1, are involved in normal palate formation.

Mice lacking the PPARγ gene in their fat cells had almost no fat tissue, severe metabolic problems, and abnormal development of other fat-related tissues.

PRP treatment improved skin pigmentation and appearance in facial lichen planus pigmentosus.

The LTF gene may help predict and manage nonspecific orbital inflammation.

Polycomb Repressive Complex 1 is crucial for keeping stem cells stable and maintaining healthy adult tissues.

CD18-deficient mice developed psoriasis-like skin disease, useful for studying inflammatory skin disorders.

Certain genetic variants may increase the risk of developing PCOS.

Over-expression of Sp2 can lead to cancer by preventing proper stem cell differentiation.

Higher levels of the DP2 receptor may lead to hair loss.

Mice with too much sPLA₂-IIA have hair loss and poor wound healing due to abnormal hair growth and stem cell depletion.