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New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

Melatonin affects gene expression in goat hair follicles, potentially increasing cashmere production.

The HPV type 11 region activates hair-specific gene expression in mice.

A specific gene mutation causes long hair in Angora rabbits.

A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

Certain genes related to sulfur metabolism are more active during the growth phase of Cashmere goat wool, and melatonin might help this process.

Variant G of the KRTAP20-1 gene improves wool curliness in Chinese Tan sheep.

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

The KRTAP36-2 gene in sheep affects wool yield.

Protein tyrosine kinases are key in male pattern baldness, affecting skin structure, hair growth, and immune responses.

The research shows that a gene called Wnt3 affects hair growth and structure, causing short hair and balding when overactive.

Planarian regeneration begins with a specific gene activation caused by injury, essential for healing and tissue regrowth.

miR-31 regulates hair growth by controlling gene expression in hair follicles.

Hair growth is controlled by specific gene clusters and proteins, and cysteine affects hair gene expression in sheep.

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

Narrowband UVB treatment increases certain gene expressions in psoriasis skin and improves symptoms.

TCDD speeds up skin barrier formation by increasing certain gene expressions.

A specific DNA region is crucial for Foxn1 gene expression in thymus cells but not in hair follicles.

Researchers used CRISPR/Cas9 to create a goat with a gene that increased cashmere production by 74.5% without affecting quality.

Hair loss in certain young mice is linked to a specific gene and can be caused by lack of iron.

Chronic stress in mice changes skin metabolism and gene expression, leading to hair loss.

SOX9 helps determine stem cell roles by interacting with DNA and proteins that control gene activity.

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

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

Activating the Sonic hedgehog gene in mice can start the hair growth phase.

Ruxolitinib effectively regrows hair in most patients with severe hair loss.

Transplant success has improved with better immunosuppressive drugs and donor matching.

Polycystic Ovary Syndrome likely starts in childhood and may be genetic and influenced by early hormone exposure.

A mother's PPARγ is crucial for preventing harmful milk that can cause inflammation and growth problems in babies.

Mutant mice help researchers understand hair growth and related genetic factors.