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The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

Keratin 17 is linked to various diseases, including cancer and skin conditions, and may be a target for diagnosis and treatment.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Poor maternal nutrition can lead to fewer wool follicles in Chinese Merino sheep.

Certain gene mutations are linked to wool quality in sheep and could help in breeding for better wool.

Hairless protein affects hair follicle structure by regulating the Dlx3 gene.

Combining skin tissue pathology with genetics has greatly improved the diagnosis and understanding of certain skin diseases.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.

Topical minoxidil may help treat a rare genetic hair condition with no fully effective treatments yet.

The document concludes that the human keratin gene cluster is complex, with a need for updated naming to reflect over 50 functional genes important for hair and skin biology.

The study found specific proteins that could mark different growth stages of cashmere goat hair and may help improve cashmere production.

Scientists have developed a method to keep chicken feather follicles alive and structurally intact in a lab for up to a week.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

Different proteins are linked to the varying thickness of sheep and goat hair types.

Hair loss in certain mice is linked to changes in keratin-related genes.

Tet2 and Tet3 enzymes are important for controlling hair growth and shape by affecting gene activity and DNA structure in hair follicles.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

DermaCult™ Keratinocyte Expansion Medium allows human skin cells to grow longer while keeping their ability to develop properly.

The man has a genetic skin condition called pachyonychia congenita.

Tet2 and Tet3 enzymes are essential for controlling hair growth by affecting DNA demethylation and gene expression in mice.

Scientists created a detailed map of gene activity in different parts of human hair follicles.

Scientists used stem cells to create a model of the skin disease Epidermolysis Bullosa simplex, which helped them understand its molecular mechanisms and could aid in finding treatments.

Li2CO3 improved skin disease in a mouse model of Focal Dermal Hypoplasia without toxicity.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

Blood cells turned into stem cells can become skin cells similar to normal ones, potentially helping in skin therapies.

New findings suggest potential treatments for melanoma, hyperpigmentation, hair defects, and multiple sclerosis, and show skin microbiome changes don't cause atopic dermatitis.

Abnormal gene expression related to keratin causes hair loss in certain mice.

Researchers found genes in sheep that may affect hair growth and wool quality.

Hairless mammals evolved quickly in both gene and non-gene areas related to skin and hair.