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The document concludes that permanent hair loss conditions are complex, require early specific treatments, and "secondary permanent alopecias" might be a more accurate term than "secondary cicatricial alopecia."

The study provides insights into hair growth mechanisms in yaks.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

TRPV3 in skin cells causes inflammation and cell death.

sPLA2-X is crucial for normal hair growth and follicle health.

Desmoglein 4 is controlled by specific proteins that affect hair growth.

P-cadherin is crucial for hair follicle pigmentation but not skin pigmentation.

Activating TRPV3 reduces skin oil production and increases inflammation, potentially causing dry skin issues.

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

Two mutations in KRT74 and EDAR genes cause sheep to have finer wool.

Understanding how acne develops in different diseases could lead to new treatments.

Regulatory γδ T cells help protect hair follicles from alopecia areata and promote hair regrowth.

White-tailed deer can get a hair loss condition that might make them more vulnerable to environmental threats.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

Certain genes on chromosomes 6, 10, 16, and 18 may increase the risk of alopecia areata.

Certain mouse strains develop a skin condition similar to a human hair loss disease due to genetic defects.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Prostasin has two roles in skin: one for normal skin development without needing activation, and another for proper hair growth that requires activation.

A specific gene mutation causes congenital hair loss.

The study concluded that similar pathways regulate hair growth in dogs and mice, and these pathways are disrupted in dogs with Alopecia X, affecting stem cells and hormone metabolism.

Hairless protein reduces Msx2 gene activity, affecting hair follicle development.

Researchers found genes and genetic variants linked to sheep wool and skin wrinkles.

Matriptase is highly active in hair follicles and sebaceous glands, especially during hair growth phases.

A new therapy for a skin blistering condition has not been developed yet.

Eyelid cells share signaling components but differ in pathway activity.

Bone marrow stem cells and their medium help hair regrowth.

A 20-year-old woman with a rare form of Turner syndrome showed improvement with hormonal therapy and needs comprehensive care.

The study found that the hair loss condition in Cesky Fousek dogs is influenced by multiple genes affecting skin and muscle structure, fat metabolism, and immunity.

Long-term use of difluprednate eye drops in dogs can lead to hair loss and hormone imbalance.