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Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

The study found that genetic differences related to hair growth and other traits help cashmere goats adapt to high-altitude environments.

A litter of cats had a hair condition similar to a mouse mutation, leading to hair loss and abnormal hair and skin.

Dermoscopy helped diagnose a rare hair disorder in a 2-year-old boy.

The girl has both monilethrix and Type 1 diabetes, but no link between the two conditions is known.

Meibomian glands are highly specialized and differ significantly from other sebaceous glands in structure and function.

Loss of Desmocollin 3 in mice causes skin blisters and hair loss.

Both Ayurvedic treatments improved hair fall, with Shirodhara being especially effective.

Basonuclin 1 (BNC1) helps skin cells multiply and move, which is crucial for wound healing.

Human hair proteins vary by individual, body site, and ethnicity, useful for forensics.

HOXC13 is essential for hair and nail development by regulating Foxn1.

The document concludes that Telogen Effluvium is a hair loss disorder that can be assessed with the modified wash test and may be treated with clobetasol foam, with patient management being important.

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

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

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

New treatments for ichthyosis, like protein replacement and gene therapy, show promise and may become standard care.

A new method was developed to extract and analyze proteins from very short human hairs.

New targeted immunotherapies are improving treatment for inflammatory skin diseases.

The study created hair-bearing skin models that lack a key protein for skin layer attachment, limiting their use for certain skin disease research.

Key genes crucial for sheep hair follicle development were identified, aiding fine wool breeding and human hair loss research.

Knocking out certain genes in mice helps understand skin and hair growth problems.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

Hair dye ingredient PPD causes cell death and aging in human hair cells by altering microRNA levels.

Different genes are active in dogs' hair growth and skin, similar to humans, which helps understand dog skin and hair diseases and can relate to human conditions.

Genomic research can help improve the quality and production of natural fibers in animals.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

Cell polarity signaling controls tissue mechanics and cell fate, with complex interactions and varying pathways across species.

A faulty KLHL24 gene leads to hair loss by damaging hair follicle stem cells.

Hair microscopy is a simple and cost-effective method to help diagnose systemic diseases in children.