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A genetic mutation in the hHa1 gene creates a smaller, but still functional, hair protein without causing hair problems.

The KRTAP7-1 gene is very similar across different cattle and yak breeds and likely plays a role in hair strength and shape.

Mutations in the ABCB6 gene cause Dyschromatosis Universalis Hereditaria.

Dermatologists should consider congenital syndromes like TRPS in young adults with early hair loss.

The Celsr1 gene is crucial for normal hair patterning in mice.

Scientists discovered a unique hair protein, KAP24.1, with a special structure, found only in the upper part of hair cuticles.

CDH3-related disease causes worsening eye and hair issues.

RpoS helps Borrelia burgdorferi survive in hosts and adapt to different environments.

Certain genetic changes in the KRT82 gene may cause patchy skin in New Zealand rabbits.

The reconstructed skin model from hair follicles functions like human skin in processing chemicals and can be used to test ingredient safety.

Gorab deficiency speeds up skin aging by disrupting protein regulation and reducing collagen.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

Early diagnosis and treatment of NCCAH can improve symptoms and fertility.

Seven genes are highly expressed in both germ-line and hematopoietic stem cells.

Gene variation affects prostate issues and hair loss.

Sheep have 17 keratin genes, similar to humans, but with different expression patterns affecting wool and hair.

The KAP13-3 gene in sheep affects wool quality by influencing keratin assembly.

Fibroblasts from healthy donors can prevent changes seen in recessive epidermolysis bullosa simplex.

The peach gene pCTG134 helps control the interaction between auxin and ethylene hormones during fruit ripening.

Congenital atrichia with papular lesions is often misdiagnosed, and new diagnostic criteria can improve accuracy.

The rs231775 genetic variant is linked to a higher risk and severity of Alopecia Areata in males.

A new rat strain with a specific gene mutation causes hair loss and kidney issues.

Researchers found a gene mutation responsible for a rare hair loss condition.

TMPRSS6 is crucial for controlling hepcidin and normal iron absorption.

RD26 controls root hair growth during drought by repressing key genes, helping plants save energy.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

The hair defect is due to abnormal inner root sheath keratinization.

The MTHFR C677T mutation may increase the risk of alopecia areata in the Turkish population.

Polycomb Repressive Complex 2 is not needed for hair regeneration.

Clouston syndrome is inherited in an autosomal dominant pattern and caused by a specific gene mutation, with no current treatment available.