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Not having the gene PLAAT3 leads to fat loss, high insulin resistance, and abnormal fat levels in the blood due to a disruption in fat cell development and function.

Topical 4-aminopyridine 5% does not improve hair growth in male pattern baldness.

ECCL should be considered in patients with specific skin and eye lesions.

Higher FABP4 levels may indicate more severe alopecia areata.

Similar treatments might work for different types of scarring hair loss.

The gene LRRC15 is more active in balding areas of the scalp compared to non-balding areas.

Tunisian children with hereditary vitamin D-resistant rickets showed improvement with calcium treatment, and new genetic mutations were identified.

Mutations in hKAP1 genes may cause hereditary hair disorders.

An American Bully with a genetic skin condition improved significantly with specific topical treatments.

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Long-term Cape Aloe use causes harmless colon pigmentation that can help detect polyps.

S100A3 protein is crucial for hair shaft formation in mice.

ACBP is crucial for healthy skin in mice.

Variation in the TCHH gene affects wool curliness in sheep.

Acidic keratin genes are on CFA9 and basic keratin genes are on CFA27 in dogs.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

Some people have genetic mutations that make them resistant to vitamin D, leading to rickets even with enough vitamin D intake.

1′S-1′-Acetoxychavicol acetate may help treat hair loss by reducing oxidative stress.

A single amino acid change in the vitamin D receptor can disrupt its function and lead to hair loss.

Researchers found a new mutation causing total hair loss from birth.

All-trans retinoic acid helps amelanotic melanocytes in hair follicles develop and produce pigment while reducing their growth.

Scientists made a carbon-14 labeled version of a drug with a 48% yield and over 99% purity.

SOX11 and SOX4 help skin cells act like embryonic cells to heal wounds in mice.

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

Researchers found a white halo around hair in most patients with a specific type of hair loss, which helps in early diagnosis and treatment.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

A new genetic mutation was found causing hair and eye issues in a boy.

The protein AtRXR3 limits root hair growth in Arabidopsis, affecting phosphorus uptake.

Cholesterol issues in skin and hair may cause permanent hair loss by triggering inflammation.