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Certain gene variations are linked to severe acne in Egyptian patients and could guide treatment choices.

Certain genetic markers on chromosome 20 are linked to hair loss in the Han Chinese from Yunnan.

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

The gene for Clouston syndrome in a large Indian family is located in the 13q11-q12.1 region.

Genetically variant peptides are reliable for forensic identification despite age-related changes in hair proteins.

The mouse hairy ears mutation causes longer ear hair due to changes in gene expression.

The CORIN gene variant causes the golden color in Siberian cats.

CTLA4 gene variants are not linked to alopecia areata in Monterrey's Mexican population.

Small amounts of DNA can be found in the hair shaft, especially near the root, but it decreases with hair treatments and washing.

Treating non-classic congenital adrenal hyperplasia is complex because the benefits of hormone treatment must be weighed against potential health risks.

Certain gene variants are linked to a higher risk of polycystic ovary syndrome, hair loss, and obesity in women from western Saudi Arabia.

Men with high genetic risk for Polycystic Ovary Syndrome (PCOS) have increased chances of obesity, type 2 diabetes, heart disease, and hair loss, showing PCOS risk factors can affect both genders.

Certain DNA regions in alpacas are linked to fiber diameter.

Hair growth serums A and C can affect hair growth genes and pathways, suggesting potential for personalized hair loss treatments.

Monitor for early signs of azathioprine toxicity and check blood counts regularly.

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.

Rare genetic variants in five specific genes are linked to male-pattern hair loss but only account for a small part of the risk.

Certain gene variations and different levels of BDNF and CRH hormones are linked to vitiligo.

Certain KIR genes in Indian SLE patients are linked to disease severity and could be biomarkers.

Genetic factors play a major role in acne.

Certain genetic variations are linked to hair loss in Mexican men.

Alopecia areata involves both innate and adaptive immunity, with specific genes linked to the disease.

Cornification is how skin cells die to form the protective outer layer of skin, hair, and nails.

Dandruff and seborrheic dermatitis are caused by yeast feeding on scalp oils, leading to irritation and flaking.

Different small areas within hair follicles send specific signals that control what type of cells stem cells become.

Dabrafenib was effective and well tolerated in treating thyroid cancer with a specific mutation.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

Mice without the vitamin D receptor are more prone to UV-induced skin tumors.

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

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.