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The KRTAP11-1 gene promoter is crucial for specific expression in sheep wool cortex.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

New genes linked to ichthyosis were found, but there's still no cure; treatment options are improving.

Longer GGN repeats in the androgen receptor gene are linked to polycystic ovary syndrome.

A new gene mutation causes hereditary coproporphyria with reduced enzyme activity.

Mouse models help understand alopecia areata and find treatments.

The document concludes that periocular hair disorders have various causes and treatments, and proper evaluation by specialists is important for management and prognosis.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

No significant link between CAG repeat numbers and female pattern hair loss in Han Chinese population.

Androgenetic alopecia, or hair loss, is most common in people in their 30s, can start early, is often inherited, and may be influenced by factors like hormones and scalp health.

Tailored treatments combining medication and hair removal methods are effective for managing excessive hair growth in women.

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

Familial frontal fibrosing alopecia is rare, mostly affects women, and often occurs between sisters or mother-daughter pairs.

Susan Lee Lindquist was a pioneering biologist who made significant contributions to understanding protein folding and its role in disease.

A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

The study found that giant pandas have more melanin in black hair follicles than white, with gene expression differences that could affect hair color and skin health.

The analysis found genes linked to skin and hair development are more active in Pashmina goats, which may explain their long-fiber production.

Certain genes related to sulfur metabolism are more active during the growth phase of Cashmere goat wool, and melatonin might help this process.

Organoid technology is advancing and entering commercial use, with applications in disease modeling, drug development, and personalized medicine.

Hair India 2012 was a successful international event focused on combating fake trichology practices and discussing various hair health topics.

Lipase H is important for hair follicle function and shaping hair fibers.

Key proteins and pathways regulate wool fiber diameter in Alpine Merino sheep.

Hypertrichosis lanuginosa causes excessive fine hair growth, often linked to genetics or cancer, with limited treatment options.

Deleting the MAD2L1 gene in mice led to rapid tumor growth despite chromosomal instability.

The document discusses various nail and hair disorders and their treatments.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

Blocking JAK-STAT5 signaling in mice leads to hair growth.

Certain genes and X chromosome patterns may significantly contribute to the development of hair loss.

Polycystic Ovary Syndrome (PCOS) is a common condition in women that can cause metabolic, reproductive, and psychological issues, and requires lifestyle changes and medication for management.

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