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Higher miR-34a levels and the A variant of the MIR-34A gene are linked to increased risk and severity of alopecia areata.

Scalp melanoma is often diagnosed late in people with hair loss, leading to worse outcomes.

All adults have Demodex mites, which vary by region.

Key genes, including KRT39 and KRT74, influence hair length in Inner Mongolia cashmere goats.

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

Chromatin state changes in hair follicle stem cells can improve cashmere growth.

Large data can lead to new medical discoveries and personalized medicine.

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

WNT10A gene mutations cause short anagen hair syndrome.

Hair follicle development in cashmere goats involves dynamic changes in proteins and metabolites, with key roles for oxytocin, MAPK, and Ca2+ pathways.

Keratosis Follicularis Spinulosa Decalvans is a rare genetic disorder causing skin and hair issues, often inherited through the X chromosome.

A boy with a new NR5A1 gene mutation has a sex development disorder without affecting his adrenal glands.

New DNA analysis and machine learning are advancing forensic science, improving accuracy and expanding into non-human applications.

Myhre syndrome symptoms worsen over time, with specific genetic variants affecting severity.

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

A woman's hyperandrogenism was caused by a genetic mutation leading to non-classic adrenogenital syndrome.

Buschke-Ollendorff syndrome is a rare genetic disorder causing skin and bone changes, with some cases also showing ADHD or developmental delays.

Non-classic congenital adrenal hyperplasia (NCCAH) can mimic PCOS and requires genetic testing for proper diagnosis and treatment.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

A new syndrome, Teelwani Syndrome, combines features of two rare genetic disorders.

Researchers developed reliable models to predict how well certain compounds bind to androgen receptors, emphasizing the importance of atomic electronegativity.

Hair proteins are complex and provide valuable genetic and biological information.

Twelve key genes may improve cashmere production by influencing hair follicle cycles.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

FGF13 gene changes cause excessive hair growth in a rare condition.

Understanding intermediate filaments helps explain hair health and related diseases.

The research suggests that Tourette syndrome is linked to both brain signaling and immune system pathways.

A Korean baby with nevus sebaceus syndrome was found to have a KRAS gene mutation.

Loose anagen hair syndrome may be caused by keratin gene mutations.