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Fewer GGC sequences in the androgen receptor gene improve finasteride treatment for hair loss.

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

Early onset hair loss linked to genetics and androgen levels.

Disrupting the FGF5 gene in rabbits leads to longer hair by extending the hair growth phase.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Melatonin affects gene expression in goat hair follicles, potentially increasing cashmere production.

Male pattern hair loss may have evolved to promote younger fathers for offspring health and survival, encouraging monogamy and paternal nurturing.

Hair loss patients have different microbes in hair follicles, possibly affecting hair loss.

Antiandrogen therapy helps treat genetic hair loss.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Researchers created human hair follicles using a new method that could help treat hair loss.

The document concludes that more research is needed to understand excessive hair growth in women with normal hormone levels and regular ovulation.

The document discussed hair loss causes and treatments but didn't give a final summary.

Sonic hedgehog proteins may help grow hair.

The PTGER2 gene is highly active in Cashmere goat skin and its activity changes with the hair growth cycle.

Alopecia areata is likely caused by a combination of genetic factors and immune system dysfunction, and may represent different diseases with various causes.

Fluconazole can cause hair loss, but the exact cause is unknown.

Melatonin treatment increases a specific RNA in goat cells that boosts cashmere growth.

UK medical students lack dermatology education, liver biopsy patients with risk factors show more fibrosis, and certain fungi resist drugs due to melanin; genetics may influence female hair loss.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

Mice without active or present vitamin D receptors maintain normal blood sugar control and islet gene expression when calcium levels are normal.

The workshop highlighted the genetic links and psychological impacts of hair loss and skin disorders.

The conclusion is that adult males with muscle weakness and hormonal imbalances should be tested for Kennedy's disease.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

Male hormones cause different growth in identical human hair follicles due to their unique epigenetic characteristics.

Thiopurines help treat IBD but require genetic testing to avoid side effects.

The NUDT15 gene variant causes severe side effects from azathioprine in some Indian patients.

Ingenol mebutate gel changes gene expression related to skin development and immune response in actinic keratosis.

Hair growth is controlled by specific gene clusters and proteins, and cysteine affects hair gene expression in sheep.