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MCHR2 gene duplications may be linked to alopecia areata.

Two brothers from Bangladesh were diagnosed with X-linked adrenoleukodystrophy, showing neurological and adrenal symptoms.

The hr gene is linked to hair loss in Valle del Belice sheep.

A new gene mutation causes vitamin D resistance and hair loss in two unrelated girls.

A Pomeranian dog had rickets due to a new gene mutation, leading to severe symptoms and euthanasia.

Gene therapy helped rats with a specific type of rickets grow hair without severe inflammation.

Male cells need DHT to respond to testosterone, while female cells do not.

A mycobacterial protein shares a similar region with a human skin protein, possibly affecting skin diseases.

FCE 28260 is a stronger and longer-lasting inhibitor of 5α-reductase than finasteride, which may make it a better treatment for certain medical conditions.

The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

PAD3 plays a key role in hair and skin protein structure and may be linked to skin diseases.

Retinoic acid-binding proteins in skin are regulated by β-catenin and Notch signalling.

Certain SPINK5 gene mutations are common in Israeli families with Comèl-Netherton syndrome.

Finasteride increases CD8+ T cells in BPH tissues.

A gene called Gk5 controls lipid production in the skin and affects hair growth.

Androgen increases VEGF expression but not VEGFR-2 in rat corpus cavernous.

A gene variant causes a skin and hair disorder by disrupting protein balance.

5-alpha-reductase inhibitors help treat urinary symptoms from an enlarged prostate.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

A reliable model for screening type II 5α-reductase inhibitors was created and validated.

The vitamin D receptor is crucial for bone health and affects various body systems, with mutations potentially leading to disease.

Mutations in the ABCB6 gene cause Dyschromatosis Universalis Hereditaria.

The SbbHLH85 protein helps sweet sorghum grow more root hairs but makes the plant more sensitive to salt.

p2y5, now called LPA6, is a receptor important for human hair growth.

The study identified a key protein involved in producing underarm odor and found ways to inhibit it.

New liposome treatment successfully delivers CRISPR to deactivate a key enzyme in androgen-related disorders.