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Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

Endocannabinoids help control mast cell activity in human skin.

Overexpressing a specific enzyme in mice causes hair loss and female infertility.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

A WNT10A gene mutation leads to ectodermal dysplasia by disrupting cell growth and differentiation.

EDA2R gene linked to hair loss.

Activating Nrf2 in skin cells causes skin disease similar to chloracne in mice.

Mice without the vitamin D receptor gene lose hair due to disrupted hair follicle cycles.

TRPV3 in skin cells causes inflammation and cell death.

FGF5 gene mutations cause long hair in domestic cats.

Vitamin D receptor is crucial for bone health and mineral metabolism.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

Certain genetic markers, especially the MICA gene, are linked to alopecia areata.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

Mice without the Sp6 gene have problems developing several body parts, including hair, teeth, limbs, and lungs.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

Activating TRPV3 reduces skin oil production and increases inflammation, potentially causing dry skin issues.

Breast cancer treatments work better with AR activation, improving results and reducing side effects.

Hormones and sex affect potassium channel gene expression in electric fish, influencing their communication signals.

The gene Msx2 is crucial for hair follicle regeneration during wound healing.

Hairless protein affects hair follicle structure by regulating the Dlx3 gene.

Nanog gene boosts stem cells, helps hair growth, and may treat hair loss.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

A specific gene mutation causes Olmsted syndrome.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

Mice with a Gsdma3 gene mutation have thicker skin and longer hair follicle openings due to increased β-catenin levels.

The gene NM_026333 slows down aging by affecting the NCX1 pathway and could be targeted for anti-aging treatments.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

Allopregnanolone changes gene expression in glioblastoma cells.