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The KRTAP36-2 gene in sheep affects wool yield.

Vitiligo is a skin condition causing white spots, more common in women, often starts before age 20, and can affect mental health.

The LRRK2-G2019S mutation in Parkinson's disease has a lifetime penetrance of 25-35%, and finasteride may help reduce symptoms in adult male Tourette syndrome patients.

Alopecia areata has a complex genetic basis that was not fully understood as of 2001.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

CSLD1 suppresses rice root hair growth with NH4+ and regulates AMT1;2 expression.

Certain surgical methods are better than routine incision for hidradenitis suppurativa, topical clindamycin and acitretin are effective treatments, men with HS have a risk of skin cancer, HS patients are more likely to die from heart problems, and specific genetic markers are linked to treatment response.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

Certain mutations in the H6PD gene cause Cortisone Reductase Deficiency by affecting hormone production.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

Researchers found a genetic region that influences the number of coat layers in dogs.

Different types of long-lasting stem cells are responsible for the growth and upkeep of the mammary gland.

Melatonin affects many body functions beyond sleep by interacting with specific receptors in various tissues.

Platelet-rich plasma can potentially promote hair growth by stimulating cell growth and increasing certain proteins.

Exposure to too much androgen before birth might cause polycystic ovary syndrome later in life.

Eph receptors and ephrins may be promising targets for treating diseases, but more understanding is needed for effective and safe therapies.

Postpartum depression is linked to changes in brain chemicals, inflammation, stress, and certain genes, and can potentially be identified by markers like specific steroids, serotonin levels, and vitamin D levels.

Prolactin contributes to hair loss by promoting hair follicle shrinkage and cell death.

Lampreys have a functional vitamin D receptor that may help detoxify harmful substances.

Both genes and environmental factors like chemicals may contribute to the increase in hypospadias, but the exact causes are still unclear.

Certain genetic variations in the AR and ERβ genes can affect androgen levels in women.

New treatments for Alopecia Areata, like JAK inhibitors, show promise for hair regrowth and are likely to change future treatment approaches.

Msx2 and Foxn1 are both crucial for hair growth and health.

Bimatoprost, a glaucoma medication, may also help treat hair loss.

The document concludes that recognizing and properly diagnosing lipodystrophy syndromes is crucial for effective management and treatment.

Certain gene variants may contribute to high androgen levels in women with polycystic ovary syndrome.

Researchers created rat liver stem cells that could help repair liver failure in rats and may be useful for studying human liver diseases.