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A new mouse gene, Keratin 17n, is mainly found in nail tissue and may explain why mice without Keratin 17 don't have nail issues.

A new mutation linked to partial Androgen Insensitivity Syndrome and prostate cancer was found in a patient unhappy with their female gender assignment.

Researchers found two genes that may explain why some Casertana pigs don't have hair.

FoxN1 overexpression in young mice harms immune cell and skin development.

Gender-affirming hormone therapy affects metabolism differently based on treatment type.

A special gene region controls the re-emergence of a primitive wool type in Merino sheep, improving their wool yield and adaptability.

The hr gene is crucial for skin and hair health, with mutations causing hair disorders.

The mTurq2-Col4a1 mouse model shows how the basement membrane develops in live mammals.

A point mutation in the androgen receptor gene causes complete androgen insensitivity.

Hereditary hyperplastic gingivitis in silver foxes may be linked to errors in the MAPK signaling pathway, influenced by androgens.

RXRα is crucial for hair growth and skin cell function.

Testosterone causes hair loss in AGA mice, which are good for testing baldness treatments, and both minoxidil and cyproterone acetate can prevent this hair loss.

A gene mutation causes monilethrix in a Chinese family.

Researchers developed a mouse model that tracks hair growth using bioluminescence, improving accuracy in studying hair cycles.

The same gene mutation can cause different symptoms in family members.

Activated erbB-2 in mice skin causes severe skin and hair abnormalities.

The Foxn1 gene is essential for normal nail and hair development.

The study concludes that a genetic mutation in TFM mice leads to reduced androgen receptor activity, affecting the body's response to male hormones.

HtrA2 activity is crucial for normal hair growth by regulating fat cell development.

Polyamines are crucial for skin tumor development, and inhibiting them can prevent tumors.

AIRE deficiency causes hair loss similar to alopecia areata in mice.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

Hairless mice lack fur due to a genetic mutation affecting skin response, not hormone issues.

Researchers created a mouse model for Cushing's syndrome to study glucocorticoid excess and potential treatments.

Melanocyte-associated antigens may play a key role in alopecia areata and could be targets for new treatments.

The hairless mutant gene causes early hair loss and affects skin and thymus development in mice.

Mutant MK6a transgenes in mice cause blistering, hair loss, and potential human alopecia.

Removing the ATR gene in adult mice causes rapid aging and stem cell loss.

Mice with alopecia areata had wider lymphatic vessels in their skin.