Search

everythinglearnresearchcommunity

for

Search:↓

The nude gene causes skin cell overgrowth and improper development, leading to hair and urinary issues.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

Men's sensitivity to male hormones might affect how severe COVID-19 gets for them.

Kennedy's disease leads to muscle weakness without a cure, but exercise and managing symptoms may help patients live a normal lifespan.

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

Foxi3 expression in developing teeth and hair is controlled by the ectodysplasin pathway.

Hirsute women have lower type 2 17β-HSD enzyme levels, which improve with treatment.

Men with hair loss have more DNA changes in back-of-head hair follicles, possibly protecting them from thinning.

The R343H mutation in the VDR gene causes vitamin D-resistant rickets with alopecia by impairing specific gene activity.

Differences in gene expression and methylation patterns found in AGA patients suggest potential targets for future treatments.

Testosterone and dihydrotestosterone treatments can help with penile growth in males with 5α-reductase type 2 deficiency, with dihydrotestosterone being more effective in infancy.

Hair follicle stem cells use specific chromatin changes to control their growth and differentiation.

Wnt signaling controls whether hair follicle stem cells stay inactive or regenerate hair.

Targeting androgen receptors could be a promising way to treat skin disorders with fewer side effects.

Fatty acid transport protein 4 is essential for skin and hair development.

BLIMP1 is essential for skin maintenance but not for defining sebaceous gland progenitors.

Adrenal disorders can cause lasting brain and behavior issues in children.

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

Finasteride works better for baldness in people with shorter gene repeats.

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

The N363S gene variant does not cause higher adrenal androgen levels in women with polycystic ovary syndrome.

Women with greater androgen sensitivity respond better to finasteride for hair loss.

Longer CAG repeats in gene linked to more severe hair loss in females.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

Dynamic, light touch is sensed through a common mechanism involving Piezo2 channels in sensory axons.

Mice with a mutated Dsg3 gene showed severe symptoms but not the typical blistering of pemphigus vulgaris.

No clear link between specific gene and hair loss in Mexican brothers.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

New drugs for Alzheimer's and rheumatoid arthritis advanced, a Zika vaccine is in development, and there were business deals in anesthesia and oncology.

Male hormones may play a role in the development of heart disease, and more research is needed to understand their effects.