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Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

The lentiviral array can monitor and predict gene activity during stem cell differentiation.

PROTO1 and PROTO2 protect against hearing damage.

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

Mycophenolate mofetil may improve lupus nephritis remission more than cyclophosphamide but with uncertain safety.

Early recognition and treatment of Peripheral Arterial Disease is crucial to improve survival and health outcomes.

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

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

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

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

PAD is common but often missed, needing lifestyle changes and medication for better outcomes.

No single treatment is clearly effective for central serous chorioretinopathy.

Different signals work together to change gene activity and guide hair follicle stem cells to become specific cell types.

Minoxidil and Finasteride are effective for male baldness; more research is needed for hair aging treatments.

The protein RSL4 is crucial for making root hairs longer by controlling genes related to cell growth.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

Oral isotretinoin may slightly improve acne but increases the risk of side effects like dry lips and skin; more research is needed to understand its full risks and benefits.

Goats with BSE or scrapie show varying symptoms, and using only clinical signs may not detect all scrapie cases.

A specific protein complex increases the activity of a plant enzyme, but this action is not required for plant root hair growth.

A protein in plants needs to bind two lipids to help with root hair growth, and this process is similar across different plant species.

Keratosis pilaris is often linked to genetic mutations and causes skin and hair abnormalities, regardless of those mutations.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

Cells with active Wnt signaling are less likely to turn into cancer when exposed to a cancer-causing gene.

Higher hair luminosity and shine mean higher perceived transparency.

PCOS causes infertility mainly due to hormonal imbalances, insulin resistance, and chronic inflammation.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Some canine hair follicle tumors contain amyloid deposits, with a protein called CK5 involved in their formation.

A new hair restoration technology was found to effectively increase hair thickness, density, and growth, while reducing hair loss and improving scalp health, with no side effects.

Activating the GDNF-GFRα1-RET signaling pathway could potentially promote skin and limb regeneration in humans and could be used to treat hair loss and promote wound healing.