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RNA aptamers can specifically block FGF5-related cell growth, potentially treating related diseases or hair disorders.

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

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

A new gene variant causes glucocorticoid resistance in a mother and son.

Mutations in the FOXN1 gene cause severe immune issues but don't affect hair and nails.

Mercuric triflate is an effective catalyst for various organic reactions, working well at room temperature with high yields.

Melanoma risk tools need improvement, a gene mutation causes a hair disorder that might be treated by managing cell stress, a potential therapy for a skin-ear disorder involves blocking cell channels, skin wrinkling may indicate lung aging regardless of smoking, and oxidative stress might contribute to common baldness.

Fluid viscosity affects fracture design and proppant placement in hydraulic fracturing.

Cathepsin L is essential for normal hair growth and development.

Scientists found a way to grow human hair cells in a lab that can create new hair when transplanted.

Docetaxel and paclitaxel for breast cancer can cause permanent, severe hair loss.

FLRG and follistatin have different roles in wound healing.

The study concludes that certain domains in Clostridium histolyticum enzymes are structurally unique, bind calcium to become more stable, and play distinct roles in breaking down collagen, with potential applications in medicine and drug delivery.

Follicular Cell Implantation might become a new treatment for hair loss and could lead to advances in organ regeneration.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

Mouse Scube3 affects teeth, tongue, vibrissae, and eye development, but not facial structure or limb growth.

Understanding how androgens work is key for creating new treatments for prostate issues and hair/skin conditions.

Hair length and thickness are related, with thickness peaking at about a quarter of the hair's maximum length.

Netherton Syndrome can cause severe skin lesions in rare cases.

Minoxidil treatment increased hair density in a young Asian girl with short anagen syndrome, but didn't improve hair length or thickness.

Chemotherapy patients don't all lose their hair due to factors like hair growth rates, age, genetics, and the type of drugs used.

Hutchinson-Gilford Progeria Syndrome causes rapid aging from a genetic mutation, with no cure but ongoing research into potential treatments.

Not having enough cystatin M/E protein causes less hair growth and dry skin.

Stem cells show promise for hair loss treatment, but no effective product for hair regeneration has been developed yet.

The document concludes that an experimental drug may help wound healing in Epidermolysis Bullosa, links Hydroa vacciniforme to EBV, discusses diagnosing hair loss disorders, finds many children with eczema have allergies, reviews the safety of a skin medication in children, notes side effects of a Duchenne's treatment, and identifies a marker for pediatric mastocytosis.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

Eating a lot of fat increases PKCβ and inflammation in skin fat cells, which affects skin and hair health.

The PON1 192R gene variant is linked to a higher risk of psoriasis and heart disease in Western Mexico.