Search

everythinglearnresearchcommunity

for

Search:↓

Dihydrotestosterone treatment on 2D and 3D-cultured skin cells slows down hair growth by affecting certain genes and could be a potential target for hair loss treatment.

Grasp protein helps maintain skin health after UVB exposure.

Noncoding dsRNA helps produce exosomes that aid in skin regeneration.

The enzyme Dgat1 is essential for healthy hair and skin by controlling retinoid levels.

Measuring 24-OHase induction helps identify defects in vitamin D processing and predict treatment response.

ARHGEF3 is essential for proper hair follicle development in mice.

A genetic defect causes males in some Mediterranean populations to be born with ambiguous genitalia and develop male traits at puberty.

A mouse gene mutation increases the risk of skin cancer.

p63 controls Satb1 to help skin develop properly.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

The Tru9I variant in the VDR gene may influence alopecia areata risk and vitamin D levels.

The N gene affects the protein makeup of mouse hair.

A new genetic mutation was found causing hair and eye issues in a boy.

Defective nuclear transport may cause gene expression changes in Progeria.

Anti-Desmocollin 3 antibodies can cause pemphigus-like symptoms in mice.

The LAMTOR3 gene is involved in cashmere goat hair growth and is affected by certain treatments and other genes.

Key genes and pathways involved in thyroid eye disease were identified, aiding potential treatment and diagnosis.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Trichothiodystrophy is a rare genetic disorder causing hair issues and sometimes linked to DNA repair defects.

The study found that tight junctions reach the top layer of the skin's stratum granulosum, not just the second top layer as previously thought.

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

Different ligands change the shape of the TRPV3 ion channel in unique ways.

Mice lacking Insig proteins had hair growth problems due to cholesterol buildup, but this was fixed by the drug simvastatin.

Certain genetic variants in ERN1, TACR3, and SPPL2C are linked to when Alzheimer's disease starts.

WIF1 helps keep skin stem cells inactive to prevent excessive cell growth.

Rat dermal papilla cells have unique genes crucial for hair growth.

Inflammation damages sweat ducts, causing sweat gland injury.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

Vitamin B3 may help prevent hair loss and promote hair growth by protecting scalp cells from stress and reducing hair growth-blocking proteins.

Immune cells might contribute to hair loss caused by a specific mutation.