Search

everythinglearnresearchcommunity

for

Search:↓

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

TGF-β1 and 2 in hair follicles may be linked to hair loss in AGA.

The new model helps understand and develop treatments for genetic skin disorders like AEC.

A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

Genetic variants in specific genes cause central centrifugal cicatricial alopecia.

Modulating the BTNL2 pathway can prevent hair loss in mice.

Recombinant thymosin β4 promotes blood vessel growth and reduces muscle damage.

A3B5 can reduce skin pigmentation and slow melanoma growth.

A unique enzyme in guinea pig hair follicles helps form protein cross-links in hair.

Endothelin-1 helps amelanotic melanocytes stick and move better on certain proteins.

Tenascin is present in normal skin and certain skin tumors but not in sebaceous glands or their tumors.

TRPV3 and TRPV6 channels change structure to regulate calcium and heat responses.

Nephronectin helps attach muscle cells to hair follicles.

A child with trichothiodystrophy also had autoimmune thyroiditis and anemia, which is a new finding.

A new protein linked to hair strength was identified, aiding in understanding brittle hair conditions.

AVT is highly conserved and may have antimicrobial properties.

NuMA-microtubule interactions are vital for proper skin structure formation and function.

CAP1 decreases the expression of a hair-related protein in young Tan sheep's skin.

Genetic changes in specific proteins contribute to hair loss in some women of African descent.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

NLRP1 helps melanoma tumors grow by boosting inflammasome activation and reducing caspase-3 activity.

TSN6 peptide improves skin thickness and hair growth.

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.

Hair differentiation starts earlier than thought, involving multiple type-II keratins.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

The study identified a key protein involved in producing underarm odor and found ways to inhibit it.