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A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

TRPV1 affects sebaceous gland function and could help treat acne.

The peach gene CTG134 helps control the interaction between auxin and ethylene, which could lead to new agricultural chemicals.

K6/ODC transgenic mice are effective for quickly identifying cancer-causing chemicals.

Scientists discovered two versions of a new human hair keratin gene.

Neuroactive steroids affect cocaine's rewarding effects through the sigma1 receptor.

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

Actinic prurigo cheilitis can occur in elderly Asians and can be treated with hydrocortisone cream and sun protection.

A more sensitive assay was developed to detect enzyme activity converting arginine to citrulline in hair follicles.

CYP154C7 enzyme can effectively modify steroids and is promising for commercial use.

The chemicals 17βC and its methyl ester can block the effects of testosterone on hamster skin but not the effects of DHT.

Hair cortisol is a reliable stress indicator in cattle but may not be valid for pigs.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

FOXN1 duplication can cause excessive hair growth.

A substance from Caulerpa racemosa seaweed may protect against skin damage caused by air pollution by reducing oxidative stress and cell death.

CXCL7 is essential for muscle repair by aiding early neutrophil infiltration.

Alpha-MSH affects mitochondrial function, and MC1R mutations may increase skin aging.

A specific DNA sequence caused hair loss in male mice by activating immune cells and increasing a certain immune signal.

Lhx2 is a crucial regulator of the Sonic Hedgehog signaling in early mouse retinal development.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

BMI1 is essential for preventing hair greying and maintaining hair color.

Alkaline ceramidase 1 is crucial for healthy skin and energy balance.

Different Hairless isoforms affect Vitamin D receptor activity in hair regulation, with one repressing and the other stimulating it.

The study created a mouse model to mimic degenerative diseases for testing tissue repair and new therapies.

Nucleic acids trigger chemokine production in skin cells, affecting skin inflammation.

A new gene mutation causes complete androgen insensitivity in a 16-year-old with a female appearance.

5α-Reductase helps regulate hormone action in toad testes, especially during breeding season.

The ACE1 gene variant doesn't affect long-COVID symptoms.

A 56-year-old man was diagnosed with Cronkhite-Canada Syndrome after showing symptoms like diarrhea, weight loss, and skin changes.