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Rabbits with Sarcoptes scabiei had thicker skin, cell death, and skin hardening.

Rapamycin treatment helps with mitochondrial disease by reducing PKC levels.

A new gene mutation causes insulin resistance in a girl and her mother.

The Hairless gene is crucial for healthy skin and hair growth.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

A patient with Rhupus was diagnosed with Rowell syndrome and treated with various medications.

The SHJH hr mice with a mutated Hr gene show signs of faster skin aging due to poor antioxidative protection.

PRC2 is essential for maintaining intestinal cell balance and aiding regeneration after damage.

Hair follicle stem cells help maintain skin health by moving to and supporting the skin's surface layers.

The mK6irs1/Krt2-6g gene likely causes wavy hair in mice.

scMC effectively separates biological signals from technical noise in single-cell genomics data.

The Notch signaling pathway helps in mouse hair development through a noncanonical mechanism that does not rely on RBPj or transcription.

ISCK03 stops melanin production in human melanoma cells and lightens skin color in mice and guinea pigs.

SkQ1 antioxidant improved health and lifespan in mice.

POUF51 and HES3 are key in controlling stem cell numbers in psoriasis.

Decreasing MIG6 can increase the movement and invasiveness of MEK-inhibited mutant NRAS melanoma, particularly when stimulated by EGF.

EGFR helps mouse hair follicles stop growing by reducing certain growth regulators.

Rhupus is a complex syndrome that combines rheumatoid arthritis and lupus, making diagnosis challenging.

The gene SDR5A1 is found in scalp hair of both hirsute and normal individuals, but it does not explain differences in hair growth.

TEDAR is crucial for skin cell differentiation and barrier formation.

Hair loss in certain mice is linked to changes in keratin-related genes.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

SRD5A2 gene variations affect PTSD symptoms differently in males and females.

The TRPV3 channel structure changes linked to severe itch and hyperkeratosis were identified using cryo-EM.

The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

SQSTM1 is linked to increased risk of alopecia areata.

SIRT7 protein is crucial for starting hair growth in mice.

Removing both KLK5 and KLK7 proteins can prevent death and skin issues in Netherton syndrome.

Hair growth-related cells need the enzyme SCD1 to help maintain the area that supports hair growth.