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Researchers found that most genes affecting drug responses are not fully covered by commercial SNP chips, suggesting the need for more comprehensive tools to optimize drug selection based on genetics.

Shift nurses show altered body temperature and stress hormone levels, suggesting their body clocks adjust to irregular schedules.

Certain genes on chromosomes 6, 10, 16, and 18 may increase the risk of alopecia areata.

Tetrahydroxystilbene Glucoside may help prevent hair loss by blocking certain pathways that lead to cell death.

WNT7A gene expression is higher in early stages of androgenetic alopecia, showing the role of WNT pathway, apoptosis, and inflammation in the disorder.

People with alopecia have shorter hair follicles and more c-kit, a stem cell factor receptor, which could predict how the condition progresses.

Genetically modified sheep with more β-catenin grew more wool without changing the wool's length or thickness.

Polycomb Repressive Complex 2 is not needed for hair regeneration.

Dihydrotestosterone (DHT) stops hair growth in mice by lowering a growth factor important for hair.

The protein STAT3 slows down cell growth by blocking the FST gene, which affects hair development in sheep.

Different genes and pathways are active in yak skin and hair cells, affecting hair growth and immune responses.

Some children in Malaysia with symptoms have either profound or partial biotinidase deficiency, and early testing and treatment are important.

Certain genetic variations in OCT1 may improve insulin sensitivity with metformin in women with PCOS.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Scientists have created a new hair loss treatment using ultrasound to deliver gene-editing particles, which resulted in up to 90% hair regrowth in mice.

The three estrogen receptor genes are highly expressed in zebrafish neuromasts during development.

Hair and skin can regenerate without bulge stem cells due to other compensating cells.

Nanog gene boosts stem cells, helps hair growth, and may treat hair loss.

Finasteride affects SRD5A2 gene pattern, possibly causing lasting side effects.

Immune activities and specific genes are important in male pattern baldness.

Pigs without the Hairless gene showed skin and thymus changes, useful for studying human hair disorders.

High-dose finasteride may help treat glioblastoma but needs localized delivery for effectiveness.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

Signaling pathways are crucial for hair growth in goats.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

GRHL3 is important for controlling gene activity in skin cells during different stages of their development.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

A gene called HDAC9 might be a new factor in male-pattern baldness.

A new therapy for a skin blistering condition has not been developed yet.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.