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Thymic transplantation normalized some T-cells but not others, maintaining immune function.

Researchers found genes that control hair color and growth change before the visible coat color changes in snowshoe hares.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

FGF9 controls which receptors it binds to through a process where two FGF9 molecules join, and changes in FGF9 can lead to incorrect receptor activation.

Gene linked to common hair loss found, may lead to new treatments.

Researchers found an RNA transcript that might help control a growth factor linked to tumor development.

African American men with prostate cancer have more androgen receptor mutations, which may lead to more aggressive cancer compared to Caucasian American men.

Topical minoxidil helps treat female pattern hair loss, but more research needed for other treatments.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

Elevated CO2 can lessen the negative impact of water shortage on soybean roots and affects specific genes.

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.

Gene differences may affect baldness treatment response in Korean men.

Finasteride side effects in young men may be linked to specific gene variations.

Ginsenoside Re from ginseng may help hair grow by blocking a specific growth-inhibiting pathway.

The conclusion is that while oral contraceptive pills are effective for PCOS-related high androgen levels, new treatments with fewer side effects are needed.

The transition from growth to regression in Cashmere goat hair follicles involves changes in expression of genes related to keratin and cell differentiation.

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.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

Hair growth is influenced by hormones and goes through different phases; androgens can both promote and inhibit hair growth depending on the body area.

N-acetyl-L-cysteine (NAC) can prevent DNA damage and protect cells from harm.

Cantu syndrome, which causes excessive hair growth and skin issues, is due to a mutation in the ABCC9 gene, and understanding this could help develop new treatments for hair diseases.

The length of CAG repeats in the androgen receptor gene is linked to ovarian reserve but does not affect how the ovaries respond to stimulation.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Progranulin overexpression leads to shorter, thinner hair and increased cell death in mouse hair follicles.

No significant link between CAG repeat numbers and female pattern hair loss in Han Chinese population.

A certain genetic variation is linked to a higher risk of polycystic ovarian syndrome.

Updated treatments for female hair loss include minoxidil, antiandrogens, hair transplants, and light therapy.

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.