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A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

Platelet lysate effectively promotes hair growth and improves hair thickness in people with androgenetic alopecia.

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

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

The research found specific proteins that affect fiber characteristics and hair growth in sheep and goats.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

Deleting the BRD4 protein in certain skin cells causes hair loss and skin inflammation.

The gene URB is more active in human hair growth cells and responds to a hair-related hormone.

Cantú syndrome is caused by mutations in the ABCC9 gene.

ARL15 is important for fat cell development and the release of the hormone adiponectin.

Vimentin is involved in regulating the hair growth cycle in Inner Mongolian Cashmere goats.

A woman's hair loss and scalp swelling, caused by a fungal infection, was wrongly treated but eventually cured with Terbinafine, emphasizing its effectiveness.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Lack of cystatin M/E causes thin hair and dry skin.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

The research identified genes and non-coding RNAs in cells that could be affected by testosterone, which may help understand hair loss and prostate cancer.

Blond hair in Solomon Islanders is due to a unique genetic variant, not European ancestry.

The study found that androgen receptors in skin cells mainly affect the focal adhesion pathway and control the caveolin-1 gene, with implications for new treatments for related diseases.

Baicalin may help reduce excessive male hormone levels in PCOS.

A mutation in the EDNRA gene causes Oro-Oto-Cardiac syndrome, affecting face and heart development.

The zinc finger protein 3 in Arabidopsis thaliana reduces plant growth and root hair development.

Some early COVID-19 mutations in patients predicted future common virus mutations.

Sons of mothers with polycystic ovary syndrome (PCOS) have a higher risk of obesity and insulin resistance, possibly due to certain genes and factors passed down from their mothers.

The research found specific genes and pathways that control fur development and color in young American minks.

The timing of when the gene Bmal1 is active affects aging and survival, with its absence during development, not adulthood, leading to premature aging.

Blocking the androgen receptor in skin cells reduces their growth response to male hormones, suggesting a possible treatment for skin conditions linked to androgens.

A special microbe helps plants absorb rock phosphate by growing on their root hairs.

Men with baldness have higher levels of specific proteins, suggesting local hormone production may play a role in hair loss.