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Wild strawberry waste extract can be a sustainable cosmetic ingredient for treating acne and hair loss.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

Epigenetic mechanisms control skin development by regulating gene expression.

A gene mutation in Lama3 is linked to a common type of hair loss.

Cells lacking the Bax protein can outcompete others, leading to better tissue repair and hair growth.

Cedrol may be an effective treatment for colorectal cancer.

Mutations in the glucocorticoid receptor gene cause reduced sensitivity to glucocorticoids and may lead to poor response to treatment.

Certain gene variations and irregular X chromosome activity may contribute to hair loss in women who can have children.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

DGAT1 enzyme is crucial for healthy skin and hair by regulating retinoid levels.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

Scientists found a specific group of itch-sensing nerve cells in mice important for feeling itch but not for sensing heat or touch.

SCD1 is crucial for skin health and overall energy balance.

GALT5 and GALT2 are important for plant growth and development because they help with protein glycosylation.

Certain genetic markers, especially the MICA gene, are linked to alopecia areata.

More research is needed to understand the genetic causes of Alopecia areata to develop better treatments.

VDR regulation varies by tissue and is crucial for its biological functions.

Keratosis pilaris is often linked to genetic mutations and causes skin and hair abnormalities, regardless of those mutations.

TGM3 is important for skin and hair structure and may help diagnose cancer.

Mutations in NIPAL4 cause skin issues by disrupting lipid layers, but some improvement is seen with topical treatment.

Lipocalin-Type Prostaglandin D2 Synthase (L-PGDS) is a protein that plays many roles in the body, including sleep regulation, pain management, food intake, and protection against harmful substances. It also affects fat metabolism, glucose intolerance, cell maturation, and is involved in various diseases like diabetes, cancer, and arthritis. It can influence sex organ development and embryonic cell differentiation, and its levels can be used as a diagnostic marker for certain conditions.

BMP4 gene is crucial for hair follicle development in Liaoning cashmere goats.

HLA-DRB5 and other genes may be linked to alopecia universalis.

Mice without certain skin enzymes have faster hair growth and bigger eye glands.

A Korean boy's skin and digestive symptoms were caused by a rare genetic disorder that affects zinc absorption, and he got better with zinc supplements.

Genetic defects in the glucocorticoid receptor gene can cause conditions with abnormal sensitivity to stress hormones, and other factors may also affect this sensitivity.

Mutations in the NR3C1 gene cause a rare condition that affects hormone signaling and can lead to various symptoms, with dexamethasone as a treatment option.

LIPH mutations in Japan cause varying degrees of hair loss and woolly hair.

The MTHFR C677T mutation may increase the risk of alopecia areata in the Turkish population.