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Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

P-cadherin is important for hair growth and health, and its problems can cause hair and skin disorders.

SV40 T antigen in hair follicles causes abnormal hair and health issues in mice.

The B2 genes are crucial for hair growth in rats.

People with myotonic dystrophy type 1 tend to develop basal cell carcinoma at a younger age but not more frequently than others.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

Melatonin given to pregnant rabbits improved their babies' fur quality.

Modifying certain signals in the body can help wounds heal without scars and regrow hair.

The HoxC gene cluster and its enhancers are essential for developing hair and nails in mammals.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

HNG may help prevent the negative effects of chemotherapy on sperm production and white blood cell counts.

Rare genetic variants in five specific genes are linked to male-pattern hair loss but only account for a small part of the risk.

Colorectal cancer development involves both genetic changes and epigenetic alterations like DNA methylation and microRNA changes.

μ-Crystallin may help hair growth by affecting thyroid hormone levels in mouse hair follicles.

Protein tyrosine kinases are key in male pattern baldness, affecting skin structure, hair growth, and immune responses.

Hard skin features like scales, feathers, and hair evolved through specific protein changes in different animal groups.

Hairless protein affects hair follicle structure by regulating the Dlx3 gene.

The TRPV3 ion channel is important for skin and hair health and could be a target for treating skin conditions.

Researchers found genes for cysteine-rich proteins that form the protective layer of hair in humans and sheep.

Ornithine decarboxylase is crucial for hair growth and follicle development.

Foxp3+ Regulatory T Cells are important for immunity and tolerance, affect hair growth and wound healing, and their dysfunction can contribute to obesity-related diseases and other health issues.

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

miR-199a-3p controls hair growth and is linked to alopecia areata.

Women with PCOS are more likely to develop kidney stones, especially those with certain PCOS types.

The symposium highlighted the importance of genetics in understanding and treating complex skin diseases.

Activating Nrf2 in skin cells causes skin disease similar to chloracne in mice.

The UD-PrOZA program successfully diagnosed 18% of adult patients with rare diseases, often using genetic testing.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

New regenerative therapies show promise for treating hair loss.

The research identified key molecules that help hair matrix and dermal papilla cells communicate and influence hair growth in cashmere goats.