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The N363S gene variant does not cause higher adrenal androgen levels in women with polycystic ovary syndrome.

Vitamin D boosts a specific gene activity in kidney cells that could improve heart and kidney function.

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.

FP-1 is a key protein in rat hair growth, active only during the growth phase.

A new gene mutation may allow some piebaldism patients to regain skin color in white patches.

Researchers found a gene in hamsters that responds to male hormones and may be indirectly controlled by them.

The KRTAP7-1 gene is very similar across different cattle and yak breeds and likely plays a role in hair strength and shape.

Pangolins have lost some skin-related genes, but kept others, leading to their unique scales and skin features.

Different types of skin stem cells can change and adapt, which is important for developing new treatments.

PTHrP is important for bone formation and may be targeted for osteoporosis treatment and longevity therapies.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

A new mutation in the AGPAT2 gene causes severe fat tissue loss and related health issues by reducing the protein's levels.

Pangolins have lost some skin-related genes, but kept others, showing complex skin evolution.

The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

Mice lacking a key DNA methylation enzyme in skin cells have a lower chance of activating stem cells necessary for hair growth, leading to progressive hair loss.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Mice without certain skin proteins had abnormal skin and hair development.

Using CRISPR for gene editing in the body is promising but needs better delivery methods to be more efficient and specific.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

Certain genetic variations in the FST gene are linked to better wool quality in Chinese Merino sheep.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

Researchers identified a new variant of the FGF5 gene in sheep that affects hair length.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Mice with a mutated Dsg3 gene showed severe symptoms but not the typical blistering of pemphigus vulgaris.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

Gene therapy helped rats with a specific type of rickets grow hair without severe inflammation.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

Future hair loss treatments should aim to extend hair growth, reactivate resting follicles, reverse shrinkage, and possibly create new follicles, with gene therapy showing promise.