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CRISPR/Cas9 gene-editing shows promise for improving sheep and goat breeding but faces challenges with efficiency and accuracy.

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

The circadian clock plays a key role in hair growth and its disruption can affect hair regeneration.

Animal models have helped understand hair loss from alopecia areata and find new treatments.

Follistatin helps hair growth and cycling, while activin prevents it.

The meeting highlighted the genetic basis of female pattern hair loss and various skin health insights.

Vitamin D Receptor is crucial for normal skin and hair growth.

Hair follicles are complex, dynamic mini-organs that help us understand cell growth, death, migration, and differentiation, as well as tissue regeneration and tumor biology.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

ATP-dependent chromatin-remodeling complexes are crucial for gene regulation, cell differentiation, and organ development in mammals.

Brain hormones significantly affect hair color and could potentially be used to prevent or reverse grey hair.

Skin abnormalities can indicate immunodeficiency due to shared origins with the immune system.

HDAC6 helps keep ovarian follicles dormant, extending female fertility.

New liposome treatment successfully delivers CRISPR to deactivate a key enzyme in androgen-related disorders.

The 2015 Hair Research Congress concluded that stem cells, maraviroc, and simvastatin could potentially treat Alopecia Areata, topical minoxidil, finasteride, and steroids could treat Frontal Fibrosing Alopecia, and PTGDR2 antagonists could also treat alopecia. They also found that low-level light therapy could help with hair loss, a robotic device could assist in hair extraction, and nutrition could aid hair growth. They suggested that Alopecia Areata is an inflammatory disorder, not a single disease, indicating a need for personalized treatments.

Twist2 is essential for proper skin healing and hair growth in developing mice.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

The Foxn1 gene mutation causes hairlessness and immune system issues, and understanding it could lead to hair growth disorder treatments.

Foxi3 expression in developing teeth and hair is controlled by the ectodysplasin pathway.

Chinese domestic goats have unique genetic traits due to domestication and geographic isolation.

External factors can cause skin cancer cells that usually don't spread to grow and form tumors in mice.

A specific mutation in the TRPV3 gene causes hair follicle cells to develop improperly, leading to hair loss.

The STIM1 R304W mutation in mice leads to bone changes and teeth hair growth.

TGFα gene mutation in mice causes abnormal skin, wavy hair, curly whiskers, and sometimes eye inflammation.

The fuzzy gene is crucial for controlling hair growth cycles.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

Mouse Scube3 affects teeth, tongue, vibrissae, and eye development, but not facial structure or limb growth.

Not having enough cystatin M/E protein causes less hair growth and dry skin.

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

A gene variant increases the risk of a type of hair loss by affecting hair protein production.