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Activating TLR5 in the gut can extend lifespan and improve health in aged mice.

MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.

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

Chemokine signaling is important for hair development.

FGF9 controls which receptors it binds to through a process where two FGF9 molecules join, and changes in FGF9 can lead to incorrect receptor activation.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

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

BeauTop improves hair growth in androgenetic alopecia patients.

Researchers identified genes in scalp hair follicles that may affect hair traits and hair loss.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

Blocking glucocorticoid receptors improves glucose metabolism in a PCOS mouse model.

The structure of SRD5A reveals how it reduces steroids, aiding drug design for related health conditions.

Let-7b helps alpaca hair grow by reducing TGFβR I protein.

The document concludes that MGRN1 affects mouse fur color by interfering with a receptor's signaling, but its full role in the body is still unknown.

A new small peptide may help hair growth by activating a specific receptor and should be tested in humans.

A specific protein complex increases the activity of a plant enzyme, but this action is not required for plant root hair growth.

The protein STAT3 slows down cell growth by blocking the FST gene, which affects hair development in sheep.

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

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

A protein called IL-36γ causes skin side effects from certain cancer treatments when combined with a common skin bacteria.

CXXC5 is a protein that controls cell growth and healing processes, and changes in its activity can lead to diseases like cancer and hair loss.

Thiazole, a sulfur and nitrogen chemical, is useful in creating potential drugs for conditions like seizures, cancer, bacterial infections, tuberculosis, inflammation, malaria, viruses, Alzheimer's, diabetes, and A1-receptor issues.

The enzyme DHHC13 is essential for healthy hair and skin, and its deficiency leads to hair loss and skin problems.

A specific gene mutation causes long hair in Angora rabbits.

Zinc is crucial for skin health and treating various skin disorders.

Certain miRNAs play a key role in the growth of cashmere by affecting hair follicle development and regeneration.

The Chinese herbal supplement BeauTop can potentially boost hair growth and thickness by increasing a protein called Vascular Endothelial Growth Factor.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

People with hypohidrotic ectodermal dysplasia are more likely to experience long-term fatigue and hair loss after COVID-19.

CXXC5 can both suppress and promote cancer, making it a complex target for treatment.