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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.

Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

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

Finasteride effectively prevents biofilm formation and treats preformed biofilms, but requires high doses.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

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

DHT is a strong androgen that may pose less risk to the prostate compared to testosterone.

Neurotrophin-4 increases calcium current in specific mouse neurons through the PI3K pathway.

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

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

A dog's skin infection caused by the fungus Chaetomium globosum was effectively treated with ketoconazole.

Washing baby socks without flipping them inside out may increase the risk of Hair Tourniquet Syndrome.

Modified stem cells that overexpress a specific protein can improve hair growth and reduce hair abnormalities in mice.

Some skin medications are safe for pregnant women, but others pose risks or should not be used.

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

Green tea component EGCG helps keep rat skin grafts viable longer.

Human hair follicle dermal cells can help repair damaged hair follicles.

Metformin, a diabetes drug, may also help fight cancer, but more research is needed to understand how.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

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

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Medicinal plants in nutricosmetics contain compounds that can improve skin and hair health.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

Eating raw cheonggukjang improves scalp hair in middle-aged women.

Cutaneous lupus patients have higher levels of certain immune cells in their blood and skin.

The document concludes that ERBB2 mutations are common in extramammary Paget disease and may respond to systemic treatments like cancer immunotherapy.

IL-17C is important in inflammatory skin diseases and could be a target for treatment.

TLR3 signaling enhances the immunosuppressive properties of human periodontal ligament stem cells.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.