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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.

Gene linked to common hair loss found, may lead to new treatments.

Blocking the FGF5 gene in sheep leads to more fine wool and active hair follicles due to changes in certain cell signaling pathways.

Mice with LSS deficiency showed hair loss and cataracts, similar to humans, and can help in understanding and treating this condition.

A new gene mutation linked to a skin condition was found in a Spanish family.

AR gene not major factor in female hair loss; different from male hair loss.

Liposomal anthracyclines are effective and safer for treating multiple myeloma, especially in elderly patients.

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

The document suggests that certain protein deficiencies and scalp blistering in Epidermolysis Bullosa may cause hair loss.

5α-Reductase inhibitors can help treat hair loss, acne, and prostate issues by reducing DHT levels.

Cat color patterns are determined early in development by gene expression and epidermal changes, with the Dickkopf 4 gene playing a crucial role.

Hes1 protein is important for hair growth and regeneration, and could be a potential treatment for hair loss.

The research suggests that autophagy-related genes might play a role in causing alopecia areata.

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

Mice can regenerate ear tissue without the p53 protein.

Blocking TSLP reduces skin inflammation and cell overgrowth in psoriasis.

Telomere damage affects skin and hair follicle stem cells by messing up important growth signals.

GPR39 is linked to certain cells in the sebaceous gland and helps with skin healing.

Intu gene is crucial for hair follicle formation by helping keratinocytes differentiate through primary cilia.

Researchers found a new mutation causing total hair loss from birth.

The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

A gene called Gk5 controls lipid production in the skin and affects hair growth.

The document concludes that Rabson-Mendenhall syndrome requires novel treatments for insulin resistance and emphasizes the importance of dental care in affected patients.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

The article concludes that hair loss is a common side effect of drugs treating skin cancer by blocking the hedgehog pathway, but treatment should continue, and more selective drugs might prevent this side effect.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

In vivo lineage labelling is better than in vitro methods for identifying and understanding stem cells.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in patients with Tourette syndrome.

Flightless I protein affects hair growth, with low levels delaying it and high levels increasing hair length in rodents.