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Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

The study suggests certain ACE gene variations are more common in women with PCOS and may be linked to increased insulin resistance.

Hairless gene not strongly linked to baldness.

The severity of symptoms in nonclassical congenital adrenal hyperplasia is not determined by CYP21A2 gene variations.

Estrogen and prolactin may play bigger roles in female hair loss than previously thought.

AHCC reduces hair loss and liver injury caused by chemotherapy in rodents.

Siblings with signs of virilization should be tested for non-classical congenital adrenal hyperplasia, which does not affect adult height but may impact fertility and well-being if untreated.

The conclusion is that young women with excessive hair growth should be quickly tested for hormonal issues and treated to improve their social well-being.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

Combining skin tissue pathology with genetics has greatly improved the diagnosis and understanding of certain skin diseases.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

Short telomeres contribute to aging and cancer, and while telomerase can delay aging, it may also promote cancer.

NEMO syndrome and systemic lupus erythematosus are linked in a new disease association.

Natural gene therapy shows promise for treating skin disorders like epidermolysis bullosa.

The document suggests a rare skin condition might be caused by a genetic phenomenon.

Damaged hair follicles make mice more prone to skin inflammation and skin cancer after UV exposure.

Targeting FGFR-1 with antisense oligonucleotides may help treat baldness by increasing hair follicle activity.

The boy with woolly hair nevus had thinner hair and abnormal hair follicles, which improved with treatment but worsened when treatment stopped.

Mice genetically modified to produce more Del1 protein had faster hair regrowth.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

Recognizing congenital triangular alopecia is crucial to avoid unnecessary treatments.

Dermatologists diagnose and manage melanoma more effectively than general practitioners.

Crossbreeding improves goat fiber quality, and specific genes affect hair traits and color.

Prunus mira Koehne is valuable for hair growth and has potential for sustainable use, but needs more research and conservation.

The most different genetic segment between Africans and East Asians is the EDA2R/AR region, with two main types influenced by population changes and natural selection, and linked to baldness.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

A patient with granuloma annulare experienced both isotopic and isomorphic responses, with skin lesions responding to steroids but relapsing after stopping treatment.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

The study showed that brown planaria can be used to cheaply test if local plants can stop cell growth.

Late diagnosis of congenital adrenal hyperplasia can greatly affect physical development, gender identity, and sexual health.