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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 document concludes that the fast-growing direct-to-consumer genetic testing market lacks sufficient regulation, posing risks to consumers due to questionable test quality and accuracy.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Piezoelectric Nanogenerators are promising for non-invasive health monitoring but need efficiency and durability improvements.

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

Identifying nonclassic congenital adrenal hyperplasia and carriers of CYP21 mutations is challenging, and genetic counseling is recommended due to their prevalence.

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.

LIPH mutations in Japan cause varying degrees of hair loss and woolly hair.

Niosomes improve minoxidil skin penetration for hair loss treatment.

Testing basal 17-HP levels is a good way to screen for nonclassic adrenal hyperplasia in women with high androgen levels.

Pregnancies in a woman with the Donohue mutation were managed with genetic testing, resulting in three healthy infants.

Niosomes are promising for skin drug delivery, offering benefits like improved drug penetration and stability.

Niosomes are a promising and effective way to deliver drugs through the skin.

Dermal Papilla cells are a promising tool for evaluating hair growth treatments.

OCT can effectively screen and diagnose various medical conditions non-invasively.

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

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Cerasus serrulata flower extracts have strong antibacterial and antioxidant effects and may help prevent hair loss.

The new caffeine cream works better for hair growth than existing products.

Living near more dermatologists and using certain cancer screening tests lowers the chance of being diagnosed with advanced skin cancer.

Blocking the Mitochondrial Pyruvate Carrier causes stress in hair follicles, which can be reduced by an ISR inhibitor.

Ethosomes are a promising method for treating hair loss by delivering drugs directly to the scalp.

The optimized caffeine formula improved hair growth and penetrated all skin layers.

A new hair loss treatment uses tiny needles to deliver a drug-loaded lipid carrier, promoting hair growth more effectively than current treatments.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

Mannosylerythritol lipids are good for skin and hair care products.

The rise in tinea capitis cases in Stockholm is linked to increased African immigration.

Innovative methods are reducing animal testing and improving biomedical research.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.