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The research suggests that the ZP4 gene is linked to egg development in women with PCOS but requires more study to understand its role in infertility.

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

Certain proteins and their receptors are more active during the growth phase of human hair and could be targeted to treat hair disorders.

A specific DNA region is crucial for Foxn1 gene expression in thymus cells but not in hair follicles.

The formula YH0618 can reduce the harmful side effects of the chemotherapy drug Doxorubicin and protect healthy cells.

Certain gene mutations are linked to wool quality in sheep and could help in breeding for better wool.

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

Early balding at 40 increases prostate cancer risk.

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

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

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

Old treatments for other skin conditions showed promise for hair regrowth in mice with a hair loss condition.

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.

Plant-based remedies may treat hair loss by reducing inflammation and improving insulin resistance.

Researchers found two genes that may explain why some Casertana pigs don't have hair.

The document concludes that pregnancy and cancer share immune evasion tactics, but more research is needed before using checkpoint blockade immunotherapy in pregnant cancer patients to avoid harm to the placenta.

Two-photon microscopy effectively tracks live stem cell activity in mouse skin with minimal harm and clear images.

The Notch signaling pathway helps in mouse hair development through a noncanonical mechanism that does not rely on RBPj or transcription.

New treatments and early diagnosis methods for permanent hair loss due to scar tissue are important for managing its psychological effects.

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

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

Over 50% of women over 50 experience hair loss, with minoxidil being the only proven effective treatment.

The monkey's hair loss was due to an autoimmune disease, not genetics.

The document concludes that more research is needed to understand and treat Beard Alopecia Areata due to limited current knowledge and evidence.

Some children who had stem cell transplants developed permanent hair loss, especially when treated with a drug called busulphan.

Hormone imbalances can cause skin diseases, and understanding these links is important for diagnosis and treatment.

Hormones and genes affect hair growth and male baldness.

No strong genetic link to other skin conditions was found, but some genetic factors may make people more likely to get seborrheic dermatitis.

Wnt proteins from certain skin cells are crucial for normal hair growth and renewal.

ACBP is essential for healthy skin and fur by maintaining the skin's barrier function.