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The research concluded that selection significantly shaped the genetic variation of the X chromosome, with certain regions affected by past selective events.

Male-pattern hair loss is largely influenced by genetics, with key genes identified.

Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

AE can have varied symptoms and genetic causes, but zinc therapy helps.

Lichen planus pigmentosus causes dark skin patches and is treated by avoiding triggers and using anti-inflammatory medications.

Two rare genetic diseases cause severe rickets in children due to defects in vitamin D metabolism.

A mother and daughter have a rare genetic hair loss disorder with no effective treatment.

Exposure to too much androgen before birth might cause polycystic ovary syndrome later in life.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

The document concludes that careful design of genetic fate mapping experiments is crucial for accurate cell lineage tracing in mice.

Pediatric endocrinologists should provide early fertility counseling and preservation options to young patients at risk of infertility.

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

Genes related to keratin, skin cell differentiation, and immune functions are key in hedgehog skin and spine development.

Improving knowledge and practices in animal fibre production is crucial to meet market demands and potentially revive natural fibres.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

Scientists identified three genes important for processing certain brain chemicals, thyroid hormones, and medications.

Cavity macrophages gather on organ surfaces but don't really invade or help repair the organs after injury.

Frontal fibrosing alopecia is a poorly understood condition with increasing cases and unclear treatment effectiveness.

The review found that different stem cell types in the skin are crucial for repair and could help treat skin diseases and cancer.

The conclusion is that proper evaluation and treatment of hair loss in midlife women is important, considering the emotional impact and potential for various treatments.

The conclusion is that understanding how feathers and hairs pattern can help in developing hair regeneration treatments.

Early-onset baldness is linked to genetics, lifestyle, and can indicate higher risk for heart and metabolic diseases, and affects mental health.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

Genetic variations greatly affect individual metabolism and can impact health and disease risk.

Changes in the HR gene have influenced hair growth and may lead to hair loss conditions in humans.

The document concludes that adult mammalian skin contains multiple stem cell populations with specific markers, important for understanding skin regeneration and related conditions.

Alopecia areata and vitiligo share immune system dysfunction but differ in specific immune responses and affected areas.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

Hair follicle stem cells are key for hair and skin regeneration, can be reprogrammed, and have potential therapeutic uses, but also carry a risk of cancer.