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Drug repositioning is becoming more targeted and efficient with new technologies, offering personalized treatment options and growing interest in the field.

The gene KAP22-1 affects wool yield and fiber shape in sheep.

Ancient Chinese goats evolved cashmere-producing traits due to selective breeding, particularly in genes affecting hair growth.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

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

PCOS may start before birth, involves metabolic issues, and can be treated with drugs like metformin and lifestyle changes.

Frontal Fibrosing Alopecia's cause is unclear, affects mainly postmenopausal women, and current treatments focus on stopping hair loss rather than regrowth.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

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

The cause of alopecia areata is likely a mix of genetics, immune system issues, and environmental factors, with more research needed to understand it fully.

Most skin changes during pregnancy are harmless and moles don't significantly change, but many women experience pigmentation changes due to hormones and sun exposure.

DNA phenotyping helps predict physical traits from DNA with varying accuracy and requires careful ethical and legal handling.

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

Young HS patients often have other physical and mental health issues, and research on HS covers a wide range of topics including genetics, triggers, treatments, and the need for more data.

Some women with PCOS have rare genetic variants linked to the condition.

Alopecia Areata is an autoimmune condition causing hair loss, influenced by genetics, environment, and possibly improved by anti-MIF therapy, with many patients experiencing regrowth within a year.

Understanding skin structure and development helps diagnose and treat skin disorders.

SFRP2 and PTGDS may be key factors in female hair loss.

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

Rare genetic variants in five specific genes are linked to male-pattern hair loss but only account for a small part of the risk.

Hairlessness in mammals is due to complex genetic changes in both genes and regulatory regions.

Stem cells control their future role by changing ERK signal timing, affecting tissue regeneration and cancer.

Cornification is the process where living skin cells die to create a protective barrier, and problems with it can cause skin diseases.

Activating Wnt in skin cells controls the number of hair follicles by directing cell movement and fate.

A thorough initial check-up is essential before sperm banking to ensure the best chance of preserving good quality sperm.

Acne vulgaris is a common skin condition that can cause low self-esteem and depression, and early treatment is important to prevent scarring.

Some vaccines, like the hepatitis B vaccine, might be linked to the hair loss condition Alopecia Areata, but more research is needed.

Keratin proteins are crucial for hair structure and strength.

Dermatoscopy is useful for identifying different hair and scalp conditions and can reduce the need for biopsies.

GABRA2 gene variations impact alcohol response, and hair loss medication finasteride reduces some effects.