Search

everythinglearnresearchcommunity

for

Search:↓

The document concludes that the development of certain tumors is influenced by genetic background and that a specific gene modification can lead to tumor regression and reduced growth.

Certain genetic markers on chromosome 20 are linked to hair loss in the Han Chinese from Yunnan.

Alopecia areata is likely caused by a combination of genetic factors and immune system dysfunction, and may represent different diseases with various causes.

Male pattern baldness is mostly inherited, involves many genes, and is linked to other traits like early puberty and strong bones.

Genetic data can predict male-pattern baldness with moderate accuracy, especially for early-onset cases in some European men.

Two specific hair keratin genes are active during hair growth and decline as hair transitions to rest.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

Hair microscopy is useful for diagnosing hair disorders, but clear definitions are needed for accurate genetic analysis.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

Using a combination of specific cell cycle regulators is better for safely keeping hair root cells alive indefinitely compared to cancer-related methods.

Faulty inflammasome activation may lead to autoimmune skin diseases and could be a target for new treatments.

Environmental factors like smoking, UV exposure, and poor diet contribute to hair loss and graying, and lifestyle changes can help manage it.

The meeting discussed various skin conditions, treatments, and unusual cases, highlighting the effectiveness of tetracycline in treating rosacea.

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

A defective gene causes hair loss and taste insensitivity in BTBR mice.

Genes and hormones cause hair loss, with four genes contributing equally.

Genes play a significant role in male-pattern baldness, and understanding them could lead to new treatments and insights into related health issues.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

Longer GGN repeats in the androgen receptor gene are linked to polycystic ovary syndrome.

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.

A person with Turner Syndrome showed severe schizophrenia that didn't respond to treatment and had brain shrinkage.

Water and fatty acids affect hair's surface differently based on hair damage, and models can help understand hair-cosmetic interactions.

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

Male genital development is driven by androgen signaling and understanding it could help address congenital anomalies.

Male pattern baldness involves hormone-related hair thinning, shorter hair, and inflammation.

Identical twins had different symptoms because one had more cells with an extra chromosome fragment in different tissues.

Researchers created immortal human skin cells with constant testosterone receptor activity to study hair loss and test treatments.

Skin problems are common in thyroid disorders, with dry skin in hypothyroidism and warm, soft skin in hyperthyroidism.

A 3-month treatment improved PCOS symptoms and reduced certain immune proteins.

People with Down syndrome have higher rates of certain immune-related conditions and need special medical attention.