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miR-22, a type of microRNA, controls hair growth and its overproduction can cause hair loss, while its absence can speed up hair growth.

Oral retinoids are effective for severe skin conditions but require careful use due to side effects.

New compounds with carborane showed anti-androgen effects similar to flutamide.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

Changing Wnt signaling can lead to more or less hair growth and might help treat hair loss and skin conditions.

A male with aromatase deficiency improved bone health with estradiol treatment.

Stress and alcohol affect brain chemicals differently in rats, mice, and humans, influenced by genetic differences.

The document explains how to identify different hair problems using a microscope.

Androgen receptor signaling causes early aging of cells important for hair growth by damaging their DNA.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

Researchers created a mouse model of a type of rickets that does not cause hair loss.

The document concludes that ongoing research using animal models is crucial for better understanding and treating Alopecia Areata.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

Finasteride may improve prostate cancer treatment outcomes.

The G60S Connexin43 mutation causes hair growth issues and poor hair quality in mice, similar to human ODDD patients.

Scientists have made progress in understanding hair follicle stem cells, identifying specific genes and markers, and suggesting their use in treating hair and skin conditions.

A woman with acromegaloidism and normal growth hormone levels had a rare X-Tetrasomy, suggesting a need to study X-chromosome genes for their role in growth and facial development.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Scientists have found specific genes linked to different hair loss conditions, which could lead to new treatments.

Eclipta alba extract may work as an anticancer agent and help reverse drug resistance.

Increased PPARGC1α relates to hair thinning in common baldness.

Advancements in nanoformulations for CRISPR-Cas9 genome editing can respond to specific triggers for controlled gene editing, showing promise in treating incurable diseases, but challenges like precision and system design complexity still need to be addressed.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

Most hair loss in children is caused by a few common conditions and is easy to diagnose, but rare types require careful evaluation.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

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

Inhibiting ALOX12 can help hair cuticle maturation by increasing S100A3 citrullination.

Some domesticated animals have the same genetic skin diseases as humans, which can help doctors understand human genetic mutations.

Mechanical forces are crucial for shaping cells and forming tissues during development.

Swiss Holstein cattle with curly, short hair carry genes from the Simmental breed.