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Retinoids increase steroid sulfatase activity in leukemia cells through RARα/RXR and involves certain pathways like phosphoinositide 3-kinase and ERK-MAP kinase.

A new eyelid shampoo improved eyelid hygiene and eyelash length in people with Meibomian Gland Dysfunction.

Men are more likely to have severe respiratory viral infections like COVID-19 due to hormonal and genetic differences, while women generally have stronger immune responses.

Many dermatologists in Saudi Arabia recommend vitamins and minerals for hair loss, often based on personal experience rather than strong evidence.

Akt2 protein is essential for normal cell division in early mouse embryos.

Acne is a common skin condition that can be influenced by diet, lifestyle, and hormones, and requires a treatment approach that includes psychological considerations.

STK11 gene variations do not predict how well metformin will work for PCOS, but may affect hair loss and excess hair growth.

Telogen Effluvium is a common, usually reversible hair loss condition, often improved by removing the trigger and possibly treated with various products, though their effectiveness is uncertain.

Netherton Syndrome is a non-treatable genetic disorder in children causing skin, hair, and allergy issues.

The document suggests more research is needed to understand the link between baldness and prostate cancer.

Protease Nexin-1 is found in human hair growth cells and is affected by male hormones.

The document highlights various patents for new compounds with potential treatments for multiple diseases, including cancer, hormonal disorders, and diabetes.

Mycophenolate helps reverse hair loss effects caused by IFN-γ by activating a key hair growth pathway.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.

Baicalin may help treat hair loss by promoting hair follicle growth and activating specific cellular pathways.

COVID-19 can cause different skin symptoms that may help with early diagnosis and show how severe the disease is.

Scientists discovered a unique hair protein, KAP24.1, with a special structure, found only in the upper part of hair cuticles.

Some vitamins and minerals are important for preventing hair loss, but treating hair loss with them without a known deficiency is not proven effective.

Some diets and supplements might help with skin disorders, but their effectiveness varies and more research is needed.

Hair analysis can help identify specific minerals and amino acids linked to various diseases.

Using enzymes to link proteins makes hair repair treatments more effective and long-lasting.

Some lesser-known causes of PCOS include autoimmune issues, genetic mutations, and changes in the body's microbiome.

Proxalutamide improved blood markers related to inflammation, immune response, and clotting in COVID-19 patients, potentially reducing hospitalizations.

A specific gene mutation causes long hair in Angora rabbits.

Imatinib mesylate can cause skin lightening, especially in Chinese patients, due to its effect on pigment production.

Different versions of the KRTAP6-2 gene in goats can lead to thinner cashmere fibers.

The study concludes that certain domains in Clostridium histolyticum enzymes are structurally unique, bind calcium to become more stable, and play distinct roles in breaking down collagen, with potential applications in medicine and drug delivery.

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

LncRNA MTC boosts growth of goat skin cells, improving cashmere quality.

The document concludes that recognizing and properly diagnosing lipodystrophy syndromes is crucial for effective management and treatment.