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Cancer rates are increasing in developed countries, with estrogen, aging, low vitamin D3, and HPV infection as common causes.

New cancer treatments are more precise and less toxic, improving survival rates, but Asia faces challenges in adopting these advancements.

Dorper sheep's wool shedding is linked to specific genes and pathways, which may help understand human hair growth.

Young women in West Bengal, India, with PCOS often have estrogen resistance, leptin receptor issues, folate deficiency, T2DM, and acanthosis, commonly linked to obesity.

Brepocitinib 30mg is most effective for moderate-to-severe alopecia areata, but ritlecitinib 50mg may offer a better balance of safety and effectiveness.

These specific gene polymorphisms are not linked to Alopecia Areata in Egyptians.

Hyperandrogenism increases heart disease risk in premenopausal women, but this risk is linked to obesity in postmenopausal women.

TNC+ fibroblasts play a key role in skin inflammation by interacting with T cells.

Multi-omics techniques help understand the molecular causes of androgenetic alopecia.

Using sunscreen and moisturizers may increase the chance of developing Frontal fibrosing alopecia (FFA), but the exact reason why is still unclear.

SIRT3 and SIRT7 genes may play a role in hair loss.

ERULUS controls root hair growth by regulating cell wall composition and pectin activity.

The same hormone can affect gene expression differently in various tissues, which could lead to new treatments for conditions like hair loss.

Vitamin C deficiency changes gene expression, affecting skin and hair health.

Androgenetic alopecia involves immune cell disruptions, especially increased CD4+ T cells around hair follicles.

N-acetylcysteine may prevent hair loss caused by chemotherapy.

Hair loss in male pattern baldness is linked to changes in specific genes and proteins that affect hair growth and scalp health.

Wounded skin cells can revert to stem cells and help heal.

Most COVID-19 patients in hospitals have androgenetic alopecia, more in men, suggesting a link between androgen sensitivity and severe COVID-19 symptoms.

New genetic locations explain much of hair color variation in Europeans.

Reducing Tyrosinase prevents mature color pigment cells from forming in mouse hair.

Immune cells in Hidradenitis suppurativa become more inflammatory and may be important for treatment targets.

New treatments for ichthyosis, like protein replacement and gene therapy, show promise and may become standard care.

Certain natural biostimulants can increase lettuce yield and improve its nutritional content.

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

Dihydrotestosterone treatment on 2D and 3D-cultured skin cells slows down hair growth by affecting certain genes and could be a potential target for hair loss treatment.

Fat tissue under the skin affects hair growth and aging; reducing its inflammation may help treat hair loss.

A patient with a rare disease had a unique genetic mutation linked to their symptoms.

A topical BRAF inhibitor, vemurafenib, can speed up wound healing and promote hair growth, especially in diabetic patients.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.