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Genes related to keratin, skin cell differentiation, and immune functions are key in hedgehog skin and spine development.

Newborn screening and gene therapy are expected to improve outcomes for Omenn syndrome patients.

Afro-textured hair is more fragile and prone to certain scalp conditions, requiring careful treatment and more research for effective management.

Nuclear shape and chromatin changes affect gene expression in skin cell differentiation.

NAC1 controls certain enzymes that reduce root hair growth in Arabidopsis.

The study found that giant pandas have more melanin in black hair follicles than white, with gene expression differences that could affect hair color and skin health.

Understanding hair surface properties is key for effective hair care products.

Pets in Egypt can pass skin fungus, especially Microsporum canis, to humans, with outdoor and young pets being more at risk.

Hidradenitis Suppurativa is a chronic skin condition best treated early with surgery for better outcomes and less recurrence.

Electrospun matrices help regenerate skin and hair follicles using PCL and collagen scaffolds.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

The document concludes that new treatments for hair loss may involve a combination of cosmetics, clinical methods, and genetic approaches.

Metreleptin treatment significantly improved metabolic health in a boy with congenital generalized lipodystrophy.

Skin aging reflects overall body aging and can indicate internal health conditions.

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

Long COVID causes various long-term health issues and needs better awareness and treatment.

New insights into cell communication in psoriasis suggest innovative drug treatments.

Androgens and androgen receptors are important for metabolic health, affecting how the body uses glucose and fats through mitochondrial function.

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

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

JAGGED1 could help regenerate tissues for bone loss and heart damage if delivered correctly.

SLFC can improve scalp health and reduce sensitive scalp symptoms.

Targeting IL-17 could help treat pattern hair loss.

Vimentin and transthyretin proteins are linked to black coat color in sheep.

The study aims to create a model to improve personalized and preventive health care.

Blocking IL-17 can reduce skin inflammation in a mouse model of pityriasis rubra pilaris.

Certain genetic variations in IL-16 may increase the risk of alopecia areata.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

A group has developed therapies that show promise for treating cancer and various other conditions.