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Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

Dermal fibroblasts have adjustable roles in wound healing, with specific cells promoting regeneration or scar formation.

GALT5 and GALT2 are important for plant growth and development because they help with protein glycosylation.

GmMAX3b gene in soybeans boosts nodulation and affects hormone levels.

GRHL3 is important for controlling gene activity in skin cells during different stages of their development.

Melanoma's complexity requires personalized treatments due to key genetic mutations and tumor-initiating cells.

Melasma's causes include genetics, sun exposure, hormones, and oxidative stress, and understanding these can help create better treatments.

Hormones during puberty increase certain receptors in the brain, and this change is influenced by estrogen levels.

The skin systems of jawed vertebrates evolved diverse appendages like hair and scales from a common structure over 420 million years ago.

The research showed how melanocytes develop, move, and respond to UV light, and their stem cells' role in hair color and skin cancer risk.

Keratin protein production in cells is controlled by a complex system that changes with cell type, health, and conditions like injury or cancer.

Keeping β-catenin levels high in mammary cells disrupts their development and branching.

New CRISPR/Cas9 variants and nanotechnology-based delivery methods are improving cancer treatment, but choosing the best variant and overcoming certain limitations remain challenges.

Softer hydrogels help wounds heal better with less scarring.

Certain gene variations in PITX2 are linked to a higher risk of male pattern baldness in Indians.

Identified genes linked to male-pattern baldness may help develop new treatments.

Genetic analysis of rabbits identified key genes for traits like coat color, body size, and fertility.

Arsenic exposure from contaminated water severely damages the skin, causing hair loss, pigmentation changes, irritation, and can lead to skin cancer.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

The Pemphigus Disease Area Index and Autoimmune Bullous Skin Disorder Intensity Score are the best tools for assessing pemphigus severity.

Skin cell behavior is influenced by the tightness of nearby cells, affecting their growth and development.

The research found that male pattern hair loss is mostly genetic and involves hair thinning due to hormonal effects and changes in gene expression.

Hair follicle stem cells are crucial for touch sensation and proper nerve structure in mice.

Lotion with fucoidan from brown seaweed improved skin and reduced allergy symptoms in mice with dermatitis.

Low oxygen areas help maintain and protect blood stem cells by using a simple sugar breakdown process for energy and managing their activity levels.

Fibroblasts are crucial for tissue repair and inflammation, and understanding them can help treat fibrotic diseases.

Activating c-Myc in skin causes rapid cell growth and changes, but these effects are reversible.

c-Myc activation in mouse skin increases sebaceous gland growth and affects hair follicle development.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.