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Certain genes related to sulfur metabolism are more active during the growth phase of Cashmere goat wool, and melatonin might help this process.

iPSCs show promise for hair regeneration but need more research to improve reliability and effectiveness.

An adult woman with scalp infection recovered after antifungal treatment, with no return of symptoms.

Melanocytes are important for normal body functions and have potential uses in regenerative medicine and disease treatment.

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

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

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

Different genes cause Female Pattern Hair Loss compared to male hair loss, and treatments vary, but more research is needed to understand it fully.

Forensic DNA Phenotyping accurately predicts physical traits and is used in investigations, but needs more diverse population data for confirmation.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

Certain KIR genes in Indian SLE patients are linked to disease severity and could be biomarkers.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Mutations in the glucocorticoid receptor gene cause reduced sensitivity to glucocorticoids and may lead to poor response to treatment.

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

OsPHR2 gene causes excessive phosphate in rice shoots, affecting plant growth and root development.

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

The Wnt/β-catenin pathway is important for body functions and diseases, and targeting it may treat conditions like cancer, but with safety challenges.

Human hair is made up of different keratins, some strong and some weak, with specific types appearing at various stages of hair growth.

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

Different small areas within hair follicles send specific signals that control what type of cells stem cells become.

Acne is linked to complex skin microbe interactions, and new findings suggest microbiome-based treatments could be effective.

Epidermolysis bullosa simplex causes easily blistered skin due to faulty skin cell proteins, leading to new treatment ideas.

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.

Innate lymphoid cells help control skin bacteria by regulating sebaceous glands.

The risk of skin tumors becoming malignant depends on the specific skin cell type affected.

Two rare genetic diseases cause severe rickets in children due to defects in vitamin D metabolism.

Bariatric surgery can cause serious mineral deficiencies, requiring better patient education and monitoring.

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

CRH in the skin acts like the body's stress response system, affecting cell behavior and immune activity.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.