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A patient with a new PLEC gene mutation showed symptoms of both muscular dystrophy and myasthenia gravis, which improved with steroid treatment.

Two mouse mutations cause similar hair loss despite different skin changes.

ILC1 cells contribute to hair loss in alopecia areata.

A new gene, mrp4, is found in mice and may play a unique role in hair follicle development in tails and ears.

mrp/plf-mRNA can indicate tumor-promoting effects in skin.

Nonionic liposomes are the best for delivering genes to skin cells.

Hair transplants can cause hair loss if done while lichen planopilaris is active; wait until it's inactive for two years and check with a scalp biopsy first.

Patients with the same vitamin D receptor mutation showed different symptoms due to other factors.

NGAL indicates abnormal skin cell differentiation.

The hairless mutant gene causes early hair loss and affects skin and thymus development in mice.

Lichen planopilaris in men often affects the scalp, eyebrows, arms, legs, and beard, with many having family members with hair loss.

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

Lysine carboxymethyl cysteinate (LCC) protects skin from UVB damage by activating autophagy.

Lichen planus on the scalp can cause scarring hair loss and has four main types.

Low-level laser therapy may reduce symptoms and increase hair thickness in lichen planopilaris patients.

Scientists found new and known long non-coding RNAs in mouse hair follicle stem cells that may be important for stem cell function and could be targets for cancer treatment.

Langerhans cells and melanocytes migrate to the skin and hair follicles during early human development.

GLI1 might protect against the start of skin cancer and is not linked to cancer severity.

New mutations in the VDR gene cause vitamin D-resistant rickets without hair loss.

New genes linked to ichthyosis were found, but there's still no cure; treatment options are improving.

SIPHL1 from tomato enhances plants' response to low phosphate levels.

848 genes related to fat and metabolism are less active in people with Central Centrifugal Cicatricial Alopecia.

Certain blood metabolites are linked to female pattern hair loss, with some increasing risk and others offering protection.

A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

Trametinib can effectively treat severe kaposiform lymphangiomatosis when other treatments fail.

FLCN helps control iron levels in cells.

A 73-year-old woman with Hypopigmented Mycosis Fungoides, a rare skin lymphoma, experienced disease progression despite treatment, emphasizing the need for ongoing monitoring.

A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

Targeting Lgr5+ stem cells and Wnt signaling may effectively treat hair loss.