Search

everythinglearnresearchcommunity

for

Search:↓

A possible link exists between minimal change nephrotic syndrome and complete hair loss.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

Platelet-rich plasma can potentially promote hair growth by stimulating cell growth and increasing certain proteins.

Hair color loss can indicate the effectiveness of a drug targeting the KIT protein in mice and humans.

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

ALA-PDT is effective and safe for chronic X-ray dermatitis, providing complete or partial remission.

Removing integrin α3β1 from hair stem cells lowers skin tumor growth by affecting CCN2 protein levels.

Guasha changed rat skin appearance and blood vessels temporarily without affecting certain nerve proteins or fiber structure.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

Chronic Telogen Effluvium is a hair loss condition in middle-aged women that usually doesn't lead to complete baldness.

Mice without the IL-6 gene had more hair growth after injury due to higher activity of a related protein, Stat3.

A 17-year-old female with adrenogenital syndrome produces very high levels of androgens, which prevent complete feminization despite high estrogen doses.

Mongolian gerbils heal wounds differently than mice, with unique protein levels and gene expression that affect skin repair.

Researchers created early-stage hair-like structures from skin cells, showing how these cells can self-organize, but more is needed for complete hair growth.

Stopping forehead irritation and using hydrocortisone helped a man's skin, Martinique has lower melanoma rates, a man had an allergy to a specific antifungal, another had unexplained cysts, certain drugs can cause skin reactions without always being interrelated, a link between Fanconi anemia and a skin condition was suggested, high levels of a certain protein may play a role in a type of psoriasis, and there's a need to study the connection between scalp pain and hair loss.

Researchers found a new mutation causing total hair loss from birth.

Dihydrotestosterone increases the activity of an enzyme in pubic skin cells that converts testosterone to dihydrotestosterone.

New cells are added to the hair's dermal papilla during the active growth phase.

The document concludes that using specific tools and tests is essential for identifying the cause of hair loss and deciding on the right treatment.

Inhibiting AP1 in mice skin causes structural changes and weakens the skin barrier.

Hairless protein affects hair follicle structure by regulating the Dlx3 gene.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

Researchers found four genes that could help diagnose severe alopecia areata early.

Fresh plasma transfusions did not help treat Leiner disease in an infant.

The document concludes that ERBB2 mutations are common in extramammary Paget disease and may respond to systemic treatments like cancer immunotherapy.

Mice with a changed Hr gene lose and regrow hair due to changes in the gene's activity.

TGF-β is crucial for tissue repair and can cause diseases if not properly regulated.

The timing of when the gene Bmal1 is active affects aging and survival, with its absence during development, not adulthood, leading to premature aging.

Keratin proteins are increasingly recognized as important for cell health and are linked to many diseases.

Wnt signaling controls whether hair follicle stem cells stay inactive or regenerate hair.