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A woman's progressive hair loss was correctly diagnosed as a rare condition called fibrosing alopecia in a pattern distribution after initially being mistaken for a more common type.

FERONIA is crucial for plant growth, pollen tube reception, and sugar signaling.

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

DNAJB9 cfRNA could help diagnose and treat female hair loss.

Some congenital hair disorders improve in childhood or with treatments like minoxidil and retinoids, while others like Netherton syndrome and trichothiodystrophy have a poor prognosis.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

Zinc, copper, and vitamin A deficiencies cause skin disorders in sheep.

Kidney cancer cells without folliculin are more sensitive to radiation due to increased self-eating cell death.

A new severe form of monilethrix syndrome includes hair loss, scalp itching, cataracts, and distinct facial features.

Dermoscopy helped diagnose a rare hair disorder in a 2-year-old boy.

A new gene mutation causes a rare type of hair loss.

The model helps test drugs for clubfoot fibrosis by mimicking cell environments and shows minoxidil reduces harmful collagen links.

Alpha-difluoromethylornithine prevents cancer in mice but causes hair loss.

A genetic mutation caused severe rickets and alopecia in an Indian patient, but high-dose calcium and phosphate treatment improved their condition.

Excessive iodine from a cystic fibrosis supplement can cause hypothyroidism.

Intermediate filaments are crucial for cell structure and function, regulated by specific genes and proteins.

Familial dyskeratotic comedones are a rare, inherited skin condition that is hard to treat but may improve slightly with topical retinoids and urea cream.

The Lanceolate hair-J mutation in mice mimics human hair disorders like Netherton's syndrome.

Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.

KIF18B is important for correctly positioning cell division machinery in skin cells, affecting hair follicle development.

Copper therapy improved health and enzyme activity in mice with copper deficiency.

Enzyme replacement therapy may help alleviate symptoms in complex cases like this.

CF patients with growth issues have more zinc in their hair than those with normal growth.

FGF5 spliceosomes inhibit rabbit hair growth by affecting gene expression.

A baby girl has a hair disorder called monilethrix, causing fragile hair that may improve over time.

ILK is essential for skin development, pigmentation, and healing.

Genetic testing can help diagnose skin conditions but needs more research for full effectiveness.

GTL1 is needed to control root hair growth and prevent problems when there are too many nutrients.

Removing the ATR gene in adult mice causes rapid aging and stem cell loss.