Search

everythingexperts & clinicslearnresearchcommunity

for

Search:↓

The skin produces and responds to thyroid-stimulating hormone, which is controlled by other thyroid-related hormones.

Telocytes have potential in therapy and tissue regeneration, but challenges in identification and cultivation remain.

A new gene mutation causes insulin resistance in a girl and her mother.

Blocking a key energy pathway in human hair follicles can trigger stress responses that stop cell growth.

Tigason improved hair growth in a boy with monilethrix without side effects.

The MTHFR C677T mutation may increase the risk of alopecia areata in the Turkish population.

The E413K mutation in the hHb6 gene causes monilethrix, a hair disorder, but doesn't show consistent symptoms.

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

A 12-year-old girl was diagnosed with monilethrix, a genetic condition causing fragile, beaded hair that breaks easily, with no effective treatment available.

Deleting the Trf1 protein in mice is safe and may help prevent cancer without major side effects.

New treatments for chronic central serous chorioretinopathy show promise in preventing permanent vision loss.

Cryptotanshinone may help treat postmenopausal osteoporosis and protect kidneys.

A specific gene mutation causes Olmsted syndrome.

Matriptase-2 helps control iron levels by suppressing hepcidin, and its deficiency can cause iron-deficiency anemia.

Netherton syndrome can cause severe dehydration, infections, and growth issues in infants.

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

A Japanese patient with a rare genetic disorder had a less severe case than others, suggesting other factors may affect symptoms.

Retinoids increase steroid sulfatase activity in leukemia cells through RARα/RXR and involves certain pathways like phosphoinositide 3-kinase and ERK-MAP kinase.

Targeting adipocyte-to-mesenchymal transition could help treat fibrosis.

Tranilast successfully treated a man's skin sarcoidosis when other treatments failed.

4-(Ethoxycarbophenyl) retinamide is much less toxic than other retinoids.

Two sisters had a rare hair condition without other usual symptoms.

The gene Endothelin 3 makes mice's fur darker by increasing pigment cells and pigment levels.

Giving dihydrotachysterol to mother rats caused skin hardening and bone issues in their babies through milk.

Trichohyalin in hair can trigger immune attacks in alopecia areata.

A specific gene mutation causes vitamin D resistance, but certain vitamin D analogs might help.

Tiger tail banding and hair abnormalities are reliable indicators for diagnosing trichothiodystrophy.