Search

everythinglearnresearchcommunity

for

Search:↓

Applying minoxidil can help improve hair growth in people with hair loss caused by LIPH gene mutations.

New genetic mutations linked to rare skin disorders were found in three newborns.

Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.

Gluconolactone products can significantly reduce skin scaling in golden retrievers with ARCI.

The conclusion is that differentiating wound types in RDEB patients is important for clinical trials and understanding the disease.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

Pregnancies in a woman with the Donohue mutation were managed with genetic testing, resulting in three healthy infants.

Topical minoxidil may help treat a rare genetic hair condition with no fully effective treatments yet.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

Hairless mice lack fur due to a genetic mutation affecting skin response, not hormone issues.

Mutations in NIPAL4 cause skin issues by disrupting lipid layers, but some improvement is seen with topical treatment.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

Some people have genetic mutations that make them resistant to vitamin D, leading to rickets even with enough vitamin D intake.

A new mouse mutation causes skin and hair defects due to a gene change.

Targeted therapy with Ustekinumab significantly improved a skin condition called ILVEN, which is caused by mutations in the CARD14 gene.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

Melanoma risk tools need improvement, a gene mutation causes a hair disorder that might be treated by managing cell stress, a potential therapy for a skin-ear disorder involves blocking cell channels, skin wrinkling may indicate lung aging regardless of smoking, and oxidative stress might contribute to common baldness.

Melanoma risk tools need improvement, certain gene mutations cause skin diseases and could be treated by targeting those mutations, skin wrinkling may relate to lung aging due to genetic factors, and oxidative stress affects hair loss but can be reduced in low oxygen.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

Lipase H is important for hair follicle function and shaping hair fibers.

Woolly hair is a rare genetic condition with no effective treatments.

No consistent link between genotype and phenotype in 5-α-Reductase type 2 deficiency.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

An infant with complete hair loss was diagnosed with a genetic disorder affecting hair growth.

An 8-year-old girl has a rare genetic disorder causing complete, irreversible hair loss and skin bumps.