Search

everythinglearnresearchcommunity

for

Search:↓

Long-term diabetes, smoking, and poor blood sugar control increase the risk of artery disease in diabetic retinopathy patients.

Vav2 changes how hair follicle stem cells' genes work as they age, which might improve regeneration but also raise cancer risk.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

Dextroamphetamine may help treat alopecia areata.

A specific group of early-stage melanocytes is reduced in vitiligo-affected skin, which may explain treatment resistance.

Removing vitamin D and calcium receptors in mice skin cells slows down skin wound healing.

Variants in the CCDC47 gene are linked to trichohepatoneurodevelopmental syndrome.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

Injecting specific cells into the skin can help improve skin structure and reduce blisters in a genetic skin disorder.

An 11-year-old girl with a rare skin disorder also had cornea issues and dry eye, needing careful management.

ESR2 gene linked to female-pattern hair loss.

DKK2 and SOSTDC1 together are necessary for the normal timing of the first regression phase in the hair growth cycle.

TTD symptoms vary widely, requiring thorough evaluations.

A small group of slow-growing cells causes basal cell carcinoma to return after treatment.

As skin cells mature, vitamin D receptor levels decrease while retinoid X receptor α levels increase.

A deep learning model was developed to help diagnose trichothiodystrophy by analyzing hair patterns.

A black-skinned woman was diagnosed with Vogt-Koyanagi-Harada disease and treated with steroids and eye drops.

The study suggests certain ACE gene variations are more common in women with PCOS and may be linked to increased insulin resistance.

Mutations in the DSG4 gene cause a severe form of brittle hair and skin issues.

Cannabidivarin (CBDV) may help brain cell growth and survival through the TRPV1 receptor.

Two new enzymes, PAD-R11 and PAD-R4, were cloned and showed activity, with PAD-R11 resembling epidermal enzymes.

Woman with diabetes had hair loss due to rare ovarian tumor; surgery improved hair growth.

A patient with total hair loss developed vitiligo after using a treatment called DCP.

Airway issues can occur in Conradi–Hünermann–Happle syndrome and can be managed with minimally invasive procedures.

Vorasidenib can cause unusual hair growth.

A child with trichothiodystrophy also had autoimmune thyroiditis and anemia, which is a new finding.

Genetic analysis is crucial for diagnosing and managing cerebral arteriopathy.

Papular acantholytic dyskeratosis of the vulva is a rare, benign skin condition that can be managed conservatively.

A woman's hair loss during Hepatitis C treatment with PEG-INF-a-2a and Ribavirin was reversible after stopping the medication.