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Increased HIF-1α is linked to the inflammation and severity of hidradenitis suppurativa, suggesting treatments that lower HIF-1α could help.

The document reports three sisters with Woodhouse-Sakati syndrome showing typical symptoms and unusual gynecological anomalies.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

Both classical and L-type atypical BSE from cattle can infect goats with different incubation times, and tests can distinguish between the two strains.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in Tourette syndrome patients.

Finasteride may help reduce tic severity in male Tourette syndrome patients.

Ellis van Creveld syndrome, a rare genetic disorder, can cause unexpected abnormalities in various body organs, requiring thorough patient evaluations.

Elkonyxis, a rare nail condition, improved when patients stopped their nail-picking habits.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

Androgens, like DHT, affect hair growth and treatments like finasteride may help.

Chronic inflammatory skin diseases are caused by disrupted interactions between skin cells and immune cells.

A woman's long-term scalp issues were diagnosed as a rare skin disorder called cutaneous Langerhans cell histiocytosis.

Young HS patients often have other physical and mental health issues, and research on HS covers a wide range of topics including genetics, triggers, treatments, and the need for more data.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

Finasteride effectively treats hair loss and enlarged prostate in men, with mild side effects.

The conclusion is that analyzing RNA from skin oils is a promising way to understand skin diseases.

The Wnt signaling pathway is not a major factor in the development of keratoacanthoma, a type of skin tumor.

Certain gene variations in EGF and EGFR may increase the risk of alopecia areata in Koreans.

Newborn screening and gene therapy are expected to improve outcomes for Omenn syndrome patients.

The congress highlighted new gene therapy techniques and cell transplantation methods for treating diseases.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

The document explains the genetic causes and characteristics of inherited hair disorders.

Most adrenal cortex tumors are benign and non-secreting, but proper diagnosis and treatment are important due to the rare possibility of cancer.

Bexxar treatment led to a high response rate in patients with advanced-stage, treatment-resistant follicular lymphoma.

Exosomes show promise for future tissue regeneration.

Certain genetic variants linked to immune response increase the risk of alopecia areata in Taiwanese people.

A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

Metreleptin treatment significantly improved metabolic health in a boy with congenital generalized lipodystrophy.

Scientists made a sensor that can detect a specific type of RNA related to androgen receptors quickly and accurately.