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Some vitamin D analogs can thicken skin and reduce pore size like a common acne treatment, with one analog also affecting skin growth factors.

A mutation in the hairless gene speeds up severe itchy skin in mice on a special diet.

A 2-year-old girl with a rare vitamin D disorder had rickets and hair loss, but treatment was ineffective due to poor compliance.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.

Three siblings with a rare genetic condition had abnormal sexual development and chose different gender identities, needing surgery and therapy.

A gene network led by RSL4 is crucial for early root hair growth in response to cold in Arabidopsis thaliana.

PRC2 is essential for maintaining intestinal cell balance and aiding regeneration after damage.

PX-12 may help treat psoriasis by blocking inflammation and cell death.

A boy with a rare skin condition and kidney disease improved with cyclosporine after steroids failed, suggesting a new treatment approach.

EREG therapy may help treat hair loss by promoting hair growth.

Activating liver X receptors can reduce fibrosis by stopping certain immune cells from releasing harmful proteins.

High flux X-ray beams quickly damage the structure of human hair.

ARQ-234, a protein designed to treat atopic dermatitis, shows increased effectiveness in early testing.

ROR-alpha may increase the growth of certain breast cancer cells by boosting aromatase, which could affect breast cancer prognosis.

NEDD4 and NEDD4L help control intestinal stem cells and prevent tumors by breaking down the LGR5 receptor.

SMR-2 and SMR-6 are much more toxic than retinoic acid, causing severe symptoms and organ damage in mice.

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

SRD5A2 gene variations affect PTSD symptoms differently in males and females.

Increasing Rps14 helps grow more inner ear cells and repair hearing cells in baby mice.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

Female rats showed more panic-related behavior than males, influenced by hormonal cycles and certain drugs.

Aromoline and DRD4 are potential targets for osteoarthritis treatment.

Finasteride inhibits enzyme activity in rhesus macaques, suggesting they're useful for evaluating similar drugs.

The vitamin D receptor is crucial for bone health and affects various body systems, with mutations potentially leading to disease.

Recognizing RSCC is crucial due to its aggressive nature and high risk of poor outcomes.

The infant was diagnosed with Rothmund-Thomson syndrome, a rare genetic disorder causing various physical and developmental issues.

Early and accurate diagnosis is crucial for managing rare genetic disorders like this localized variant of junctional epidermolysis bullosa.

Scientists found new genetic areas that affect how rice root hairs grow and develop.