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Scientists created a long-lasting stem cell line from human hair that can turn into different skin and hair cell types.

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

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

Physical inactivity is a primary cause of many human illnesses.

Taiwanese women with PCOS experience different symptoms based on age, with younger women facing more hormone imbalances and older women dealing with more metabolic issues.

Different types of PCOS in Chinese Han women show varying levels of male hormone and metabolic issues.

A girl with Becker's nevus syndrome showed good improvement in breast development using spironolactone.

Mouse Scube3 affects teeth, tongue, vibrissae, and eye development, but not facial structure or limb growth.

Progranulin overexpression leads to shorter, thinner hair and increased cell death in mouse hair follicles.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

PNKP is essential for keeping adult mouse progenitor cells healthy and growing normally.

Low Vitamin D is common in people with Alopecia Areata, but its impact on the condition needs more research.

A litter of cats had a hair condition similar to a mouse mutation, leading to hair loss and abnormal hair and skin.

Women with PCOS and polycystic ovaries have higher male hormone levels and more insulin resistance, especially if they are overweight.

Blocking IL-17 signaling can delay skin aging and improve skin and hair health.

Electrospun matrices help regenerate skin and hair follicles using PCL and collagen scaffolds.

Acute leukemias with the Philadelphia chromosome may be biphenotypic, and identifying this is important for proper treatment.

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

Different people show different symptoms for genetic diseases because of how sensitive their bodies are to small changes in important factors.

A 15-year-old girl with no menstrual period was diagnosed with a genetic condition that makes her body unable to respond to male hormones, leading to female characteristics despite having male genetic makeup.

Different PCOS subgroups have similar metabolic features, but those without menstrual problems have milder issues.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

The 18-year-old girl likely has a condition called müllerian agenesis, which caused her to not have a uterus and experience no menstrual periods.

Androgen affects oil production and hair growth in the skin.

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

Hair follicles produce IL-7, which is essential for certain skin lymphoma cells to survive.

Girls with PCOS and menstrual disorders have notably higher androgen hormone levels.

Early over-expression of FoxN1 harms immune and skin development.

MPA increases cancer spread by boosting Eph A2 activity.

TGFα gene mutation in mice causes abnormal skin, wavy hair, curly whiskers, and sometimes eye inflammation.