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Environmental factors like diet and vitamin levels, especially Vitamin D, can affect autoimmune diseases differently, with lifestyle changes potentially improving outcomes.

The Rotterdam Study aims to understand various diseases in older adults.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

Cells in hair follicles help create fat cells in the skin by releasing a protein called Sonic Hedgehog.

Six new genetic regions linked to early hair loss also connect to Parkinson's disease and prostate cancer, possibly leading to new treatments.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

The IRS-2 Asp/Asp genotype may increase the risk of PCOS in Chinese women, especially if they are not obese.

Too much β-catenin activity can mess up the development of mammary glands and make them more like hair follicles.

Certain gene variants may contribute to high androgen levels in women with polycystic ovary syndrome.

Hair and skin can regenerate without bulge stem cells due to other compensating cells.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

HNG may help prevent the negative effects of chemotherapy on sperm production and white blood cell counts.

The review found no clear link between vitamin D receptor gene variations and polycystic ovary syndrome.

A gene called HDAC9 might be a new factor in male-pattern baldness.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

The conclusion is that genetic changes in the glucocorticoid receptor can lead to conditions affecting stress response, immunity, and metabolism, requiring personalized treatment.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

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

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

Certain mutations in the H6PD gene cause Cortisone Reductase Deficiency by affecting hormone production.

The report concludes that PCOS is mainly a condition of excess male hormones and its definition may change as new information is discovered.

Scientists made a mouse that shows how a specific protein in the skin changes and affects hair growth and shape.

Lower PPARγ levels and specific gene variations are linked to more severe Frontal Fibrosing Alopecia.

Men with more vanadium in their blood and who drink less soy milk are more likely to have hair loss.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

No strong genetic link to other skin conditions was found, but some genetic factors may make people more likely to get seborrheic dermatitis.

Blocking JAK/STAT pathways can help treat hair loss from alopecia areata.

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

Methotrexate side effects vary by race and sex.