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Bacteria in our hair can affect its health and growth, and studying these bacteria could help us understand hair diseases better.

Aging causes skin stem cells to work less effectively.

Platelet-rich Plasma Gel may help treat en coup de sabre scleroderma, improving symptoms and skin quality with minimal side effects.

The EDAR gene mutation leads to thinner and more deformed hair shafts.

Chemicals and body size might change when puberty starts and progresses, but more research is needed to confirm this.

ATP-dependent chromatin-remodeling complexes are crucial for gene regulation, cell differentiation, and organ development in mammals.

Women with polycystic ovary syndrome tend to have a longer distance between the clitoris and anus.

Engineered skin substitutes can grow hair but have limitations like missing sebaceous glands and hair not breaking through the skin naturally.

Retinoids increase steroid sulfatase activity in leukemia cells through RARα/RXR and involves certain pathways like phosphoinositide 3-kinase and ERK-MAP kinase.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

Indian jujube has many medicinal properties and can help treat ailments like diabetes, inflammation, and cancer.

Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.

The study identified a key protein involved in producing underarm odor and found ways to inhibit it.

Finasteride, a hair loss drug, may cause long-term sexual side effects due to changes in hormone receptor levels.

The study found that alopecia areata and hypothyroidism increase the risk of each other, but androgenetic alopecia and hypothyroidism do not.

Researchers created a mouse model of a type of rickets that does not cause hair loss.

Mice without the vitamin D receptor have bone issues and other health problems, suggesting vitamin D is important for preventing various diseases in humans.

Removing the ATR gene in adult mice causes rapid aging and stem cell loss.

The HR protein helps hair grow by blocking a hair growth inhibitor, aiding in hair follicle regeneration.

A mutation in the EDNRA gene causes Oro-Oto-Cardiac syndrome, affecting face and heart development.

Genetic factors affect hair loss, and molecular testing may help predict, diagnose, and treat it.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

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

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

The conference presented findings on how vitamin D levels, genetic factors, and lifestyle choices like smoking and yoga affect various health conditions and diseases.

Melanocytes produce melanin; their defects cause vitiligo and hair graying, with treatments available for vitiligo.

Wild African goats have genetic adaptations for surviving harsh desert conditions.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

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