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Genetic testing can help diagnose skin conditions but needs more research for full effectiveness.

Passiflora incarnata may help with anxiety and sleep issues but has side effects; teleconsultation for heart failure can improve quality of life; increased screen time for children during the pandemic led to more clinical complaints; older and severely affected COVID-19 patients are more likely to have long-term symptoms.

The first Japanese family with Marie Unna hereditary hypotrichosis showed hair condition improvement in a child and highlighted the risk of misdiagnosis.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

Rhodococcus equi causes severe pneumonia in young foals, and effective vaccines are needed due to foals' weak immune responses.

The research found how GPCR Class A Rhodopsin receptors are related and suggested possible substances they interact with.

Targeted cancer therapies have a significant but lower risk of causing hair loss compared to chemotherapy.

Two siblings with a genetic mutation had a form of rickets that doesn't respond to vitamin D.

Certain cells in the adult mouse ear come from cranial neural crest cells, but muscle and hair cells do not.

Keratin-associated proteins have ancient origins and were used for different purposes before being adapted for hair in mammals.

The document concludes that better targeted treatments are needed for wound healing, and single-cell technologies may improve cell-based therapies.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

Scientists found gene mutations that affect hair loss, skin stem cells, and skin disorders, and identified drugs that may help treat blood vessel and skin conditions.

Dabrafenib was effective and well tolerated in treating thyroid cancer with a specific mutation.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Nagashima-type palmoplantar keratosis in Asians is caused by a SERPINB7 gene mutation.

Researchers found eight natural compounds and essential oils in the Italian plant Bituminaria basaltica, which are typical for its genus and known for bioactivity.

Not having enough cystatin M/E protein causes less hair growth and dry skin.

Melanoma risk tools need improvement, certain gene mutations cause skin diseases and could be treated by targeting those mutations, skin wrinkling may relate to lung aging due to genetic factors, and oxidative stress affects hair loss but can be reduced in low oxygen.

The document concludes that rapid identification, isolation, and strict infection control are crucial to manage SARS outbreaks.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

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

This is the first known case of parathyroid cancer in a patient with Birt Hogg Dube Syndrome.

Blocking IL-17 can reduce skin inflammation in a mouse model of pityriasis rubra pilaris.

Darier-White disease causes skin and nail issues, starts around age 20, worsens until 40-50, and has poor treatment options.

CK 5/6 expression in breast cancer is linked to negative hormone receptor status and higher tumor grade.

CDP is crucial for lung and hair follicle cell development.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.