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Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

AP-2α and AP-2β proteins are essential for healthy adult skin and hair.

One twin girl has Loose anagen syndrome with poorly anchored hair, diagnosed with a simple hair pull test, while her identical twin does not have the condition.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

Hair diversity is influenced by complex genetics and environmental factors, requiring more research for practical solutions.

The conclusion is that managing hair loss conditions like FFA and melanoma requires individualized approaches, considering new findings and balancing treatment benefits with potential risks.

Netherton Syndrome is a non-treatable genetic disorder in children causing skin, hair, and allergy issues.

People with Down syndrome are more likely to experience hair loss, and using dermoscopy can help diagnose it.

Early signs of PCOS in girls, like irregular periods and polycystic ovaries, suggest a need for early diagnosis and intervention to prevent further health issues.

The study found that certain genes are important for hedgehog skin appendage development and immunity, with spines possibly evolving for protection and infection resistance.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

S100A3 protein is crucial for hair shaft formation in mice.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

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

Gene linked to common hair loss found, may lead to new treatments.

Gene regulation could revolutionize hair color by altering pigmentation from within.

Haplogroup X found in Altaian population supports Amerindian origin.

Minoxidil foam helps hair growth by increasing good proteins and decreasing bad pathways in men with hair loss.

No clear link between specific gene and hair loss in Mexican brothers.

Gene variation affects prostate issues and hair loss.

Stem cell offspring help control their parent stem cells, affecting tissue health, healing, and cancer.

The TGM3 gene's promoter region is key for skin and hair cell function and may aid gene therapy.

Aromatase gene variation may increase female hair loss risk.

Fadrozole and finasteride change gene expression related to sex hormones and thyroid hormones in frog larvae development.

Men with a family history of hair loss are more likely to experience it themselves, especially if both parents have hair loss.

Using a gene therapy with the Sonic Hedgehog gene helps mice regrow hair faster after losing it from chemotherapy.

Genetically-altered adult stem cells can help in wound healing and are becoming crucial in regenerative medicine and drug design.

KFSD is a genetic disorder causing hair loss and skin issues, with no effective treatment.

Signaling pathways are crucial for hair growth in goats.

Sp6 promotes tooth development by reducing follistatin levels.