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The document concludes that pregnancy and cancer share immune evasion tactics, but more research is needed before using checkpoint blockade immunotherapy in pregnant cancer patients to avoid harm to the placenta.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

New single-cell analysis techniques are improving our understanding of stem cells and could help in treating diseases.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

Hair microscopy is useful for diagnosing hair disorders, but clear definitions are needed for accurate genetic analysis.

A gene in Arabidopsis thaliana, AtPRPL1, affects root hair length but not cell wall composition.

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

A genetic mutation in the LIPH gene causes tightly curled hair that stops growing in some Japanese individuals.

Innovative methods are reducing animal testing and improving biomedical research.

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

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

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

The research suggests that Tourette syndrome is linked to both brain signaling and immune system pathways.

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

Nonclassic adrenal hyperplasia is a genetic condition that can cause early puberty and fertility problems, treated with specific steroids.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

Cancer rates are increasing in developed countries, with estrogen, aging, low vitamin D3, and HPV infection as common causes.

Most clinicians follow discharge guidelines, many lupus patients don't use sunscreen regularly, dithranol is effective for psoriasis, biopsy methods should be based on lesion type, voriconazole may raise skin cancer risk, a new scale can help diagnose female hair loss early, and most melanomas may develop from existing moles.

Activating Notch signaling can kill basal cell carcinoma cells.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

Different miRNAs in Rex rabbit skin affect cell processes and hair growth.

Lower SMAD2/3 activation predicts more severe skin cancer.

FOXN1 is crucial for thymus development and immune response in Xenopus laevis.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

Scientists made a mouse model of a serious skin cancer by changing skin cells with a virus and a specific gene, which is similar to the disease in humans.

No consistent link between genotype and phenotype in 5-α-Reductase type 2 deficiency.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

Targeting colon cancer stem cells might lead to better treatment results.

Increasing olanzapine caused hair loss in a woman, which stopped after changing medication.