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Researchers developed a cost-effective 66 K SNP chip for cashmere goats that is accurate and useful for genetic studies.

A woman with both Cronkhite-Canada syndrome and myelodysplastic syndrome improved significantly with corticosteroid treatment.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

The ACE1 gene variant doesn't affect long-COVID symptoms.

MX1 and AR genes are linked to milder COVID-19, while TMPRSS2 increases severe risk, especially in women.

pCLCA2 protein may help maintain skin structure and function.

The CORT, FGF5, and CD36 genes are crucial for the cold weather adaptation of Yanbian cattle.

Specific gene variants affect wool traits in Chinese Tan sheep.

Genetic variants in specific genes cause central centrifugal cicatricial alopecia.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

The KRTAP13-3 gene affects wool fibre diameter variability in Chinese Tan sheep.

UC.145 may be a new biomarker for predicting gastric cancer.

Cepharanthine may help treat gastric cancer by causing cancer cell death and affecting energy use.

CCCA can occur in children and needs early diagnosis to prevent permanent hair loss.

Metastatic cervical cancer can cause rare, severe Cushing's syndrome with high risk of death.

The rs231775 genetic variant is linked to a higher risk and severity of Alopecia Areata in males.

CXXC5 is a protein that controls cell growth and healing processes, and changes in its activity can lead to diseases like cancer and hair loss.

The document confirms the structures of major metabolites of the CRTh2 antagonist Setipiprant and identifies minor metabolites.

Scientists made a carbon-14 labeled version of a drug with a 48% yield and over 99% purity.

Cronkhite-Canada syndrome can cause multiple gastrointestinal polyps and various physical symptoms.

Cyclic ADP-ribose helps regulate calcium and signals that promote hair growth in hair follicle cells.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

Connexin-26 gene mutations may increase cancer risk in KID syndrome patients.