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WNT10A mutations often cause ectodermal dysplasias, with males showing more tooth issues than females.

Wharton’s Jelly stem cells from the umbilical cord improve skin healing and hair growth without scarring.

Men who start losing hair at age 30 may have a lower risk of prostate cancer.

Spironolactone harms fish reproduction and is more potent in fish than invertebrates, needing environmental monitoring.

The article concludes that global standardization in PCOS research is crucial for accurate diagnosis and understanding of the condition.

SIPHL1 from tomato enhances plants' response to low phosphate levels.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

IL16 gene variations may affect the risk of alopecia areata in Koreans.

White piedra, a rare fungal infection, was diagnosed in two women in a northern climate.

Hair diameter and curvature are mostly determined by genetics.

New genetic mutations causing hair loss were found in a Chinese family.

The UK's EDS National Diagnostic Service found that early diagnosis, lifestyle advice, and regular check-ups are crucial for managing vascular Ehlers-Danlos syndrome. A combination of losartan and bisoprolol can reduce vascular events, improving survival and quality of life.

The study identified key genes and pathways linked to hair disorders, aiding precision medicine.

Male-pattern hair loss is largely influenced by genetics, with key genes identified.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

The study found that diseases can be grouped by symptoms and that the accuracy of predicting disease-related genes varies with the data source.

The current methods for diagnosing polycystic ovary syndrome are too vague and may lead to misdiagnosis and problems in research.

CLE40 and CRN/CLV2 pathways have opposite effects on root growth in Arabidopsis.

Neuregulin3 affects cell development in the skin and mammary glands.

The study concludes that a genetic mutation in TFM mice leads to reduced androgen receptor activity, affecting the body's response to male hormones.

Lack of Vitamin D receptor changes skin structure and increases certain immune cells in the skin.

Four new cases of Bachmann-Bupp syndrome suggest potential for targeted treatment.

New DNA analysis and machine learning are advancing forensic science, improving accuracy and expanding into non-human applications.

Polycystic ovary syndrome (PCOS) lowers women's quality of life, especially mentally and socially, but nursing guidelines can improve their understanding of the condition.

Certain skin proteins can form anchoring structures without the protein AMACO.

DNA markers can predict physical traits for forensic use, but there are ethical and technical challenges.

The meeting highlighted the importance of genetic testing and multidisciplinary approaches in pediatric dermatology.

Ethnicity affects how polycystic ovary syndrome shows up in women, with white women having higher metabolic risks but less diabetes, and South Asian women showing more androgenic symptoms and being younger at presentation.

Overexpressing a specific enzyme in mice causes hair loss and female infertility.

Researchers identified genes linked to coat color, body size, cashmere production, and high altitude adaptation in goats.