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A 12-year-old girl in Saudi Arabia with Focal dermal hypoplasia showed skin and dental symptoms, highlighting the condition's variability and the need for personalized treatment.

People with Down's syndrome are more likely to have syringomas.

New treatments targeting specific genes show promise for treating keratin disorders.

5α‐reductase isozymes are crucial for prostate development and health, and targeting them can help prevent and treat prostate issues.

Semecarpus anacardium Linn. has many medicinal benefits.

Equisetum debile extract, especially the ethyl acetate type, may be a promising natural ingredient for anti-hair loss products.

Low-potency steroids can cause serious side effects in people with skin conditions like Netherton syndrome.

Gene therapy has potential as a future treatment for Hutchinson-Gilford progeria syndrome.

Nonclassic congenital adrenal hyperplasia is a genetic disorder causing hormone imbalances, affecting fertility and requiring personalized treatment.

Certain genetic variations are linked to increased androgen levels in PCOS, but more research is needed to understand these connections fully.

Proper control of β-catenin activity is crucial for development and preventing diseases like cancer.

lncRNA XLOC_008679 and gene KRT35 affect cashmere fineness in goats.

DNA methylation and long non-coding RNAs are key in controlling hair growth in Cashmere goats.

lncRNAs may regulate hair follicle development in Hu sheep.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

Testosterone therapy improved physical and social health in a male with 49,XXXXY syndrome.

Longer CAG repeats in gene linked to more severe hair loss in females.

Hairless HRS/J mice resist Bacillus anthracis skin infections due to high numbers of immune cells, not because they lack hair follicles.

Women with myotonic dystrophy might get diseases related to male hormones because their body tissues are extra sensitive to these hormones.

The document concludes that AFA should be considered in patients with acromegaly-like features but normal hormone levels, and more cases need to be identified to understand the condition fully.

The research reveals how early embryonic mouse skin develops from simple to complex structures, identifying various cell types and their roles in this process.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

A protein called FERONIA helps control root hair growth in response to cold and low nitrogen by activating nutrient-sensing pathways in a plant called Arabidopsis.

Hairless mammals have genetic changes in both their protein-coding and regulatory sequences related to hair.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

Keratin gene expression helps understand different types of skin cells and their development, and should be used carefully as biological markers.

Low-coverage sequencing is a cost-effective way to identify genes related to wool traits in rabbits.

The document does not determine if adults with aphallia are fertile.

Removing centrosomes from skin cells leads to thinner skin and stops hair growth, but does not greatly affect skin cell differentiation.

Goat skin changes with the seasons due to genes affected by daylight and hormones.