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Androgen is important in controlling stem cell differentiation, reducing fat development, and increasing lean mass.

TCDD speeds up skin barrier formation by increasing certain gene expressions.

New LPA receptors (LPA4, LPA5, LPA6) have diverse roles in the body.

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

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Finasteride reduces Tourette syndrome symptoms, but results may be limited due to potential biases.

Finasteride may help reduce symptoms in male Tourette syndrome patients.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in patients with Tourette syndrome.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

A boy with a rare skin condition and kidney disease improved with cyclosporine after steroids failed, suggesting a new treatment approach.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Relatives of women with PCOS symptoms are more likely to have similar health issues.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in Tourette syndrome patients.

Finasteride may help reduce tic severity in male Tourette syndrome patients.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

The document concludes that the 5 alpha-reductase enzymes are important in steroid metabolism and related to various human diseases, with inhibitors used to treat conditions like male pattern baldness and prostate issues.

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

New treatments for male hair loss show promise but need more research for safety and effectiveness.

A mutation in the Adam10 gene causes freckle-like spots on Hairless mice.

A new mutation in the AGPAT2 gene causes severe fat tissue loss and related health issues by reducing the protein's levels.

Women with hair loss have more androgen receptors in certain hair follicles.

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

Deleting the Trf1 protein in mice is safe and may help prevent cancer without major side effects.

KLF4 is important for maintaining stem cells and has potential in cancer treatment and wound healing.

Hair follicle sampling is a feasible method to measure FMRP and FMR1 mRNA levels in children.

WNT10B is linked to cancer development and affects survival and disease progression in various cancers.

The conclusion is that the nuclear lamina and LINC complex in skin cells respond to mechanical signals, affecting gene expression and cell differentiation, which is important for skin health and can impact skin diseases.

K_ATP channel gene mutations are linked to heart diseases, but more research is needed to understand the connection and treatment potential.

The document concludes that early diagnosis and treatment of Congenital Adrenal Hyperplasia are crucial for preventing serious health issues and improving patient outcomes.

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.