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Topiramate impairs gene transmission in zebrafish, while Ginkgo biloba reduces harmful effects of high β-catenin levels.

Diagnosing and managing monilethrix is harder when it occurs with other hair loss conditions.

Diagnosing and managing monilethrix is harder when it occurs with other hair loss conditions.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

The secretome from mesenchymal stem cells is a promising treatment that may repair tissue and avoid side effects of stem cell transplantation.

Exosomes have potential in skin treatments but need more research and are only used topically in the U.S.

Advancements in reproductive technologies for carnivores help conserve species and offer insights into human reproductive issues.

Hair loss in certain young mice is linked to a specific gene and can be caused by lack of iron.

Hair fiber research combines multiple sciences to improve hair care products.

NIPT can help detect potential maternal cancer, and GIPXplore can identify immune diseases in pregnancies.

A mother's diet at conception can cause lasting genetic changes in her child.

Prenatal genetic diagnosis may not predict MELAS syndrome severity in offspring.

Older parental age, rural living, and specific genetic mutations increase hypospadias risk in children.

CD28 is a promising target for treating alopecia areata with belatacept.

CD28 is a promising target for treating alopecia areata with belatacept.

The new model helps understand and develop treatments for genetic skin disorders like AEC.

The number of CAG repeats in the androgen receptor gene doesn't significantly affect female pattern hair loss in the Han Chinese population.

Exposure to too much androgen before birth might cause polycystic ovary syndrome later in life.

Different genes cause Female Pattern Hair Loss compared to male hair loss, and treatments vary, but more research is needed to understand it fully.

Polyelectrolytes can improve cell surfaces for better medical applications.

Mutations in mitochondrial DNA might significantly contribute to the development of Polycystic Ovarian Syndrome.

Both genes and environmental factors like chemicals may contribute to the increase in hypospadias, but the exact causes are still unclear.

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

New methods to improve the healing abilities of mesenchymal stem cells for disease treatment are promising but need more research.

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

Half-siblings with a rare skin condition improved with treatment for a fungal infection, but hair loss remained.

Testosterone therapy in transgender men can lead to hair loss, with the risk increasing over time and influenced by family history.

Cutaneous lupus erythematosus is a chronic skin disease that can progress to systemic lupus in some cases and requires treatment to prevent recurrences and scarring.

Both gene and non-gene areas of DNA evolved to make some mammals hairless.

Hair root sheaths can be used to accurately analyze genetic markers.