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Certain gene variants in estrogen receptors are linked to polycystic ovary syndrome, mainly affecting metabolism, in Tunisian women.

FGF10 and non-coding RNAs are important for cashmere goat hair follicle development.

The conclusion is that obesity should be managed with a slow, balanced approach to diet and exercise, with medication and surgery as additional options, and education and access to care are important.

Eph receptors and ephrins may be promising targets for treating diseases, but more understanding is needed for effective and safe therapies.

Androgenetic alopecia is mainly caused by genetic factors and increased androgen activity, leading to hair follicle miniaturization.

AGA is caused by genetics and androgens, treatable with finasteride and minoxidil.

Genes and hormones cause hair loss, with four genes contributing equally.

A person with Turner Syndrome showed severe schizophrenia that didn't respond to treatment and had brain shrinkage.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

Men have worse COVID-19 outcomes than women due to genetic and hormonal differences.

Society's pressure to have children later in life favors genes that increase the risk of early baldness in male offspring.

Genes play a significant role in male-pattern baldness, and understanding them could lead to new treatments and insights into related health issues.

Environmental factors like smoking, UV exposure, and poor diet contribute to hair loss and graying, and lifestyle changes can help manage it.

Longer GGN repeats in the androgen receptor gene are linked to polycystic ovary syndrome.

Dermatologists give better information on pathology forms, hypersensitivity vasculitis is a common skin issue, misdiagnoses can occur, and various skin conditions are linked to loss of elastin or genetic factors.

Certain genes and X chromosome patterns may significantly contribute to the development of hair loss.

A complex X chromosome rearrangement can increase the risk of multiple autoimmune diseases.

A 6-year-old girl with Turner syndrome also had psoriasis, alopecia areata, and trachyonychia.

Certain gene variations and irregular X chromosome activity may contribute to hair loss in women who can have children.

A woman with acromegaloidism and normal growth hormone levels had a rare X-Tetrasomy, suggesting a need to study X-chromosome genes for their role in growth and facial development.

Keratosis Follicularis Spinulosa Decalvans is a rare genetic disorder causing skin and hair issues, often inherited through the X chromosome.

Loss of the Y chromosome and UTY gene activity increases cancer risk in men.

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

Male pattern baldness is partly caused by specific genes, but most genetic factors are still unknown.

FGF13 gene changes cause excessive hair growth in a rare condition.

Hair loss gene found on chromosome 3q26.

Steroid sulfatase is important for activating hormones that affect memory, brain function, and certain diseases, and could be a target for treating hormone-related disorders.

Protoporphyrin IX is useful in cancer treatment but can cause health problems if not properly regulated.

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

Ectodermal dysplasia causes various symptoms and early treatment is important for eye, dental, and skin issues.