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An imbalance between certain immune cells is linked to a chronic skin condition and may be influenced by obesity, smoking, and autoimmune issues.

Amenorrhea is when a woman doesn't have periods, with primary amenorrhea starting by age 15 or within five years of breast development, and secondary amenorrhea when periods stop for three months. It affects 3-4% of women not pregnant, breastfeeding, or in menopause, mainly due to polycystic ovary syndrome, hypothalamic amenorrhea, hyperprolactinemia, and ovarian failure.

Some stem cells in the body rarely divide, which could help create better treatments for diseases and aging.

Amenorrhea, or the absence of periods, should be evaluated by age 15 or within five years of early breast development, and is most commonly caused by conditions like polycystic ovary syndrome and hypothalamic amenorrhea.

Flightless I protein affects hair growth, with low levels delaying it and high levels increasing hair length in rodents.

New partnerships, clinical trials, and drug approvals marked progress in therapeutic delivery in July 2018.

Hair proteins in preschool children and their mothers could indicate developmental changes and health status.

Skin and nail problems like hair loss, dry skin, and fungal infections are common in people with long-term Type 2 Diabetes and can be prevented with good blood sugar control and foot care.

Genetic testing can help diagnose skin conditions but needs more research for full effectiveness.

The research provided new insights into the genetic factors contributing to hair loss and skin conditions by analyzing individual cells from the human scalp.

Genetic factors could lead to personalized treatments for hair loss.

Different human traits like skin color and hair type vary between populations due to genetic adaptations to the environment.

A mutation in mice causes hair loss and immune problems.

Sheep have a unique gene, KAP8-2, that humans don't have, which may affect wool properties.

Recent selection on immune response genes was identified across seven ethnicities.

Multi-omics techniques help understand the molecular causes of androgenetic alopecia.

The document concludes that careful design of genetic fate mapping experiments is crucial for accurate cell lineage tracing in mice.

PCOS has a strong genetic basis, but more research is needed to fully understand it.

Genetic analysis of rabbits identified key genes for traits like coat color, body size, and fertility.

Genetic factors affect hair loss, and molecular testing may help predict, diagnose, and treat it.

Certain genetic variants linked to immune response increase the risk of alopecia areata in Taiwanese people.

Certain gut bacteria may increase or decrease the risk of male pattern baldness.

Immune cells are essential for early hair and skin development and healing.

Genetic variants can affect valproic acid's effectiveness, side effects, and levels in epilepsy treatment.

Understanding the immune-related causes of Alopecia Areata has led to potential treatments like JAK inhibitors.

Genomic approach finds new possible treatments for hair loss.

DNA methylation is essential for skin and hair follicle development, and could be a target for treating skin diseases.

FGF9 controls which receptors it binds to through a process where two FGF9 molecules join, and changes in FGF9 can lead to incorrect receptor activation.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

The research provides a gene-based framework for hair biology, highlighting the Hippo pathway's importance and suggesting links between hair disorders, cancer pathways, and the immune system.