Search

everythinglearnresearchcommunity

for

Search:↓

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

Humans lost body hair relatively recently in evolution.

Hair, teeth, and mammary glands develop similarly at first but use different genes later.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

Four genetic risk spots found for hair loss, with WNT signaling involved and a link to curly hair.

People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

Hormones and their receptors, especially androgens, play a key role in hair growth and disorders like baldness.

Genetics play a role in acne, but how exactly they contribute is not fully understood.

Early onset hair loss linked to genetics and androgen levels.

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

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

Cavity macrophages gather on organ surfaces but don't really invade or help repair the organs after injury.

The document concludes that PCOS has a strong genetic component, but more research is needed to fully understand the specific genes involved.

Genetic counselors should be culturally skilled and aware of transgender patients' unique health risks and needs.

Monotreme hair structure and protein distribution are similar to other mammals, but their inner root sheath cornifies differently, suggesting a unique evolution from reptile skin.

Certain genetic differences may affect how likely someone is to get COVID-19 and how severe it might be.

Certain mutations in the PADI3 gene may increase the risk of developing a type of scarring hair loss common in women of African descent.

The EDAR gene mutation leads to thinner and more deformed hair shafts.

A genetic variant in the androgen receptor gene increases heart disease risk in women but not in men.

Different types of Armillaria fungus have a high genetic variety when partnering with Polyporus umbellatus mushrooms in China.

The structure of SRD5A reveals how it reduces steroids, aiding drug design for related health conditions.

Genetic mutations can affect female sexual development, requiring personalized medical care.

Human skin has multiple layers and functions, with key roles in protection, temperature control, and appearance.

Changing protein kinase levels in pituitary cells affects calcium flow and beta-endorphin release.

A genetic mutation in the LIPH gene causes tightly curled hair that stops growing in some Japanese individuals.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

Scientists made the first metal-based compounds from a nonsteroidal antiandrogen drug, which showed potential in fighting both hormone-dependent and independent prostate cancer cells.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

Endo-HSE helps grow hair-like structures from human skin cells in the lab.

Finasteride irreversibly affects human steroid 5α-reductase 2, providing insight into its catalytic mechanism and disease-related mutations.