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The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

Skin reactions to drugs are common and can be deadly, usually requiring stopping the drug and may be better prevented with genetic testing in the future.

Biotin supplements improved skin and hair problems in a girl with biotinidase deficiency.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

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

Mutations in the CYP21A2 gene are not a major factor in causing PCOS.

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

The conclusion is that accurately identifying folliculosebaceous tumors requires understanding their clinical signs and microscopic features.

Two gene variations, rs6493497 and rs7176005, may be linked to female hair loss in Chinese people.

Certain bacteria can boost lentil growth and improve soil used for farming.

Adding yeast extract and methyl jasmonate to Eclipta alba cell cultures increased the production of the compound wedelolactone.

Environmental factors like diet and vitamin levels, especially Vitamin D, can affect autoimmune diseases differently, with lifestyle changes potentially improving outcomes.

Women with congenital adrenal hyperplasia (CAH) have more sexual function issues than those with polycystic ovary syndrome (PCOS), but physical activity can improve sexual functioning in all women.

Genetic differences within ethnic groups may affect prostate cancer treatment effectiveness.

The most different genetic segment between Africans and East Asians is the EDA2R/AR region, with two main types influenced by population changes and natural selection, and linked to baldness.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Harlequin mutant mice have hair loss due to low AIF protein levels and retroviral element activity.

The research reveals how early embryonic mouse skin develops from simple to complex structures, identifying various cell types and their roles in this process.

Vav2 and Vav3 proteins help control skin stem cell numbers and activity in both healthy and cancerous cells.

The article concludes that studying how skin forms is key to understanding skin diseases and improving regenerative medicine.

The Wnt signaling pathway is not a major factor in the development of keratoacanthoma, a type of skin tumor.

The KRTAP7-1 gene is very similar across different cattle and yak breeds and likely plays a role in hair strength and shape.

Henna has potential health benefits and can treat various conditions, but more research is needed to confirm safety and effectiveness.

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

NAC1 controls certain enzymes that reduce root hair growth in Arabidopsis.

Pangolins have lost some skin-related genes, but kept others, showing complex skin evolution.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.