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Certain genes in Iranian sheep are linked to wool production and heat adaptation.

Frizzled 3 and Frizzled 6 together control the orientation of mouse hair follicles.

Hairless mammals have genetic changes in both their protein-coding and regulatory sequences related to hair.

Epidermolysis bullosa simplex causes easily blistered skin due to faulty skin cell proteins, leading to new treatment ideas.

Finasteride may cause lasting sexual and mental health issues, and genetic screening could help prevent them.

PCOS is a genetic disorder affecting women's reproductive health, with treatments focused on symptoms like insulin resistance and fertility.

Researchers found genes and genetic variants linked to sheep wool and skin wrinkles.

The workshop highlighted the genetic links and psychological impacts of hair loss and skin disorders.

Early diagnosis and genetic evaluation of ADULT syndrome are crucial to reduce stress and medical costs.

Scientists found gene mutations that affect hair loss, skin stem cells, and skin disorders, and identified drugs that may help treat blood vessel and skin conditions.

PCOS is caused by both genetics and environmental factors like diet and obesity.

Researchers found genes and microRNAs that control curly fleece in Chinese Tan sheep.

Transverse sections are better for non-scarring hair loss, vertical sections are better for lichen planopilaris, and either method works for other scarring hair loss types.

Exosome treatment safely increases hair density in male patients with androgenetic alopecia.

New findings explain how genetic changes, body clocks, and certain molecules affect tissue response to stress hormones.

Some human genetic markers work for genetic studies in pig-tailed and stump-tailed macaques, which can help in their conservation.

Scientists found new genetic areas that affect how rice root hairs grow and develop.

Atopic dermatitis may have genetic causes and can be treated with pharmacologic methods, glycerin creams, and controlling Staphylococcus aureus colonization.

The best animal model for studying male-pattern baldness is the stumptailed macaque, not rats or mice.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

Keratosis pilaris is often linked to genetic mutations and causes skin and hair abnormalities, regardless of those mutations.

No link found between specific genes and female pattern hair loss.

The chapter explains that there are many genetic skin disorders affecting skin cell formation, including both common and rare types.

The document concludes that understanding genetic mutations in the PI3K-AKT-mTOR pathway can lead to better diagnosis and treatment for certain genetic skin disorders.

The EDAR gene greatly affects hair thickness in Asian populations.

Nonclassic congenital adrenal hyperplasia is a genetic disorder causing hormone imbalances, affecting fertility and requiring personalized treatment.

The conclusion is that many small genetic variations influence claw disorders in cows, and using genomic selection could help reduce these disorders.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

The RapidHIT ID system can effectively get DNA profiles from hair roots with enough cells.

New treatments for male hair loss show promise but need more research for safety and effectiveness.