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The conclusion is that young women with excessive hair growth should be quickly tested for hormonal issues and treated to improve their social well-being.

Two siblings have a rare genetic condition causing curly, coarse hair.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.

Chinese domestic goats have unique genetic traits due to domestication and geographic isolation.

Certain genetic markers linked to wool quality in Rambouillet sheep were identified, which can guide better breeding choices.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

Many treatments for hair loss lack proper testing and FDA approval, so their effectiveness is uncertain.

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

New method finds genetic links between Type 2 Diabetes and Prostate Cancer not seen before.

Changes in the HR gene have influenced hair growth and may lead to hair loss conditions in humans.

A patient with Werner syndrome showed a range of aging-like symptoms and metabolic issues, underscoring the need for early detection and treatment.

Minoxidil helps stabilize hair loss, increase density, and reduce shedding after hair transplant surgery.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Researchers found genes linked to feather growth speed in Shouguang chickens, highlighting two genes that might explain differences in feathering.

Minoxidil can increase hair density, speed up regrowth in transplanted hair, and slow down further hair loss, especially beneficial for women, young men with thinning hair, and those wanting to reconstruct the back of the scalp.

Different people show different symptoms for genetic diseases because of how sensitive their bodies are to small changes in important factors.

Male-pattern hair loss is largely influenced by genetics, with key genes identified.

Hormones and genes affect hair growth and male baldness.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

The 18-year-old girl likely has a condition called müllerian agenesis, which caused her to not have a uterus and experience no menstrual periods.

Mice are useful for researching human hair loss and testing treatments, despite some differences between species.

Hormones and genetics play key roles in male and female baldness, which can affect mental health and may be linked to other health issues.

Alopecia areata is likely an autoimmune disease with unclear triggers, involving various immune cells and molecules, and currently has no cure.

Some growth factors, while important for normal body functions, can cause diseases when not regulated properly.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

Neurohormones help control skin health and could treat skin disorders.

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.