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Vitamin D receptor can control the hairless gene linked to hair loss even without vitamin D.

Hair thinning and loss in a girl with a rare metabolic disorder was linked to her condition.

A new mutation in the HR gene causes hair loss in a specific family.

The mouse hairy ears mutation causes longer ear hair due to changes in gene expression.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

Hair loss in certain young mice is linked to a specific gene and can be caused by lack of iron.

All-trans retinoic acid causes hair loss by increasing TGF-β2 in hair follicle cells.

Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.

Hyperandrogenism increases heart disease risk in premenopausal women, but this risk is linked to obesity in postmenopausal women.

Researchers found 71 genetic regions linked to male pattern baldness, which account for 38% of its genetic risk.

Autoimmune liver diseases are likely linked to certain skin conditions like vitiligo and psoriasis.

Different hair loss patterns may be linked to varying male hormone levels.

The 2003 consensus updated PCOS diagnosis criteria and linked PCOS to higher risks of diabetes and heart problems, recommending lifestyle changes to lower these risks.

Premature balding in some men may be linked to altered hormones, but it's not the male equivalent to polycystic ovary syndrome or metabolic syndrome.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

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.

A specific thyroid hormone resistance mutation may be linked to different types of hair loss.

These specific gene polymorphisms are not linked to Alopecia Areata in Egyptians.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

Keloid skin disorder involves abnormal fibroblast activation and immune response, linked to a group of genes including FGF11.

The conference concluded that understanding hair and nail disorders is important, iron deficiency may be linked to hair loss, and while some treatments for skin conditions are effective, they may have risks and high costs.

Scalp involvement is common in pemphigus and can lead to hair loss, with the severity of scalp lesions linked to overall disease severity.

Low-dose acitretin helps nail psoriasis, stem cells may treat scarring alopecia, Chinese men have lower baldness rates, lateral foldplasty is good for ingrown toenails, hair diameter helps diagnose female baldness, childhood trauma linked to alopecia areata, certain hair-weaving leads to scalp conditions in African American women, and new methods for hair research and understanding hair and sweat gland development were introduced.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

Lipase H is important for hair follicle function and shaping hair fibers.

The document concludes that proper diagnosis and a multidisciplinary approach are crucial for managing Congenital Adrenal Hyperplasia effectively.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

Researchers found 15 new genetic links to skin traits in Japanese women.