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Increasing mir-302 turns human hair cells into stem cells by changing gene regulation and demethylation.

An 11-year-old child with total hair loss may have a genetic autoimmune disease, and the outlook for hair regrowth is not good.

Patients with a specific genetic variant have more severe alopecia areata and higher recurrence rates.

PCOS has no cure, but treatments can manage symptoms and improve health.

The document concludes that better understanding the wound microbiome can improve chronic wound care by preserving helpful bacteria and targeting harmful ones.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

A gene mutation in mice causes hair loss, weak bones, and protein buildup, showing how protein processing issues can lead to diseases.

Fibroblasts can be turned into melanocytes for potential skin treatments.

Foxi3 expression in developing teeth and hair is controlled by the ectodysplasin pathway.

A specific genetic mutation may increase male pattern baldness risk, especially in Europeans.

lncRNA XLOC_008679 and gene KRT35 affect cashmere fineness in goats.

Cashmere and milk goats have different hair growth cycles and gene expressions, which could help improve wool production.

Six new hair loss factors in men not linked to female hair loss.

DNA methylation and long non-coding RNAs are key in controlling hair growth in Cashmere goats.

The conclusion suggests that PCOS may persist due to genetic traits that, while harmful for female fertility, could have provided survival and reproductive benefits to males.

DNA phenotyping helps predict physical traits from DNA with varying accuracy and requires careful ethical and legal handling.

The research identified two types of keratinocytes in chicken scales: one for hard scales and another for soft skin, with similarities to human skin differentiation.

The meeting highlighted important advances in stem cell research and its potential for creating new medical treatments.

The document says a skin condition called alopecia areata causes hair loss and stress, and is treated with strong skin creams, injections, or other therapies, but treatment success varies.

New treatments and management strategies for skin conditions like melanoma and Spitz naevi were discussed at the dermatologists' meeting.

Higher basal metabolic rate increases the risk of non-alcoholic fatty liver disease, especially in Chinese people, and may require tailored management.

JAK inhibitors effectively regrow hair in alopecia areata but hair loss often returns after stopping treatment.

The study suggests that hypothyroidism may cause alopecia areata.

Certain genes and nutrients like vitamin D, zinc, and omega fatty acids affect COVID-19 severity and infection risk.

The gene Prss53 affects hair shape and bone development in rabbits.

Discoid Lupus Erythematosus often causes scarring hair loss, is influenced by genetics and environment, and requires early treatment to prevent worsening.

The PON1 192R gene variant is linked to a higher risk of psoriasis and heart disease in Western Mexico.

Eating a lot of fat increases PKCβ and inflammation in skin fat cells, which affects skin and hair health.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.