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Non-hormonal treatments should be used first for sexual dysfunction in postmenopausal breast cancer patients on aromatase inhibitors, with hormones as a second option.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

Non-coding RNAs are important for hair growth and could lead to new hair loss treatments, but more research is needed.

PPARγ is essential for maintaining healthy skin, controlling inflammation, and ensuring proper skin barrier function.

Hair and skin healing involve complex cell interactions controlled by specific molecules and pathways, and hair follicle cells can help repair skin wounds.

Fat tissue under the skin affects hair growth and aging; reducing its inflammation may help treat hair loss.

A patient with a rare disease had a unique genetic mutation linked to their symptoms.

Our microbiome may affect the development of the hair loss condition Alopecia Areata, but more research is needed to understand this relationship.

A specific pathway involving AR, miR-221, and IGF-1 plays a key role in causing common hair loss.

Human hair keratins K85 and K35 create unique filament patterns important for early hair formation.

Aesthetic rehabilitation techniques can improve life quality and wellbeing for disabled patients.

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.

Different stem cells are key for hair growth and health, and understanding their regulation could help treat hair loss.

Melatonin increased the activity of a hair growth gene in Cashmere goats.

A woman's hair loss during Hepatitis C treatment with PEG-INF-a-2a and Ribavirin was reversible after stopping the medication.

The combination therapy of PEG-IFN α-2a and Ribavirin can cause widespread hair loss and skin reactions.

Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

The document concludes that detailed clinical descriptions of seven family cases help understand dominant dystrophic epidermolysis bullosa's symptoms and inheritance.

The gene therapy showed significant wound healing and was safe for treating severe RDEB.

The conclusion is that differentiating wound types in RDEB patients is important for clinical trials and understanding the disease.

The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

Antiviral drugs, especially daclatasvir, may be a new treatment for a rare skin disease, improving survival and reducing symptoms in mice.

Most Recessive Dystrophic Epidermolysis Bullosa patients with a specific mutation likely have Sephardic ancestry from about 500 years ago.

Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

Skin grafts from related donors significantly healed chronic wounds in patients with a severe skin condition over a year.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

Corkscrew hair may be a new sign for quickly diagnosing scalp fungus in black children.

The document concludes that assessing hair follicle damage due to cyclophosphamide in mice involves analyzing structural changes and suggests a scoring system for standardized evaluation.

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

The document concludes that certain rats and mice are useful for studying hair loss in humans and testing treatments.