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Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Disrupting the FGF5 gene in rabbits leads to longer hair by extending the hair growth phase.

Lychee fruit polyphenol (Oligonol®) may regulate genes linked to cell growth and inflammation in human scalp cells.

Removing a specific gene in certain skin cells causes hair loss on the body by disrupting normal hair development.

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

Efficient delivery systems are needed for the clinical use of CRISPR-Cas9 gene editing.

The nucleus is key in controlling skin growth and repair by coordinating signals, gene regulators, and epigenetic changes.

A new gene mutation causes hereditary coproporphyria with reduced enzyme activity.

Researchers made a mouse model with curly hair and hair loss by editing a gene.

Clouston's syndrome is a rare disorder affecting nails, hair, teeth, and skin, caused by a gene mutation, and currently has no treatment, only supportive care.

Vitamin D helps protect skin, PSORS1 gene's risk interval for psoriasis is expanded, hair follicles can be generated from mouse cells, and interferon-γ may cause pigmented skin lesions.

Both genes and environmental factors like chemicals may contribute to the increase in hypospadias, but the exact causes are still unclear.

Cells in hair follicles help create fat cells in the skin by releasing a protein called Sonic Hedgehog.

Exosomes from dermal papilla cells help hair growth by making hair follicle stem cells multiply and change.

The review recommends hormone replacement therapy for women with premature ovarian insufficiency to manage symptoms and protect health, with specific approaches for different groups.

miR-22, a type of microRNA, controls hair growth and its overproduction can cause hair loss, while its absence can speed up hair growth.

Stress and alcohol affect brain chemicals differently in rats, mice, and humans, influenced by genetic differences.

The gel made of minoxidil and hydroxypropyl-β-cyclodextrin improves hair growth and is good for long-term use.

Mice with autoimmune hair loss showed signs of heart problems.

P-cadherin is important for hair growth and health, and its problems can cause hair and skin disorders.

Skin abnormalities can indicate immunodeficiency due to shared origins with the immune system.

A gene mutation in mice causes increased mast cells and disorganized hair follicles in their skin.

A gene mutation in Lama3 is linked to a common type of hair loss.

Chrousos Syndrome is caused by mutations that make the body less sensitive to glucocorticoids, leading to various symptoms and requiring high-dose treatment.

Two new compounds can block androgen receptor activity in different ways and may lead to new treatments for androgen-related diseases.

Hair growth phase and certain genes can speed up wound healing, while an inflammatory mediator can slow down new hair growth after a wound. Understanding these factors can improve tissue regeneration during wound healing.

Different types of skin cells have unique genetic markers that affect how likely they are to spread cancer.

Scientists found a new, less invasive way to study body clocks using hair cells, which shows shift workers' body clocks don't match their lifestyles.

Hair greying is caused by oxidative stress damaging hair follicles and melanocytes.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.