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Some people experience severe, long-lasting side effects from fluoroquinolone antibiotics, leading to the recommendation of limited use and increased awareness of these risks.

Deleting Snai2 and Snai3 causes fatal autoimmunity.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

Melatonin affects many body functions beyond sleep by interacting with specific receptors in various tissues.

Hair follicle stem cells are key for hair and skin regeneration, can be reprogrammed, and have potential therapeutic uses, but also carry a risk of cancer.

CDP is crucial for lung and hair follicle cell development.

Estrogens significantly influence hair growth by interacting with receptors in hair follicles and may help regulate the hair growth cycle.

Targeting the IL-23/IL-17 pathway effectively treats several inflammatory skin diseases.

Lampreys have a functional vitamin D receptor that may help detoxify harmful substances.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

The study found that immune responses disrupt hair growth cycles, causing hair loss in alopecia areata.

Tcf3 helps cells move and heal wounds by controlling lipocalin 2.

Keratins are important for skin cell health and their problems can cause diseases.

The document concludes that mouse models are crucial for studying hair biology and that all mutant mice may have hair growth abnormalities that require detailed analysis to identify.

Dupilumab is being tested for many new skin, respiratory, and gastrointestinal conditions.

RANK is a key target in breast cancer treatment due to its role in tumor growth and bone metastasis.

Phosphatidic acid may help hair grow by affecting cell growth pathways.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

Hair loss involves immune responses, inflammation, and disrupted signaling pathways.

A specific protein in chicken embryos links early skin layers to feather development.

Minoxidil foam 5% effectively treats hair loss in both frontal and vertex scalp regions.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

The document concludes that various findings in rheumatology offer insights into disease severity, treatment responses, and potential risks in medication, with some limitations due to unspecified participant numbers.

Lymphatic vessels are essential for health and can be targeted to treat various diseases.

Young HS patients often have other physical and mental health issues, and research on HS covers a wide range of topics including genetics, triggers, treatments, and the need for more data.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

Hair loss improved with treatment and successful transplant.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

New insights into cell communication in psoriasis suggest innovative drug treatments.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.