Search

everythinglearnresearchcommunity

for

Search:↓

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

The local environment is crucial for cell development in the tongue.

The gene Foxq1, controlled by Hoxc13, is crucial for hair follicle differentiation.

Skin issues can indicate immune system problems.

Tissue stiffness affects hair follicle regeneration, and Twist1 is a key regulator.

Mice with LSS deficiency showed hair loss and cataracts, similar to humans, and can help in understanding and treating this condition.

The conclusion is that young women with excessive hair growth should be quickly tested for hormonal issues and treated to improve their social well-being.

Genetic defects in testosterone production can cause hormonal and developmental disorders, and more research is needed to understand androgen regulation and develop safer treatments.

The conclusion is that hair growth can be improved by activating hair cycles, changing the surrounding environment, healing wounds to create new hair follicles, and using stem cell technology.

A cross-bred lamb with severe skin and movement issues had ichthyosis fetalis but normal vitamin A levels.

Computational methods can speed up and improve the development and safety of herbal drugs.

Genetic counselors should be culturally skilled and aware of transgender patients' unique health risks and needs.

The FDA approved the first gene therapy for a blood disorder after overcoming early challenges and demonstrating patient benefits.

The document concludes that accurate diagnosis and understanding the type of hair disorder are crucial for treating hair loss in children.

Diagnosing sex development disorders requires combining medical history, physical exams, imaging, lab tests, and genetic data.

Melanoma's complexity requires personalized treatments due to key genetic mutations and tumor-initiating cells.

FGF12 is important for hair growth and could be targeted for hair loss treatment.

Type 2 immunity helps control mite growth in hair follicles, preventing damage.

Manipulating cell cleanup processes could help treat hair loss.

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

Female donor to male recipient sex mismatch and positive ACA-IgG are key risk factors for vitiligo and alopecia areata in chronic GvHD patients.

Memory regulatory T cells need IL-7, not IL-2, to stay in peripheral tissues.

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

The review shows how to properly diagnose and treat the loss of eyebrow and eyelash hair.

Sex neurosteroids cause different effects on hippocampal synaptic plasticity in males and females.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

NF-κB signaling is crucial in many diseases and can be targeted for new treatments.

A new medical syndrome may include skin changes, hair loss, sweating issues, bone malformations, leg swelling, and low cortisol.

Steroidogenic isoenzymes may help improve treatments for common hair loss.