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B2m-free HLA variants may be a new class of HLA important in immune responses and diseases.

Human fetal placental stromal cell injections speed up healing and improve skin and hair recovery after radiation damage.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

The secretions of mesenchymal stem cells could be used for healing without using the cells themselves.

The meeting discussed vitamin D3's role in fighting tuberculosis, potential treatments for skin conditions like psoriasis, and hair follicle regeneration as a possible solution for hair loss.

Fetal-maternal stem cells in a mother's hair can help with tissue repair and regeneration long after childbirth.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

The circadian clock influences the behavior and regeneration of stem cells in the body.

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

Most pregnant women experience skin changes like darkening and itching, while serious skin conditions are rare but need early treatment.

Fetal death was caused by umbilical cord stricture with hair growth in the Wharton jelly.

Understanding skin structure and development helps diagnose and treat skin disorders.

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.

The secretome from mesenchymal stem cells is a promising treatment that may repair tissue and avoid side effects of stem cell transplantation.

Msx and Dlx genes are crucial for development, controlling cell behaviors like growth and differentiation through their roles as gene regulators.

Pregnancy can cause various skin changes and diseases, with PUPPP being the most common skin condition specific to pregnancy.

Mouse amnion can turn into skin and hair follicles with help from certain cells and factors.

ICL is a condition with low CD4+ T cells like AIDS but not caused by HIV, and normal CD4+ T cell counts may vary between men and women.

Zouboulis syndrome is a rare condition that helps diagnose monosomy 18p early.

The research found that a complex gene network, controlled by microRNAs, is important for hair growth in cashmere goats.

People with Mucopolysaccharidoses often have skin problems like thick skin and extra hair, and recognizing these can help diagnose and treat the condition early.

Melatonin affects cashmere growth in goats by influencing stem cell and certain signaling pathways.

A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

Women with nonclassical congenital adrenal hyperplasia may have a higher risk of fertility issues and miscarriages, and should get genetic counseling.

Doctors should consider Netherton syndrome in patients with chronic skin and hair issues to avoid misdiagnosis.

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

The document is a detailed medical reference on skin and genetic disorders.

EDA signaling is linked to skin disorders, various cancers, and liver disease.

New genetic mutations linked to rare skin disorders were found in three newborns.

Using powdered umbilical remnant allograft can effectively treat chronic scalp wounds resistant to traditional treatments.