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FOXN1 gene variants cause low T cells and immune issues from birth.

Scientists created early-stage hairs from mouse cells that grew into normal, pigmented hair when implanted into other mice.

Ectodermal dysplasia causes various symptoms and early treatment is important for eye, dental, and skin issues.

People who carry the 21-Hydroxylase Deficiency gene are not more likely to have excessive male hormone levels.

Changes in keratin affect skin health and can lead to skin disorders like blistering diseases and psoriasis.

Infertile men are more likely to produce sperm with abnormal chromosome numbers, which can affect pregnancy success and embryo health.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

Wnt7a protein is crucial for development and tissue maintenance and plays varying roles in diseases and potential treatments.

Conditioned media from human amniotic fluid-derived stem cells helps skin heal and protects against aging from sun exposure.

CD90 is present on specific cells in dog hair follicles.

Women with nonclassic 21-hydroxylase deficiency can have successful pregnancies through IVF, with certain factors affecting their chances.

Two patients with the same genetic mutation had both blistering skin and easily pulled out hair.

Understanding fetal skin development helps diagnose congenital skin diseases.

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

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

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

The document concluded that stem cells are crucial for skin repair, regeneration, and may help in developing advanced skin substitutes.

New dermatology leaders and events were announced.

The meeting highlighted the genetic basis of female pattern hair loss and various skin health insights.

The Seoul International Dermatology Symposium was a successful event that highlighted new dermatology treatments and fostered international relations.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

A 15-year-old girl with no menstrual period was diagnosed with a genetic condition that makes her body unable to respond to male hormones, leading to female characteristics despite having male genetic makeup.

Epidermolysis bullosa is an inherited condition causing fragile skin with no cure, managed by wound care and experimental treatments show promise.

The commentary stresses the importance of using historical control data and proper interpretation in evaluating developmental toxicity.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

Regenerative cellular therapies show promise for treating non-scarring hair loss but need more research.

Epidermolysis bullosa simplex causes easily blistered skin due to faulty skin cell proteins, leading to new treatment ideas.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.