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Patients with Bohring-Opitz syndrome and ASXL1 mutations need regular kidney ultrasounds to check for tumors.

K16 can partially replace K14 but causes hair loss and skin issues.

Mothers and newborns with dental fillings had higher mercury in their hair, but getting fillings during pregnancy didn't raise mercury levels further.

Regenerative pharmacology, which combines drugs with regenerative medicine, shows promise for repairing damaged body parts and needs more interdisciplinary research.

A mother's western diet can make her milk toxic, causing inflammation and hair loss in babies.

EGF and FGF help hair growth by affecting cell differentiation and fiber growth.

Melanocyte precursors in human fetal skin follow a specific migration pattern and some remain in the skin's deeper layers.

Low-potency steroids can cause serious side effects in people with skin conditions like Netherton syndrome.

Systemic glucocorticosteroids are a primary treatment for various skin conditions but require careful management due to potential side effects and relapses.

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

Eating glucoraphanin can help prevent psychosis in offspring whose mothers had immune system activation.

Finasteride may affect fetal brain development and increase arousal, but more research is needed for safety confirmation.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

Skin and hair can help us understand organ regeneration, especially how certain stem cells might be used to form new organs.

The conclusion is that formalizing how past decisions influence current health technology assessments could improve the credibility and defense of coverage decisions.

Activating Notch in adult skin causes T cells and neural crest cells to gather, leading to skin issues.

Not enough vitamin B6 in pregnant rats' diets caused poor development and health in their babies.

New treatments for immune disorders caused by FOXN1 deficiency are promising.

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

Loss of Fz6 disrupts hair follicle and associated structures' orientation.

Wounds heal without scarring in early development but later result in scars, and studying Wnt signaling could help control scarring.

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

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.

Cat color patterns are determined early in development by gene expression and epidermal changes, with the Dickkopf 4 gene playing a crucial role.

Two siblings were the first reported cases of inheriting both eye coloboma and loose anagen syndrome together.

Neurosteroids can influence behavior by modulating brain inhibition, with potential for treating psychiatric disorders.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

A 2-year-old boy with a rare brain malformation may have Gomez–López-Hernández syndrome.

Scientists developed a method to grow human fetal skin and digits in a lab for 3-4 weeks, which could help study skin features and understand genetic interactions in tissue formation.