Search

everythinglearnresearchcommunity

for

Search:↓

A new EDA gene mutation was found in a Chinese family with a specific skin disorder.

New RIPK4 gene mutations were found to cause a type of skin and limb birth defect.

Dermoscopy can help diagnose oral lichen planus by identifying specific patterns.

Egfl6 is not needed for zebrafish face development.

Integumentary organs adapt and evolve for survival, with potential uses in regenerative medicine.

The case suggests a possible link between severe acne and certain bone deformities.

P-cadherin is important for hair growth and health, and its problems can cause hair and skin disorders.

A 4-year-old girl has a rare hair condition causing fragile, short hair.

Keratin 2e shows a unique pattern in developing fetal skin, different from other keratins.

Two cases showed skin abnormalities without bone or neural defects.

Retinoic acid can change skin development, like turning scales into feathers or forming glands.

Human placental extract may be better for tooth repair than current materials.

A 15-year-old with KID syndrome developed a rare skin condition called PEHFN.

A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.

Neonatal hair can help determine drug exposure during pregnancy.

Eyelid cells share signaling components but differ in pathway activity.

Understanding fetal skin development helps diagnose congenital skin diseases.

Trichocytic differentiation starts in cells with epithelial cytokeratins, transitioning to trichocytic cytokeratins in hair and gradually in nails.

Atoh1 expression can create new Merkel cells in the skin.

Reptilian scales, feathers, and hairs evolved from changes in skin cell interactions.

LHX2, with other markers, can identify hair placodes in rats.

EBF1 controls hair type and length.

Nestin-expressing progenitor cells become outer root sheath keratinocytes.

Hair in mammals likely evolved from glandular structures, not scales.

Eruptive vellus hair cysts likely originate from the infrainfundibulum and sebaceous duct.

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

A mutation in the EDNRA gene causes Oro-Oto-Cardiac syndrome, affecting face and heart development.

XEDAR deficiency prevents muscle degeneration in EDA-A2 transgenic mice.

Dermal EZH2 controls skin cell growth and differentiation in mice.