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The modified stem cells with VEGF165 in a special scaffold improved blood vessel growth and wound healing for skin repair.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

A 21-year-old male has a rare scalp condition with excessive skin folds.

A 12-year-old boy had severe shingles and skin damage after a stem-cell transplant.

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

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

Stem cells in the eye have different roles and behaviors, helping maintain and repair the eye's surface.

AtCSLD3 and GhCSLD3 genes enhance root growth and cell elongation in plants.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Removing SIX1 in fat cells reduces skin fibrosis.

The technique successfully promoted hair growth and skin renewal in mice.

Clouston syndrome can lead to skin cancer, so monitoring is crucial.

Acyclovir can prevent rejection of skin grafts in herpes-related lip leucoderma.

A man had two rare autoimmune diseases that might be connected.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

Vertical sleeve gastrectomy improved metabolism, behavior, and reproduction in obese rats with PCOS.

The patient has a leg condition caused by vein issues, needing lifestyle changes and leg care.

Suplatast tosilate successfully treated a woman's systemic sclerosis symptoms.

Early diagnosis and treatment are crucial for managing Berardinelli–Seip syndrome.

Parental socioeconomic status doesn't improve dietary habits or reduce disease severity in children with sickle cell disease.

Dermal lymphatic vessels help hair growth by affecting hair cycle phases.

Hoyeraal-Hreidarsson syndrome in infants causes severe gastrointestinal issues.

The family has a unique form of ectodermal dysplasia similar to Clouston syndrome but with different hair and skin symptoms.

Modified rat hair follicle stem cells can help create artificial hair follicles, blood vessels, and skin.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

HTLV-1-associated lichenoid dermatitis (HALD) is linked to an immune response against HTLV-1-infected cells.

A specific gene mutation causes sparse, brittle hair in a family.