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Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Tofacitinib successfully treated a woman's severe symptoms from a rare autoimmune condition.

Actin and alpha-smooth muscle actin help skin heal in mouse fetuses.

People with Lichen Planus, especially with mucosal involvement, are more likely to have Metabolic Syndrome, which increases their risk for heart disease and diabetes.

Different types of fibroblasts play various roles in diseases and healing, and more research on them could improve treatments.

Three Iranian men had reddish-brown facial pigmentation with no effective treatment.

Fibroblast and endothelial cell interactions are crucial in forming hypertrophic scars.

Trichodysplasia spinulosa is a rare skin condition caused by a virus, treatable with antiviral medication.

CMG2 and TEM8 receptors have distinct roles in skin and growth disorders, affecting collagen breakdown and growth.

TNC+ fibroblasts play a key role in skin inflammation by interacting with T cells.

A one-year-old cat had multiple benign skin tumors similar to those known in humans.

Histopathological examination is crucial to avoid misdiagnosis and ensure proper treatment for skin lesions.

Collagenous gastritis is a rare condition causing chronic diarrhea and weight loss, often misdiagnosed due to nonspecific symptoms.

The glassy layer of hair follicles has different fibril sizes and arrangements in guinea pigs and young mice.

The pseudo 'fringe sign' can also appear in frontal fibrosing alopecia, not just in traction alopecia, showing that this condition may be more common than thought.

Harlequin ichthyosis involves abnormal skin cell structures and giant mitochondria, affecting skin and hair.

Radiotherapy can cause skin fibrosis, which is often overlooked and needs better treatment and evaluation.

A rare case showed basal cell carcinoma and leiomyosarcoma coexisting, needing careful diagnosis and treatment.

GRF is not safe for tubal occlusion.

A 23-year-old Syrian woman has two rare hair disorders, and avoiding hair treatments plus using vitamins and minoxidil may help.

A mutation in the SREBF1 gene causes both hereditary mucoepithelial dysplasia and IFAP syndrome, which are related conditions.

Folliculin slows hair growth, and blocking it might help treat hair loss.

Skin heals with scars because only one type of fibroblast is used, not a mix.

Hair follicle hyperplasia is common in both benign and malignant skin lymphoproliferative disorders, with a proposed new term "pseudolymphomatous adnexitis."

A guinea pig with ovarian cysts had a uterine infection and abnormal uterus lining due to a piece of hay inside it.

Folliculotropic Mycosis Fungoides requires stage-based treatment, with early stages using skin therapies and advanced stages needing aggressive treatments.

A 3D model of Dupuytren’s disease was developed for better drug testing.

Keloid skin disorder involves abnormal fibroblast activation and immune response, linked to a group of genes including FGF11.