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A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

The document concludes that inhalation of oxygen and sumatriptan injections are primary for cluster headaches, indomethacin for paroxysmal hemicrania, and lidocaine and lamotrigine for SUNCT, but SUNCT often resists treatment.

People with chronic hives should be tested for thyroid autoimmunity to manage their condition better.

Aδ-LTMRs have complex synapses with glycine, while Aβ-LTMRs have simpler ones.

Scientists are still unsure what triggers the immune system to attack hair follicles in Alopecia areata.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

CTHRC1 is essential for healing and preventing heart rupture after a heart attack.

A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

Enzyme replacement therapy improved multiple symptoms of homocystinuria in mice.

Overexpressing ATF3 in mice's epithelial cells may lead to oral cancer.

Citrullus colocynthis has pain-relieving, anti-inflammatory, antidiabetic, and hair growth benefits, but can cause side effects like colic and diarrhea.

CCCA may be caused by both hair traction and an immune response.

Trichothiodystrophy causes abnormal protein deposits and distortion in hair follicles.

Vitamin C supplementation can resolve pulmonary arterial hypertension caused by vitamin C deficiency.

Genetic variants in specific genes cause central centrifugal cicatricial alopecia.

Mast cells and the CB1 receptor may be key in causing IgA vasculitis.

A high-fat diet worsens neutrophilic folliculitis by increasing certain chemokines.

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

Hyperaesthetic leucotrichia in horses causes painful, recurring skin lesions and hair color changes, especially in Arabian and American paint horses.

Ritlecitinib can reduce inflammation and help hair regrow in Alopecia Areata.

Acetylcholine receptors might be involved in the development of acne inversa and smoking could worsen the condition.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

Small bowel lesions in Cronkhite-Canada syndrome persist despite steroid treatment.

Trichothiodystrophy involves brittle hair due to low sulfur amino acids, not a transport defect.

Citrullus colocynthis fruit extract may effectively treat testosterone-related hair loss, similar to finasteride.

Higher activity in lichen planopilaris is linked to certain immune and tissue genes.

PADI4 enzyme slows down cell growth in developing hair follicles.