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The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

Ruxolitinib significantly improves multiple autoimmune conditions in APS-1 patients.

People in Jeddah know about Vitamin D and its sources but are unclear on how much they need daily, and while many women take supplements, attitudes towards increasing Vitamin D levels vary.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Different human traits like skin color and hair type vary between populations due to genetic adaptations to the environment.

Cats lose fur due to various reasons, including allergies, infections, genetics, hormones, diet, cancer, stress, and some conditions are treatable while others are not.

Young women in West Bengal, India, with PCOS often have estrogen resistance, leptin receptor issues, folate deficiency, T2DM, and acanthosis, commonly linked to obesity.

A new gene mutation causes insulin resistance in a girl and her mother.

An 11-year-old child with total hair loss may have a genetic autoimmune disease, and the outlook for hair regrowth is not good.

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

The symposium showed that stem cells are key for understanding and treating skin diseases and for developing new skin models and therapies.

Experts met to improve care for ichthyosis patients in Spain.

Leptin-deficient mice, used as a model for Type 2 Diabetes, have delayed wound healing due to impaired contraction and other dysfunctional cellular responses.

Autism's genetics are linked with early age of puberty and less hair loss, but not with hormone levels or polycystic ovary syndrome.

Hair follicles are normally protected from the immune system, but when this protection fails, it can cause hair loss in alopecia areata.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

Fibrodysplasia ossificans progressiva is a rare genetic disorder that causes extra bone growth and symptoms of premature aging.

Brothers of women with PCOS tend to have higher levels of a hormone called DHEAS, indicating a possible genetic link.

Recognizing scalp symptoms in PRP is crucial for proper diagnosis and treatment.

Lack of sleep in mice leads to prostatitis by reducing certain hormones and activating an inflammatory pathway, which can be temporarily fixed with normal sleep.

The JAK/STAT pathway is important in cell processes and disease, and JAK inhibitors are promising for treating related conditions.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

IL-1 family cytokines are crucial for skin defense and healing, but their imbalance can cause skin diseases.

The genes KRT25 and SP6 affect curly hair in horses, with KRT25 also causing hair loss. If both genes are mutated, the horse gets curly hair and hair loss. KRT25 can hide the effect of SP6.

Linear Discoid Lupus Erythematosus of the scalp can cause hair loss and should be considered in similar cases.

Topical corticosteroids are the main treatment for Erosive Pustular Dermatosis, but recurrence is common after stopping treatment.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

Different people show different symptoms for genetic diseases because of how sensitive their bodies are to small changes in important factors.

New treatments for alopecia areata show promise, but more research is needed to confirm their effectiveness.

New treatments for alopecia areata show promise, but standardized guidelines are needed.