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A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

The early Iron Age settlement at Raposal shows diverse cultural influences and challenges previous ideas about settlement types in the Ebro Valley.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

The keratin 5 mutation in a family with epidermolysis bullosa simplex was due to mosaicism, not a new mutation.

The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

Biopsy is crucial to accurately distinguish Erosive Pustular Dermatosis of the Scalp from Squamous Cell Carcinoma.

SLE patients in eastern Saudi Arabia have a generally good prognosis despite multi-organ involvement.

A prostate cancer drug can lower the levels of a protein that the coronavirus uses to enter lung cells.

The research showed that CRISPR/Cas9 can fix mutations causing a skin disease in stem cells, which then improved skin grafts in mice, but more work on safety and efficiency is needed.

ILC1-like cells can cause alopecia areata by themselves.

The MDR1 C3435T polymorphism does not significantly affect methotrexate response in rheumatoid arthritis patients.

The gene therapy showed significant wound healing and was safe for treating severe RDEB.

Raman spectroscopy can help identify cancerous skin tissue during surgery.

GLABRA 2 controls ethylene production to help root hair growth during nutrient deficiency.

Systemic sclerosis skin shows varied gene patterns, suggesting potential for personalized treatment.

RAR-gamma 1 is important for normal skin maintenance and differentiation.

The frizzy mouse and hairless rat mutations are due to changes in the Prss8 gene.

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.

Sox13 is a marker for early hair follicle development but not essential for skin and hair growth.

CDKN2AIP gene is less active in nevus sebaceous, affecting related RNA networks.

Targeting CD200 could be a new treatment for rheumatoid arthritis.

Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

Two patients with the same genetic mutation had both blistering skin and easily pulled out hair.

Keratin 14 may be an autoantigen in autoimmune skin diseases.

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

Targeting ACE2 and TMPRSS2 may help prevent or treat COVID-19 in cancer patients.

Calreticulin has roles in healing, immune response, and disease beyond its known functions in the endoplasmic reticulum.