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Severe CCCA may be biologically and clinically different from milder forms.

Some patients with a type of skin lymphoma can experience a rare, non-scarring hair loss that looks like another hair loss condition but has distinct features.

Monilethrix is linked to a gene cluster on chromosome 12.

ECM1-modified stem cells can effectively treat liver cirrhosis.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

Copper supplements during pregnancy improve survival and development in mutant mice.

People who carry the 21-Hydroxylase Deficiency gene are not more likely to have excessive male hormone levels.

The LncRNA AC010789.1 slows down hair loss by promoting hair follicle growth and interacting with miR-21 and the Wnt/β-catenin pathway.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

The E413K mutation in the hHb6 gene causes monilethrix, a hair disorder, but doesn't show consistent symptoms.

Lamins are vital for cell survival, organ development, and preventing premature aging.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

CT-707 is effective and safe for treating certain Chinese lung cancer patients.

Non-classic congenital adrenal hyperplasia is a common disorder causing symptoms like acne and infertility, and it's managed based on symptoms, not just test results. Treatment can improve fertility and reduce miscarriage risk.

CCCA may be a fibroproliferative disorder, and anti-fibrotic therapies could help.

SQSTM1 gene issues may increase the risk of alopecia areata.

Monilethrix involves multiple genes affecting hair structure, including DSG4 mutations.

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

Colchicine can inhibit hair growth by affecting cell activity and protein expression in hair follicles.

ALRN-6924 may prevent hair loss caused by chemotherapy.

Genetic screening for NUDT15 polymorphisms is crucial for patients taking azathioprine, especially in Asians.

Mutations in the p63 gene affect skin adhesion, barrier integrity, and hair growth.

A specific gene mutation causes monilethrix in this family, and minoxidil treatment improves hair condition.

Cladribine has known risks and potential new safety concerns, requiring careful monitoring.

A woman's hyperandrogenism was caused by a genetic mutation leading to non-classic adrenogenital syndrome.

Higher Lnk protein levels in ovaries may lead to insulin resistance in women with PCOS.

Replacing defective mesenchymal cells with normal ones fixes thymic growth issues in 22q11.2DS mouse models.

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.