Search

everythingexperts & clinicslearnresearchcommunity

for

Search:↓

Children with alopecia areata, especially with Down syndrome or thyroid issues, should be screened for thyroid disease.

Follicular mucinosis in a 15-year-old is usually harmless but needs monitoring for possible lymphoma.

A new mutation caused a rare hair disorder in a Polish girl, not inherited from her family.

Some cells may slow melanoma growth, a protein could affect skin pigmentation, a gene-silencing method might treat hair defects, skin bacteria changes likely result from eczema, and a defensin protein could help treat multiple sclerosis.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

Activating PKM2 and Wnt/β-catenin signaling together can potentially enhance hair growth and could be a treatment for hair loss.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

A Japanese patient with a rare genetic disorder had a less severe case than others, suggesting other factors may affect symptoms.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

A new type of hereditary hair loss in a Chinese family is linked to chromosome 2p25.1–2p23.2.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

It's important to understand the differences between FMF and PFM in children.

The mouse model showed defects in adult stem cell maintenance related to Hutchinson-Gilford progeria syndrome.

A mutation in the VDR gene affects hair cycling without needing ligand binding.

TMPRSS2 helps viruses enter cells and protects the prostate from inflammation-related cancer.

HDAC1 is crucial for skin development and preventing tumors.

Removing both Atr and Trp53 genes in adult mice causes severe tissue damage and death due to DNA damage.

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

Mutations in the LSS gene cause hair loss and may affect brain development, with varying severity.

Mutant MK6a transgenes in mice cause blistering, hair loss, and potential human alopecia.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

Pyruvate Kinase M2 helps hair grow by linking energy production and a key hair growth pathway.

PKM2 is a promising target for heart repair and regeneration.

Id2 gene helps keep hair follicle stem cells inactive.

A new mouse mutation causes skin and hair issues, influenced by another gene.

A new genetic mutation causing Werner's syndrome was found in an Indian man.

The LTF gene may help predict and manage nonspecific orbital inflammation.

Gefitinib treatment led to unexpected hair growth in two lung cancer patients.

FOXN1 mutations cause severe immunodeficiency, hair loss, nail issues, and thymus defects.

A rare EGFR mutation in newborns leads to severe health issues and early death.