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Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

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

Ancient DNA blocks are still present in human genomes, possibly due to advantages they provide.

Baricitinib and its combination with lonafarnib improve fat cell formation in certain genetic disorders.

The UK's EDS National Diagnostic Service found that early diagnosis, lifestyle advice, and regular check-ups are crucial for managing vascular Ehlers-Danlos syndrome. A combination of losartan and bisoprolol can reduce vascular events, improving survival and quality of life.

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

Colorectal cancer development involves both genetic changes and epigenetic alterations like DNA methylation and microRNA changes.

Wounded skin cells can revert to stem cells and help heal.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

A small group of slow-growing cells causes basal cell carcinoma to return after treatment.

Different signals work together to change gene activity and guide hair follicle stem cells to become specific cell types.

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

Researchers found that certain RNA circles in the brain are linked to disease risk, but their exact role in disease is still unknown.

A mutation in the IKZF1 gene causes immune system overactivity, linked to autoimmune diseases like lupus.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

A protein called IL-36γ causes skin side effects from certain cancer treatments when combined with a common skin bacteria.

Conditioned medium from keratinocytes can improve hair growth potential in cultured dermal papilla cells.

Chinese domestic goats have unique genetic traits due to domestication and geographic isolation.

Genetic variations greatly affect individual metabolism and can impact health and disease risk.

The document suggests a possible link between FAM111B gene mutations and increased cancer risk, particularly pancreatic cancer.

Topical immunotherapy can treat alopecia areata, but its effectiveness varies and the exact mechanism is unclear.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

KCNQ potassium channels help control the sensitivity of touch receptors in the skin.

HLA-DRB5 and other genes may be linked to alopecia universalis.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

Chemotherapy-induced hair loss is partly due to decreased laminin-511 and increased laminin-332.

Asparagus racemosus and Withania somnifera can help reduce side effects of a cancer drug.

New genetic mutations linked to rare skin disorders were found in three newborns.

Dihydrotestosterone treatment on 2D and 3D-cultured skin cells slows down hair growth by affecting certain genes and could be a potential target for hair loss treatment.

Researchers used a laser to create advanced skin models with hair-like structures.