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A new mutation linked to partial Androgen Insensitivity Syndrome and prostate cancer was found in a patient unhappy with their female gender assignment.

Defects in certain proteins cause major heart abnormalities during early development.

Polycomb Repressive Complex 1 is crucial for keeping stem cells stable and maintaining healthy adult tissues.

Monilethrix is linked to a gene cluster on chromosome 12.

New probes were created to effectively measure specific enzymes involved in fat metabolism, which could help develop new drugs.

CEP135 may predict cancer outcomes, and targeting PLK1 could help treat certain sarcomas.

The tumor suppressor BRCA2 helps in cell division by bringing key proteins to the area where cells split.

Human hair keratin genes hHa2 and hHb1 are located on chromosomes 17 and 12.

A protein called PLC2 is important for the growth and development of plant roots influenced by auxin.

The PIP5K1A gene helps cashmere growth in goats by promoting cell proliferation, and melatonin boosts its expression.

A specific hair protein variant increases the spread of breast cancer and is linked to worse survival rates.

K6/ODC transgenic mice are effective for quickly identifying cancer-causing chemicals.

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

A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

New mutations in KRT83 and KRT86 are linked to the hair disorder monilethrix.

Keratin 79 marks a new group of cells that are key for creating and repairing the hair follicle's structure.

MultiKano accurately identifies cell types in complex data better than existing methods.

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

PCAT1 helps hair growth by controlling miR-329/Wnt10b.

Protein kinase C epsilon may increase skin cancer risk by affecting nearby cells.

WNT10A helps esophageal cancer cells spread and keep renewing themselves.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

Cronkhite-Canada syndrome can cause multiple gastrointestinal polyps and various physical symptoms.

Plakophilin 1 helps control skin cell immune responses to prevent excessive inflammation.

NBCCS and BFHS might be the same syndrome, helping better identify and manage cases.

Key genes, including KRT39 and KRT74, influence hair length in Inner Mongolia cashmere goats.

Inflammation may cause nail issues in Cronkhite–Canada Syndrome.

TBX5 gene influences feathered feet in Guangxi chickens by affecting cell growth and movement.