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Not having the gene PLAAT3 leads to fat loss, high insulin resistance, and abnormal fat levels in the blood due to a disruption in fat cell development and function.

Removing REDD1 in mice increases skin fat by making fat cells larger and more numerous.

The study found genetic differences related to hair development that may explain hair loss in a patient with Trichorhinophalangeal syndrome type I.

Trichotillomania may have a genetic link to psychiatric disorders.

A rare case of isolated trichothiodystrophy was identified, marked by brittle hair with low sulfur content.

The study suggests that higher levels of SIRT1 and SIRT2 may improve overall cell health and aging processes.

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

Female Pattern Hair Loss is linked to genetics, diet, stress, and certain health conditions.

Old people have less hair because their hair follicles don't regenerate as well, not because of fewer stem cells, and a protein called follistatin might help reactivate hair growth.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

The type of tumor suppressor affects the form of skin cancer from hair follicle stem cells.

Researchers made a mouse model with curly hair and hair loss by editing a gene.

Prairie dogs with fewer neighbors are more stressed but their number of babies isn't affected.

The agouti gene may help understand and treat obesity.

RXRα is crucial for proper immune response and links diet to immune function.

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

Different types of polycystic ovary syndrome show varying levels of insulin resistance, with the 'PHO' type being the most insulin resistant.

Researchers created a new mouse model for studying scleroderma.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

A specific gene mutation causes different hair defects in Indian monilethrix families.

Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.

TrichoScan helps identify subtle hair thinning in women with androgenetic alopecia.

The TG5 gene affects beef cattle weight, and the CC genotype leads to higher weights.

RXRa is crucial for Th2 immune cell development and may link nutrition to immune health.

Using trait prevalence priors in genetic prediction models for appearance traits is currently impractical due to limited knowledge and potential accuracy issues.

Trichothiodystrophy is a condition with brittle hair and various physical and mental issues due to low sulfur in proteins.

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

OsPHR3 can help breed rice that efficiently uses phosphate without growth issues.

A rare case of trichothiodystrophy was found with autism, seizures, and mental retardation.