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

Keratin protein production in cells is controlled by a complex system that changes with cell type, health, and conditions like injury or cancer.

The HoxC gene cluster and its enhancers are essential for developing hair and nails in mammals.

The KRT84 gene is linked to better wool quality in Gansu Alpine Fine-wool sheep.

Mexican patients had a lower incidence of skin reactions to drugs and no significant link between these reactions and the TNF2 gene variant.

The review shows that skin symptoms like chronic fungal infections, hair loss, and skin depigmentation are key for early detection and management of APECED.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

TRPV4 helps cells repair tissue and reduce scarring by controlling calcium levels.

The trial aims to understand how obesity and lifestyle affect circadian rhythms in people with schizophrenia and bipolar disorder.

Both gene and non-gene areas of DNA evolved to make some mammals hairless.

Peps help Arabidopsis plants grow more root hairs by affecting specific genes and calcium signaling.

Disrupting the Flcn gene in mice causes early kidney cysts and tumors, which can be treated with rapamycin.

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.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

The document reports three sisters with Woodhouse-Sakati syndrome showing typical symptoms and unusual gynecological anomalies.

A genetic mutation in the LIPH gene causes tightly curled hair that stops growing in some Japanese individuals.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

Foxn1 gene regulation is crucial for thymus development but not for hair growth.

Crossbreeding improves goat fiber quality, and specific genes affect hair traits and color.

Topical ceramide treatment partially improves the skin condition in Jack Russell Terriers with a genetic skin disorder.

Deleting the MAD2L1 gene is tolerated in certain mouse cancer models.

Mutations in mitochondrial DNA might significantly contribute to the development of Polycystic Ovarian Syndrome.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

A patient with Werner syndrome showed a range of aging-like symptoms and metabolic issues, underscoring the need for early detection and treatment.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

Delta-opioid receptors affect skin cell circadian rhythms, possibly impacting wound healing and cancer.

DAVID syndrome is a condition with immune system and hormone deficiencies, needing early diagnosis to avoid serious complications.