Search

everythinglearnresearchcommunity

for

Search:↓

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

Longer GGN repeats in the androgen receptor gene are linked to polycystic ovary syndrome.

Certain genes are linked to type 1 and type 2 diabetes in kids, and changes in these genes can also cause other diabetes-related conditions.

The research identified genes linked to male-pattern baldness and potential drug targets for treatment.

A new genetic model may improve treatment and diagnosis for certain inherited skin diseases.

A gene mutation causes monilethrix in a Chinese family.

The document concludes that the development of certain tumors is influenced by genetic background and that a specific gene modification can lead to tumor regression and reduced growth.

The length of the CAG repeat in the androgen receptor gene affects the risk and progression of prostate cancer, BPH, infertility, and undermasculinized genitalia.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

A girl had rickets due to a gene mutation affecting vitamin D response.

Certain genetic variations are linked to increased androgen levels in PCOS, but more research is needed to understand these connections fully.

Certain gene variants are linked to severe acne, especially in males.

The 1298CC genotype in RA patients leads to higher methotrexate toxicity, while the 1298AA genotype results in better treatment response.

PrrH sRNA controls pyochelin production in *Pseudomonas aeruginosa*.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

Seven new genetic risk areas for prostate cancer were found.

A specific gene mutation causes a severe skin disorder in a family.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Mutations in the SNRPE gene cause hereditary hair loss.

Some people have genetic mutations that make them resistant to vitamin D, leading to rickets even with enough vitamin D intake.

Mutations in hKAP1 genes may cause hereditary hair disorders.

PC-associated alopecia has unique microscopic features.

A new genetic mutation was found causing hair and eye issues in a boy.

Genetic variations may affect how well finasteride works for BPH patients.

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

PCOS should be reclassified into two types based on hormone levels and symptoms.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Screening for the NUDT15 gene variant can prevent severe side effects from thiopurine drugs in East-Asian people.