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The peach gene CTG134 helps control the interaction between auxin and ethylene, which could lead to new agricultural chemicals.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

Robertsonian translocation can cause recurrent miscarriages.

Mouse and human keratin 16 can both form filaments, with differences likely due to the tail domain, not the helical domain.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

Metreleptin treatment significantly improved metabolic health in a boy with congenital generalized lipodystrophy.

A new gene mutation causes insulin resistance in a girl and her mother.

Androsterone and finasteride have different solid forms, with new findings correcting previous errors and identifying a new form.

Defective nuclear transport may cause gene expression changes in Progeria.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

A new gene mutation may cause cyclic thrombocytopenia by affecting platelet production.

ChatGPT-5 can pass the endocrinology exam but isn't fully reliable for clinical decisions yet.

Keratin K80 is an ancient protein found in various tissues, important for cell structure and tissue differentiation.

Certain gene variations in the Vitamin D receptor may increase the risk of chronic hair loss.

The hamster polyomavirus middle T antigen is linked to tumors in hamsters and associates with a specific tyrosine kinase.

BioPlex-11 improves DNA profiling from telogen hair roots in forensic work.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

Overexpression of PTHrP in chondrocytes causes short-limbed dwarfism and delayed bone formation in mice.

Genetic factors in PCOS are complex, with potential influences from the MC4R gene.

The PCL/PHB blend allows for slower, more controlled curcumin release than individual polymers.

Certain gene variations and different levels of BDNF and CRH hormones are linked to vitiligo.

Keratin2-6g is crucial for hair follicle development, with mutations causing cell degeneration and vacuolation.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

Certain changes in the VEGF gene can increase or decrease the risk of polycystic ovary syndrome.

Anastrozole and cyproterone acetate treatment can help increase adult height in boys with testotoxicosis.

The study showed that a specific DNA sequence can control gene expression in hair growth areas of mice.

The STIM1 R304W mutation in mice leads to bone changes and teeth hair growth.

Certain gene variations might help protect against insulin resistance and glucose intolerance in people with Polycystic Ovary Syndrome.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

Thiopurines help treat IBD but require genetic testing to avoid side effects.