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A specific gene region can control targeted and responsive gene expression in mice, useful for skin disorder treatments.

Nelfb is essential for dermal fat development and survival.

Certain gene variations in Jiangnan cashmere goats are linked to important traits like birth weight and fiber quality, useful for breeding.

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

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

Vitamin D and glucocorticoids affect bone growth, metabolism, and immune response.

Tunisian children with hereditary vitamin D-resistant rickets showed improvement with calcium treatment, and new genetic mutations were identified.

There is no significant link between the MMP-1 rs1799750 polymorphism and androgenetic alopecia in the Indonesian population.

Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

High levels of TNF-α may contribute to obesity and insulin resistance in PCOS, but not due to the C850T genetic variation.

Two genetic variations in Moa buffalo help them adapt to heat.

Vitamin D receptor binds similarly to natural and synthetic ligands, affecting gene regulation.

Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.

Severe genetic variants in children with a specific adrenal condition match predicted symptoms well, but milder variants do not.

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

C57BL/6 mice and SD rats have different sweat gland and hair follicle patterns, useful for skin research.

The Msx2 gene affects feather development in Hungarian white geese and a specific gene variation could indicate feather quality.

The modified stem cells with VEGF165 in a special scaffold improved blood vessel growth and wound healing for skin repair.

Shorter GGC triplet repeats in the androgen receptor gene are linked to less hair loss in Han men.

G allele of AR Stul polymorphism linked to higher hair loss risk, especially in white people.

Genetic differences affect COVID-19 severity and treatment effectiveness.

Certain genetic variations are linked to hair loss in Mexican men.

Hair loss gene linked to prostate issues.

The FAT1 gene and its variations can help improve wool quality in Chinese Merino sheep through selective breeding.

Researchers created a mouse model of a type of rickets that does not cause hair loss.

A new mutation in the AGPAT2 gene causes severe fat tissue loss and related health issues by reducing the protein's levels.

A new mutation in the HJV gene was found in a young woman with juvenile hemochromatosis, causing unusual symptoms like secondary hypothyroidism.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.