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The transcription factor Meis2 is essential for touch sensation and proper nerve development in touch receptors.

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

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.

Genes linked to wool fineness in sheep have been identified.

Different people show different symptoms for genetic diseases because of how sensitive their bodies are to small changes in important factors.

Heat stress changes goats' skin and hair at the microscopic level and affects their genes and skin bacteria.

Neurosteroids help regulate oxytocin levels, especially during stress and pregnancy, to protect against premature labor.

The document concludes that inflammation markers can be used in diabetes, vitamin D3 affects immune pathways, hyperthyroidism changes hormone levels, androgen levels help diagnose Adrenocortical Carcinoma, erectile dysfunction is linked to diabetes, hypogonadism is common in HIV-infected males, and hormones can be biomarkers for various conditions.

Six genetic conditions are often linked to complete scalp hair loss in children.

Forensic DNA Phenotyping accurately predicts physical traits and is used in investigations, but needs more diverse population data for confirmation.

Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.

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

Deleting the MAD2L1 gene in mice led to rapid tumor growth despite chromosomal instability.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

Androgenetic alopecia is linked to a higher risk of coronary heart disease due to certain genetic factors and high homocysteine levels.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

New treatments targeting specific genes show promise for treating keratin disorders.

A new gene mutation causes female pseudohermaphroditism due to glucocorticoid resistance.

The skin protects the body and is constantly renewed by stem cells; disruptions can lead to cancer.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

N-acetyl-L-cysteine (NAC) can prevent DNA damage and protect cells from harm.

Pattern baldness is likely caused by a dominant gene influenced by testosterone levels, making it more common in men.

The document concluded that more research is needed to understand how estrogen affects the enzyme involved in hirsutism development.

Diagnosing both systemic lupus and hemoglobinopathy is challenging due to overlapping symptoms.

A new gene variant causes glucocorticoid resistance in a mother and son.

Netherton syndrome can cause severe dehydration, infections, and growth issues in infants.

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

Exposure to certain sex hormones can increase health risks, while some hormone therapies may offer benefits for specific conditions.