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Hair follicle development in cashmere goats involves dynamic changes in proteins and metabolites, with key roles for oxytocin, MAPK, and Ca2+ pathways.

Genetic variants can affect valproic acid's effectiveness, side effects, and levels in epilepsy treatment.

Epidermolysis bullosa simplex causes easily blistered skin due to faulty skin cell proteins, leading to new treatment ideas.

Fish teeth and taste bud densities are linked and can change between types due to shared genetic and molecular factors.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

The KRTAP21-2 gene affects wool length and quality in sheep.

New genes linked to ichthyosis were found, but there's still no cure; treatment options are improving.

The specific skin disease variant p.(Arg2000Trp) in plectin can cause a wide range of symptoms, which should be considered when diagnosing patients.

Some parents have a mild form of congenital adrenal hyperplasia without symptoms, and they usually don't need treatment.

WNT10A mutations often cause ectodermal dysplasias, with males showing more tooth issues than females.

Understanding phenotypic plasticity is crucial for developing effective cancer therapies.

Caucasian and Asian women with PCOS generally show similar symptoms, except Asian women have less chest hair.

Staphylococcus epidermidis A/C strains are more antibiotic-resistant and infection-adapted, while B strains thrive in hair follicles.

T-cells in alopecia areata scalp show abnormal regulation, leading to less inflammation.

No consistent link between genotype and phenotype in 5-α-Reductase type 2 deficiency.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

Finger length ratios don't predict baldness in men.

Polycystic ovary syndrome affects about 6-10% of women, with varying symptoms and the need for standardized global definitions.

No clear link between specific gene and hair loss in Mexican brothers.

Woodhouse-Sakati syndrome shows varied symptoms, including hair loss and diabetes, and is common in Qatar due to a specific genetic variant.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

Women with Polycystic Ovary Syndrome (PCOS) have a higher risk of developing type 2 diabetes due to insulin resistance.

The transgene likely activated an oncogene or interrupted a tumor suppressor gene, causing melanoma in mice.

The study concludes that a genetic mutation in TFM mice leads to reduced androgen receptor activity, affecting the body's response to male hormones.

Low Vitamin D receptor levels in breast cancer are linked to worse outcomes and more bone metastases, and could be a marker for prognosis.

The editor suggests removing "race" and "ethnicity" from dermatology and creating tools to objectively assess skin color and hair texture.

Early hair loss in men may signal broader health issues similar to PCOS in women.

Men with early baldness often have low vitamin D levels.

Higher EULAR/ACR scores in SLE patients predict more organ damage.

Clinical signs of hyperandrogenism are related to female pattern hair loss severity, but biochemical markers are not.