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Patients with both connective tissue disease and acid reflux are more likely to have certain symptoms and physical signs.

Maize hybrids show better early growth due to complex gene interactions from their parent strains.

Different human traits like skin color and hair type vary between populations due to genetic adaptations to the environment.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

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

Minoxidil affects collagen-related genes, potentially helping treat fibrosis.

Mice skin has components that could help with hair growth and might be used for diabetes treatment.

Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.

Beige and leaden pigment genes act within melanocytes, affecting pigment patterns.

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

Combining genetic and physical trait analysis improves diagnosis accuracy for monogenic diabetes.

Harlequin mutant mice have hair loss due to low AIF protein levels and retroviral element activity.

The study found that mouse sweat glands develop before birth, mature after birth, and have specific keratin patterns.

Tongue cancer cells show more plectin-1 than non-cancer cells, but both have similar levels of trichohyalin.

Researchers found that certain RNA circles in the brain are linked to disease risk, but their exact role in disease is still unknown.

Plucked hairs can be used instead of skin biopsies to study hair traits because they contain specific cells related to hair.

mEphA1 receptor tyrosine kinase is important for skin and hair development and may play a role in certain diseases.

DNA changes in tetraploid wheat improve root growth and nitrogen use.

sPLA2-X is crucial for normal hair growth and follicle health.

Cattle skin has leptin which might control skin and hair growth.

The mouse hairy ears mutation causes longer ear hair due to changes in gene expression.

Lower levels of certain genes in hair cells improve hair loss treatment outcomes.

Nuclear shape and chromatin changes affect gene expression in skin cell differentiation.

Pregnant women with PCOS have higher levels of Neurokinin B in the placenta, especially with female babies.

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

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

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

VDR regulation varies by tissue and is crucial for its biological functions.

Sox21 is crucial for tooth development and enamel formation by preventing cells from changing into a different type.

As skin cells mature, vitamin D receptor levels decrease while retinoid X receptor α levels increase.