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A complex X chromosome rearrangement can increase the risk of multiple autoimmune diseases.

Ancient DNA blocks are still present in human genomes, possibly due to advantages they provide.

Increased FGFR2b signaling, influenced by androgens, plays a role in causing acne.

Epidermal nevi are skin cell clusters linked to various syndromes.

New treatments for ichthyosis, like protein replacement and gene therapy, show promise and may become standard care.

The new anti-acne treatment HA-P5 effectively reduces acne by targeting two key receptors and avoids an enzyme that can hinder treatment.

Autism's genetics are linked with early age of puberty and less hair loss, but not with hormone levels or polycystic ovary syndrome.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

CRISPR/Cas9 gene-editing shows promise for improving sheep and goat breeding but faces challenges with efficiency and accuracy.

The symposium concluded that understanding the molecular mechanisms of skin aging could lead to better clinical practices and treatments.

Key genes are crucial for Drosophila wing development and could be insecticide targets.

Human skin's melanocytes respond to light by changing shape, producing pigments and hormones, which may affect sleep patterns.

Stem cells regenerate tissues and their behavior varies by environment, suggesting the hematopoietic system model may need revision.

Follistatin and LIN28B together improve the ability of inner ear cells in mice to regenerate into hearing cells.

Scientists made a mouse model of a serious skin cancer by changing skin cells with a virus and a specific gene, which is similar to the disease in humans.

Different types of stem cells with unique roles exist in blood, skin, and intestines, and this variety is important for tissue repair.

A new method can detect mutations in mice by observing changes in hair follicle cells.

Early and precise nutritional intervention is crucial for managing anorexia nervosa.

Cutaneous Lymphadenoma is a unique skin tumor with specific protein markers and common gene mutations that may cause continuous cell growth.

Increasing mir-302 turns human hair cells into stem cells by changing gene regulation and demethylation.

Pregnant women with isolated hypothyroxinemia face more health issues, so iodine and folic acid supplements are important before and during early pregnancy.

Certain medications can reduce sexual desire and function, especially in women.

Childhood cancer diagnosis leads to long-term physical and emotional health issues in parents.

The two-factor model fits better for Chinese patients' understanding of illness causes than the original four-factor model.

Hair samples can be used to create stem cells easily and non-invasively.

TGF-β signaling is crucial for stem cell maintenance, differentiation, and has implications for cancer treatment.

Proper control of β-catenin activity is crucial for development and preventing diseases like cancer.

African American men with prostate cancer have more androgen receptor mutations, which may lead to more aggressive cancer compared to Caucasian American men.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

Women with PCOS often have more sleep problems than the general population.