Search

everythinglearnresearchcommunity

for

Search:↓

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

The gene for slick hair in Senepol cattle is located on chromosome 20 and may involve the SRD5A2 gene.

The document concludes that current treatments for androgenic alopecia are not fully effective, but new therapies like botulinum toxin and PRP show promise, and future gene therapy could be beneficial.

A teenager's hair with alternating white and dark bands, known as Pili annulati, is a genetic condition that is usually harmless and often considered attractive.

Using a combination of specific cell cycle regulators is better for safely keeping hair root cells alive indefinitely compared to cancer-related methods.

Researchers found two genes that may explain why some Casertana pigs don't have hair.

The scraggly mutation causes hair loss and skin defects in mice.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

Genetic data can predict male-pattern baldness with moderate accuracy, especially for early-onset cases in some European men.

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

Dermatologists give better information on pathology forms, hypersensitivity vasculitis is a common skin issue, misdiagnoses can occur, and various skin conditions are linked to loss of elastin or genetic factors.

Men have worse COVID-19 outcomes than women due to genetic and hormonal differences.

Certain genes and X chromosome patterns may significantly contribute to the development of hair loss.

Society's pressure to have children later in life favors genes that increase the risk of early baldness in male offspring.

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

The most different genetic segment between Africans and East Asians is the EDA2R/AR region, with two main types influenced by population changes and natural selection, and linked to baldness.

Chromosomal differences affect how muscle cells respond to testosterone.

Two mouse mutations cause similar hair loss despite different skin changes.

The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

The document concludes that careful diagnosis is crucial for chromosome 13q deletion syndrome, tamoxifen can cause reversible eye damage, finasteride may be linked to cataracts, and OCT is useful for diagnosing macular diseases.

Eye exams are crucial for kids with 13q deletion syndrome, tamoxifen can cause vision loss, Propecia may lead to cataracts, Lipoid Proteinosis causes skin bumps, and OCT is useful for diagnosing macular diseases.

Taking Propecia might lead to the development of cataracts.

Multiple eye conditions were studied, highlighting the importance of various imaging methods for diagnosis, the vision side effects of drugs tamoxifen and Propecia, and the usefulness of optical coherence tomography for diagnosing and monitoring macular and retinal diseases.

S100A3 protein is crucial for hair shaft formation in mice.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Trichoscopy helps accurately diagnose Netherton syndrome, often mistaken for atopic dermatitis.

A woman with acromegaloidism and normal growth hormone levels had a rare X-Tetrasomy, suggesting a need to study X-chromosome genes for their role in growth and facial development.

Keratosis Follicularis Spinulosa Decalvans is a rare genetic disorder causing skin and hair issues, often inherited through the X chromosome.

DNA profiling in forensics has improved, but predicting physical traits and ancestry from DNA has limitations and requires ethical consideration.