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Fasting in hens affects thyroid hormones, which regulate feather and hair growth.

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

Chinese domestic goats have unique genetic traits due to domestication and geographic isolation.

The study found that PCOS affects about 6.5-6.8% of women in both urban and rural areas of Telangana, India, and highlighted the importance of lifestyle changes for management.

Topical ceramide treatment partially improves the skin condition in Jack Russell Terriers with a genetic skin disorder.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

Plant sterols have health benefits like lowering cholesterol, but more research is needed to understand their effects and improve their extraction and sustainability.

Hair microscopy is useful for diagnosing hair disorders, but clear definitions are needed for accurate genetic analysis.

Higher miR-34a levels and the A variant of the MIR-34A gene are linked to increased risk and severity of alopecia areata.

Two new reliable Arabic questionnaires for measuring quality of life in women with PCOS were created, one for married and one for unmarried women.

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

Human hair follicle cells can grow hair when put into mouse skin if they stay in contact with mouse cells.

The study showed that hair follicle stem cells can maintain and organize themselves in a lab setting, keeping their ability to renew and form hair and skin.

Hair diameter and curvature are mostly determined by genetics.

A man with hypoparathyroidism had other health issues that led to a diagnosis of a rare autoimmune disorder, APS-1.

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

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

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

The document concludes that recognizing and properly diagnosing lipodystrophy syndromes is crucial for effective management and treatment.

Spironolactone harms fish reproduction and is more potent in fish than invertebrates, needing environmental monitoring.

Bleaching hair damages protein structure, especially keratin, leading to weakened hair.

The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

The article concludes that global standardization in PCOS research is crucial for accurate diagnosis and understanding of the condition.

DNA phenotyping helps predict physical traits from DNA with varying accuracy and requires careful ethical and legal handling.

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

Tiny particles from 3D-grown skin cells speed up wound healing by promoting blood vessel growth.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

A thorough initial check-up is essential before sperm banking to ensure the best chance of preserving good quality sperm.

Triptolide effectively and safely reduces actinic keratosis lesions in mice.