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The document concludes that AFA should be considered in patients with acromegaly-like features but normal hormone levels, and more cases need to be identified to understand the condition fully.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

A 20-year-old woman with a rare form of Turner syndrome showed improvement with hormonal therapy and needs comprehensive care.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

The SOSTDC1 gene is crucial for determining sheep wool type.

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

Alopecia areata has a complex genetic basis that was not fully understood as of 2001.

Doxazosin mesylate and saw palmetto cause genetic changes in fruit flies.

Chromosomal differences affect how muscle cells respond to testosterone.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

A gene called HDAC9 might be a new factor in male-pattern baldness.

Infertile men are more likely to produce sperm with abnormal chromosome numbers, which can affect pregnancy success and embryo health.

Researchers developed a cost-effective 66 K SNP chip for cashmere goats that is accurate and useful for genetic studies.

Researchers created specific antibodies that detect a protein important in development and various conditions, and can be used for research and diagnosis.

Rice bran oil extracted by supercritical CO2 is considered non-genotoxic.

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

Wharton’s Jelly stem cells from the umbilical cord improve skin healing and hair growth without scarring.

Sheep and goat hair fibers are complex due to keratin-associated proteins, which are important for fiber properties and growth.

Understanding wool keratin-associated proteins in sheep can help improve wool quality through selective breeding.

FGF13 gene changes cause excessive hair growth in a rare condition.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

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

No significant link between male pattern baldness and COVID-19 severity was found.

Male-pattern hair loss is largely influenced by genetics, with key genes identified.

Busulfan/cyclophosphamide and total bone irradiation are equally effective for AML transplants.

Polyamines help fix DNA damage accurately in cells.

The conclusion is that certain genetic factors and blood types may affect COVID-19 severity, but changes in ACE2 and TMPRSS2 genes are not clearly linked to it.

The research provides a gene-based framework for hair biology, highlighting the Hippo pathway's importance and suggesting links between hair disorders, cancer pathways, and the immune system.

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

The document concludes that the 5 alpha-reductase enzymes are important in steroid metabolism and related to various human diseases, with inhibitors used to treat conditions like male pattern baldness and prostate issues.