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Certain genetic markers linked to wool quality in Rambouillet sheep were identified, which can guide better breeding choices.

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.

Two siblings with a genetic mutation had a form of rickets that doesn't respond to vitamin D.

Five new mutations in the androgen receptor gene were found, helping to understand androgen insensitivity syndrome better.

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

Transplanted hair follicles can resist hair loss from an autoimmune condition better than natural hair.

Vitiligo is linked to autoimmune diseases and hearing issues, so hearing tests are recommended for patients.

Male pattern baldness is mostly inherited, involves many genes, and is linked to other traits like early puberty and strong bones.

Feather patterns form through genetic and epigenetic controls, with cells self-organizing into periodic patterns.

A special gene region controls the re-emergence of a primitive wool type in Merino sheep, improving their wool yield and adaptability.

An 11-year-old child with total hair loss may have a genetic autoimmune disease, and the outlook for hair regrowth is not good.

Prunus mira Koehne is valuable for hair growth and has potential for sustainable use, but needs more research and conservation.

Six genetic conditions are often linked to complete scalp hair loss in children.

Cancer development is like natural selection, involving mutated cells and environmental factors.

New genetic discoveries may lead to better treatments for alopecia areata.

Using 17-hydroxyprogesterone levels to diagnose nonclassic congenital adrenal hyperplasia can result in many incorrect diagnoses.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

Certain genetic variations in IL18 may increase the risk of alopecia areata in Koreans.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

Researchers identified genes and proteins that may influence wool thickness in sheep.

Baricitinib and its combination with lonafarnib improve fat cell formation in certain genetic disorders.

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.

Sardinians were historically short due to a mix of genetics and factors like disease and poor nutrition, but recent height increases suggest better living conditions had a bigger impact.

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

The document concludes that alopecia areata is an unpredictable autoimmune hair loss condition with no cure, but various treatments exist that require personalized approaches.

Diagnosing alopecia areata is challenging and requires careful examination and various tests to distinguish it from other hair loss types.

New treatments like nanotechnology show promise in improving skin cancer therapy.

Researchers found genes that may explain why some pigs grow winter hair, which could help breed cold-resistant pigs.

People with hypohidrotic ectodermal dysplasia are more likely to experience long-term fatigue and hair loss after COVID-19.

Hair follicle development in cashmere goats involves dynamic changes in proteins and metabolites, with key roles for oxytocin, MAPK, and Ca2+ pathways.