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A specific RNA molecule, circCOL1A1, affects the growth and quality of goat hair by interacting with miR-149-5p and influencing cell growth pathways.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

Box A of HMGB1 can improve stem cell function, aiding anti-aging therapy.

Young women in West Bengal, India, with PCOS often have estrogen resistance, leptin receptor issues, folate deficiency, T2DM, and acanthosis, commonly linked to obesity.

Combining genetic and physical trait analysis improves diagnosis accuracy for monogenic diabetes.

The mTurq2-Col4a1 mouse model shows that cells can divide while attached to stable basement membranes during development.

Wild African goats have genetic adaptations for surviving harsh desert conditions.

New treatments and diagnostic methods for various animal skin conditions showed promising results.

The document is a detailed medical reference on skin and genetic disorders.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

Multi-omics techniques help understand the molecular causes of androgenetic alopecia.

The mTurq2-Col4a1 mouse model shows how the basement membrane develops in live mammals.

Genetic variations greatly affect individual metabolism and can impact health and disease risk.

Autofluorescence can sort plant cells without labeling.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

Colorectal cancer development involves both genetic changes and epigenetic alterations like DNA methylation and microRNA changes.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

New genetic locations explain much of hair color variation in Europeans.

Researchers found that certain RNA circles in the brain are linked to disease risk, but their exact role in disease is still unknown.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

HLA-DRB5 and other genes may be linked to alopecia universalis.

The research confirms that Hidradenitis Suppurativa is characterized by increased inflammation, disrupted skin cell organization, and abnormal metabolic processes.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

Two mutations in KRT74 and EDAR genes cause sheep to have finer wool.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

DAVID syndrome is a condition with immune system and hormone deficiencies, needing early diagnosis to avoid serious complications.

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.