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

Mice without certain skin enzymes have faster hair growth and bigger eye glands.

Type 1 diabetes often occurs with other autoimmune diseases, and personalized treatment based on genetics can improve outcomes.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

lncRNA2919 slows down rabbit hair growth by stopping cell growth and causing cell death.

Keratin protein production in cells is controlled by a complex system that changes with cell type, health, and conditions like injury or cancer.

The SOSTDC1 gene is crucial for determining sheep wool type.

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.

Certain genes related to sulfur metabolism are more active during the growth phase of Cashmere goat wool, and melatonin might help this process.

CRISPR/Cas9 has improved precision and control but still faces clinical challenges.

Epigenetic mechanisms control skin development by regulating gene expression.

A gene mutation in Lama3 is linked to a common type of hair loss.

There are effective treatments available for baldness.

Researchers made a mouse model with curly hair and hair loss by editing a gene.

Protein tyrosine kinases are key in male pattern baldness, affecting skin structure, hair growth, and immune responses.

Polycystic Ovary Syndrome (PCOS) is a common but often undiagnosed disorder in women that can cause irregular periods, infertility, and other symptoms, and can be managed with lifestyle changes, medication, and sometimes surgery.

The document's conclusion cannot be provided because the document is not accessible or understandable.

Certain surgical methods are better than routine incision for hidradenitis suppurativa, topical clindamycin and acitretin are effective treatments, men with HS have a risk of skin cancer, HS patients are more likely to die from heart problems, and specific genetic markers are linked to treatment response.

Alopecia areata is an autoimmune disease where T cells attack hair follicles.

Patched1 helps prevent tumors by controlling cell growth.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

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

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

Actinic keratosis can lead to skin cancer, is more common in fair-skinned people, and can be reduced with sunscreen and treated effectively.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

Different hair types in mammals are linked to variations in specific protein genes, with changes influenced by their living environments.

Mice with too much Claudin-6 have skin barrier problems and abnormal hair growth.

Certain genes in Iranian sheep are linked to wool production and heat adaptation.