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A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

Deleting Snai2 and Snai3 causes fatal autoimmunity.

Mice lacking the PPARγ gene in their fat cells had almost no fat tissue, severe metabolic problems, and abnormal development of other fat-related tissues.

The document concludes that careful diagnosis is crucial for chromosome 13q deletion syndrome, tamoxifen can cause reversible eye damage, finasteride may be linked to cataracts, and OCT is useful for diagnosing macular diseases.

Bexxar treatment led to a high response rate in patients with advanced-stage, treatment-resistant follicular lymphoma.

Mice lacking a key DNA methylation enzyme in skin cells have a lower chance of activating stem cells necessary for hair growth, leading to progressive hair loss.

Mice without certain skin proteins had abnormal skin and hair development.

Brain-Derived Neurotrophic Factor (BDNF) slows down hair growth and promotes hair follicle regression.

Certain mouse strains develop a skin condition similar to a human hair loss disease due to genetic defects.

Epidermal Growth Factor helps hair follicle cells grow and move by activating a specific cell signaling pathway.

sPLA2-X is crucial for normal hair growth and follicle health.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

Eye exams are crucial for kids with 13q deletion syndrome, tamoxifen can cause vision loss, Propecia may lead to cataracts, Lipoid Proteinosis causes skin bumps, and OCT is useful for diagnosing macular diseases.

Vitamin D receptor is important for regulating hair growth and wound healing in mice.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

A patient with myotonic dystrophy had several autoimmune disorders and thyroid cancer, suggesting a possible link between these conditions.

UVB radiation harms hair growth and health, causing cell death and other changes in human hair follicles.

Zouboulis syndrome is a rare condition that helps diagnose monosomy 18p early.

Examining scalp tissue under a microscope helps diagnose and understand hair loss diseases.

Lichen planopilaris is a rare, chronic condition causing hair loss, mainly in middle-aged women, and early treatment is important to prevent permanent baldness.

Fat-related cells are important for initiating hair growth.

Testing basal 17-HP levels is a good way to screen for nonclassic adrenal hyperplasia in women with high androgen levels.

Some people with pattern hair loss may also have scalp inflammation and scarring similar to lichen planopilaris.

Manipulating the catagen and telogen phases of hair growth could lead to treatments for hair disorders.

Hair greying is caused by oxidative stress damaging hair follicles and melanocytes.

Pitx2 helps outer root sheath cells differentiate but can't start hair growth on its own.

Scientists found cells in hair that are key for growth and color.

AGA patients have fewer hairs and smaller follicles; T:V ratio above 4:1 may indicate AGA.