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A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

2011 dermatological research found new skin aging markers, hair loss causes, skin defense mechanisms, and potential for new treatments.

Dermatologists give better information on pathology forms, hypersensitivity vasculitis is a common skin issue, misdiagnoses can occur, and various skin conditions are linked to loss of elastin or genetic factors.

Certain gene variations might help protect against insulin resistance and glucose intolerance in people with Polycystic Ovary Syndrome.

Porphyra-334 may help reduce wrinkles and promote hair growth.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

Rhodococcus equi causes severe pneumonia in young foals, and effective vaccines are needed due to foals' weak immune responses.

Identical twins had different symptoms because one had more cells with an extra chromosome fragment in different tissues.

Accurate diagnosis of APL is crucial to avoid unnecessary treatments.

Understanding how EDC genes are regulated can help develop better drugs for skin diseases.

Anticancer drugs are increasingly found in surface waters, and their long-term environmental effects are not well understood, requiring better testing methods.

The document concludes that eyelash trichomegaly, which is the abnormal growth of eyelashes, can be present from birth, caused by diseases, or result from certain medications.

The gene KAP22-1 affects wool yield and fiber shape in sheep.

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.

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 gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

Obesity is linked to various skin problems and may increase the risk of skin cancer.

Researchers found two genes that may explain why some Casertana pigs don't have hair.

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

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

Different types of long-lasting stem cells are responsible for the growth and upkeep of the mammary gland.

The document concludes that proper diagnosis and a multidisciplinary approach are crucial for managing Congenital Adrenal Hyperplasia effectively.

Genetics play a role in acne, but how exactly they contribute is not fully understood.

Weight loss and metformin don't significantly change vaspin levels in women with PCOS.

Light microscopy is useful for diagnosing different hair disorders.

Researchers found a genetic region that influences the number of coat layers in dogs.

Researchers found a gene mutation responsible for a rare hair loss condition.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.