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TRPV4 helps cells repair tissue and reduce scarring by controlling calcium levels.

The Msx2 gene affects feather development in Hungarian white geese and a specific gene variation could indicate feather quality.

Forensic DNA Phenotyping accurately predicts physical traits and is used in investigations, but needs more diverse population data for confirmation.

Forensic medicine is crucial for justice and needs continuous innovation and technology integration.

Early diagnosis and genetic evaluation of ADULT syndrome are crucial to reduce stress and medical costs.

The review concludes that accurate diagnosis of different types of hair loss requires proper biopsy techniques and understanding the hair growth cycle and underlying causes.

The book details skin conditions in older adults, their link to mental health, cancer treatment importance, hair loss remedies, and managing autoimmune and itchy skin.

Different fish use the same genes to regrow teeth.

The conclusion is that understanding how patterns form in biology is crucial for advancing research and medical science.

The Wnt/β-catenin pathway is important for body functions and diseases, and targeting it may treat conditions like cancer, but with safety challenges.

Different species use the same genes for tooth regeneration.

Lichen Planus is a less common condition affecting skin and mucous membranes, with various types and associated risk factors, challenging to diagnose, significantly impacts life quality, and may have a risk of cancerous changes in oral lesions.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

Blood vessels and specific genes help turn cartilage into bone when bones heal.

Hair microscopy is useful for diagnosing certain hair loss conditions but has limitations and must be interpreted carefully.

The document concludes that a thorough history, physical exam, and specific tests are crucial for diagnosing and managing hair loss effectively.

A Saudi girl was diagnosed with Loose Anagen Hair Syndrome, a rare condition causing easy hair loss without scarring.

Eruptive vellus hair cysts are a cosmetic skin condition, more common in young adults, with few effective treatments.

Hair follicles are complex, dynamic mini-organs that help us understand cell growth, death, migration, and differentiation, as well as tissue regeneration and tumor biology.

Bovines can have rare inherited skin diseases with specific symptoms like hair loss, fragile skin, and abnormal porphyrin buildup.

Accurate diagnosis and tailored treatments are crucial for managing hair loss in humans and animals.

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

Skin abnormalities can indicate immunodeficiency due to shared origins with the immune system.

Lactic acid cream can help improve skin bumps known as eruptive vellus hair cysts.

The study found no common cause for a girl's crystalline cataract and uncombable hair, suggesting their co-occurrence might be coincidental.

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

Two siblings were found to have a genetic condition causing progressive hair loss and woolly hair, which may often be misdiagnosed.

Mother and son diagnosed with a rare genetic hair loss condition with no effective treatment.

The conclusion is that proper signaling is crucial for hair growth and development, and errors can lead to cancer or hair loss.

Alopecia areata is an autoimmune condition causing hair loss due to the immune system attacking hair follicles, often influenced by genetics and stress.