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The study found genetic differences related to hair development that may explain hair loss in a patient with Trichorhinophalangeal syndrome type I.

The research found specific genes that may cause longer hair in Tianzhu White Yak.

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

The most different genetic segment between Africans and East Asians is the EDA2R/AR region, with two main types influenced by population changes and natural selection, and linked to baldness.

Keratin-associated proteins have ancient origins and were used for different purposes before being adapted for hair in mammals.

A specific genetic deletion in goats affects cashmere yield and thickness.

The workshop highlighted the genetic links and psychological impacts of hair loss and skin disorders.

Different types of skin cells have unique genetic markers that affect how likely they are to spread cancer.

Polycystic Ovary Syndrome likely starts in childhood and may be genetic and influenced by early hormone exposure.

The review suggests thorough evaluation and genetic testing for proper diagnosis and treatment of Chrousos syndrome.

Chinese domestic goats have unique genetic traits due to domestication and geographic isolation.

The Asiatic lion has very low genetic diversity and unique genetic traits, highlighting the need for its conservation.

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.

Skin patterns form through molecular signals and genetic factors, affecting healing and dermatology.

A mother's diet at conception can cause lasting genetic changes in her child.

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

The document concludes that PCOS is a complex disorder caused by both genetic and environmental factors, affecting women's health in various ways, and requires personalized treatment.

The Rotterdam Study aims to understand disease causes in the elderly and has found new risk factors and genetic influences on various conditions.

LGR5 and LGR6 are expressed differently in various skin tumors, which may offer clues about their origins.

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

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

Dermatologists need to understand diverse cultural hair practices to offer better care.

Hair follicle stem cells are a promising source for tissue repair and treating skin or hair diseases.

Hairlessness in mammals is due to complex genetic changes in both genes and regulatory regions.

The Rotterdam Study found risk factors for elderly diseases, links between lifestyle and genetics with health conditions, and aimed to explore new areas like DNA methylation and sensory input effects on brain function.

Stem cell niches are crucial for regulating stem cell behavior and tissue health, and their decline can impact aging and cancer.

Insulin resistance and obesity are key factors in the development and worsening of polycystic ovary syndrome, and lifestyle changes are important for managing it.

Biomaterials with MSC-derived substances could improve tissue repair and have advantages over direct cell therapy.

Cancer development is like natural selection, involving mutated cells and environmental factors.

Skin grafts are effective for chronic leg ulcers, especially autologous split-thickness grafts for venous ulcers, but more data is needed for diabetic ulcers.