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Chitosan-encapsulated Cordyceps militaris reduces lung cell damage from pollution.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

The document suggests treating individuals with nonclassic congenital adrenal hyperplasia who show symptoms, especially those related to excess male hormones.

The hr gene is crucial for skin and hair health, with mutations causing hair disorders.

Standard reference values for hair analysis in healthy Indian males were established.

CCC1 is essential for pH balance and normal cell function in plants.

Shh and Dhh affect skin development and can cause tumors, while Ihh does not.

CCCA can appear as patchy hair loss in younger men, not just the usual pattern.

Elderly patients with CCCA were all African American with low vitamin D, but no iron or zinc deficiencies, and no hormonal imbalances compared to younger patients.

The research found that the properties of solid-state Electronic Circular Dichroism (ss-ECD) are influenced by the orientation of local crystals, which could help in examining and mapping chiral materials like pharmaceutical ingredients.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Cronkhite-Canada syndrome is a rare, non-inherited condition causing various symptoms like polyps, hair loss, and weight loss.

Damaged hair follicles make mice more prone to skin inflammation and skin cancer after UV exposure.

Genetic mutation and carcinogen treatment are both needed for skin cancer to develop in these specific mice.

Some Chrysanthemum samples from the USA, Europe, and China differ in quality and some contain harmful cadmium.

A 12-year-old boy has a rare, harmless hair loss on his chin with no need for treatment.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

CCCA causes progressive hair loss in Black women, starting from a central scalp patch.

CCCA is a common hair loss condition in African American women, often inherited and influenced by hairstyling, with unique scalp features detectable by special tools.

Cronkhite-Canada syndrome can cause multiple gastrointestinal polyps and various physical symptoms.

The study found that Central Centrifugal Cicatricial Alopecia mainly affects middle-aged African descent women, is linked to certain hair care practices and genetics, and often goes undiagnosed for years.

Some parents have a mild form of congenital adrenal hyperplasia without symptoms, and they usually don't need treatment.

Chikungunya can cause hyperpigmentation in children and should be considered in diagnosis.

Genetic factors, especially PADI3 gene variants, contribute to CCCA in women of African descent.

Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.

Chitin nanofibrils can improve skin health and help deliver active ingredients into the skin.

The gene for Clouston syndrome in a large Indian family is located in the 13q11-q12.1 region.

CTCF protein is essential for skin and hair follicle development in mice.

HAIRCARECUBE TM (HCC) helps hair products work better by getting active ingredients deeper into the hair.

GCN reduces lung inflammation and damage from air pollution in mice.