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A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

A genetic mutation caused severe rickets and alopecia in an Indian patient, but high-dose calcium and phosphate treatment improved their condition.

Scientists successfully created and analyzed the structure of a part of the human androgen receptor with specific modulators and a peptide to understand how it binds differently in various tissues.

A mutation in the vitamin D receptor causes severe resistance to vitamin D, affecting bone health but not hair growth.

A 12-year-old boy with PAIS successfully developed male characteristics using high-dose testosterone and anastrozole.

The vitamin D receptor is essential for normal hair growth, even without its usual binding.

A mutation in the VDR gene affects hair cycling without needing ligand binding.

Vitamin D receptor and hairless protein are essential for hair growth.

Vitamin D receptor is essential for hair growth and preventing hair loss.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

The study found that certain mutations in the vitamin D receptor can cause rickets and potentially affect hair growth.

Riboflavin 5′-phosphate (FMN) shows potential for treating androgen-related conditions but may be limited in treating prostate cancer.

DHT enhances androgen receptor activity more than testosterone, and MAGE-11 influences this activity through specific interactions.

New androgen receptor modulators show promise for treating diseases like prostate cancer and muscle wasting.

The androgen receptor's shape-changing ability helps it function but can lead to cancer treatment resistance.

Tunisian children with hereditary vitamin D-resistant rickets showed improvement with calcium treatment, and new genetic mutations were identified.

Teicoplanin may help treat hair loss by reducing androgen receptors and boosting hair cell growth.

Removing part of the vitamin D receptor stops vitamin D from working properly.

Mutations in the enzyme don't significantly change how it binds to its specific substances.

LEF1 interacts with Vitamin D Receptor, affecting hair follicle regeneration and this could be linked to hair loss conditions.

A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

Certain changes to the B-ring of androgen receptor ligands can increase their effectiveness for potential treatments of muscle and bone conditions.

The study concludes that certain domains in Clostridium histolyticum enzymes are structurally unique, bind calcium to become more stable, and play distinct roles in breaking down collagen, with potential applications in medicine and drug delivery.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Specific mutations in a receptor cause facial abnormalities and hair loss.

A single amino acid change in the vitamin D receptor can disrupt its function and lead to hair loss.

A new mutation linked to partial Androgen Insensitivity Syndrome and prostate cancer was found in a patient unhappy with their female gender assignment.

KATP channels are important for energy balance and are targeted by drugs for diabetes, hypoglycemia, hypertension, and hair loss.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

A compound from Calophyllum inophyllum L. leaf may help treat non-small cell lung cancer.