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Increased Toll-like receptors in blood cells may contribute to alopecia areata and could be a target for new treatments.

Certain NK cell changes in blood may indicate alopecia areata progression.

Black hairy tongue can be an early sign of graft-versus-host disease after stem cell transplants.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

The dense fine speckled pattern in ANA tests is common in autoimmune diseases, challenging previous beliefs that it was unrelated.

The guidelines ensure accurate genetic testing and reporting for 21-hydroxylase deficiency.

CD44 variant changes start alopecia areata, but don't maintain it.

CT60 polymorphism might increase the risk of Alopecia Areata.

A specific type of immune cell plays a key role in causing alopecia areata and could be a target for treatment.

Certain blood markers, especially MLR, can help diagnose alopecia areata.

Er:YAG laser therapy effectively treats Hailey-Hailey disease, leading to long-term remission and improved quality of life.

A girl had rickets due to a gene mutation affecting vitamin D response.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

Low quality of life and high HSS-29 scores increase risk of losing patients during treatment.

LHTric-1 is a specific antibody useful for studying hair and nail formation.

Disease-specific tools better assess quality of life in alopecia areata patients.

BTNL2 helps protect hair follicles from immune attacks.

Female donor to male recipient sex mismatch and positive ACA-IgG are key risk factors for vitiligo and alopecia areata in chronic GvHD patients.

DDS treatment for LABD can cause severe side effects like anemia and hair loss, requiring careful monitoring.

Vδ1+ T-cells in the skin contribute to hair loss in alopecia areata and could be targeted for treatment.

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.

Farudodstat can prevent hair follicle immune damage linked to alopecia areata.

CD117 and platelet-derived growth factor receptor α may play a role in alopecia areata.

The document provides 70 multiple choice questions to improve haematology skills.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

IL-15 helps protect hair follicles from immune attacks and encourages hair growth.

A new tool helps study hair follicle cells to develop better treatments for hair disorders.

The A allele of the C2 gene increases the risk of lupus, while the G allele may protect against it.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.