Search
for
Sort by
Research 511–540 of 1000+
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Genetic Hair Disorders: A Review
- YAP/TAZ Signalling Controls Epidermal Keratinocyte Fate
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- Abstract 14
- A Kaleidoscope of Keratin Gene Expression and the Mosaic of Its Regulatory Mechanisms
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report
- Functional Enhancers As Master Regulators of Tissue-Specific Gene Regulation and Cancer Development.
- Monilethrix: a typical case report with microscopic and dermatoscopic findings
- Pili annulati with fragility: Electron microscopic findings of a case
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Ichthyosis linearis circumflexa in a child. Response to narrowband UVB therapy.
- A phase 2a study investigating the effects of ritlecitinib on brainstem auditory evoked potentials and intraepidermal nerve fiber histology in adults with alopecia areata
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- The emerging roles of N6-methyladenosine (m6A) deregulation in polycystic ovary syndrome
- Pathophysiology and Nutritional Approaches in Polycystic Ovary Syndrome (PCOS): A Comprehensive Review
- Zebrafish Model of Hereditary Pigmentary Disorders
- Ectodermal Dysplasia: Variable Expressions
- Coordinating the Sculptors: Ectodysplasin-A (EDA) Signaling Cross-Talk with Skeletogenic Pathways
- A missense mutation in Lama3 causes androgen alopecia
- Omenn syndrome in a 10-month-old male with athymia and VACTERL association
- Genome Wide Differential Expression Profiles in Nevus Sebaceous Uncovered Low Expression of CDKN2AIP and Construction of a ceRNA Network
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- Society for Endocrinology guidelines for testosterone replacement therapy in male hypogonadism
- Adenolipoma—Eccrine and Apocrine Variants With Evidence for a Hamartomatous Process
- Hub biomarkers in ultrasound-guided bladder cancer and osteosarcoma: Myosin light chain kinase and caldesmon
- Genetic and other epidemiological risk factors of infants and children with hypospadias: a case control study
- Molecular landscape of lung cancer: insights into therapeutic targets and clinical outcomes
- Relationship between Platelets, Plateletcrit and Lymphocytes in the Complete Blood Count and Recurrent Implantation Failure: A Retrospective Study
- Conditional telomerase induction causes proliferation of hair follicle stem cells