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Research 31–60 of 1000+
- Association of mtDNA M/N haplogroups with systemic lupus erythematosus: a case-control study of Han Chinese women
- An adult case of suspected A20 haploinsufficiency mimicking polyarteritis nodosa
- Lack of concordance and linkage disequilibrium among brothers for androgenetic alopecia and CAG/GGC haplotypes of the androgen receptor gene in Mexican families
- An open-label, single-arm, clinical study to evaluate the efficacy and safety of Nyumi happy hair gummies in healthy adult subjects with hair fall
- Alopecia Areata is associated with MICA and an extended HLA haplotype
- Pioneers in Dermatology and Venereology: An interview with Professor Rudolf Happle
- What happens when simulations get real and cosmetic dermatology goes virtual?
- Does haphazard implantation of follicular units affect the long term outcome of hair growth redirection in hair restoration surgery in male baldness?
- Whatever Happened to Lasers?
- Study of Human Leukocyte Antigen ( HLA ) in 13 cases of familial frontal fibrosing alopecia: CYP 21A2 gene p.V281L mutation from congenital adrenal hyperplasia linked to HLA class I haplotype HLA ‐ A*33:01 ; B*14:02; C*08:02 as a genetic marker
- Early Skin Biopsy in Conradi‐Hünermann‐Happle Syndrome (X‐Linked Dominant Chondrodysplasia Punctata)
- Alopecia areata susceptibility variant identified by MHC risk haplotype sequencing reproduces symptomatic patched hair loss in mice
- Androgenetic Alopecia: How It Happens
- Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness
- Airway Involvement in Conradi–Hünermann–Happle Syndrome: A Novel Clinical Manifestation
- The Noggin null mouse phenotype is strain dependent and haploinsufficiency leads to skeletal defects
- Major Histocompatibility Complex Class I Chain-Related Gene A Polymorphisms and Extended Haplotypes Are Associated with Familial Alopecia Areata
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- <i>IGF2BP2</i> and <i>IGFBP3</i> Genotypes, Haplotypes, and Genetic Models Studies in Polycystic Ovary Syndrome
- The Impact of Perceived Stress, Happiness, and Religiosity on Political Orientation
- Genome-wide association study for cashmere traits in Inner Mongolia cashmere goat population reveals new candidate genes and haplotypes
- Centrifugation Determines What Is in the Syringe, Not What Happens to the Patient: A Systematic Meta-Analysis of Platelet-Rich Plasma Preparation, Platelet Integrity, Cell Counts, Growth Factors and Clinical Outcomes in Regenerative Medicine
- Faculty Opinions recommendation of The Venus flytrap trigger hair-specific potassium channel KDM1 can reestablish the K+ gradient required for hapto-electric signaling.
- A splice variant in KRT71 is associated with curly coat phenotype of Selkirk Rex cats
- Nestin-Expressing Hair Follicle-Accessible Pluripotent Stem Cells for Nerve and Spinal Cord Repair
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- Common Variants in the Sex Hormone-Binding Globulin (SHBG) Gene Influence SHBG Levels in Women with Polycystic Ovary Syndrome
- Hydrogel from Acellular Porcine Adipose Tissue Accelerates Wound Healing by Inducing Intradermal Adipocyte Regeneration
- Aging hair follicles rejuvenated by transplantation to a young subcutaneous environment
- The Associations of Androgen-Related Genes CYP21A2 and CYP19A1 with Severe Acne Vulgaris in Patients from Southwest China