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Research 421–450 of 1000+
- Dimorphic regulation of the MafB gene by sex steroids in hamsters (Mesocricetus auratus)
- The association of Wnt – Factor TCF7L2 (TCF4) gene polymorphism and treated Alopecia Areata (Platelet rich plasma Vs conventional)
- Molecular Genetic Characteristics of the Hoxc13 Gene and Association Analysis of Wool Traits
- Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men
- Molecular characterisation of keratin-associated protein-7 (KRTAP7) gene for hair quality in Indian Dromedary Camel
- DEFINING THE ROLE OF ABI1 GENE IN PROSTATE CANCER PROGRESSION AND TREATMENT RESISTANCE
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- Pharmacological investigation of vitamin E with combined oral contraceptives on INHBA gene against PCOS that intricate through melatonin PKC pathway
- The FRZB gene regulates hair follicle development in rabbits via the Wnt/β-catenin signaling pathway
- ANALYSIS OF CTLA 4 GENE +49A/G AND CT60 A/G POLYMORPHISMS IN ALOPECIA AREATA PATIENTS
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis
- Finasteride Induces Epigenetic Alteration of TMPRss2 Gene Expression: A Potential role in Severe Acute Respiratory Syndrome-Corona Virus-2 Inhibition
- 468 Use of calcitonin gene-related peptide monoclonal antibodies in patients with rosacea: An exploratory, comparative case series
- 1440 DNA dioxygenases Tet2/3 regulate gene promoter accessibility and chromatin topology in lineage-specific loci to control keratinocyte differentiation and hair growth
- 157 Analysis of the hybrid schwannoma and neurofibroma including a case report of schwannomatosis caused by a mutation in the LZTR1 gene
- The Relation of the SHBG Gene Polymorphism (rs1799941) with PCOS in a Group of Iraqi Women
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- Alymphoid cystic thymic dysgenesis - FOXN1 gene mutation: a rare case report of two siblings
- 764 DNA dioxygenases Tet1/2/3 control hair matrix keratinocyte differentiation and hair shaft shape via regulation of hair keratin gene expression
- In silico analysis of imprinted gene expression in the mouse skin
- Spectrum of clinical manifestations of SLE patients from India and its correlation with KIR gene polymorphism
- 1392 Activation of Id2 gene regulatory network ruling quiescence of hair follicle stem cells
- AKT2 Gene Polymorphisms, sRANKL/OPG and Hormone Measurements in Polycystic Ovarian Syndrome (PCOS) Women
- A homozygous single T deletion found in the GGCX gene with PXE-like phenotypes
- Genetic screening of non-classic CAH females with hyperandrogenemia identifies a novel CYP11B1 gene mutation
- Association between epidermal growth factor and epidermal growth factor receptor gene polymorphisms and susceptibility to alopecia areata in Korean population
- Evolution in action: highlighting a role for the Agouti gene in development?
- Construction and Activity Analysis of K14/K5 Promoter Vector Containing Luciferase Gene
- Mutation analysis of type II hair keratin gene in a pedigree with monilethrix
- 026 Altered Skin Wound Healing in Homeobox Gene Msx-2 Knockout Mice