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Research 31–60 of 32
- Proteolysis‐Targeting Chimera (PROTAC): Current Applications and Future Directions
- Advancing Design Strategy of PROTACs for Cancer Therapy
- Case Report: A Chinese Family of Woodhouse-Sakati Syndrome With Diabetes Mellitus, With a Novel Biallelic Deletion Mutation of the DCAF17 Gene
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
- Woodhouse-Sakati Syndrome: The New Genetic Variant of DCAF17 In 2 Adult Sisters
- Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati Syndrome
- Endocrine disorders in Woodhouse-Sakati syndrome: a systematic review of the literature
- Woodhouse-Sakati syndrome (WSS)
- Writer’s Cramp Presentation of Woodhouse–Sakati Syndrome – “Out of the Woods”
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- Expanding on the phenotypic spectrum of Woodhouse‐Sakati syndrome due to founder pathogenic variant in <i>DCAF17</i>: Report of 58 additional patients from Qatar and literature review
- Genomic prediction and genome-wide association studies of morphological traits and distraction index in Korean Sapsaree dogs
- Cost-effectively dissecting the genetic architecture of complex wool traits in rabbits by low-coverage sequencing
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Woodhouse-Sakati Syndrome with Unique Unreported Previous Findings
- Cost-effectively dissecting the genetic architecture of complex wool traits in rabbits by low-coverage sequencing
- Identification of Candidate Genes for Min Pig Villi Hair Traits by Genome-Wide Association of Copy Number Variation
- <i>C2orf37</i> mutational spectrum in Woodhouse–Sakati syndrome patients
- Genome-Wide Associations with Body and Fleece Weight in United States Sheep
- Tissue-Specific Multi-Omics Integration Demonstrates Molecular Signatures Connecting Obesity to Immune Vulnerability
- Increasing GSH-Px Activity and Activating Wnt Pathway Promote Fine Wool Growth in FGF5-Edited Sheep
- Progress on genome-wide association studies and selection signature analysis for agronomic traits in Chinese sheep and goats: review
- Molecular Morbidity Score–Can MicroRNAs Assess the Burden of Disease?
- Table_1_Bioinformatics and Network Pharmacology Identify the Therapeutic Role and Potential Mechanism of Melatonin in AD and Rosacea.xlsx
- Novel circRNAs from cashmere goats: Discovery, integrated regulatory network, and their putative roles in the regeneration and growth of secondary hair follicles
- Polyglandular autoimmune syndrome type 4 with GAD antibody and dystonia
- FOXP3 <sup>+</sup> regulatory T cells and age‐related diseases