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Research 961–990 of 1000+
- Exact, time-independent estimation of clone size distributions in normal and mutated cells
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Genome-wide DNA methylation and transcriptome analyses reveal the key gene for wool type variation in sheep
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- Regulation of somatic cell reprogramming through inducible mir-302 expression
- The JAK/STAT signaling pathway: from bench to clinic
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- Pioneer factors govern super-enhancer dynamics in stem cell plasticity and lineage choice
- ERG induces androgen receptor-mediated regulation of SOX9 in prostate cancer
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Drug Repositioning: New Approaches and Future Prospects for Life-Debilitating Diseases and the COVID-19 Pandemic Outbreak
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- FGF5 is a crucial regulator of hair length in humans
- Molecular evolution of the keratin associated protein gene family in mammals, role in the evolution of mammalian hair
- A Nonredundant Human Protein Chip for Antibody Screening and Serum Profiling
- Comprehensive transcriptome and methylome analysis delineates the biological basis of hair follicle development and wool-related traits in Merino sheep
- The Krüppel-like Factor Epiprofin Is Expressed by Epithelium of Developing Teeth, Hair Follicles, and Limb Buds and Promotes Cell Proliferation
- Temporal Layering of Signaling Effectors Drives Chromatin Remodeling during Hair Follicle Stem Cell Lineage Progression
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- PRC 2 preserves intestinal progenitors and restricts secretory lineage commitment
- Four Independent Mutations in the Feline Fibroblast Growth Factor 5 Gene Determine the Long-Haired Phenotype in Domestic Cats
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- Tinea genitalis: a new entity of sexually transmitted infection? Case series and review of the literature
- Exploring Differentially Expressed Genes by RNA-Seq in Cashmere Goat (Capra hircus) Skin during Hair Follicle Development and Cycling
- Identification of Key Pathways and Genes Related to the Development of Hair Follicle Cycle in Cashmere Goats
- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3
- Signature selection analysis reveals candidate genes associated with production traits in Iranian sheep breeds
- WNT10A promotes an invasive and self-renewing phenotype in esophageal squamous cell carcinoma
- Functional Enhancers As Master Regulators of Tissue-Specific Gene Regulation and Cancer Development.
- Scalp bacterial shift in Alopecia areata