Search
for
Sort by
Research 721–750 of 1000+
- Skin transcriptome reveals the periodic changes in genes underlying cashmere (ground hair) follicle transition in cashmere goats
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Molecular characterization of caprine<i>KRTAP13-3</i>in Liaoning cashmere goat in China
- Shedding light on cashmere goat hair follicle biology: from morphology analyses to transcriptomic landascape
- Analysis of Genome DNA Methylation at Inherited Coat Color Dilutions of Rex Rabbits
- Selective Janus kinase 1 inhibition resolves inflammation and restores hair growth offering a viable treatment option for alopecia areata
- Application of lncRNA-miRNA-mRNA ceRNA network analysis in the treatment of androgenic alopecia.
- Medicinal Plants as Reservoirs of Endophytic Bacterial Genes Regulating Stress Tolerance: A Metagenomic Study on Eclipta prostrata (L.) L.
- Exosomal miRNA-218–5p derived from low-passage dermal papilla cells modulates hair follicle growth and development
- Differential expression of keratin and keratin associated proteins are linked with hair loss condition in spontaneously mutated inbred mice
- 766 H3K9me3 methyltransferase SETDB1 controls retrotransposon silencing, DNA methylation, constitutive heterochromatin maintenance and 3D-chromatin structure in epidermal keratinocytes
- Genome-wide detection of RNA editing events during the hair follicles cycle of Tianzhu white yak
- Video2_BBS7–SHH Signaling Activity Regulates Primary Cilia for Periodontal Homeostasis.MP4
- 376 Tsc2 disruption in mesenchymal progenitors regulates hair follicles and TGF beta signaling
- Hereditary Vitamin D Resistant Rickets: Clinical, Laboratory, and Genetic Characteristics of 2 Iranian Siblings
- Transforming 300 billion points of data into diagnostics, therapeutics and new insights into disease
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Adipose transcriptome in the scalp of androgenetic alopecia
- Transcriptome Profiling of Pilosebaceous Units in Male Androgenetic Alopecia Reveals Altered Junctional Networks
- ATP-dependent chromatin remodeling during mammalian development
- Cantú Syndrome Is Caused by Mutations in ABCC9
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Planar Cell Polarity Cadherin Celsr1 Regulates Skin Hair Patterning in the Mouse
- Temporal Layering of Signaling Effectors Drives Chromatin Remodeling during Hair Follicle Stem Cell Lineage Progression
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Significance of stress keratin expression in normal and diseased epithelia
- Sustained Exosome‐Guided Macrophage Polarization Using Hydrolytically Degradable PEG Hydrogels for Cutaneous Wound Healing: Identification of Key Proteins and MiRNAs, and Sustained Release Formulation
- The vitamin D receptor functions as a transcription regulator in the absence of 1,25-dihydroxyvitamin D3
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients