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<title>Channels - Bone Marrow Failure Associated With Short Telomeres and Digenic Variants of Uncertain Significance in Telomere Biology Genes :: FRELIP Discovery
Channels Bone Marrow Failure Associated With Short Telomeres and Digenic Variants of Uncertain Significance in Telomere Biology Genes
Telomere DNA in the insect order Dermaptera and the first evidence for the non-canonical telomeric motif TTCGG in Arthropoda
Epigenetic gene regulation is controlled by distinct regulatory complexes utilizing specialized paralogs of TELOMERE REPEAT BINDING FACTORS
Non-canonical telomeric motif TTAGGGGTGG in the true bug species Geocoris dispar Waga, 1839 (Heteroptera, Geocoridae)
Telomere to Telomere Genome Assembly and Efficient Transformation and Genome Editing in Populus euphratica
Giant chromosomes of a tiny plant—the complete telomere-to-telomere genome assembly of the simple thalloid liverwort Apopellia endiviifolia (Jungermanniopsida, Marchantiophyta)
Human herpesvirus 7 integrates into host telomeres via its telomeric repeat arrays
New insights into the chromosomes of stoneflies: I. Karyotype, C-banding and localization of ribosomal and telomeric DNA markers in Skwala compacta (McLachlan, 1872) (Polyneoptera, Plecoptera, Perlodidae) from Siberia
A Near Telomere‐to‐Telomere Genome of Belamcanda chinensis Provides Insights Into Genome Evolution and the Biosynthesis of Characteristic Isoflavones
Hereditary Myopathy With Early Respiratory Failure Associated With an Incidental COL4A5 Variant: A Case Report
Telomere Dysfunction and Proteostasis Decline Define Distinct Pathways of Cellular Senescence in the Human Respiratory Tract
A Novel Variant in the BICRA Gene, Expanding the Phenotype: A Case Report
Application Strategies of Bone Marrow Mesenchymal Stromal Cells in Bone‐Related Diseases
A Pilot Study of ANXA2, MED12, CALM1 and MAPK1 Gene Variants in Primary Hyperparathyroidism
Identification of a Rare Variant in the SRD5A2 Gene in Siblings With 46,XY Disorders of Sexual Development
Kufor–Rakeb Syndrome in a Guatemalan Patient With an ATP13A2 Gene Pathogenic Variant: A Case Report
RAPSN-Associated Congenital Myasthenic Syndrome due to Biallelic Single Nucleotide Variants at the Same Position
Clinical Heterogeneity of a TP53 Variant in a Consanguineous Omani Family: A Case Report Featuring a Homozygous Pathogenic Variant
Telomerization of Vinyl Chloride with Chloroform Initiated by Ferrous Chloride-Dimethylacetamide under Ultrasonic Conditions
Autologous Bone Marrow-Derived Mesenchymal Stem Cells in the Reversal of Unobstructed Azoospermia in Rats
Understanding the prevalence of germline oncogenic biomarker variants across the Indian population
Single-cell lineage tracing identifies hemogenic endothelial cells in the adult mouse bone marrow
Hypokalemic Periodic Paralysis Associated With a Rare CACNA1S Variant (p.Leu1243Val): Expanding the Mutational Spectrum
Novel KIF11 Variants with New Clinical Features: Expanding the Clinical Phenotype
Novel SIAH1 Frameshift Variant in a Chilean Patient With Buratti–Harel Syndrome
