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3. Functional annotation of the animal genomes: An integrated annotation resource for the horse

4. First reported case of fragile foal syndrome type 1 in the Thoroughbred caused by PLOD1 c.2032G>A

5. Breed Distribution and Allele Frequencies of Base Coat Color, Dilution, and White Patterning Variants across 28 Horse Breeds.

6. Analysis of Genetic Diversity in the American Standardbred Horse Utilizing Short Tandem Repeats and Single Nucleotide Polymorphisms

8. Prevalence of clinical signs and factors impacting expression of myosin heavy chain myopathy in Quarter Horse‐related breeds with the MYH1E321G mutation

9. Prediction of histone post-translational modification patterns based on nascent transcription data.

10. DNA methylation aging and transcriptomic studies in horses

11. Mining the 99 Lives Cat Genome Sequencing Consortium database implicates genes and variants for the Ticked locus in domestic cats (Felis catus)

12. A novel DDB2 mutation causes defective recognition of UV-induced DNA damages and prevalent equine squamous cell carcinoma

14. Generation of a Biobank From Two Adult Thoroughbred Stallions for the Functional Annotation of Animal Genomes Initiative.

15. Identification of W13 in the American Miniature Horse and Shetland Pony Populations

16. Decoding the Equine Genome: Lessons from ENCODE

17. Comparison of Poly-A+ Selection and rRNA Depletion in Detection of lncRNA in Two Equine Tissues Using RNA-seq.

18. A de novo MITF Deletion Explains a Novel Splashed White Phenotype in an American Paint Horse

19. Functionally Annotating Regulatory Elements in the Equine Genome Using Histone Mark ChIP-Seq

20. DDB2 Genetic Risk Factor for Ocular Squamous Cell Carcinoma Identified in Three Additional Horse Breeds

21. Distribution of the Warmblood Fragile Foal Syndrome Type 1 Mutation (PLOD1 c.2032G>A) in Different Horse Breeds from Europe and the United States

22. Horses with equine recurrent uveitis have an activated CD4+ T-cell phenotype that can be modulated by mesenchymal stem cells in vitro.

23. Functionally Annotating Regulatory Elements in the Equine Genome Using Histone Mark ChIP-Seq.

24. Author Correction: Improved reference genome for the domestic horse increases assembly contiguity and composition

25. Frameshift Variant in MFSD12 Explains the Mushroom Coat Color Dilution in Shetland Ponies.

26. Additional Evidence for DDB2 T338M as a Genetic Risk Factor for Ocular Squamous Cell Carcinoma in Horses

27. Effects of high fat diet-induced obesity on mammary tumorigenesis in the PyMT/MMTV murine model

28. Erratum: Author Correction: Improved reference genome for the domestic horse increases assembly contiguity and composition.

30. Breed predispositions to congenital and juvenile cataracts in horses at two academic institutions.

31. Improved reference genome for the domestic horse increases assembly contiguity and composition.

32. Redundant contribution of a Transient Receptor Potential cation channel Member 1 exon 11 single nucleotide polymorphism to equine congenital stationary night blindness

33. Naturally occurring horse model of miscarriage reveals temporal relationship between chromosomal aberration type and point of lethality.

35. GO‐FAANG meeting: a Gathering On Functional Annotation of Animal Genomes

36. Additional evidence supports GRM6 p.Thr178Met as a cause of congenital stationary night blindness in three horse breeds.

37. An intronic copy number variation inSyntaxin 17determines speed of greying and melanoma incidence in Grey horses

38. Additional evidence supports GRM6 p.Thr178Met as a cause of congenital stationary night blindness in three horse breeds

39. Evidence for a retroviral insertion in TRPM1 as the cause of congenital stationary night blindness and leopard complex spotting in the horse.

41. Delayed embryonic development or a long sperm survival in two mares—A registration conundrum.

44. Risk factors for insidious uveitis in the Knabstrupper breed.

45. Risk factors for insidious uveitis in the Knabstrupper breed

49. Prevalence of the RAPGEF5 c.2624C>A and PLOD1 c.2032G>A variants associated with equine familial isolated hypoparathyroidism and fragile foal syndrome in the US Thoroughbred population (1988–2019).

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