Connection

BRENDAN LEE to Animals

This is a "connection" page, showing publications BRENDAN LEE has written about Animals.
Connection Strength

1.018
  1. De novo variants in RYBP are associated with a severe neurodevelopmental disorder and congenital anomalies. Genet Med. 2025 Apr; 27(4):101369.
    View in: PubMed
    Score: 0.051
  2. The IFITM5 mutation in osteogenesis imperfecta type V is associated with an ERK/SOX9-dependent osteoprogenitor differentiation defect. J Clin Invest. 2024 Jun 17; 134(15).
    View in: PubMed
    Score: 0.049
  3. Boosting glycolysis to combat fragile bone in type 1 diabetes. Cell Chem Biol. 2023 09 21; 30(9):1002-1003.
    View in: PubMed
    Score: 0.046
  4. Molecular alterations due to Col5a1 haploinsufficiency in a mouse model of classic Ehlers-Danlos syndrome. Hum Mol Genet. 2022 04 22; 31(8):1325-1335.
    View in: PubMed
    Score: 0.042
  5. Localized chondro-ossification underlies joint dysfunction and motor deficits in the Fkbp10 mouse model of osteogenesis imperfecta. Proc Natl Acad Sci U S A. 2021 06 22; 118(25).
    View in: PubMed
    Score: 0.040
  6. Tendon and motor phenotypes in the Crtap-/- mouse model of recessive osteogenesis imperfecta. Elife. 2021 05 26; 10.
    View in: PubMed
    Score: 0.039
  7. Combinatorial Prg4 and Il-1ra Gene Therapy Protects Against Hyperalgesia and Cartilage Degeneration in Post-Traumatic Osteoarthritis. Hum Gene Ther. 2019 02; 30(2):225-235.
    View in: PubMed
    Score: 0.033
  8. Argininosuccinate Lyase Deficiency Causes an Endothelial-Dependent Form of Hypertension. Am J Hum Genet. 2018 08 02; 103(2):276-287.
    View in: PubMed
    Score: 0.032
  9. Arginase overexpression in neurons and its effect on traumatic brain injury. Mol Genet Metab. 2018 09; 125(1-2):112-117.
    View in: PubMed
    Score: 0.032
  10. Gene therapy for repair and regeneration of bone and cartilage. Curr Opin Pharmacol. 2018 06; 40:59-66.
    View in: PubMed
    Score: 0.032
  11. Osteocyte-specific WNT1 regulates osteoblast function during bone homeostasis. J Clin Invest. 2017 Jun 30; 127(7):2678-2688.
    View in: PubMed
    Score: 0.030
  12. MicroRNA miR-23a cluster promotes osteocyte differentiation by regulating TGF-? signalling in osteoblasts. Nat Commun. 2017 04 11; 8:15000.
    View in: PubMed
    Score: 0.030
  13. Fkbp10 Deletion in Osteoblasts Leads to Qualitative Defects in Bone. J Bone Miner Res. 2017 Jun; 32(6):1354-1367.
    View in: PubMed
    Score: 0.030
  14. Loss of DDRGK1 modulates SOX9 ubiquitination in spondyloepimetaphyseal dysplasia. J Clin Invest. 2017 Apr 03; 127(4):1475-1484.
    View in: PubMed
    Score: 0.029
  15. Genetic causes and mechanisms of Osteogenesis Imperfecta. Bone. 2017 Sep; 102:40-49.
    View in: PubMed
    Score: 0.029
  16. Restoration of the serum level of SERPINF1 does not correct the bone phenotype in Serpinf1 null mice. Mol Genet Metab. 2016 Mar; 117(3):378-82.
    View in: PubMed
    Score: 0.027
  17. Human recombinant arginase enzyme reduces plasma arginine in mouse models of arginase deficiency. Hum Mol Genet. 2015 Nov 15; 24(22):6417-27.
    View in: PubMed
    Score: 0.027
  18. Notch activation as a driver of osteogenic sarcoma. Cancer Cell. 2014 Sep 08; 26(3):390-401.
    View in: PubMed
    Score: 0.025
  19. Argininosuccinate lyase in enterocytes protects from development of necrotizing enterocolitis. Am J Physiol Gastrointest Liver Physiol. 2014 Aug 01; 307(3):G347-54.
    View in: PubMed
    Score: 0.024
  20. Branched-chain amino acid metabolism: from rare Mendelian diseases to more common disorders. Hum Mol Genet. 2014 Sep 15; 23(R1):R1-8.
    View in: PubMed
    Score: 0.024
  21. The swaying mouse as a model of osteogenesis imperfecta caused by WNT1 mutations. Hum Mol Genet. 2014 Aug 01; 23(15):4035-42.
    View in: PubMed
    Score: 0.024
  22. Differential effects of collagen prolyl 3-hydroxylation on skeletal tissues. PLoS Genet. 2014 Jan; 10(1):e1004121.
    View in: PubMed
    Score: 0.024
  23. Proteoglycan 4 expression protects against the development of osteoarthritis. Sci Transl Med. 2013 Mar 13; 5(176):176ra34.
    View in: PubMed
    Score: 0.022
  24. Quantitative imaging of murine osteoarthritic cartilage by phase-contrast micro-computed tomography. Arthritis Rheum. 2013 Feb; 65(2):388-96.
    View in: PubMed
    Score: 0.022
  25. miRNA-34c regulates Notch signaling during bone development. Hum Mol Genet. 2012 Jul 01; 21(13):2991-3000.
    View in: PubMed
    Score: 0.021
  26. C-terminal frameshift variants in GPKOW are associated with a multisystemic X-linked disorder. Genet Med. 2025 Jul; 27(7):101429.
    View in: PubMed
    Score: 0.013
  27. A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3. Am J Hum Genet. 2024 01 04; 111(1):96-118.
    View in: PubMed
    Score: 0.012
  28. Dominant negative variants in KIF5B cause osteogenesis imperfecta via down regulation of mTOR signaling. PLoS Genet. 2023 Nov; 19(11):e1011005.
    View in: PubMed
    Score: 0.012
  29. Yap and Taz promote osteogenesis and prevent chondrogenesis in neural crest cells in vitro and in vivo. Sci Signal. 2022 10 25; 15(757):eabn9009.
    View in: PubMed
    Score: 0.011
  30. 4-PBA Treatment Improves Bone Phenotypes in the Aga2 Mouse Model of Osteogenesis Imperfecta. J Bone Miner Res. 2022 04; 37(4):675-686.
    View in: PubMed
    Score: 0.010
  31. COPB2 loss of function causes a coatopathy with osteoporosis and developmental delay. Am J Hum Genet. 2021 09 02; 108(9):1710-1724.
    View in: PubMed
    Score: 0.010
  32. Leukocyte-dependent effects of platelet-rich plasma on cartilage loss and thermal hyperalgesia in a mouse model of post-traumatic osteoarthritis. Osteoarthritis Cartilage. 2020 10; 28(10):1385-1393.
    View in: PubMed
    Score: 0.009
  33. ATRAID regulates the action of nitrogen-containing bisphosphonates on bone. Sci Transl Med. 2020 05 20; 12(544).
    View in: PubMed
    Score: 0.009
  34. Notch Signaling in Skeletal Development, Homeostasis and Pathogenesis. Biomolecules. 2020 02 19; 10(2).
    View in: PubMed
    Score: 0.009
  35. Bmi1 Suppresses Adipogenesis in the Hematopoietic Stem Cell Niche. Stem Cell Reports. 2019 09 10; 13(3):545-558.
    View in: PubMed
    Score: 0.009
  36. Bi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes. Am J Hum Genet. 2019 03 07; 104(3):422-438.
    View in: PubMed
    Score: 0.008
  37. Effect of Genetic Diagnosis on Patients with Previously Undiagnosed Disease. N Engl J Med. 2018 11 29; 379(22):2131-2139.
    View in: PubMed
    Score: 0.008
  38. Disease-Modifying Osteoarthritis Treatment With Interleukin-1 Receptor Antagonist Gene Therapy in Small and Large Animal Models. Arthritis Rheumatol. 2018 11; 70(11):1757-1768.
    View in: PubMed
    Score: 0.008
  39. Therapeutic Antibody Targeting Tumor- and Osteoblastic Niche-Derived Jagged1 Sensitizes Bone Metastasis to Chemotherapy. Cancer Cell. 2017 Dec 11; 32(6):731-747.e6.
    View in: PubMed
    Score: 0.008
  40. mTORC1 Signaling is a Critical Regulator of Postnatal Tendon Development. Sci Rep. 2017 12 07; 7(1):17175.
    View in: PubMed
    Score: 0.008
  41. P3h3-null and Sc65-null Mice Phenocopy the Collagen Lysine Under-hydroxylation and Cross-linking Abnormality of Ehlers-Danlos Syndrome Type VIA. J Biol Chem. 2017 03 03; 292(9):3877-3887.
    View in: PubMed
    Score: 0.007
  42. Intra-iliac Artery Injection for Efficient and Selective Modeling of Microscopic Bone Metastasis. J Vis Exp. 2016 09 26; (115).
    View in: PubMed
    Score: 0.007
  43. Post-translationally abnormal collagens of prolyl 3-hydroxylase-2 null mice offer a pathobiological mechanism for the high myopia linked to human LEPREL1 mutations. J Biol Chem. 2015 Mar 27; 290(13):8613-22.
    View in: PubMed
    Score: 0.006
  44. Mice expressing mutant Trpv4 recapitulate the human TRPV4 disorders. J Bone Miner Res. 2014 Aug; 29(8):1815-1822.
    View in: PubMed
    Score: 0.006
  45. Benzothiophene carboxylate derivatives as novel allosteric inhibitors of branched-chain a-ketoacid dehydrogenase kinase. J Biol Chem. 2014 Jul 25; 289(30):20583-93.
    View in: PubMed
    Score: 0.006
  46. Excessive transforming growth factor-? signaling is a common mechanism in osteogenesis imperfecta. Nat Med. 2014 Jun; 20(6):670-5.
    View in: PubMed
    Score: 0.006
  47. Connective tissue alterations in Fkbp10-/- mice. Hum Mol Genet. 2014 Sep 15; 23(18):4822-31.
    View in: PubMed
    Score: 0.006
  48. Notch signaling in skeletal stem cells. Calcif Tissue Int. 2014 Jan; 94(1):68-77.
    View in: PubMed
    Score: 0.006
  49. ADAMTS-7 forms a positive feedback loop with TNF-a in the pathogenesis of osteoarthritis. Ann Rheum Dis. 2014 Aug; 73(8):1575-84.
    View in: PubMed
    Score: 0.006
  50. Structure-based design and mechanisms of allosteric inhibitors for mitochondrial branched-chain a-ketoacid dehydrogenase kinase. Proc Natl Acad Sci U S A. 2013 Jun 11; 110(24):9728-33.
    View in: PubMed
    Score: 0.006
  51. WNT1 mutations in early-onset osteoporosis and osteogenesis imperfecta. N Engl J Med. 2013 May 09; 368(19):1809-16.
    View in: PubMed
    Score: 0.006
  52. Yunis-Var?n syndrome is caused by mutations in FIG4, encoding a phosphoinositide phosphatase. Am J Hum Genet. 2013 May 02; 92(5):781-91.
    View in: PubMed
    Score: 0.006
  53. Whole-exome sequencing identifies mutations in the nucleoside transporter gene SLC29A3 in dysosteosclerosis, a form of osteopetrosis. Hum Mol Genet. 2012 Nov 15; 21(22):4904-9.
    View in: PubMed
    Score: 0.005
  54. Mutations in KAT6B, encoding a histone acetyltransferase, cause Genitopatellar syndrome. Am J Hum Genet. 2012 Feb 10; 90(2):282-9.
    View in: PubMed
    Score: 0.005
  55. Neonatal helper-dependent adenoviral vector gene therapy mediates correction of hemophilia A and tolerance to human factor VIII. Proc Natl Acad Sci U S A. 2011 Feb 01; 108(5):2082-7.
    View in: PubMed
    Score: 0.005
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.