Brendan Lee
Affiliations: | Chair of Genetics | Baylor College of Medicine, Houston, TX |
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Publications
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Couasnay G, Madel MB, Lim J, et al. (2021) Sites of Cre-recombinase activity in mouse lines targeting skeletal cells. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research |
Rauch D, Robinson ME, Seiltgens C, et al. (2020) Assessment of Longitudinal Bone Growth in Osteogenesis Imperfecta Using Metacarpophalangeal Pattern Profiles. Bone. 115547 |
Stroup BM, Marom R, Li X, et al. (2020) A Global Slc7a7 Knockout Mouse Model Demonstrates Characteristic Phenotypes of Human Lysinuric Protein Intolerance. Human Molecular Genetics |
Samsa WE, Mamidi MK, Bashur LA, et al. (2020) The crucial p53-dependent oncogenic role of JAB1 in osteosarcoma in vivo. Oncogene |
Chung HL, Wangler MF, Marcogliese PC, et al. (2020) Loss- or Gain-of-Function Mutations in ACOX1 Cause Axonal Loss via Different Mechanisms. Neuron |
Ortinau LC, Wang H, Lei K, et al. (2019) Identification of Functionally Distinct Mx1+αSMA+ Periosteal Skeletal Stem Cells. Cell Stem Cell. 25: 784-796.e5 |
Cho KY, Kelley BP, Monier D, et al. (2019) Trps1 Regulates Development of Craniofacial Skeleton and Is Required for the Initiation of Palatal Shelves Fusion. Frontiers in Physiology. 10: 513 |
Kruger KM, Caudill A, Rodriguez Celin M, et al. (2019) Mobility in osteogenesis imperfecta: a multicenter North American study. Genetics in Medicine : Official Journal of the American College of Medical Genetics |
Burrage LC, Reynolds JJ, Baratang NV, et al. (2019) Bi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes. American Journal of Human Genetics |
Retrouvey JM, Taqi D, Tamimi F, et al. (2018) Oro-dental and cranio-facial characteristics of osteogenesis imperfecta type V. European Journal of Medical Genetics |