Dr. Timothy Clyde Cox MD
Hematologist-Oncologist | Hematology & Oncology
560 W MITCHELL ST PETOSKEY MI, 49770About
Dr. Timothy Cox is a hematologist oncologist practicing in Port Huron, MI. Dr. Cox specializes in the diagnosis, treatment and prevention of blood diseases such as anemia, hemophilia, sickle-cell disease, leukemia and lymphoma. Hematologist Oncologists are also trained in the study of cancer and its attack on other organs.
Education and Training
Univ Di Roma-La Sapienza, Fac Di Med E Chirurgia, Roma, Italy 1989
Board Certification
Internal MedicineAmerican Board of Internal MedicineABIM- Medical Oncology
Provider Details
Expert Publications
Data provided by the National Library of Medicine- MID1 and MID2 homo- and heterodimerise to tether the rapamycin-sensitive PP2A regulatory subunit, alpha 4, to microtubules: implications for the clinical variability of X-linked Opitz GBBB syndrome and other developmental disorders.
- Complementation of a yeast CYC3 deficiency identifies an X-linked mammalian activator of apocytochrome c.
- Isolation and characterisation of the chick orthologue of the Opitz syndrome gene, Mid1, supports a conserved role in vertebrate development.
- The jugular foramen in complex and syndromic craniosynostosis and its relationship to raised intracranial pressure.
- Expression of three spalt (sal) gene homologues in zebrafish embryos.
- A new X-linked syndrome with agenesis of the corpus callosum, mental retardation, coloboma, micrognathia, and a mutation in the Alpha 4 gene at Xq13.
- Intensity-based 2-D-3-D registration of cerebral angiograms.
- Hyperacute head injuries and the timing of computed tomography.
- A comparison of a similarity-based and a feature-based 2-D-3-D registration method for neurointerventional use.
- Subclassification of the RBCC/TRIM superfamily reveals a novel motif necessary for microtubule binding.
- Evolution of cerebral arteriopathies in childhood arterial ischemic stroke.
- Solution structure of the RBCC/TRIM B-box1 domain of human MID1: B-box with a RING.
- Expression profiles of cIRF6, cLHX6 and cLHX7 in the facial primordia suggest specific roles during primary palatogenesis.
- Somatic FGFR and TWIST mutations are not a common cause of isolated nonsyndromic single suture craniosynostosis.
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