Latoya Brown MAADC II
Counselor/Therapist | Addiction (Substance Use Disorder)
1803 SUN VALLEY DR JEFFERSON CITY MO, 65109About
Latoya Brown is an Addiction Medicine Counselor in JEFFERSON CITY, MO. Latoya evaluates patients using many different procedures, in order to determine what treatments must be carried out in order to properly assess their symptoms. Addiction Medicine counselors provide patient care and consultation for each patient and their families.
Provider Details
Expert Publications
Data provided by the National Library of Medicine- An estrogen receptor-selective coregulator that potentiates the effectiveness of antiestrogens and represses the activity of estrogens.
- Identification and characterization of a novel factor that regulates quinone reductase gene transcriptional activity.
- Qualitative and quantitative assessment of interactions.
- hPMC2 is required for recruiting an ERbeta coactivator complex to mediate transcriptional upregulation of NQO1 and protection against oxidative DNA damage by tamoxifen.
- Effects of social stress and intrauterine position on sexual phenotype in wild-type house mice (Mus musculus).
- HEXIM1 modulates vascular endothelial growth factor expression and function in breast epithelial cells and mammary gland.
- HEXIM1 is a critical determinant of the response to tamoxifen.
- The exonuclease activity of hPMC2 is required for transcriptional regulation of the QR gene and repair of estrogen-induced abasic sites.
- Inhibition of metastasis by HEXIM1 through effects on cell invasion and
- The carboxy-terminal F domain of the human estrogen receptor: role in the transcriptional activity of the receptor and the effectiveness of antiestrogens as estrogen antagonists.
- Activation of transcriptionally inactive human estrogen receptors by cyclic adenosine 3',5'-monophosphate and ligands including antiestrogens.
- Responses to pure antiestrogens (ICI 164384, ICI 182780) in estrogen-sensitive and -resistant experimental and clinical breast cancer.
- Antiestrogens: mechanisms and actions in target cells.
- Identification of multiple, widely spaced estrogen-responsive regions in the rat progesterone receptor gene.
- Cloning of the rat progesterone receptor gene 5'-region and identification of two functionally distinct promoters.
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