Dr. Phyllis J Byrd MD
Family Practitioner
4242 Farnam St #150 Omaha NE, 68131About
Dr. Phyllis Byrd is a family practitioner practicing in Omaha, NE. Dr. Byrd specializes in comprehensive health care for people of all ages. In addition to diagnosing and treating illnesses, family practitioners also put focus on preventative care with routine checkups, tests and personalized coaching on how to maintain a healthy lifestyle. Dr. Byrd possesses immense general knowledge on maintaining health and today, family practitioners provide more care for the underserved and rural populations than any other medical specialty.
Education and Training
Univ of Ne Coll of Med, Omaha Ne 1994
Board Certification
Family MedicineAmerican Board of Family MedicineABFM
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Inactivation of ataxia telangiectasia mutated gene in B-cell chronic lymphocytic leukaemia.
- The DNA double-strand break repair gene hMRE11 is mutated in individuals with an ataxia-telangiectasia-like disorder.
- hMRE11: genomic structure and a null mutation identified in a transcript protected from nonsense-mediated mRNA decay.
- Residual ataxia telangiectasia mutated protein function in cells from ataxia telangiectasia patients, with 5762ins137 and 7271T-->G mutations, showing a less severe phenotype.
- Ataxia-telangiectasia-like disorder (ATLD)-its clinical presentation and molecular basis.
- Molecular pathology of ataxia telangiectasia.
- Immunodeficiency in ataxia telangiectasia is correlated strongly with the presence of two null mutations in the ataxia telangiectasia mutated gene.
- The expression of the adenovirus 12 early region 1B 19K protein using a recombinant simian virus 40 system.
- Lymphoid tumours and breast cancer in ataxia telangiectasia; substantial protective effect of residual ATM kinase activity against childhood tumours.
- Ataxia telangiectasia: more variation at clinical and cellular levels.
- The binding of guanine nucleotide to N-ras p21--a phosphorous and proton magnetic resonance study.
- A haplotype common to intermediate radiosensitivity variants of ataxia-telangiectasia in the UK.
- Differentiation of normal and adenovirus-12 E1 transformed human embryo retinal cells.
- A Haplotype Common to Intermediate Radiosensitivity Variants of Ataxia-telangiectasia in the UK.
- The level of expression of class-I MHC antigens in adenovirus-transformed human cell lines.
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