Faculty Detail   
Name FREDERICK D. GOLDMAN
  
Campus Address ACC 512 Zip 0011
Phone  (205) 638-5855
E-mail  fgoldman@uab.edu
Other websites
    

Faculty Appointment(s)
Appointment Type Department Division Rank
Primary  Ped - Hematology/Oncology  Ped - Hematology/Oncology Professor Emeritus

Graduate Biomedical Sciences Affiliations
Biochemistry and Structural Biology 

Biographical Sketch 
1975-1979 B.S., Biology Tulane University, New Orleans, LA

1979-1981 M.S., Immunology University of New Orleans, New Orleans, LA

1981-1985 M.D.Louisiana State University, New Orleans, LA

1985-1988 Pediatric Residency Tulane University School of Medicine
New Orleans, LA

1988-1991 Clinical Fellow in Pediatric Hematology/Oncology University of Colorado Health Sciences Center
Children’s Hospital, Denver, CO

1989-1992 Postdoctoral Research Fellowship Immunology
National Jewish Center for and Respiratory Medicine, Denver, CO
1993-1999 Assistant Professor University of Iowa College of Medicine
Department of Pediatrics

1999-2009 Associate Professor University of Iowa College of Medicine
Department of Pediatrics

2001-2009 Director, Pediatric Immune Disorders Clinic, University of Iowa College of Medicine
2001-2006 Director, Pediatric Bone Marrow Transplant Program, University of Iowa College of Medicine
2003-2009 Director, University of Iowa Hematopoietic Stem Cell Bank

2009-Present Professor of Pediatrics University of Alabama at Birmingham
Division of Pediatric Hematology & Oncology
Birmingham, AL
2009-Present Medical Director University of Alabama at Birmingham
Lowder Bone Marrow Transplant Program

Society Memberships
Organization Name Position Held Org Link
American Society for Blood and Marrow Transplantation  Member   
American Society of Hematology  Member   
American Society of Pediatric Hematology/Oncology  Member   
International Bone Marrow Transplant `Registry  MemberNon-Malignant Marrow Disorders Working Committee   
Pediatric Bone Marrow Transplant Consortium  Member   
 

Research/Clinical Interest
Title
Creation of patient-specific gene corrected hematopoietic stem cells in inherited bone marrow failure syndromes using inducible pluripotent stem cell technology
Description
The major research interest of Dr. Goldman’s laboratory relates to understanding the molecular and immunologic mechanisms of bone marrow failure syndromes and congenital immune deficiencies, and translating this information to the promotion of novel stem therapies for these disorders. His work previously focused on Dyskeratosis congenita (DC) and he was involved in the discovery of the autosomal dominant form of this disease, AD DC. More recently, he has been involved in studies assessing the defect in hematopoietic stem cells in DC, and in collaboration with the Daley Lab at Dana Farber, applied iPS cell technology to correct the underlying deficiency in telomerase in reprogrammed DC cells. Studies are currently being performed that are assessing the role of telomerase in defects in oxidative stress and DNA repair. Dr. Goldman has also participated in pre-clinical gene therapy studies for a number of other bone marrow failure disorders and immune deficiencies, and has created an extensive tissue repository with patient samples from many different conditions, including Diamond Blackfan Anemia (DBA), Shwachman Diamond Syndrome, and Fanconi’s anemia. More recently his research interests have shifted to DBA, and in concert with the Townes laboratory, is actively working on gene correction strategies for this condition using iPS cell technology and homologous recombineering. Through our collaboration with Dr. Lamb, the Director of the Stem Cell Processing laboratory and GMP facility at UAB, it is our collective hope that corrected patient iPS cells can be differentiated into hematopoietic stem cells for future transplantation into patients with DBA or other disorders of hematopoiesis.

Selected Publications 
2.Horvis R, Donovan J, Musci M, Motto D, Goldman F, Ross S, Koretzky G. Rescue of signaling by a chimeric protein containing the cytoplasmic domain of CD45. Science, 260:544-546, 1993  8475387 
3.Ross S, Goldman F, Crabtree J, Schraven B, Koretzky G. The association between CD45 and lck does not require CD4 and is independent of TCR stimulation. Biochemical and Biophysical Research Communications, 198:88-94, 1994.  8292053 
4.Donovan J, Goldman F, Koretzky G. Restoration of CD2-mediated signaling by chimeric membrane protein including the cytoplasmic sequence of CD45. Human Immunology, 40:123-30, 1994  7928441  
5.Goldman F, Jensen WA, Johnson GL, Heasley L, Cambier JC. gp120 ligation of CD4 induces p56lck activation and TCR desensitization independent of TCR tyrosine phosphorylation. Journal of Immunology, 153:2905-2917, 1994.  7522245  
1.Goldman F, Rotbardt H, Guitterez K, Ambruso D. Parvovirus associated aplastic crisis in a patient with red cell glucose 6-phosphate dehydrogenase deficiency. Pediatric Infectious Disease Journal, 9:593-594, 1990.  2172909 
10.Goldman FD, Trigg, ME. Bone marrow transplantation for relapsed ALL. International Journal of Pediatric Hematology/Oncology, 5(2-4):215-230, 1998.   
13.Trigg ME, Goldman FD. Removing T-lymphocytes from bone marrow: present dangers and future benefits. Cancer Research Therapy and Control, January, 1998.   
36.Filipovich AH, Bleesing J, Goldman F. Emerging Targets for Hematopoietic Cell Transplantation (HCT): Genetic Disorders of Hematopoiesis and Immunity. Biol Blood Marrow Transplant, 2007, Jan;13S1:58-63.   
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Keywords
gene therapy, telomerase, hematopoiesis, inducible pluripotent stem cells, oxidative stress, DNA damage response pathways