-J A Kessler Researcher Activity Profile

Research Author Detailed Information 

J A Kessler Publication Rate By Year

J A Kessler has published 1 paper(s) in 1999, 2 paper(s) in 2000, 1 paper(s) in 2004, 1 paper(s) in 2005, 1 paper(s) in 2006, 6 paper(s) in 2007, 4 paper(s) in 2008, for a total of 16 research publications in total.

J A Ja Kessler Author Information

LAST NAME: kessler

FIRST NAME: J A

INITIALS: ja

AFFILIATION:

Papers

J A Kessler's Publication Record

1. Developmental changes in progenitor cell responsiveness to bone morphogenetic proteins differentially modulate progressive CNS lineage fate. Year Published: 2000
Department of Neurology, the Rose F. Kennedy Center for Research in Mental Retardation and Developmental Disabilities, Albert Einstein College of Medicine, Bronx, N.Y., USA. mehler@aecom.yu.edu
2. Bone morphogenetic protein-2 and -4 limit the number of enteric neurons but promote development of a TrkC-expressing neurotrophin-3-dependent subset. Year Published: 2004
Department of Anatomy and Cell Biology, Columbia University, College of Physicians and Surgeons, New York, New York 10032, USA. ac83@columbia.edu
3. Developmental changes in progenitor cell responsiveness to cytokines. Year Published: 2000
Departments of Neurology and Neuroscience, Albert Einstein College of Medicine, Bronx, New York, USA. gzhu@aecom.yu.edu
4. Sonic hedgehog and BMP2 exert opposing actions on proliferation and differentiation of embryonic neural progenitor cells. Year Published: 1999
Department of Neurology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, New York, 10461, USA. gzhu@aecom.yu.edu
5. LIF and BMP signaling generate separate and discrete types of GFAP-expressing cells. Year Published: 2005
Davee Department of Neurology, Northwestern University's Feinberg School of Medicine, Chicago, IL 60611, USA. m-bonaguidi@northwestern.edu
6. Neural tube defects and folate pathway genes: family-based association tests of gene-gene and gene-environment interactions. Year Published: 2006
Center for Human Genetics, Duke University Medical Center, Durham, North Carolina 27710, USA.
7. Hematopoietic growth factors pass through the blood-brain barrier in intact rats. Year Published: 2007
Department of Neurology, Northwestern University, Feinberg School of Medicine, 303 East Chicago Avenue, Chicago, IL 60611, USA. lzhao@lsuhsc.edu
8. Dual function of Sox1 in telencephalic progenitor cells. Year Published: 2007
Department of Neurology, Northwestern University Feinberg School of Medicine, 303 E. Chicago Ave., Ward 10-233, Chicago, IL 60611-3008, USA. l-kan@northwestern.edu
9. Age-dependent effects of TWEAK/Fn14 receptor activation on neural progenitor cells. Year Published: 2007
Department of Neurology, Northwestern University Medical School, Chicago, Illinois.
10. Dual function of Sox1 in telencephalic progenitor cells. Year Published: 2007
Department of Neurology, Northwestern University Feinberg School of Medicine, 303 E. Chicago Ave., Ward 10-233, Chicago, IL 60611-3008, USA. l-kan@northwestern.edu
11. Age-dependent effects of TWEAK/Fn14 receptor activation on neural progenitor cells. Year Published: 2007
Department of Neurology, Northwestern University Medical School, 303 East Chicago Avenue, Chicago, IL 60611, USA. c-hamill@northwestern.edu
12. Breathtaking advances in stem cell biology. Year Published: 2008
JA Kessler is an Advisory Board member of Nature Clinical Practice Neurology.
13. Breathtaking advances in stem cell biology. Year Published: 2008
JA Kessler is an Advisory Board member of Nature Clinical Practice Neurology.
14. Age-dependent effects of TWEAK/Fn14 receptor activation on neural progenitor cells. Year Published: 2007
Department of Neurology, Northwestern University Medical School, 303 East Chicago Avenue, Chicago, IL 60611, USA. c-hamill@northwestern.edu
15. Self-assembling nanofibers inhibit glial scar formation and promote axon elongation after spinal cord injury. Year Published: 2008
Department of Neurology, Northwestern University, Chicago, Illinois 60611, USA.
16. Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneity. Year Published: 2008
Department of Neurology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA, ajalali004@md.northwestern.edu