Hamed Jafar-Nejad

Hamed Jafar-Nejad

Department of Molecular and Human Genetics, Baylor College of Medicine

Affiliated withBaylor College of Medicine

Research Area

Biography

Hamed Jafar-Nejad is an Associate Professor in the Department of Molecular & Human Genetics and the Program in Developmental Biology at Baylor College of Medicine. His group is interested in the roles of glycosylation and deglycosylation in the regulation of animal development and human disease pathogenesis.

He received his MD degree from Tehran University of Medical Sciences and learned basic molecular biology techniques in a research institute in Iran. He spent one year in the Neuroscience Research Institute at the University of Ottawa, studying the transcriptional regulation of a serotonin receptor implicated in mood disorders with Dr. Paul Albert. He then moved to Houston and started his postdoctoral training in the area of Notch signaling and Drosophila neurogenesis with Dr. Hugo Bellen at Baylor College of Medicine/HHMI. In December 2006, he joined the faculty at the University of Texas Health Science Center at Houston, focusing on a glycosyltransferase called Rumi which he had identified in Drosophila as a key regulator of the Notch signaling pathway.

In 2012, he was recruited back to the Department of Molecular & Human Genetics at Baylor, where his group continues their work on the role of glycosylation in animal development and human disease. Hamed’s lab has established a mouse model for a rare disease called Alagille syndrome and has identified Rumi (Poglut1) as a dominant genetic suppressor of the Alagille biliary phenotypes in the mouse. The Jafar-Nejad group is also using Drosophila and mammalian cell culture assays to understand the role of a deglycosylation enzyme called N-glycanase 1 (NGLY1) in animal development and BMP signaling, in hopes of shedding light on the pathophysiology of NGLY1 deficiency in human patients and identifying drug targets for this disease.

JoVE Journal Publications

ArticleTotal : 2
Year
Cell Aggregation Assays to Evaluate the Binding of the <em>Drosophila</em> Notch with <em>Trans</em>-Ligands and its Inhibition by <em>Cis</em>-Ligands
Publication title

Cited by 3

2018
2019

Other Publications

Article
Year
Mapping Drosophila mutations with molecularly defined P element insertions.

Proceedings of the National Academy of Sciences of the United States of America| PubMed ID: 12960394

2003
2003
Gfi/Pag-3/senseless zinc finger proteins: a unifying theme?

Molecular and cellular biology| PubMed ID: 15456856

2004
2005
2005
2006
2006
2006
2008
2008
2010
2011
2011
Negative regulation of notch signaling by xylose.

PLoS genetics| PubMed ID: 23754965

2013
Structure-function analysis of Drosophila Notch using genomic rescue transgenes.

Methods in molecular biology (Clifton, N.J.)| PubMed ID: 25053479

2014
2014
2014
2015
2015
2016
Mapping Sites of O-Glycosylation and Fringe Elongation on Drosophila Notch.

The Journal of biological chemistry| PubMed ID: 27268051

2016
2016
2017
2017
2017
2018
2018
Unbiased glycomics: a powerful tool in rare disease diagnosis and research.

Translational research : the journal of laboratory and clinical medicine| PubMed ID: 30528322

2019