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Martin, Martin G

Title(s)Professor, Pediatrics
SchoolPeds - Gastroenterology
Phone45532
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    Collapse Research 
    Collapse Research Activities and Funding
    COngenital Diarrhea and Enteropathy (PediCODE) Consortium and BioRepository
    NIH/NIDDK RC2DK118640Sep 15, 2019 - Jun 30, 2024
    Role: Principal Investigator
    Smooth Muscle Cell-Based Assesment and Therapy for Myopathic forms of CIPO
    NIH/NIDDK R21DK111216Jun 1, 2017 - May 31, 2019
    Role: Principal Investigator
    Intestinal Stem Cell Culture and Entero-Endocrine Lineage Development
    NIH/NIDDK U01DK085535Sep 30, 2009 - Aug 31, 2019
    Role: Principal Investigator
    Neurogenin3 and Intestinal Failure
    NIH/NIDDK R01DK083762Jul 1, 2009 - Jun 30, 2014
    Role: Principal Investigator
    Cell Fate Determination of the Intestine and Chronic Diarrhea in Children
    NIH/NIDDK R21DK075009May 15, 2006 - Apr 30, 2009
    Role: Principal Investigator
    Regulation of Intestinal Nutrient Transporters
    NIH/NICHD R03HD041034Sep 24, 2001 - Jun 30, 2004
    Role: Principal Investigator
    MOLECULAR BASIS OF ENTEROCYTE REGULATION DURING ONTOGENY
    NIH/NICHD R01HD034706Mar 1, 1998 - Feb 28, 2004
    Role: Principal Investigator

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    Collapse Publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help.
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    1. Lee H, Huang AY, Wang LK, Yoon AJ, Renteria G, Eskin A, Signer RH, Dorrani N, Nieves-Rodriguez S, Wan J, Douine ED, Woods JD, Dell'Angelica EC, Fogel BL, Martin MG, Butte MJ, Parker NH, Wang RT, Shieh PB, Wong DA, Gallant N, Singh KE, Tavyev Asher YJ, Sinsheimer JS, Krakow D, Loo SK, Allard P, Papp JC, Palmer CGS, Martinez-Agosto JA, Nelson SF. Diagnostic utility of transcriptome sequencing for rare Mendelian diseases. Genet Med. 2019 Oct 14. PMID: 31607746.
      View in: PubMed
    2. Meriwether D, Sulaiman D, Volpe C, Dorfman A, Grijalva V, Dorreh N, Solorzano-Vargas RS, Wang J, O'Connor E, Papesh J, Larauche M, Trost H, Palgunachari MN, Anantharamaiah GM, Herschman HR, Martin MG, Fogelman AM, Reddy ST. Apolipoprotein A-I mimetics mitigate intestinal inflammation in COX2-dependent inflammatory bowel disease model. J Clin Invest. 2019 Jun 11; 130:3670-3685. PMID: 31184596.
      View in: PubMed
    3. Khalil HA, Hong SN, Rouch JD, Scott A, Cho Y, Wang J, Lewis MS, Martin MG, Dunn JCY, Stelzner MG. Intestinal epithelial replacement by transplantation of cultured murine and human cells into the small intestine. PLoS One. 2019; 14(5):e0216326. PMID: 31150401.
      View in: PubMed
    4. Wang TC, Martin MG, Kuo CJ, Klein OD, Niland J. Introduction to themed series on intestinal stem cells and the NIDDK Intestinal Stem Cell Consortium. Am J Physiol Gastrointest Liver Physiol. 2019 02 01; 316(2):G247-G250. PMID: 30548077.
      View in: PubMed
    5. Pathak SJ, Mueller JL, Okamoto K, Das B, Hertecant J, Greenhalgh L, Cole T, Pinsk V, Yerushalmi B, Gurkan OE, Yourshaw M, Hernandez E, Oesterreicher S, Naik S, Sanderson IR, Axelsson I, Agardh D, Boland CR, Martin MG, Putnam CD, Sivagnanam M. EPCAM mutation update: Variants associated with congenital tufting enteropathy and Lynch syndrome. Hum Mutat. 2019 02; 40(2):142-161. PMID: 30461124.
      View in: PubMed
    6. Schlegel C, Weis VG, Knowles BC, Lapierre LA, Martin MG, Dickman P, Goldenring JR, Shub MD. Apical Membrane Alterations in Non-intestinal Organs in Microvillus Inclusion Disease. Dig Dis Sci. 2018 02; 63(2):356-365. PMID: 29218485.
      View in: PubMed
    7. Bandsma RH, Sokollik C, Chami R, Cutz E, Brubaker PL, Hamilton JK, Perlman K, Zlotkin S, Sigalet DL, Sherman PM, Martin MG, Avitzur Y. From diarrhea to obesity in prohormone convertase 1/3 deficiency: age-dependent clinical, pathologic, and enteroendocrine characteristics. J Clin Gastroenterol. 2013 Nov-Dec; 47(10):834-43. PMID: 24135795.
      View in: PubMed
    8. Magness ST, Puthoff BJ, Crissey MA, Dunn J, Henning SJ, Houchen C, Kaddis JS, Kuo CJ, Li L, Lynch J, Martin MG, May R, Niland JC, Olack B, Qian D, Stelzner M, Swain JR, Wang F, Wang J, Wang X, Yan K, Yu J, Wong MH. A multicenter study to standardize reporting and analyses of fluorescence-activated cell-sorted murine intestinal epithelial cells. Am J Physiol Gastrointest Liver Physiol. 2013 Oct 15; 305(8):G542-51. PMID: 23928185.
      View in: PubMed
    9. Martín MG, Lindberg I, Solorzano-Vargas RS, Wang J, Avitzur Y, Bandsma R, Sokollik C, Lawrence S, Pickett LA, Chen Z, Egritas O, Dalgic B, Albornoz V, de Ridder L, Hulst J, Gok F, Aydogan A, Al-Hussaini A, Gok DE, Yourshaw M, Wu SV, Cortina G, Stanford S, Georgia S. Congenital proprotein convertase 1/3 deficiency causes malabsorptive diarrhea and other endocrinopathies in a pediatric cohort. Gastroenterology. 2013 Jul; 145(1):138-148. PMID: 23562752.
      View in: PubMed
    10. Kanji MS, Martin MG, Bhushan A. Dicer1 is required to repress neuronal fate during endocrine cell maturation. Diabetes. 2013 May; 62(5):1602-11. PMID: 23382448.
      View in: PubMed
    11. Stelzner M, Helmrath M, Dunn JC, Henning SJ, Houchen CW, Kuo C, Lynch J, Li L, Magness ST, Martin MG, Wong MH, Yu J. A nomenclature for intestinal in vitro cultures. Am J Physiol Gastrointest Liver Physiol. 2012 Jun 15; 302(12):G1359-63. PMID: 22461030.
      View in: PubMed
    12. Baum M, Martin MG, Booth IW, Holmberg C, Twombley K, Zhang Q, Gattineni J, Moe O. Nucleotide sequence of the Na+/H+ exchanger-8 in patients with congenital sodium diarrhea. J Pediatr Gastroenterol Nutr. 2011 Nov; 53(5):474-7. PMID: 21666503.
      View in: PubMed
    13. Watanabe J, Lin JA, Narasimha AJ, Shahbazian A, Ishikawa TO, Martin MG, Herschman HR, Reddy ST. Novel anti-inflammatory functions for endothelial and myeloid cyclooxygenase-2 in a new mouse model of Crohn's disease. Am J Physiol Gastrointest Liver Physiol. 2010 Jun; 298(6):G842-50. PMID: 20299600.
      View in: PubMed
    14. Pacini-Edelstein SJ, Mehra M, Ament ME, Vargas JH, Martin MG, McDiarmid SV. Varicella in pediatric liver transplant patients: a retrospective analysis of treatment and outcome. J Pediatr Gastroenterol Nutr. 2003 Aug; 37(2):183-6. PMID: 12883306.
      View in: PubMed
    15. Pacini-Edelstein SJ, Bahar RJ, McDiarmid SV, Vargas JH, Martin MG, Mehra M, Ament ME. The unique occurrence of hepatic failure from type 1 autoimmune hepatitis with concurrent brain abscess. J Pediatr Gastroenterol Nutr. 2003 Mar; 36(3):414-7. PMID: 12604986.
      View in: PubMed
    16. Wright EM, Turk E, Martin MG. Molecular basis for glucose-galactose malabsorption. Cell Biochem Biophys. 2002; 36(2-3):115-21. PMID: 12139397.
      View in: PubMed
    17. Martín MG, Wang J, Solorzano-Vargas RS, Lam JT, Turk E, Wright EM. Regulation of the human Na(+)-glucose cotransporter gene, SGLT1, by HNF-1 and Sp1. Am J Physiol Gastrointest Liver Physiol. 2000 Apr; 278(4):G591-603. PMID: 10762614.
      View in: PubMed