Hasil Pencarian - Michael L Cunningham

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  1. 1
    Calvarial osteoblast gene expression in patients with craniosynostosis leads to novel polygenic mouse model.

    Calvarial osteoblast gene expression in patients with craniosynostosis leads to novel polygenic mouse model. oleh Jonas A Gustafson, Sarah S Park, Michael L Cunningham

    Diterbitkan 2019-01-01
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  2. 2
    PPARs and Xenobiotic-Induced Adverse Effects: Relevance to Human Health

    PPARs and Xenobiotic-Induced Adverse Effects: Relevance to Human Health oleh Christopher Lau, Barbara D. Abbott, J. Christopher Corton, Michael L. Cunningham

    Diterbitkan 2010-01-01
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  3. 3
    Quantitative trait loci affecting the 3D skull shape and size in mouse and prioritization of candidate genes in-silico.

    Quantitative trait loci affecting the 3D skull shape and size in mouse and prioritization of candidate genes in-silico. oleh A. Murat eMaga, A. Murat eMaga, Nicolas eNavarro, Nicolas eNavarro, Michael L Cunningham, Michael L Cunningham, Timothy C Cox, Timothy C Cox, Timothy C Cox

    Diterbitkan 2015-03-01
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  4. 4
    Mechanism of Disease: Recessive ADAMTSL4 Mutations and Craniosynostosis with Ectopia Lentis

    Mechanism of Disease: Recessive ADAMTSL4 Mutations and Craniosynostosis with Ectopia Lentis oleh Jonas Gustafson, Maria Bjork, Conny M. A. van Ravenswaaij-Arts, Michael L. Cunningham

    Diterbitkan 2022-01-01
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  5. 5
    Transcriptomic Signatures of Single-Suture Craniosynostosis Phenotypes

    Transcriptomic Signatures of Single-Suture Craniosynostosis Phenotypes oleh Samantha Lapehn, Jonas A. Gustafson, Andrew E. Timms, Michael L. Cunningham, Alison G. Paquette

    Diterbitkan 2023-03-01
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  6. 6
    A randomized crossover trial comparing the Nifty cup to a medicine cup in preterm infants who have difficulty breastfeeding at Komfo Anokye Teaching Hospital (KATH) in Kumasi, Ghana.

    A randomized crossover trial comparing the Nifty cup to a medicine cup in preterm infants who have difficulty breastfeeding at Komfo Anokye Teaching Hospital (KATH) in Kumasi, Ghan... oleh Christy M McKinney, Gyikua Plange-Rhule, Daniel Ansong, Michael L Cunningham, Irene Agyeman, Patricia S Coffey

    Diterbitkan 2019-01-01
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  7. 7
    Differential expression of extracellular matrix-mediated pathways in single-suture craniosynostosis.

    Differential expression of extracellular matrix-mediated pathways in single-suture craniosynostosis. oleh Brendan D Stamper, Sarah S Park, Richard P Beyer, Theo K Bammler, Frederico M Farin, Brig Mecham, Michael L Cunningham

    Diterbitkan 2011-01-01
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  8. 8
    Genetic associations and phenotypic heterogeneity in the craniosynostotic rabbit.

    Genetic associations and phenotypic heterogeneity in the craniosynostotic rabbit. oleh James R Gilbert, Joseph E Losee, Mark P Mooney, James J Cray, Jennifer Gustafson, Michael L Cunningham, Gregory M Cooper

    Diterbitkan 2018-01-01
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  9. 9
    Effects of the PPARα Agonist and Widely Used Antihyperlipidemic Drug Gemfibrozil on Hepatic Toxicity and Lipid Metabolism

    Effects of the PPARĪ± Agonist and Widely Used Antihyperlipidemic Drug Gemfibrozil on Hepatic Toxicity and Lipid Metabolism oleh Michael L. Cunningham, Bradley J. Collins, Milton R. Hejtmancik, Ronald A. Herbert, Gregory S. Travlos, Molly K. Vallant, Matthew D. Stout

    Diterbitkan 2010-01-01
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  10. 10
    Phthalate-Induced Liver Protection against Deleterious Effects of the Th1 Response: A Potentially Serious Health Hazard

    Phthalate-Induced Liver Protection against Deleterious Effects of the Th1 Response: A Potentially Serious Health Hazard oleh Mostafa Z. Badr, Alexander Shnyra, Mikhail Zoubine, Maxim Norkin, Betty Herndon, Tim Quinn, Roberto N. Miranda, Michael L. Cunningham, Agostino Molteni

    Diterbitkan 2007-01-01
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  11. 11
    Auriculocondylar syndrome 2 results from the dominant-negative action of PLCB4 variants

    Auriculocondylar syndrome 2 results from the dominant-negative action of PLCB4 variants oleh Stanley M. Kanai, Caleb Heffner, Timothy C. Cox, Michael L. Cunningham, Francisco A. Perez, Aaron M. Bauer, Philip Reigan, Cristan Carter, Stephen A. Murray, David E. Clouthier

    Diterbitkan 2022-04-01
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  12. 12
    PC16. Mutations in FOXI3 Cause Microtia and Craniofacial Microsomia

    PC16. Mutations in FOXI3 Cause Microtia and Craniofacial Microsomia oleh Andrew T. Timberlake, MD, PhD, Daniel Quiat, MD, Michael L. Cunningham, MD, PhD, John Persing, MD, Daniela Luquetti, MD PhD, Carrie L. Heike, MD, Jonathan Seidman, PhD, Christine Seidman, PhD

    Diterbitkan 2023-04-01
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  13. 13
    Whole genome sequencing identifies associations for nonsyndromic sagittal craniosynostosis with the intergenic region of BMP2 and noncoding RNA gene LINC01428

    Whole genome sequencing identifies associations for nonsyndromic sagittal craniosynostosis with the intergenic region of BMP2 and noncoding RNA gene LINC01428 oleh Anthony M. Musolf, Cristina M. Justice, Zeynep Erdogan-Yildirim, Seppe Goovaerts, Araceli Cuellar, John R. Shaffer, Mary L. Marazita, Peter Claes, Seth M. Weinberg, Jae Li, Craig Senders, Marike Zwienenberg, Emil Simeonov, Radka Kaneva, Tony Roscioli, Lorena Di Pietro, Marta Barba, Wanda Lattanzi, Michael L. Cunningham, Paul A. Romitti, Simeon A. Boyadjiev

    Diterbitkan 2024-04-01
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  14. 14
    Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and mice.

    Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and mice. oleh Lisenka E L M Vissers, Timothy C Cox, A Murat Maga, Kieran M Short, Fenny Wiradjaja, Irene M Janssen, Fernanda Jehee, Debora Bertola, Jia Liu, Garima Yagnik, Kiyotoshi Sekiguchi, Daiji Kiyozumi, Hans van Bokhoven, Carlo Marcelis, Michael L Cunningham, Peter J Anderson, Simeon A Boyadjiev, Maria Rita Passos-Bueno, Joris A Veltman, Ian Smyth, Michael F Buckley, Tony Roscioli

    Diterbitkan 2011-09-01
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  15. 15
    Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology.

    Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology. oleh John R Shaffer, Ekaterina Orlova, Myoung Keun Lee, Elizabeth J Leslie, Zachary D Raffensperger, Carrie L Heike, Michael L Cunningham, Jacqueline T Hecht, Chung How Kau, Nichole L Nidey, Lina M Moreno, George L Wehby, Jeffrey C Murray, Cecelia A Laurie, Cathy C Laurie, Joanne Cole, Tracey Ferrara, Stephanie Santorico, Ophir Klein, Washington Mio, Eleanor Feingold, Benedikt Hallgrimsson, Richard A Spritz, Mary L Marazita, Seth M Weinberg

    Diterbitkan 2016-08-01
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  16. 16
    Haploinsufficiency of SF3B2 causes craniofacial microsomia

    Haploinsufficiency of SF3B2 causes craniofacial microsomia oleh Andrew T. Timberlake, Casey Griffin, Carrie L. Heike, Anne V. Hing, Michael L. Cunningham, David Chitayat, Mark R. Davis, Soghra J. Doust, Amelia F. Drake, Milagros M. Duenas-Roque, Jack Goldblatt, Jonas A. Gustafson, Paula Hurtado-Villa, Alexis Johns, Natalya Karp, Nigel G. Laing, Leanne Magee, University of Washington Center for Mendelian Genomics, Sureni V. Mullegama, Harry Pachajoa, Gloria L. Porras-Hurtado, Rhonda E. Schnur, Jennie Slee, Steven L. Singer, David A. Staffenberg, Andrew E. Timms, Cheryl A. Wise, Ignacio Zarante, Jean-Pierre Saint-Jeannet, Daniela V. Luquetti

    Diterbitkan 2021-08-01
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