Martine Tetreault, Ph.D. - Publications

Affiliations: 
2013 Molecular Biology Université de Montréal, Montréal, Canada 
Area:
Neurogenetics, neurodegenerative disorders, neuromuscular disorders, hereditary ataxias

36/103 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2017 Alcantara D, Elmslie F, Tetreault M, Bareke E, Hartley T, Majewski J, Boycott K, Innes AM, Dyment DA, O'Driscoll M. SHORT syndrome due to a novel de novo mutation in PRKCE (Protein Kinase Cɛ) impairing TORC2-dependent AKT activation. Human Molecular Genetics. 26: 3713-3721. PMID 28934384 DOI: 10.1093/hmg/ddx256  0.48
2017 Ylikallio E, Woldegebriel R, Tumiati M, Isohanni P, Ryan MM, Stark Z, Walsh M, Sawyer SL, Bell KM, Oshlack A, Lockhart PJ, Shcherbii M, Estrada-Cuzcano A, Atkinson D, Hartley T, ... Tetreault M, et al. MCM3AP in recessive Charcot-Marie-Tooth neuropathy and mild intellectual disability. Brain : a Journal of Neurology. PMID 28633435 DOI: 10.1093/brain/awx138  0.48
2017 Kernohan KD, Dyment DA, Pupavac M, Cramer Z, McBride A, Bernard G, Straub I, Tetreault M, Hartley T, Huang L, Sell E, Majewski J, Rosenblatt DS, Shoubridge E, Mhanni A, et al. Matchmaking facilitates the diagnosis of an autosomal-recessive mitochondrial disease caused by biallelic mutation of the tRNA isopentenyltransferase (TRIT1) gene. Human Mutation. PMID 28185376 DOI: 10.1002/humu.23196  0.52
2017 La Piana R, Weraarpachai W, Ospina LH, Tetreault M, Majewski J, Bruce Pike G, Decarie JC, Tampieri D, Brais B, Shoubridge EA. Identification and functional characterization of a novel MTFMT mutation associated with selective vulnerability of the visual pathway and a mild neurological phenotype. Neurogenetics. PMID 28058511 DOI: 10.1007/s10048-016-0506-0  0.52
2016 Ejaz R, Qin W, Huang L, Blaser S, Tetreault M, Hartley T, Boycott KM, Carter MT. Lateral meningocele (Lehman) syndrome: A child with a novel NOTCH3 mutation. American Journal of Medical Genetics. Part A. PMID 26754023 DOI: 10.1002/ajmg.a.37541  0.52
2015 Stray-Pedersen A, Cobben JM, Prescott TE, Lee S, Cang C, Aranda K, Ahmed S, Alders M, Gerstner T, Aslaksen K, Tétreault M, Qin W, Hartley T, Jhangiani SN, Muzny DM, et al. Biallelic Mutations in UNC80 Cause Persistent Hypotonia, Encephalopathy, Growth Retardation, and Severe Intellectual Disability. American Journal of Human Genetics. PMID 26708751 DOI: 10.1016/j.ajhg.2015.11.004  0.52
2015 Choquet K, Zurita-Rendón O, La Piana R, Yang S, Dicaire MJ, Boycott KM, Majewski J, Shoubridge EA, Brais B, Tétreault M. Autosomal recessive cerebellar ataxia caused by a homozygous mutation in PMPCA. Brain : a Journal of Neurology. PMID 26657514 DOI: 10.1093/brain/awv362  0.52
2015 Boycott KM, Beaulieu CL, Kernohan KD, Gebril OH, Mhanni A, Chudley AE, Redl D, Qin W, Hampson S, Küry S, Tetreault M, Puffenberger EG, Scott JN, Bezieau S, Reis A, et al. Autosomal-Recessive Intellectual Disability with Cerebellar Atrophy Syndrome Caused by Mutation of the Manganese and Zinc Transporter Gene SLC39A8. American Journal of Human Genetics. 97: 886-93. PMID 26637978 DOI: 10.1016/j.ajhg.2015.11.002  0.52
2015 Choquet K, Tétreault M, Yang S, La Piana R, Dicaire MJ, Vanstone MR, Mathieu J, Bouchard JP, Rioux MF, Rouleau GA, Boycott KM, Majewski J, Brais B. SPG7 mutations explain a significant proportion of French Canadian spastic ataxia cases. European Journal of Human Genetics : Ejhg. PMID 26626314 DOI: 10.1038/ejhg.2015.240  0.52
2015 Vanstone JR, Smith AM, McBride S, Naas T, Holcik M, Antoun G, Harper ME, Michaud J, Sell E, Chakraborty P, Tetreault M, Majewski J, Baird S, Boycott KM, et al. DNM1L-related mitochondrial fission defect presenting as refractory epilepsy. European Journal of Human Genetics : Ejhg. PMID 26604000 DOI: 10.1038/ejhg.2015.243  0.52
2015 Faden M, AlZahrani F, Mendoza-Londono R, Dupuis L, Hartley T, Kannu P, Raiman JA, Howard A, Qin W, Tetreault M, Xi JQ, Al-Thamer I, Maas RL, Boycott K, et al. Identification of a Recognizable Progressive Skeletal Dysplasia Caused by RSPRY1 Mutations. American Journal of Human Genetics. 97: 608-15. PMID 26365341 DOI: 10.1016/j.ajhg.2015.08.007  0.52
2015 Kernohan KD, Tétreault M, Liwak-Muir U, Geraghty MT, Qin W, Venkateswaran S, Davila J, Holcik M, Majewski J, Richer J, Boycott KM. Homozygous mutation in the eukaryotic translation initiation factor 2alpha phosphatase gene, PPP1R15B, is associated with severe microcephaly, short stature and intellectual disability. Human Molecular Genetics. 24: 6293-300. PMID 26307080 DOI: 10.1093/hmg/ddv337  0.52
2015 Wagner JD, Huang L, Tetreault M, Majewski J, Boycott KM, Bulman DE, Dyment DA, McMillan HJ. Autosomal recessive axonal polyneuropathy in a sibling pair due to a novel homozygous mutation in IGHMBP2. Neuromuscular Disorders : Nmd. 25: 794-9. PMID 26298607 DOI: 10.1016/j.nmd.2015.07.017  0.52
2015 Imai A, Nakaya A, Fahiminiya S, Tétreault M, Majewski J, Sakata Y, Takashima S, Lathrop M, Ott J. Beyond Homozygosity Mapping: Family-Control analysis based on Hamming distance for prioritizing variants in exome sequencing. Scientific Reports. 5: 12028. PMID 26143870 DOI: 10.1038/srep12028  0.52
2015 Tetreault M, Fahiminiya S, Antonicka H, Mitchell GA, Geraghty MT, Lines M, Boycott KM, Shoubridge EA, Mitchell JJ, Michaud JL, Majewski J. Whole-exome sequencing identifies novel ECHS1 mutations in Leigh syndrome. Human Genetics. 134: 981-91. PMID 26099313 DOI: 10.1007/s00439-015-1577-y  0.52
2015 Sawyer SL, Cheuk-Him Ng A, Innes AM, Wagner JD, Dyment DA, Tetreault M, Majewski J, Boycott KM, Screaton RA, Nicholson G. Homozygous mutations in MFN2 cause multiple symmetric lipomatosis associated with neuropathy. Human Molecular Genetics. PMID 26085578 DOI: 10.1093/hmg/ddv229  0.52
2015 Mendoza-Londono R, Fahiminiya S, Majewski J, Tétreault M, Nadaf J, Kannu P, Sochett E, Howard A, Stimec J, Dupuis L, Roschger P, Klaushofer K, Palomo T, Ouellet J, et al. Recessive osteogenesis imperfecta caused by missense mutations in SPARC. American Journal of Human Genetics. 96: 979-85. PMID 26027498 DOI: 10.1016/j.ajhg.2015.04.021  0.52
2015 Tetreault M, Bareke E, Nadaf J, Alirezaie N, Majewski J. Whole-exome sequencing as a diagnostic tool: current challenges and future opportunities. Expert Review of Molecular Diagnostics. 15: 749-60. PMID 25959410 DOI: 10.1586/14737159.2015.1039516  0.52
2015 Tétreault M, Gonzalez M, Dicaire MJ, Allard P, Gehring K, Leblanc D, Leclerc N, Schondorf R, Mathieu J, Zuchner S, Brais B. Adult-onset painful axonal polyneuropathy caused by a dominant NAGLU mutation. Brain : a Journal of Neurology. 138: 1477-83. PMID 25818867 DOI: 10.1093/brain/awv074  0.52
2015 Xi Y, Honeywell C, Zhang D, Schwartzentruber J, Beaulieu CL, Tetreault M, Hartley T, Marton J, Vidal SM, Majewski J, Aravind L, Gollob M, Boycott KM, Gow RM. Whole exome sequencing identifies the TNNI3K gene as a cause of familial conduction system disease and congenital junctional ectopic tachycardia. International Journal of Cardiology. 185: 114-6. PMID 25791106 DOI: 10.1016/j.ijcard.2015.03.130  0.52
2015 Dyment DA, Tétreault M, Beaulieu CL, Hartley T, Ferreira P, Chardon JW, Marcadier J, Sawyer SL, Mosca SJ, Innes AM, Parboosingh JS, Bulman DE, Schwartzentruber J, Majewski J, Tarnopolsky M, et al. Whole-exome sequencing broadens the phenotypic spectrum of rare pediatric epilepsy: a retrospective study. Clinical Genetics. 88: 34-40. PMID 25046240 DOI: 10.1111/cge.12464  0.52
2014 Aldinger KA, Mosca SJ, Tétreault M, Dempsey JC, Ishak GE, Hartley T, Phelps IG, Lamont RE, O'Day DR, Basel D, Gripp KW, Baker L, Stephan MJ, Bernier FP, Boycott KM, et al. Mutations in LAMA1 cause cerebellar dysplasia and cysts with and without retinal dystrophy. American Journal of Human Genetics. 95: 227-34. PMID 25105227 DOI: 10.1016/j.ajhg.2014.07.007  0.52
2013 Daoud H, Tétreault M, Gibson W, Guerrero K, Cohen A, Gburek-Augustat J, Synofzik M, Brais B, Stevens CA, Sanchez-Carpintero R, Goizet C, Naidu S, Vanderver A, Bernard G. Mutations in POLR3A and POLR3B are a major cause of hypomyelinating leukodystrophies with or without dental abnormalities and/or hypogonadotropic hypogonadism. Journal of Medical Genetics. 50: 194-7. PMID 23355746 DOI: 10.1136/jmedgenet-2012-101357  0.52
2013 Thiffault I, Dicaire MJ, Tetreault M, Huang KN, Demers-Lamarche J, Bernard G, Duquette A, Larivière R, Gehring K, Montpetit A, McPherson PS, Richter A, Montermini L, Mercier J, Mitchell GA, et al. Diversity of ARSACS mutations in French-Canadians. The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques. 40: 61-6. PMID 23250129  0.52
2012 Bayat V, Thiffault I, Jaiswal M, Tétreault M, Donti T, Sasarman F, Bernard G, Demers-Lamarche J, Dicaire MJ, Mathieu J, Vanasse M, Bouchard JP, Rioux MF, Lourenco CM, Li Z, et al. Mutations in the mitochondrial methionyl-tRNA synthetase cause a neurodegenerative phenotype in flies and a recessive ataxia (ARSAL) in humans. Plos Biology. 10: e1001288. PMID 22448145 DOI: 10.1371/journal.pbio.1001288  0.52
2012 Tétreault M, Putorti ML, Thiffault I, Sylvain M, Venderver A, Schiffmann R, Brais B, Bernard G. TACH leukodystrophy: locus refinement to chromosome 10q22.3-23.1. The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques. 39: 122-3. PMID 22384513  0.52
2011 Tétreault M, Choquet K, Orcesi S, Tonduti D, Balottin U, Teichmann M, Fribourg S, Schiffmann R, Brais B, Vanderver A, Bernard G. Recessive mutations in POLR3B, encoding the second largest subunit of Pol III, cause a rare hypomyelinating leukodystrophy. American Journal of Human Genetics. 89: 652-5. PMID 22036172 DOI: 10.1016/j.ajhg.2011.10.006  0.52
2011 Tétreault M, Srour M, Allyson J, Thiffault I, Loisel L, Robitaille Y, Bouchard JP, Brais B. Founder mutation for α-sarcoglycan-LGMD2D in a Magdalen Islands Acadian cluster. The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques. 38: 747-52. PMID 21856579  0.52
2011 Bernard G, Chouery E, Putorti ML, Tétreault M, Takanohashi A, Carosso G, Clément I, Boespflug-Tanguy O, Rodriguez D, Delague V, Abou Ghoch J, Jalkh N, Dorboz I, Fribourg S, Teichmann M, et al. Mutations of POLR3A encoding a catalytic subunit of RNA polymerase Pol III cause a recessive hypomyelinating leukodystrophy. American Journal of Human Genetics. 89: 415-23. PMID 21855841 DOI: 10.1016/j.ajhg.2011.07.014  0.52
2010 Bernard G, Thiffault I, Tetreault M, Putorti ML, Bouchard I, Sylvain M, Melançon S, Laframboise R, Langevin P, Bouchard JP, Vanasse M, Vanderver A, Sébire G, Brais B. Tremor-ataxia with central hypomyelination (TACH) leukodystrophy maps to chromosome 10q22.3-10q23.31. Neurogenetics. 11: 457-64. PMID 20640464 DOI: 10.1007/s10048-010-0251-8  0.52
2009 Loggia ML, Bushnell MC, Tétreault M, Thiffault I, Bhérer C, Mohammed NK, Kuchinad AA, Laferrière A, Dicaire MJ, Loisel L, Mogil JS, Brais B. Carriers of recessive WNK1/HSN2 mutations for hereditary sensory and autonomic neuropathy type 2 (HSAN2) are more sensitive to thermal stimuli. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 2162-6. PMID 19228968 DOI: 10.1523/JNEUROSCI.4633-08.2009  0.52
2008 Gosselin I, Thiffault I, Tétreault M, Chau V, Dicaire MJ, Loisel L, Emond M, Senderek J, Mathieu J, Dupré N, Vanasse M, Puymirat J, Brais B. Founder SH3TC2 mutations are responsible for a CMT4C French-Canadians cluster. Neuromuscular Disorders : Nmd. 18: 483-92. PMID 18511281 DOI: 10.1016/j.nmd.2008.04.001  0.52
2007 Rossignol E, Mathieu J, Thiffault I, Tétreault M, Dicaire MJ, Chrestian N, Dupré N, Puymirat J, Brais B. A novel founder SCN4A mutation causes painful cold-induced myotonia in French-Canadians. Neurology. 69: 1937-41. PMID 17998485 DOI: 10.1212/01.wnl.0000290831.08585.2c  0.52
2007 Jarry J, Rioux MF, Bolduc V, Robitaille Y, Khoury V, Thiffault I, Tétreault M, Loisel L, Bouchard JP, Brais B. A novel autosomal recessive limb-girdle muscular dystrophy with quadriceps atrophy maps to 11p13-p12. Brain : a Journal of Neurology. 130: 368-80. PMID 17008331 DOI: 10.1093/brain/awl270  0.52
2006 Tétreault M, Duquette A, Thiffault I, Bherer C, Jarry J, Loisel L, Banwell B, D'Anjou G, Mathieu J, Robitaille Y, Vanasse M, Brais B. A new form of congenital muscular dystrophy with joint hyperlaxity maps to 3p23-21. Brain : a Journal of Neurology. 129: 2077-84. PMID 16760198 DOI: 10.1093/brain/awl146  0.52
2006 Thiffault I, Rioux MF, Tetreault M, Jarry J, Loiselle L, Poirier J, Gros-Louis F, Mathieu J, Vanasse M, Rouleau GA, Bouchard JP, Lesage J, Brais B. A new autosomal recessive spastic ataxia associated with frequent white matter changes maps to 2q33-34. Brain : a Journal of Neurology. 129: 2332-40. PMID 16672289 DOI: 10.1093/brain/awl110  0.52
Low-probability matches
2018 Fitzsimons PE, Alston CL, Bonnen PE, Hughes J, Crushell E, Geraghty MT, Tetreault M, O'Reilly P, Twomey E, Sheikh Y, Walsh R, Waterham HR, Ferdinandusse S, Wanders RJA, Taylor RW, et al. Clinical, biochemical, and genetic features of four patients with short-chain enoyl-CoA hydratase (ECHS1) deficiency. American Journal of Medical Genetics. Part A. PMID 29575569 DOI: 10.1002/ajmg.a.38658  0.01
2017 Tarnopolsky MA, Brady L, Tetreault M. TRMT5 mutations are associated with features of complex hereditary spastic paraparesis. Neurology. PMID 29021354 DOI: 10.1212/WNL.0000000000004657  0.01
2015 Tetreault MW, Della Valle CJ, Bohl DD, Lodha SJ, Biswas D, Wysocki RW. What Factors Influence the Success of Medial Gastrocnemius Flaps in the Treatment of Infected TKAs? Clinical Orthopaedics and Related Research. PMID 26573319 DOI: 10.1007/s11999-015-4624-z  0.01
2015 Tétreault MP. Esophageal Cancer: Insights From Mouse Models. Cancer Growth and Metastasis. 8: 37-46. PMID 26380556 DOI: 10.4137/CGM.S21218  0.01
2015 Huddleston JI, Tetreault MW, Yu M, Bedair H, Hansen VJ, Choi HR, Goodman SB, Sporer SM, Della Valle CJ. Is There a Benefit to Modularity in 'Simpler' Femoral Revisions? Clinical Orthopaedics and Related Research. PMID 26245164 DOI: 10.1007/s11999-015-4474-8  0.01
2015 Long A, Giroux V, Whelan KA, Hamilton KE, Tétreault MP, Tanaka K, Lee JS, Klein-Szanto AJ, Nakagawa H, Rustgi AK. WNT10A promotes an invasive and self-renewing phenotype in esophageal squamous cell carcinoma. Carcinogenesis. 36: 598-606. PMID 25795715 DOI: 10.1093/carcin/bgv025  0.01
2015 Nair A, Gan J, Bush-Joseph C, Verma N, Tetreault MW, Saha K, Margulis A, Fogg L, Scanzello CR. Synovial chemokine expression and relationship with knee symptoms in patients with meniscal tears. Osteoarthritis and Cartilage / Oars, Osteoarthritis Research Society. 23: 1158-64. PMID 25724256 DOI: 10.1016/j.joca.2015.02.016  0.01
2015 Bourdin B, Shakeri B, Tétreault MP, Sauvé R, Lesage S, Parent L. Functional characterization of CaVα2δ mutations associated with sudden cardiac death. The Journal of Biological Chemistry. 290: 2854-69. PMID 25527503 DOI: 10.1074/jbc.M114.597930  0.01
2015 Brown NM, Tetreault M, Cipriano CA, Della Valle CJ, Paprosky W, Sporer S. Modular tapered implants for severe femoral bone loss in THA: reliable osseointegration but frequent complications. Clinical Orthopaedics and Related Research. 473: 555-60. PMID 25053289 DOI: 10.1007/s11999-014-3811-7  0.01
2015 Wilde P, Tetreault M, Franco SB. Talking back: Writing assistants renegotiate the public memory of writing centers Pedagogies of Public Memory: Teaching Writing and Rhetoric At Museums, Archives, and Memorials. 105-116. DOI: 10.4324/9781315696676  0.01
2015 Huddleston JI, Tetreault MW, Yu M, Bedair H, Hansen VJ, Choi HR, Goodman SB, Sporer SM, della Valle CJ. Is There a Benefit to Modularity in ‘Simpler’ Femoral Revisions? Clinical Orthopaedics and Related Research. DOI: 10.1007/s11999-015-4474-8  0.01
2014 Erickson BJ, Harris JD, Tetreault M, Bush-Joseph C, Cohen M, Romeo AA. Is Tommy John Surgery Performed More Frequently in Major League Baseball Pitchers From Warm Weather Areas? Orthopaedic Journal of Sports Medicine. 2: 2325967114553916. PMID 26535277 DOI: 10.1177/2325967114553916  0.01
2014 Chen AF, Tetreault MW, Levicoff EA, Fedorka CJ, Rothenberg AC, Klatt BA. Increased incidence of patella baja after total knee arthroplasty revision for infection. American Journal of Orthopedics (Belle Mead, N.J.). 43: 562-6. PMID 25490011  0.01
2014 Tetreault MW, Wetters NG, Moric M, Gross CE, Della Valle CJ. Is synovial C-reactive protein a useful marker for periprosthetic joint infection? Clinical Orthopaedics and Related Research. 472: 3997-4003. PMID 25070920 DOI: 10.1007/s11999-014-3828-y  0.01
2014 Sundman EA, Cole BJ, Karas V, Della Valle C, Tetreault MW, Mohammed HO, Fortier LA. The anti-inflammatory and matrix restorative mechanisms of platelet-rich plasma in osteoarthritis. The American Journal of Sports Medicine. 42: 35-41. PMID 24192391 DOI: 10.1177/0363546513507766  0.01
2014 Tetreault MW, Shukla SK, Yi PH, Sporer SM, Della Valle CJ. Are short fully coated stems adequate for "simple" femoral revisions? Clinical Orthopaedics and Related Research. 472: 577-83. PMID 23846608 DOI: 10.1007/s11999-013-3167-4  0.01
2014 Tetreault MW, Wetters NG, Aggarwal V, Mont M, Parvizi J, Della Valle CJ. The Chitranjan Ranawat Award: Should prophylactic antibiotics be withheld before revision surgery to obtain appropriate cultures? Clinical Orthopaedics and Related Research. 472: 52-6. PMID 23633187 DOI: 10.1007/s11999-013-3016-5  0.01
2013 Tetreault MP, Yang Y, Katz JP. Krüppel-like factors in cancer. Nature Reviews. Cancer. 13: 701-13. PMID 24060862 DOI: 10.1038/nrc3582  0.01
2013 Tetreault MW, Wetters NG, Aggarwal VK, Moric M, Segreti J, Huddleston JI, Parvizi J, Della Valle CJ. Should draining wounds and sinuses associated with hip and knee arthroplasties be cultured? The Journal of Arthroplasty. 28: 133-6. PMID 23906868 DOI: 10.1016/j.arth.2013.04.057  0.01
2013 Hamilton KE, Tétreault MP, Lund PK. Opportunities and challenges for women PhD investigators in gastrointestinal research. Gastroenterology. 145: 266-71. PMID 23792200 DOI: 10.1053/j.gastro.2013.06.024  0.01
2013 Hansen E, Tetreault M, Zmistowski B, Della Valle CJ, Parvizi J, Haddad FS, Hozack WJ. Outcome of one-stage cementless exchange for acute postoperative periprosthetic hip infection. Clinical Orthopaedics and Related Research. 471: 3214-22. PMID 23775569 DOI: 10.1007/s11999-013-3079-3  0.01
2013 Zmistowski B, Tetreault MW, Alijanipour P, Chen AF, Della Valle CJ, Parvizi J. Recurrent periprosthetic joint infection: persistent or new infection? The Journal of Arthroplasty. 28: 1486-9. PMID 23587491 DOI: 10.1016/j.arth.2013.02.021  0.01
2012 Cooper HJ, Della Valle CJ, Berger RA, Tetreault M, Paprosky WG, Sporer SM, Jacobs JJ. Corrosion at the head-neck taper as a cause for adverse local tissue reactions after total hip arthroplasty. The Journal of Bone and Joint Surgery. American Volume. 94: 1655-61. PMID 23289127 DOI: 10.2106/JBJS.K.01352  0.01
2012 Yang Y, Tarapore RS, Jarmel MH, Tetreault MP, Katz JP. p53 mutation alters the effect of the esophageal tumor suppressor KLF5 on keratinocyte proliferation. Cell Cycle (Georgetown, Tex.). 11: 4033-9. PMID 22990386 DOI: 10.4161/cc.22265  0.01
2012 Tetreault MP, Alrabaa R, McGeehan M, Katz JP. Krüppel-like factor 5 protects against murine colitis and activates JAK-STAT signaling in vivo. Plos One. 7: e38338. PMID 22675454 DOI: 10.1371/journal.pone.0038338  0.01
2012 Chen AF, Chivukula S, Jacobs LJ, Tetreault MW, Lee JY. What is the prevalence of MRSA colonization in elective spine cases? Clinical Orthopaedics and Related Research. 470: 2684-9. PMID 22441994 DOI: 10.1007/s11999-012-2316-5  0.01
2012 Tetreault MP, Katz JP. Transgenic Animal Models of Gastrointestinal Function Physiology of the Gastrointestinal Tract. 1: 97-113. DOI: 10.1016/B978-0-12-382026-6.00005-1  0.01
2011 Yang Y, Nakagawa H, Tetreault MP, Billig J, Victor N, Goyal A, Sepulveda AR, Katz JP. Loss of transcription factor KLF5 in the context of p53 ablation drives invasive progression of human squamous cell cancer. Cancer Research. 71: 6475-84. PMID 21868761 DOI: 10.1158/0008-5472.CAN-11-1702  0.01
2011 Maher FA, Tetreault MKT. Long-term transformations: Excavating privilege and diversity in the academy Gender and Education. 23: 281-297. DOI: 10.1080/09540253.2010.491790  0.01
2011 Tetreault M, Hogan R, Stanton F, Rom E. RINSC thermal column cooling system upgrade Transactions of the American Nuclear Society. 105: 75-76.  0.01
2010 Tetreault MP, Wang ML, Yang Y, Travis J, Yu QC, Klein-Szanto AJ, Katz JP. Klf4 overexpression activates epithelial cytokines and inflammation-mediated esophageal squamous cell cancer in mice. Gastroenterology. 139: 2124-2134.e9. PMID 20816834 DOI: 10.1053/j.gastro.2010.08.048  0.01
2010 Tetreault MP, Yang Y, Travis J, Yu QC, Klein-Szanto A, Tobias JW, Katz JP. Esophageal squamous cell dysplasia and delayed differentiation with deletion of krüppel-like factor 4 in murine esophagus. Gastroenterology. 139: 171-81.e9. PMID 20347813 DOI: 10.1053/j.gastro.2010.03.048  0.01
2010 Basora N, Tétreault MP, Boucher MP, Herring E, Beaulieu JF. Polycystin-1 is a microtubule-driven desmosome-associated component in polarized epithelial cells. Experimental Cell Research. 316: 1454-64. PMID 20211617 DOI: 10.1016/j.yexcr.2010.02.033  0.01
2010 Khan S, Perry C, Tetreault ML, Henry D, Trimmer JS, Zimmerman AL, Matthews G. A novel cyclic nucleotide-gated ion channel enriched in synaptic terminals of isotocin neurons in zebrafish brain and pituitary. Neuroscience. 165: 79-89. PMID 19778592 DOI: 10.1016/j.neuroscience.2009.09.040  0.01
2009 Rangiah K, Tippornwong M, Sangar V, Austin D, Tétreault MP, Rustgi AK, Blair IA, Yu KH. Differential secreted proteome approach in murine model for candidate biomarker discovery in colon cancer. Journal of Proteome Research. 8: 5153-64. PMID 19769411 DOI: 10.1021/pr900518v  0.01
2009 Tetreault MA. La longue durée and energy security in the gulf British Journal of Middle Eastern Studies. 36: 375-393. DOI: 10.1080/13530190903338920  0.01
2009 Maher FA, Tetreault MK. Diversity and privilege Academe. 95: 17-20.  0.01
2008 Tétreault MP, Chailler P, Beaulieu JF, Rivard N, Ménard D. Specific signaling cascades involved in cell spreading during healing of micro-wounded gastric epithelial monolayers. Journal of Cellular Biochemistry. 105: 1240-9. PMID 18802922 DOI: 10.1002/jcb.21924  0.01
2008 Yang Y, Tetreault MP, Yermolina YA, Goldstein BG, Katz JP. Krüppel-like factor 5 controls keratinocyte migration via the integrin-linked kinase. The Journal of Biological Chemistry. 283: 18812-20. PMID 18450752 DOI: 10.1074/jbc.M801384200  0.01
2008 Tétreault MP, Chailler P, Beaulieu JF, Rivard N, Ménard D. Epidermal growth factor receptor-dependent PI3K-activation promotes restitution of wounded human gastric epithelial monolayers. Journal of Cellular Physiology. 214: 545-57. PMID 17708540 DOI: 10.1002/jcp.21239  0.01
2006 Tetreault ML, Horrigan DM, Kim JA, Zimmerman AL. Retinoids restore normal cyclic nucleotide sensitivity of mutant ion channels associated with cone dystrophy. Molecular Vision. 12: 1699-705. PMID 17213799  0.01
2006 Tetreault ML, Henry D, Horrigan DM, Matthews G, Zimmerman AL. Characterization of a novel cyclic nucleotide-gated channel from zebrafish brain. Biochemical and Biophysical Research Communications. 348: 441-9. PMID 16887101 DOI: 10.1016/j.bbrc.2006.07.074  0.01
2006 Maher FA, Tetreault MKT. Privilege and diversity in the academy Privilege and Diversity in the Academy. 1-232. DOI: 10.4324/9780203944561  0.01
2005 Pralong E, Pollo C, Coubes P, Bloch J, Roulet E, Tétreault MH, Debatisse D, Villemure JG. Electrophysiological characteristics of limbic and motor globus pallidus internus (GPI) neurons in two cases of Lesch-Nyhan syndrome. Neurophysiologie Clinique = Clinical Neurophysiology. 35: 168-73. PMID 16530134 DOI: 10.1016/j.neucli.2005.12.004  0.01
2005 Horrigan DM, Tetreault ML, Tsomaia N, Vasileiou C, Borhan B, Mierke DF, Crouch RK, Zimmerman AL. Defining the retinoid binding site in the rod cyclic nucleotide-gated channel. The Journal of General Physiology. 126: 453-60. PMID 16230468 DOI: 10.1085/jgp.200509387  0.01
2005 Tétreault MP, Chailler P, Rivard N, Ménard D. Differential growth factor induction and modulation of human gastric epithelial regeneration. Experimental Cell Research. 306: 285-97. PMID 15878352 DOI: 10.1016/j.yexcr.2005.02.019  0.01
2004 Pralong E, Villemure JG, Bloch J, Pollo C, Daniels RT, Ghika J, Vingerhoets F, Tetreault MH, Debatisse D. Quality index for the quantification of the information recorded along standard microelectrode tracks to the subthalamic nucleus in parkinsonian patients. Neurophysiologie Clinique = Clinical Neurophysiology. 34: 209-15. PMID 15639130 DOI: 10.1016/j.neucli.2004.08.001  0.01
2004 Pralong E, Pollo C, Bloch J, Villemure JG, Daniel RT, Tétreault MH, Debatisse D. Recording of ventral posterior lateral thalamus neuron response to contact heat evoked potential in patient with neurogenic pain. Neuroscience Letters. 367: 332-5. PMID 15337260 DOI: 10.1016/j.neulet.2004.06.024  0.01
2004 McCabe SL, Pelosi DM, Tetreault M, Miri A, Nguitragool W, Kovithvathanaphong P, Mahajan R, Zimmerman AL. All-trans-retinal is a closed-state inhibitor of rod cyclic nucleotide-gated ion channels. The Journal of General Physiology. 123: 521-31. PMID 15078915 DOI: 10.1085/jgp.200409011  0.01
2002 Tetreault M, Cusanovich M, Meyer T, Axelrod H, Okamura MY. Double mutant studies identify electrostatic interactions that are important for docking cytochrome c2 onto the bacterial reaction center Biochemistry. 41: 5807-5815. PMID 11980484 DOI: 10.1021/bi012053e  0.01
2001 Tetreault M, Rongey SH, Feher G, Okamura MY. Interaction between cytochrome c2 and the photosynthetic reaction center from Rhodobacter sphaeroides: effects of charge-modifying mutations on binding and electron transfer. Biochemistry. 40: 8452-62. PMID 11456482 DOI: 10.1021/bi010222p  0.01
1999 Tetreault MA. Sex and violence: Social reactions to economic restructuring in Kuwait International Feminist Journal of Politics. 1: 237-255. DOI: 10.1080/146167499359907  0.01
1999 Messenger JR, Smith JC, Tetreault MJ, Vitasovic C, Zhou S, Scott P, Kozicki M. The use of dynamic BNR and two-dimensional clarifier modelling to investigate nitrogen removal at Eastern Treatment Plant, Melbourne, Australia Water Science and Technology. 39: 89-96. DOI: 10.1016/S0273-1223(99)00126-2  0.01
1997 Maher FA, Tetreault MKT. Learning in the Dark: How Assumptions of Whiteness Shape Classroom Knowledge Harvard Educational Review. 67: 321-349.  0.01
1996 Young RR, Tetreault MA. Brief field experiences: An instructional tool for undergraduate political science classes Ps - Political Science and Politics. 29: 695-700.  0.01
1996 Tetreault MA. Gulf winds: Inclement political weather in the Arabian peninsula Current History. 95: 23-27.  0.01
1995 Tetreault MA, Al-Mughni H. Gender, citizenship and nationalism in kuwait British Journal of Middle Eastern Studies. 22: 64-80. DOI: 10.1080/13530199508705612  0.01
1993 Maher FA, Tetreault MKT. Doing feminist ethnography: Lessons from feminist classrooms International Journal of Qualitative Studies in Education. 6: 19-32. DOI: 10.1080/0951839930060103  0.01
1993 Tetreault MA. Independence, sovereignty, and vested glory: oil and politics in the second Gulf War Orient. 34: 87-103.  0.01
1993 Tetreault M, Marcos B, Lapointe J. Forcing function and time delay in qualitative simulation Applications of Artificial Intelligence in Engineering. 2: 109-120.  0.01
1992 Parker DS, Merrill MS, Tetreault MJ. Wastewater treatment process theory and practice: The emerging convergence Water Science and Technology. 25: 301-315.  0.01
1988 Fahim A, Tetreault M, Necsulescu DS. Robot trajectory optimisation with dynamic constraints The International Journal of Advanced Manufacturing Technology. 3: 71-76. DOI: 10.1007/BF02601502  0.01
1988 Tetreault MA. Energy policy and the Reagan administration Forum For Applied Research & Public Policy. 3: 70-79.  0.01
1987 Tetreault MJ, Diemer DM. Control of anaerobic digester foaming Journal of the Water Pollution Control Federation. 59: 987-988.  0.01
1986 Tetreault MJ, Benedict AH, Kaempfer C, Barth EF. Biological phosphorus removal: A technology evaluation Journal of the Water Pollution Control Federation. 58: 823-837.  0.01
1985 Tétreault M. [Not Available]. Historical Papers / the Canadian Historical Association = Communications Historiques / La SociéTé Historique Du Canada. Canadian Historical Association. Meeting. 29-44. PMID 11617099  0.01
1983 Tétreault M. [Not Available]. Revue D'Histoire De L'AméRique FrançAise. 36: 507-26. PMID 11632928  0.01
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