Philippe Campeau: search on Z-Library

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1

Palladium-Catalyzed Direct Arylation of Azine and Azole N -Oxides: Reaction Development, Scope and Applications in Synthesis

Campeau, Louis-Charles, Stuart, David R., Leclerc, Jean-Philippe, Bertrand-Laperle, Mégan, Villemure, Elisia, Sun, Ho-Yan, Lasserre, Sandrine, Guimond, Nicolas, Lecavallier, Melanie, Fagnou, Keith

Journal:

Journal of the American Chemical Society

Year:

2009

Language:

english

File:

PDF, 915 KB

english, 2009

2

Mutation of KCNJ8 in a patient with Cantú syndrome with unique vascular abnormalities – Support for the role of K(ATP) channels in this condition

Brownstein, Catherine A., Towne, Meghan C., Luquette, Lovelace J., Harris, David J., Marinakis, Nicholas S., Meinecke, Peter, Kutsche, Kerstin, Campeau, Philippe M., Yu, Timothy W., Margulies, David M

Journal:

European Journal of Medical Genetics

Year:

2013

Language:

english

File:

PDF, 1.19 MB

english, 2013

3

Modeling a Crowdsourced Definition of Molecular Complexity

Sheridan, Robert P., Zorn, Nicolas, Sherer, Edward C., Campeau, Louis-Charles, Chang, Charlie (Zhenyu), Cumming, Jared, Maddess, Matthew L., Nantermet, Philippe G., Sinz, Christopher J., O’Shea, Paul

Journal:

Journal of Chemical Information and Modeling

Year:

2014

Language:

english

File:

PDF, 5.53 MB

english, 2014

4

Requirement of argininosuccinate lyase for systemic nitric oxide production

Erez, Ayelet, Nagamani, Sandesh C S, Shchelochkov, Oleg A, Premkumar, Muralidhar H, Campeau, Philippe M, Chen, Yuqing, Garg, Harsha K, Li, Li, Mian, Asad, Bertin, Terry K, Black, Jennifer O, Zeng, Hen

Journal:

Nature Medicine

Year:

2011

Language:

english

File:

PDF, 991 KB

english, 2011

5

Kaufman oculo-cerebro-facial syndrome in a child with small and absent terminal phalanges and absent nails

Kariminejad, Ariana, Ajeawung, Norbert Fonya, Bozorgmehr, Bita, Dionne-Laporte, Alexandre, Molidperee, Sirinart, Najafi, Kimia, Gibbs, Richard A, Lee, Brendan H, Hennekam, Raoul C, Campeau, Philippe M

Journal:

Journal of Human Genetics

Year:

2017

Language:

english

File:

PDF, 654 KB

english, 2017

6

Hot water epilepsy and SYN1 variants

Peron, Angela, Baratang, Nissan V., Canevini, Maria Paola, Campeau, Philippe M., Vignoli, Aglaia

Journal:

Year:

2018

Language:

english

File:

PDF, 258 KB

english, 2018

7

Kinova Modular Robot Arms for Service Robotics Applications

Campeau-Lecours, Alexandre, Lamontagne, Hugo, Latour, Simon, Fauteux, Philippe, Maheu, Véronique, Boucher, François, Deguire, Charles, L'Ecuyer, Louis-Joseph Caron

Journal:

International Journal of Robotics Applications and Technologies

Year:

2017

Language:

english

File:

PDF, 2.00 MB

english, 2017

8

BAFopathies’ DNA methylation epi-signatures demonstrate diagnostic utility and functional continuum of Coffin–Siris and Nicolaides–Baraitser syndromes

Aref-Eshghi, Erfan, Bend, Eric G., Hood, Rebecca L., Schenkel, Laila C., Carere, Deanna Alexis, Chakrabarti, Rana, Nagamani, Sandesh C. S., Cheung, Sau Wai, Campeau, Philippe M., Prasad, Chitra, Siu,

Journal:

Nature Communications

Year:

2018

Language:

english

File:

PDF, 2.97 MB

english, 2018

9

Assistive robotic arm: Evaluation of the performance of intelligent algorithms

Lebrasseur, Audrey, Lettre, Josiane, Routhier, François, Archambault, Philippe S., Campeau-Lecours, Alexandre

Journal:

Assistive Technology

Year:

2019

Language:

english

File:

PDF, 1.97 MB

english, 2019

10

[IEEE 2019 IEEE 16th International Conference on Rehabilitation Robotics (ICORR) - Toronto, ON, Canada (2019.6.24-2019.6.28)] 2019 IEEE 16th International Conference on Rehabilitation Robotics (ICORR) - Preliminary Design of an Active Stabilization Assistive Eating Device for People Living with Movement Disorders

Turgeon, Philippe, Laliberte, Thierry, Routhier, Francois, Campeau-Lecours, Alexandre

Year:

2019

Language:

english

File:

PDF, 844 KB

english, 2019

11

Clinical characteristics of patients from Quebec, Canada, with Morquio A syndrome: a longitudinal observational study

Moisan, Lina, Iannuzzi, David, Maranda, Bruno, Campeau, Philippe M., Mitchell, John J.

Journal:

Orphanet Journal of Rare Diseases

Year:

2020

File:

PDF, 1.12 MB

2020

12

Prenatal diagnosis of monosomy 1p36: A focus on brain abnormalities and a review of the literature

Philippe M. Campeau, Nicholas Ah Mew, Lola Cartier, Katherine L. Mackay, Lisa G. Shaffer, Vazken M. Der Kaloustian, Mary Ann Thomas

Journal:

American Journal of Medical Genetics Part A

Year:

2008

Language:

english

File:

PDF, 143 KB

english, 2008

13

ChemInform Abstract: Palladium-Catalyzed Direct Arylation of Azine and Azole N-Oxides: Reaction Development, Scope and Applications in Synthesis.

Louis-Charles Campeau, David R. Stuart, Jean-Philippe Leclerc, Megan Bertrand-Laperle, Elisia Villemure, Ho-Yan Sun, Sandrine Lasserre, Nicolas Guimond, Melanie Lecavallier, Keith Fagnou

Journal:

Year:

2009

Language:

english

File:

PDF, 65 KB

english, 2009

14

ChemInform Abstract: Palladium-Catalyzed Direct Arylation of Azine and Azole N-Oxides: Reaction Development, Scope and Applications in Synthesis.

Louis-Charles Campeau, David R. Stuart, Jean-Philippe Leclerc, Megan Bertrand-Laperle, Elisia Villemure, Ho-Yan Sun, Sandrine Lasserre, Nicolas Guimond, Melanie Lecavallier, Keith Fagnou

Journal:

Year:

2009

File:

PDF, 55 KB

2009

15

Hereditary breast cancer: new genetic developments, new therapeutic avenues

Philippe M. Campeau, William D. Foulkes, Marc D. Tischkowitz

Journal:

Year:

2008

Language:

english

File:

PDF, 471 KB

english, 2008

16

Persistent DNA damage signalling triggers senescence-associated inflammatory cytokine secretion

Rodier, Francis, Coppé, Jean-Philippe, Patil, Christopher K., Hoeijmakers, Wieteke A. M., Muñoz, Denise P., Raza, Saba R., Freund, Adam, Campeau, Eric, Davalos, Albert R., Campisi, Judith

Journal:

Nature Cell Biology

Year:

2009

Language:

english

File:

PDF, 316 KB

english, 2009

17

Persistent DNA damage signalling triggers senescence-associated inflammatory cytokine secretion

Rodier, Francis, Coppé, Jean-Philippe, Patil, Christopher K., Hoeijmakers, Wieteke A. M., Muñoz, Denise P., Raza, Saba R., Freund, Adam, Campeau, Eric, Davalos, Albert R., Campisi, Judith

Journal:

Nature Cell Biology

Year:

2009

Language:

english

File:

PDF, 2.31 MB

english, 2009

18

The KAT6B-related disorders genitopatellar syndrome and Ohdo/SBBYS syndrome have distinct clinical features reflecting distinct molecular mechanisms

Philippe M. Campeau, James T. Lu, Brian C. Dawson, Ivo F. A. C. Fokkema, Stephen P. Robertson, Richard A. Gibbs, Brendan H. Lee

Journal:

Year:

2012

Language:

english

File:

PDF, 374 KB

english, 2012

19

Mutations in KAT6B, Encoding a Histone Acetyltransferase, Cause Genitopatellar Syndrome

Philippe M. Campeau, Jaeseung C. Kim, James T. Lu, Jeremy A. Schwartzentruber, Omar A. Abdul-Rahman, Silke Schlaubitz, David M. Murdock, Ming-Ming Jiang, Edward J. Lammer, Gregory M. Enns, William J.

Journal:

The American Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 1.10 MB

english, 2012

20

Nitric-Oxide Supplementation for Treatment of Long-Term Complications in Argininosuccinic Aciduria

Sandesh C.S. Nagamani, Philippe M. Campeau, Oleg A. Shchelochkov, Muralidhar H. Premkumar, Kilian Guse, Nicola Brunetti-Pierri, Yuqing Chen, Qin Sun, Yaoping Tang, Donna Palmer, Anilkumar K. Reddy, Li

Journal:

The American Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 588 KB

english, 2012

21

57 Neo-organoid of mesenchymal stem cells engineered to secrete a CC-chemokine chimeric fusokine reverses EAE

Moutih Rafei, Philippe Campeau, Elena Birman, Jacques Galipeau

Journal:

Year:

2008

Language:

english

File:

PDF, 47 KB

english, 2008

22

A 25-year longitudinal analysis of treatment efficacy in inborn errors of metabolism

Philippe M. Campeau, Charles R. Scriver, John J. Mitchell

Journal:

Molecular Genetics and Metabolism

Year:

2008

Language:

english

File:

PDF, 571 KB

english, 2008

23

Early orthotopic liver transplantation in urea cycle defects: Follow up of a developmental outcome study

Philippe M. Campeau, Penelope J. Pivalizza, Geoffrey Miller, Kim McBride, Saul Karpen, John Goss, Brendan H. Lee

Journal:

Molecular Genetics and Metabolism

Year:

2010

Language:

english

File:

PDF, 266 KB

english, 2010

24

Identification of Novel Mutations Confirms Pde4d as a Major Gene Causing Acrodysostosis

Lynch, Danielle C., Dyment, David A., Huang, Lijia, Nikkel, Sarah M., Lacombe, Didier, Campeau, Philippe M., Lee, Brendan, Bacino, Carlos A., Michaud, Jacques L., Bernier, Francois P., Consortium, FOR

Journal:

Year:

2013

Language:

english

File:

PDF, 296 KB

english, 2013

25

WNT1 Mutations in Early-Onset Osteoporosis and Osteogenesis Imperfecta

Laine, Christine M., Joeng, Kyu Sang, Campeau, Philippe M., Kiviranta, Riku, Tarkkonen, Kati, Grover, Monica, Lu, James T., Pekkinen, Minna, Wessman, Maija, Heino, Terhi J., Nieminen-Pihala, Vappu, Ar

Journal:

Boston Medical and Surgical Journal

Year:

2013

Language:

english

File:

PDF, 804 KB

english, 2013

26

C2, C5, and C4 Azole N -Oxide Direct Arylation Including Room-Temperature Reactions

Campeau, Louis-Charles, Bertrand-Laperle, Mégan, Leclerc, Jean-Philippe, Villemure, Elisia, Gorelsky, Serge, Fagnou, Keith

Journal:

Journal of the American Chemical Society

Year:

2008

Language:

english

File:

PDF, 78 KB

english, 2008

27

The genetic basis of DOORS syndrome: an exome-sequencing study

Campeau, Philippe M, Kasperaviciute, Dalia, Lu, James T, Burrage, Lindsay C, Kim, Choel, Hori, Mutsuki, Powell, Berkley R, Stewart, Fiona, Félix, Têmis Maria, van den Ende, Jenneke, Wisniewska, Marzen

Journal:

The Lancet Neurology

Year:

2014

Language:

english

File:

PDF, 2.11 MB

english, 2014

28

Yunis-Varón Syndrome Is Caused by Mutations in FIG4, Encoding a Phosphoinositide Phosphatase

Campeau, Philippe M., Lenk, Guy M., Lu, James T., Bae, Yangjin, Burrage, Lindsay, Turnpenny, Peter, Román Corona-Rivera, Jorge, Morandi, Lucia, Mora, Marina, Reutter, Heiko, Vulto-van Silfhout, Anneke

Journal:

The American Journal of Human Genetics

Year:

2013

Language:

english

File:

PDF, 1.30 MB

english, 2013

29

A Recurrent PDGFRB Mutation Causes Familial Infantile Myofibromatosis

Cheung, Yee Him, Gayden, Tenzin, Campeau, Philippe M., LeDuc, Charles A., Russo, Donna, Nguyen, Van-Hung, Guo, Jiancheng, Qi, Ming, Guan, Yanfang, Albrecht, Steffen, Moroz, Brenda, Eldin, Karen W., Lu

Journal:

The American Journal of Human Genetics

Year:

2013

Language:

english

File:

PDF, 523 KB

english, 2013

30

184 Serial measurement of baseline — Normalized fibrinogen/plasminogen ratio in systemic thrombolytic therapy with streptokinase for acute myocardial infarction

Murali, Chaya, Lu, James T., Jain, Mahim, Liu, David S., Lachman, Ralph, Gibbs, Richard A., Lee, Brendan H., Cohn, Daniel, Campeau, Philippe M.

Journal:

Fibrinolysis and Proteolysis

Year:

1988

Language:

english

File:

PDF, 98 KB

english, 1988

31

Diagnosis of ALG12-CDG by exome sequencing in a case of severe skeletal dysplasia

Murali, Chaya, Lu, James T., Jain, Mahim, Liu, David S., Lachman, Ralph, Gibbs, Richard A., Lee, Brendan H., Cohn, Daniel, Campeau, Philippe M.

Journal:

Molecular Genetics and Metabolism Reports

Year:

2014

Language:

english

File:

PDF, 785 KB

english, 2014

32

Genotype–Phenotype Correlation — Promiscuity in the Era of Next-Generation Sequencing

Lu, James T., Campeau, Philippe M., Lee, Brendan H.

Journal:

New England Journal of Medicine

Year:

2014

Language:

english

File:

PDF, 507 KB

english, 2014

33

Osteogenesis imperfecta without features of type V caused by a mutation in the IFITM 5 gene

Grover, Monica, Campeau, Philippe M, Lietman, Caressa Dee, Lu, James T, Gibbs, Richard A, Schlesinger, Alan E, Lee, Brendan H

Journal:

Journal of Bone and Mineral Research

Year:

2013

Language:

english

File:

PDF, 1.58 MB

english, 2013

34

Identification of Novel Mutations Confirms PDE4D as a Major Gene Causing Acrodysostosis

Lynch, Danielle C., Dyment, David A., Huang, Lijia, Nikkel, Sarah M., Lacombe, Didier, Campeau, Philippe M., Lee, Brendan, Bacino, Carlos A., Michaud, Jacques L., Bernier, Francois P., Consortium, FOR

Journal:

Year:

2013

Language:

english

File:

PDF, 74 KB

english, 2013

35

DOORS syndrome: Phenotype, genotype and comparison with Coffin-Siris syndrome

Campeau, Philippe M., Hennekam, Raoul C.

Journal:

American Journal of Medical Genetics Part C: Seminars in Medical Genetics

Year:

2014

Language:

english

File:

PDF, 503 KB

english, 2014

36

Myhre and LAPS syndromes: clinical and molecular review of 32 patients

Michot, Caroline, Le Goff, Carine, Mahaut, Clémentine, Afenjar, Alexandra, Brooks, Alice S, Campeau, Philippe M, Destree, Anne, Di Rocco, Maja, Donnai, Dian, Hennekam, Raoul, Heron, Delphine, Jacquemo

Journal:

European Journal of Human Genetics

Year:

2014

Language:

english

File:

PDF, 937 KB

english, 2014

37

Genotype-Phenotype Correlation

Lu, James T., Campeau, Philippe M., Lee, Brendan H.

Journal:

Obstetric and Gynecologic Survey

Year:

2014

Language:

english

File:

PDF, 210 KB

english, 2014

38

Early childhood presentation of Czech dysplasia

Burrage, Lindsay C., Lu, James T., Liu, David S., Moss, Timothy J., Gibbs, Richard, Schlesinger, Alan E., Bacino, Carlos A., Campeau, Philippe M., Lee, Brendan H.

Journal:

Clinical Dysmorphology

Year:

2013

Language:

english

File:

PDF, 375 KB

english, 2013

39

FBN1 contributing to familial congenital diaphragmatic hernia

Beck, Tyler F., Campeau, Philippe M., Jhangiani, Shalini N., Gambin, Tomasz, Li, Alexander H., Abo-Zahrah, Reem, Jordan, Valerie K., Hernandez-Garcia, Andres, Wiszniewski, Wojciech K., Muzny, Donna, G

Journal:

American Journal of Medical Genetics Part A

Year:

2015

Language:

english

File:

PDF, 1.13 MB

english, 2015

40

Myhre and LAPS syndromes: clinical and molecular review of 32 patients

Michot, Caroline, Le Goff, Carine, Mahaut, Clémentine, Afenjar, Alexandra, Brooks, Alice S, Campeau, Philippe M, Destree, Anne, Di Rocco, Maja, Donnai, Dian, Hennekam, Raoul, Heron, Delphine, Jacquemo

Journal:

European Journal of Human Genetics

Year:

2014

Language:

english

File:

PDF, 63 KB

english, 2014

41

Mesenchymal Stromal Cells Engineered to Express Erythropoietin Induce Anti-erythropoietin Antibodies and Anemia in Allorecipients

Campeau, Philippe M, Rafei, Moutih, François, Moïra, Birman, Elena, Forner, Kathy-Ann, Galipeau, Jacques

Journal:

Molecular Therapy

Year:

2009

File:

PDF, 831 KB

2009

42

Mesenchymal Stromal Cells Engineered to Express Erythropoietin Induce Anti-erythropoietin Antibodies and Anemia in Allorecipients

Campeau, Philippe M, Rafei, Moutih, François, Moïra, Birman, Elena, Forner, Kathy-Ann, Galipeau, Jacques

Journal:

Molecular Therapy

Year:

2009

Language:

english

File:

PDF, 831 KB

english, 2009

43

Biosynthesis of glycosaminoglycans: associated disorders and biochemical tests

Sasarman, Florin, Maftei, Catalina, Campeau, Philippe M., Brunel-Guitton, Catherine, Mitchell, Grant A., Allard, Pierre

Journal:

Journal of Inherited Metabolic Disease

Year:

2016

Language:

english

File:

PDF, 1.87 MB

english, 2016

44

Small 6q16.1 Deletions Encompassing POU3F2 Cause Susceptibility to Obesity and Variable Developmental Delay with Intellectual Disability

Kasher, Paul R., Schertz, Katherine E., Thomas, Megan, Jackson, Adam, Annunziata, Silvia, Ballesta-Martinez, María J., Campeau, Philippe M., Clayton, Peter E., Eaton, Jennifer L., Granata, Tiziana, Gu

Journal:

The American Journal of Human Genetics

Year:

2016

Language:

english

File:

PDF, 1.19 MB

english, 2016

45

Adult presentation of X-linked Conradi-Hünermann-Happle syndrome

Posey, Jennifer E., Burrage, Lindsay C., Campeau, Philippe M., Lu, James T., Eble, Tanya N., Kratz, Lisa, Schlesinger, Alan E., Gibbs, Richard A., Lee, Brendan H., Nagamani, Sandesh C.S.

Journal:

American Journal of Medical Genetics Part A

Year:

2015

Language:

english

File:

PDF, 1018 KB

english, 2015

46

Genomic approaches to diagnose rare bone disorders

Falardeau, Félix, Camurri, Maria Vittoria, Campeau, Philippe M.

Journal:

Year:

2016

Language:

english

File:

PDF, 516 KB

english, 2016

47

[IEEE 2016 IEEE/RSJ International Conference on Intelligent Robots and Systems (IROS) - Daejeon, South Korea (2016.10.9-2016.10.14)] 2016 IEEE/RSJ International Conference on Intelligent Robots and Systems (IROS) - Improving cable driven parallel robot accuracy through angular position sensors

Fortin-Cote, Alexis, Cardou, Philippe, Campeau-Lecours, Alexandre

Year:

2016

Language:

english

File:

PDF, 1.80 MB

english, 2016

48

Mutations in the phosphatidylinositol glycan C ( PIGC ) gene are associated with epilepsy and intellectual disability

Edvardson, Simon, Murakami, Yoshiko, Nguyen, Thi Tuyet Mai, Shahrour, Maher, St-Denis, Anik, Shaag, Avraham, Damseh, Nadira, Le Deist, Françoise, Bryceson, Yenan, Abu-Libdeh, Bassam, Campeau, Philippe

Journal:

Journal of Medical Genetics

Year:

2017

Language:

english

File:

PDF, 1.17 MB

english, 2017

49

MicroRNA miR-23a cluster promotes osteocyte differentiation by regulating TGF-β signalling in osteoblasts

Zeng, Huan-Chang, Bae, Yangjin, Dawson, Brian C., Chen, Yuqing, Bertin, Terry, Munivez, Elda, Campeau, Philippe M., Tao, Jianning, Chen, Rui, Lee, Brendan H.

Journal:

Nature Communications

Year:

2017

Language:

english

File:

PDF, 1.35 MB

english, 2017

50

Succinate, increased in metabolic syndrome, activates GPR91 receptor signaling in urothelial cells

Mossa, Abubakr H., Flores, Monica Velasquez, Cammisotto, Philippe G., Campeau, Lysanne

Journal:

Cellular Signalling

Year:

2017

Language:

english

File:

PDF, 1.12 MB

english, 2017