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Atypical Omenn Syndrome due to Adenosine Deaminase Deficiency.

Case reports in immunology

Joshi AY, Ham EK, Shah NB, Dong X, Khan SP, Abraham RS.
PMID: 25954555
Case Reports Immunol. 2012;2012:919241. doi: 10.1155/2012/919241. Epub 2012 May 31.

We present here a novel case of an atypical Omenn syndrome (OS) phenotype due to mutations in the ADA gene encoding adenosine deaminase. This case is noteworthy for a significant increase in circulating CD56(bright)CD16- cytokine-producing NK cells after treatment...

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Joshi AY, Ham EK, Shah NB, et al. Atypical Omenn Syndrome due to Adenosine Deaminase Deficiency. Case Reports Immunol. 2012;2012:919241doi: 10.1155/2012/919241.
Joshi, A. Y., Ham, E. K., Shah, N. B., Dong, X., Khan, S. P., & Abraham, R. S. (2012). Atypical Omenn Syndrome due to Adenosine Deaminase Deficiency. Case reports in immunology, 2012919241. https://doi.org/10.1155/2012/919241
Joshi, Avni Y, et al. "Atypical Omenn Syndrome due to Adenosine Deaminase Deficiency." Case reports in immunology vol. 2012 (2012): 919241. doi: https://doi.org/10.1155/2012/919241
Joshi AY, Ham EK, Shah NB, Dong X, Khan SP, Abraham RS. Atypical Omenn Syndrome due to Adenosine Deaminase Deficiency. Case Reports Immunol. 2012;2012:919241. doi: 10.1155/2012/919241. Epub 2012 May 31. PMID: 25954555; PMCID: PMC4412092.
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Simple to simplest: the tubeless technique.

Journal of thoracic disease

Li J, Liu J, Hamblin L, Liu H, Liang L, Dong Q, He J.
PMID: 28275463
J Thorac Dis. 2017 Feb;9(2):222-224. doi: 10.21037/jtd.2017.02.55.

No abstract available.

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Li J, Liu J, Hamblin L, et al. Simple to simplest: the tubeless technique. J Thorac Dis. 2017;9(2):222-224doi: 10.21037/jtd.2017.02.55.
Li, J., Liu, J., Hamblin, L., Liu, H., Liang, L., Dong, Q., & He, J. (2017). Simple to simplest: the tubeless technique. Journal of thoracic disease, 9(2), 222-224. https://doi.org/10.21037/jtd.2017.02.55
Li, Jingpei, et al. "Simple to simplest: the tubeless technique." Journal of thoracic disease vol. 9,2 (2017): 222-224. doi: https://doi.org/10.21037/jtd.2017.02.55
Li J, Liu J, Hamblin L, Liu H, Liang L, Dong Q, He J. Simple to simplest: the tubeless technique. J Thorac Dis. 2017 Feb;9(2):222-224. doi: 10.21037/jtd.2017.02.55. PMID: 28275463; PMCID: PMC5334079.
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Crystallization-induced asymmetric transformation of chiral-at-metal ruthenium(II) complexes bearing achiral ligands.

Chemistry (Weinheim an der Bergstrasse, Germany)

Hamelin O, Pécaut J, Fontecave M.
PMID: 15146526
Chemistry. 2004 May 17;10(10):2548-54. doi: 10.1002/chem.200305749.

Recently, we observed that the enantiopure Lambda form of the tributylammonium salt of the chiral anion tris[tetrachlorobenzene-1,2-bis(olato)]phosphate, also named Trisphat, was able to induce an efficient resolution of a Delta,Lambda racemic mixture of cis-[Ru(dmp)2(NCCH3)2](PF6)2 (dmp=2,9-dimethyl-1,10-phenanthroline) due to the spontaneous...

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Hamelin O, Pécaut J, Fontecave M. Crystallization-induced asymmetric transformation of chiral-at-metal ruthenium(II) complexes bearing achiral ligands. Chemistry. 2004;10(10):2548-54doi: 10.1002/chem.200305749.
Hamelin, O., Pécaut, J., & Fontecave, M. (2004). Crystallization-induced asymmetric transformation of chiral-at-metal ruthenium(II) complexes bearing achiral ligands. Chemistry (Weinheim an der Bergstrasse, Germany), 10(10), 2548-54. https://doi.org/10.1002/chem.200305749
Hamelin, Olivier, et al. "Crystallization-induced asymmetric transformation of chiral-at-metal ruthenium(II) complexes bearing achiral ligands." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 10,10 (2004): 2548-54. doi: https://doi.org/10.1002/chem.200305749
Hamelin O, Pécaut J, Fontecave M. Crystallization-induced asymmetric transformation of chiral-at-metal ruthenium(II) complexes bearing achiral ligands. Chemistry. 2004 May 17;10(10):2548-54. doi: 10.1002/chem.200305749. PMID: 15146526.
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Catalytic asymmetric sulfoxidation by chiral manganese complexes: acetylacetonate anions as chirality switches.

Inorganic chemistry

Schoumacker S, Hamelin O, Pécaut J, Fontecave M.
PMID: 14632533
Inorg Chem. 2003 Dec 01;42(24):8110-6. doi: 10.1021/ic0346533.

Three manganese(II) complexes, namely [Mn(1)(ClO(4))(2)] (3), [Mn(1)(acac)(2)] (4), and [Mn(2)(1)(acac)(4)] (5), were isolated from solutions of Mn(ClO(4))(2) or Mn(acac)(2), and an easily accessible diimine ligand (1S,2S)-N,N'-bis-pyridin-2-ylmethylene-cyclohexane-1,2-diamine (1). Their structure was determined by X-ray crystallography, and these complexes proved to...

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Schoumacker S, Hamelin O, Pécaut J, et al. Catalytic asymmetric sulfoxidation by chiral manganese complexes: acetylacetonate anions as chirality switches. Inorg Chem. 2003;42(24):8110-6doi: 10.1021/ic0346533.
Schoumacker, S., Hamelin, O., Pécaut, J., & Fontecave, M. (2003). Catalytic asymmetric sulfoxidation by chiral manganese complexes: acetylacetonate anions as chirality switches. Inorganic chemistry, 42(24), 8110-6. https://doi.org/10.1021/ic0346533
Schoumacker, Sébastien, et al. "Catalytic asymmetric sulfoxidation by chiral manganese complexes: acetylacetonate anions as chirality switches." Inorganic chemistry vol. 42,24 (2003): 8110-6. doi: https://doi.org/10.1021/ic0346533
Schoumacker S, Hamelin O, Pécaut J, Fontecave M. Catalytic asymmetric sulfoxidation by chiral manganese complexes: acetylacetonate anions as chirality switches. Inorg Chem. 2003 Dec 01;42(24):8110-6. doi: 10.1021/ic0346533. PMID: 14632533.
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Improved proteome coverage by using iTRAQ labelling and peptide OFFGEL fractionation.

Proteome science

Ernoult E, Gamelin E, Guette C.
PMID: 18851748
Proteome Sci. 2008 Oct 13;6:27. doi: 10.1186/1477-5956-6-27.

BACKGROUND: The development of mass spectrometric techniques and fractionation methods now allows the investigation of very complex protein mixtures ranging from subcellular structures to tissues. Nevertheless, this work is particularly difficult due to the wide dynamic range of protein...

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Ernoult E, Gamelin E, Guette C. Improved proteome coverage by using iTRAQ labelling and peptide OFFGEL fractionation. Proteome Sci. 2008;6:27doi: 10.1186/1477-5956-6-27.
Ernoult, E., Gamelin, E., & Guette, C. (2008). Improved proteome coverage by using iTRAQ labelling and peptide OFFGEL fractionation. Proteome science, 627. https://doi.org/10.1186/1477-5956-6-27
Ernoult, Emilie, et al. "Improved proteome coverage by using iTRAQ labelling and peptide OFFGEL fractionation." Proteome science vol. 6 (2008): 27. doi: https://doi.org/10.1186/1477-5956-6-27
Ernoult E, Gamelin E, Guette C. Improved proteome coverage by using iTRAQ labelling and peptide OFFGEL fractionation. Proteome Sci. 2008 Oct 13;6:27. doi: 10.1186/1477-5956-6-27. PMID: 18851748; PMCID: PMC2572582.
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Examination of Gould's modified S1 (mS1) selective medium and Angle's non-selective medium for describing the diversity of Pseudomonas spp. in soil and root environments.

FEMS microbiology ecology

Tarnawski S, Hamelin J, Locatelli L, Aragno M, Fromin N.
PMID: 19719620
FEMS Microbiol Ecol. 2003 Jul 01;45(2):97-104. doi: 10.1016/S0168-6496(03)00130-2.

Abstract Studies on the diversity of environmental culturable Pseudomonas populations are dependent on the isolation procedure. This procedure includes the use of selective media which may influence the recovery of strains and thus the diversity described. In this study,...

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Tarnawski S, Hamelin J, Locatelli L, et al. Examination of Gould's modified S1 (mS1) selective medium and Angle's non-selective medium for describing the diversity of Pseudomonas spp. in soil and root environments. FEMS Microbiol Ecol. 2003;45(2):97-104doi: 10.1016/S0168-6496(03)00130-2.
Tarnawski, S., Hamelin, J., Locatelli, L., Aragno, M., & Fromin, N. (2003). Examination of Gould's modified S1 (mS1) selective medium and Angle's non-selective medium for describing the diversity of Pseudomonas spp. in soil and root environments. FEMS microbiology ecology, 45(2), 97-104. https://doi.org/10.1016/S0168-6496(03)00130-2
Tarnawski, Sonia, et al. "Examination of Gould's modified S1 (mS1) selective medium and Angle's non-selective medium for describing the diversity of Pseudomonas spp. in soil and root environments." FEMS microbiology ecology vol. 45,2 (2003): 97-104. doi: https://doi.org/10.1016/S0168-6496(03)00130-2
Tarnawski S, Hamelin J, Locatelli L, Aragno M, Fromin N. Examination of Gould's modified S1 (mS1) selective medium and Angle's non-selective medium for describing the diversity of Pseudomonas spp. in soil and root environments. FEMS Microbiol Ecol. 2003 Jul 01;45(2):97-104. doi: 10.1016/S0168-6496(03)00130-2. PMID: 19719620.
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Characterization of the surfaceome of the metal-reducing bacterium Desulfotomaculum reducens.

Frontiers in microbiology

Dalla Vecchia E, Shao PP, Suvorova E, Chiappe D, Hamelin R, Bernier-Latmani R.
PMID: 25191310
Front Microbiol. 2014 Aug 19;5:432. doi: 10.3389/fmicb.2014.00432. eCollection 2014.

Desulfotomaculum reducens strain MI-1 is a Gram-positive, sulfate-reducing bacterium also capable of reducing Fe(III). Metal reduction in Gram-positive bacteria is poorly understood. Here, we investigated Fe(III) reduction with lactate, a non-fermentable substrate, as the electron donor. Lactate consumption is...

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Dalla Vecchia E, Shao PP, Suvorova E, et al. Characterization of the surfaceome of the metal-reducing bacterium Desulfotomaculum reducens. Front Microbiol. 2014;5:432doi: 10.3389/fmicb.2014.00432.
Dalla Vecchia, E., Shao, P. P., Suvorova, E., Chiappe, D., Hamelin, R., & Bernier-Latmani, R. (2014). Characterization of the surfaceome of the metal-reducing bacterium Desulfotomaculum reducens. Frontiers in microbiology, 5432. https://doi.org/10.3389/fmicb.2014.00432
Dalla Vecchia, Elena, et al. "Characterization of the surfaceome of the metal-reducing bacterium Desulfotomaculum reducens." Frontiers in microbiology vol. 5 (2014): 432. doi: https://doi.org/10.3389/fmicb.2014.00432
Dalla Vecchia E, Shao PP, Suvorova E, Chiappe D, Hamelin R, Bernier-Latmani R. Characterization of the surfaceome of the metal-reducing bacterium Desulfotomaculum reducens. Front Microbiol. 2014 Aug 19;5:432. doi: 10.3389/fmicb.2014.00432. eCollection 2014. PMID: 25191310; PMCID: PMC4137172.
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Inactivation of Bacillus cereus vegetative cells by gastric acid and bile during in vitro gastrointestinal transit.

Gut pathogens

Ceuppens S, Uyttendaele M, Hamelink S, Boon N, Van de Wiele T.
PMID: 23034184
Gut Pathog. 2012 Oct 03;4(1):11. doi: 10.1186/1757-4749-4-11.

BACKGROUND: The foodborne pathogen Bacillus cereus can cause diarrhoeal food poisoning by production of enterotoxins in the small intestine. The prerequisite for diarrhoeal disease is thus survival during gastrointestinal passage.METHODS: Vegetative cells of 3 different B. cereus strains were...

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Ceuppens S, Uyttendaele M, Hamelink S, et al. Inactivation of Bacillus cereus vegetative cells by gastric acid and bile during in vitro gastrointestinal transit. Gut Pathog. 2012;4(1):11doi: 10.1186/1757-4749-4-11.
Ceuppens, S., Uyttendaele, M., Hamelink, S., Boon, N., & Van de Wiele, T. (2012). Inactivation of Bacillus cereus vegetative cells by gastric acid and bile during in vitro gastrointestinal transit. Gut pathogens, 4(1), 11. https://doi.org/10.1186/1757-4749-4-11
Ceuppens, Siele, et al. "Inactivation of Bacillus cereus vegetative cells by gastric acid and bile during in vitro gastrointestinal transit." Gut pathogens vol. 4,1 (2012): 11. doi: https://doi.org/10.1186/1757-4749-4-11
Ceuppens S, Uyttendaele M, Hamelink S, Boon N, Van de Wiele T. Inactivation of Bacillus cereus vegetative cells by gastric acid and bile during in vitro gastrointestinal transit. Gut Pathog. 2012 Oct 03;4(1):11. doi: 10.1186/1757-4749-4-11. PMID: 23034184; PMCID: PMC3500208.
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Intrinsic Dielectric Constant Anomaly in Critical Liquid Mixtures.

Physical review letters

Bose TK, Gopal BR, Hamelin J, Thoen J.
PMID: 10058004
Phys Rev Lett. 1995 Apr 03;74(14):2733-2736. doi: 10.1103/PhysRevLett.74.2733.

No abstract available.

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Bose TK, Gopal BR, Hamelin J, et al. Intrinsic Dielectric Constant Anomaly in Critical Liquid Mixtures. Phys Rev Lett. 1995;74(14):2733-2736doi: 10.1103/PhysRevLett.74.2733.
Bose, T. K., Gopal, B. R., Hamelin, J., & Thoen, J. (1995). Intrinsic Dielectric Constant Anomaly in Critical Liquid Mixtures. Physical review letters, 74(14), 2733-2736. https://doi.org/10.1103/PhysRevLett.74.2733
Bose, et al. "Intrinsic Dielectric Constant Anomaly in Critical Liquid Mixtures." Physical review letters vol. 74,14 (1995): 2733-2736. doi: https://doi.org/10.1103/PhysRevLett.74.2733
Bose TK, Gopal BR, Hamelin J, Thoen J. Intrinsic Dielectric Constant Anomaly in Critical Liquid Mixtures. Phys Rev Lett. 1995 Apr 03;74(14):2733-2736. doi: 10.1103/PhysRevLett.74.2733. PMID: 10058004.
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Mitochondrial roles and cytoprotection in chronic liver injury.

Biochemistry research international

Degli Esposti D, Hamelin J, Bosselut N, Saffroy R, Sebagh M, Pommier A, Martel C, Lemoine A.
PMID: 22745910
Biochem Res Int. 2012;2012:387626. doi: 10.1155/2012/387626. Epub 2012 Jun 15.

The liver is one of the richest organs in terms of number and density of mitochondria. Most chronic liver diseases are associated with the accumulation of damaged mitochondria. Hepatic mitochondria have unique features compared to other organs' mitochondria, since...

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Degli Esposti D, Hamelin J, Bosselut N, et al. Mitochondrial roles and cytoprotection in chronic liver injury. Biochem Res Int. 2012;2012:387626doi: 10.1155/2012/387626.
Degli Esposti, D., Hamelin, J., Bosselut, N., Saffroy, R., Sebagh, M., Pommier, A., Martel, C., & Lemoine, A. (2012). Mitochondrial roles and cytoprotection in chronic liver injury. Biochemistry research international, 2012387626. https://doi.org/10.1155/2012/387626
Degli Esposti, Davide, et al. "Mitochondrial roles and cytoprotection in chronic liver injury." Biochemistry research international vol. 2012 (2012): 387626. doi: https://doi.org/10.1155/2012/387626
Degli Esposti D, Hamelin J, Bosselut N, Saffroy R, Sebagh M, Pommier A, Martel C, Lemoine A. Mitochondrial roles and cytoprotection in chronic liver injury. Biochem Res Int. 2012;2012:387626. doi: 10.1155/2012/387626. Epub 2012 Jun 15. PMID: 22745910; PMCID: PMC3382253.
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The Membrane-Bound C Subunit of Reductive Dehalogenases: Topology Analysis and Reconstitution of the FMN-Binding Domain of PceC.

Frontiers in microbiology

Buttet GF, Willemin MS, Hamelin R, Rupakula A, Maillard J.
PMID: 29740408
Front Microbiol. 2018 Apr 24;9:755. doi: 10.3389/fmicb.2018.00755. eCollection 2018.

Organohalide respiration (OHR) is the energy metabolism of anaerobic bacteria able to use halogenated organic compounds as terminal electron acceptors. While the terminal enzymes in OHR, so-called reductive dehalogenases, are well-characterized, the identity of proteins potentially involved in electron...

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Buttet GF, Willemin MS, Hamelin R, et al. The Membrane-Bound C Subunit of Reductive Dehalogenases: Topology Analysis and Reconstitution of the FMN-Binding Domain of PceC. Front Microbiol. 2018;9:755doi: 10.3389/fmicb.2018.00755.
Buttet, G. F., Willemin, M. S., Hamelin, R., Rupakula, A., & Maillard, J. (2018). The Membrane-Bound C Subunit of Reductive Dehalogenases: Topology Analysis and Reconstitution of the FMN-Binding Domain of PceC. Frontiers in microbiology, 9755. https://doi.org/10.3389/fmicb.2018.00755
Buttet, Géraldine F, et al. "The Membrane-Bound C Subunit of Reductive Dehalogenases: Topology Analysis and Reconstitution of the FMN-Binding Domain of PceC." Frontiers in microbiology vol. 9 (2018): 755. doi: https://doi.org/10.3389/fmicb.2018.00755
Buttet GF, Willemin MS, Hamelin R, Rupakula A, Maillard J. The Membrane-Bound C Subunit of Reductive Dehalogenases: Topology Analysis and Reconstitution of the FMN-Binding Domain of PceC. Front Microbiol. 2018 Apr 24;9:755. doi: 10.3389/fmicb.2018.00755. eCollection 2018. PMID: 29740408; PMCID: PMC5928378.
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A paired training curriculum and internal monitoring program for clinical research regulatory compliance in the emerging era of the single Institutional Review Board.

Journal of clinical and translational science

Jarrell TC, Hamblin F, Ford DE, Powell SR, Ellen JM, Goldenberg NA.
PMID: 31660212
J Clin Transl Sci. 2017 Oct 09;1(4):211-217. doi: 10.1017/cts.2017.12. eCollection 2017 Aug.

BACKGROUND: Academic health systems and their investigators are challenged to systematically assure clinical research regulatory compliance. This challenge is heightened in the emerging era of centralized single Institutional Review Boards for multicenter studies, which rely on monitoring programs at...

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Jarrell TC, Hamblin F, Ford DE, et al. A paired training curriculum and internal monitoring program for clinical research regulatory compliance in the emerging era of the single Institutional Review Board. J Clin Transl Sci. 2017;1(4):211-217doi: 10.1017/cts.2017.12.
Jarrell, T. C., Hamblin, F., Ford, D. E., Powell, S. R., Ellen, J. M., & Goldenberg, N. A. (2017). A paired training curriculum and internal monitoring program for clinical research regulatory compliance in the emerging era of the single Institutional Review Board. Journal of clinical and translational science, 1(4), 211-217. https://doi.org/10.1017/cts.2017.12
Jarrell, T Che, et al. "A paired training curriculum and internal monitoring program for clinical research regulatory compliance in the emerging era of the single Institutional Review Board." Journal of clinical and translational science vol. 1,4 (2017): 211-217. doi: https://doi.org/10.1017/cts.2017.12
Jarrell TC, Hamblin F, Ford DE, Powell SR, Ellen JM, Goldenberg NA. A paired training curriculum and internal monitoring program for clinical research regulatory compliance in the emerging era of the single Institutional Review Board. J Clin Transl Sci. 2017 Oct 09;1(4):211-217. doi: 10.1017/cts.2017.12. eCollection 2017 Aug. PMID: 31660212; PMCID: PMC6798223.
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Showing 1 to 12 of 151 entries