-
1
-
-
48349136889
-
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease
-
J.C. Barrett et al., Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease, Nat Genet 40 (2008), 955-962.
-
(2008)
Nat Genet
, vol.40
, pp. 955-962
-
-
Barrett, J.C.1
-
2
-
-
17944372335
-
CARD15 mutations in Blau syndrome
-
DOI 10.1038/ng720
-
C. Miceli-Richard, S. Lesage, M. Rybojad et al., CARD15 mutations in Blau syndrome, Nat Genet 29 (2001), 19-20. (Pubitemid 32801800)
-
(2001)
Nature Genetics
, vol.29
, Issue.1
, pp. 19-20
-
-
Miceli-Richard, C.1
Lesage, S.2
Rybojad, M.3
Prieur, A.-M.4
Manouvrier-Hanu, S.5
Hafner, R.6
Chamaillard, M.7
Zouali, H.8
Thomas, G.9
Hugot, J.-P.10
-
3
-
-
3242771408
-
Both donor and recipient NOD2/CARD15 mutations associate with transplant-related mortality and GvHD following allogeneic stem cell transplantation
-
DOI 10.1182/blood-2003-10-3543
-
E. Holler, G. Rogler, H. Herfarth et al., Both donor and recipient NOD2/CARD15 mutations associate with transplant-related mortality and Gv HD following allogeneic stem cell transplantation, Blood 104 (2004), 889-894. (Pubitemid 38970589)
-
(2004)
Blood
, vol.104
, Issue.3
, pp. 889-894
-
-
Holler, E.1
Rogler, G.2
Herfarth, H.3
Brenmoehl, J.4
Wild, P.J.5
Hahn, J.6
Eissner, G.7
Scholmerich, J.8
Andreesen, R.9
-
4
-
-
34249877249
-
Simultaneous mutation scanning and genotyping by high-resolution DNA melting analysis
-
DOI 10.1038/nprot.2007.10, PII NPROT.2007.10
-
J. Montgomery, C.T. Wittwer, R. Palais and L. Zhou, Simultaneous mutation scanning and genotyping by high-resolution DNA melting analysis, Nat Protocols 2 (2007), 59-66. (Pubitemid 47040069)
-
(2007)
Nature Protocols
, vol.2
, Issue.1
, pp. 59-66
-
-
Montgomery, J.1
Wittwer, C.T.2
Palais, R.3
Zhou, L.4
-
5
-
-
0035283211
-
Fluorescein-labeled oligonucleotides for real-time PCR: Using the inherent quenching of deoxyguanosine nucleotides
-
DOI 10.1006/abio.2000.4957
-
A.O. Crockett and C.T. Wittwer, Fluorescein-labeled oligonucleotides for real-time PCR: Using the inherent quenching of deoxyguanosine nucleotides, Anal Biochem 290 (2001), 89-97. (Pubitemid 32182273)
-
(2001)
Analytical Biochemistry
, vol.290
, Issue.1
, pp. 89-97
-
-
Crockett, A.O.1
Wittwer, C.T.2
-
6
-
-
0037371570
-
Amplicon melting analysis with labeled primers: A closed-tube method for differentiating homozygotes and heterozygotes
-
DOI 10.1373/49.3.396
-
C.N. Gundry, J.G. Vandersteen, G.H. Reed, R.J. Pryor, J. Chen and C.T. Wittwer, Amplicon melting analysis with labeled primers: A closed-tube method for differentiating homozy-gotes and heterozygotes, Clin Chem 49 (2003), 396-406. (Pubitemid 36250200)
-
(2003)
Clinical Chemistry
, vol.49
, Issue.3
, pp. 396-406
-
-
Gundry, C.N.1
Vandersteen, J.G.2
Reed, G.H.3
Pryor, R.J.4
Chen, J.5
Wittwer, C.T.6
-
7
-
-
66349090454
-
High-resolution melting analysis (HRMA) - More than just sequence variant screening
-
R.H.A.M. Vossen, E. Aten, A. Roos and J.T. den Dunnen, High-resolution melting analysis (HRMA) - More than just sequence variant screening, Hum Mut 30 (2009), 860-866.
-
(2009)
Hum Mut
, vol.30
, pp. 860-866
-
-
Vossen, R.H.A.M.1
Aten, E.2
Roos, A.3
Den Dunnen, J.T.4
-
8
-
-
65549160923
-
Mutation scanning using high-resolution melting
-
C.F. Taylor, Mutation scanning using high-resolution melting, Biochem Soc Trans 37 (2009), 433-437.
-
(2009)
Biochem Soc Trans
, vol.37
, pp. 433-437
-
-
Taylor, C.F.1
-
9
-
-
66349095408
-
High-resolution DNA melting analysis: Advancements and limitations
-
C.T. Wittwer, High-resolution DNA melting analysis: advancements and limitations, Hum Mut 30 (2009), 857-859.
-
(2009)
Hum Mut
, vol.30
, pp. 857-859
-
-
Wittwer, C.T.1
-
10
-
-
73349109122
-
High-resolution melting analysis (HRMA): A highly sensitive inexpensive genotyping alternative for population studies
-
B.L. Smith, C.P Lu and J.R. Alvarado Bremer, High-resolution melting analysis (HRMA): a highly sensitive inexpensive genotyping alternative for population studies, Mol Ecol Res 10 (2010), 193-196.
-
(2010)
Mol Ecol Res
, vol.10
, pp. 193-196
-
-
Smith, B.L.1
Lu, C.P.2
Alvarado Bremer, J.R.3
-
11
-
-
34247872951
-
Closed-tube SNP genotyping without labeled probes: A comparison between unlabeled probe and amplicon melting
-
DOI 10.1309/N7RARXH3623AVKDV
-
M. Liew, M. Seipp, J. Durtschi, R.L. Margraf, S. Dames, M. Erali, K. Voelkerding and C.T. Wittwer, Closed-tube genotyping without labeled probes: A comparison between unlabeled probe and amplicon melting, Am J Clin Pathol 127 (2007), 341-348. (Pubitemid 46806326)
-
(2007)
American Journal of Clinical Pathology
, vol.127
, Issue.3
, pp. 341-348
-
-
Liew, M.1
Seipp, M.2
Durtschi, J.3
Margraf, R.L.4
Darmes, S.5
Erali, M.6
Voelkerding, K.7
Wittwer, C.8
-
12
-
-
67650744534
-
Diagnostic method validation: High resolution melting (HRM) of small amplicons genotyping for most common variants in the MTHFR gene
-
PA. Norambuena, J.A. Copeland, P. Krenkova, A. Štambergova and M. Macek, Jr., Diagnostic method validation: High resolution melting (HRM) of small amplicons genotyping for most common variants in the MTHFR gene, Clin Biochem 42 (2009), 1308-1316.
-
(2009)
Clin Biochem
, vol.42
, pp. 1308-1316
-
-
Norambuena, P.A.1
Copeland, J.A.2
Krenkova, P.3
Štambergova, A.4
MacEk, M.5
-
13
-
-
40749117206
-
Rapid detection of carriers with BRCA1 and BRCA2 mutations using high resolution melting analysis
-
E. Takano, G. Mitchell, S. Fox and A. Dobrovic, Rapid detection of carriers with BRCA1 and BRCA2 mutations using high resolution melting analysis, BMC Cancer 8 (2008), 59.
-
(2008)
BMC Cancer
, vol.8
, pp. 59
-
-
Takano, E.1
Mitchell, G.2
Fox, S.3
Dobrovic, A.4
-
14
-
-
66849099848
-
Rapid diagnosis of spinal muscular atrophy using high-resolution melting analysis
-
W.J. Chen, W.J. Dong, X.Z. Lin, M.T. Lin, S.X. Murong, Z.Y. Wu and N. Wang, Rapid diagnosis of spinal muscular atrophy using high-resolution melting analysis, BMC Medical Genetics 10 (2009), 45-48.
-
(2009)
BMC Medical Genetics
, vol.10
, pp. 45-48
-
-
Chen, W.J.1
Dong, W.J.2
Lin, X.Z.3
Lin, M.T.4
Murong, S.X.5
Wu, Z.Y.6
Wang, N.7
-
15
-
-
8844229534
-
Polymorphisms in multidrug resistance 1 (MDR1) gene are associated with refractory Crohn disease and ulcerative colitis
-
DOI 10.1038/sj.gene.6364123
-
U. Potocnik, I. Ferkolj, D. Glavac and M. Dean, Polymorphisms in multidrug resistance 1 (MDR1) gene are associated with refractory Crohn disease and ulcerative colitis, Genes Immun 5 (2004), 530-539. (Pubitemid 39529969)
-
(2004)
Genes and Immunity
, vol.5
, Issue.7
, pp. 530-539
-
-
Potocnik, U.1
Ferkolj, I.2
Glavac, D.3
Dean, M.4
-
16
-
-
84965308844
-
Human experimentation: Code of ethics of W.M.A
-
Human Experimentation: Code of Ethics of W.M.A, Br Med J 2 (1964), 177.
-
(1964)
Br Med J
, vol.2
, pp. 177
-
-
-
17
-
-
0033990048
-
Primer3 on the WWW for general users and for biologist programmers
-
S. Krawetz and S. Misener, eds, Humana Press, Totowa
-
S. Rozen and H.J. Skaletsky, Primer3 on the WWW for general users and for biologist programmers, in: Bioinformatics Methods and Protocols: Methods in Molecular Biology, S. Krawetz and S. Misener, eds, Humana Press, Totowa, 2000, pp. 365-386.
-
(2000)
Bioinformatics Methods and Protocols: Methods in Molecular Biology
, pp. 365-386
-
-
Rozen, S.1
Skaletsky, H.J.2
-
18
-
-
0033596964
-
Nearest-neighbor thermodynamics and NMR of DNA sequences with internal A·A, C·C, G·G, and T·T mismatches
-
N. Peyret, P.A. Seneviratne, H.T. Allawi and J. Santa Lucia, Nearest-Neighbor Thermodynamics and NMR of DNA Sequences with Internal A·A, C·C, G·G, and T·T Mismatches, Biochem 38 (1999), 3468-3477.
-
(1999)
Biochem
, vol.38
, pp. 3468-3477
-
-
Peyret, N.1
Seneviratne, P.A.2
Allawi, H.T.3
Santa Lucia, J.4
-
19
-
-
62149125915
-
Rapid, sensitive and inexpensive detection of SCN5a genetic variations by high resolution melting analysis
-
G. Millat, V. Chanavat, C. Rodriguez-Lafrasse and R. Rous-son, Rapid, sensitive and inexpensive detection of SCN5a genetic variations by high resolution melting analysis, Clin Biochem 42 (2009), 491-499.
-
(2009)
Clin Biochem
, vol.42
, pp. 491-499
-
-
Millat, G.1
Chanavat, V.2
Rodriguez-Lafrasse, C.3
Rous-Son, R.4
-
20
-
-
74049151955
-
Rapid detection of SMARCB1 sequence variation using high resolution melting
-
V. Dagar, C.W. Chow, D.M. Ashley and E.M. Algar, Rapid detection of SMARCB1 sequence variation using high resolution melting, BMC Cancer 9 (2009), 437-461.
-
(2009)
BMC Cancer
, vol.9
, pp. 437-461
-
-
Dagar, V.1
Chow, C.W.2
Ashley, D.M.3
Algar, E.M.4
-
21
-
-
64249120879
-
High-resolution melting analysis for JAK2 exon 14 and exon 12 mutations
-
I. Rapado, S. Grande, E. Albizua, R. Ayala, J.A. Hernandez, M. Gallardo, F. Gilsanz and J. Martinez-Lopez, High-resolution melting analysis for JAK2 exon 14 and exon 12 mutations, J Mol Diag 11 (2009), 155-161.
-
(2009)
J Mol Diag
, vol.11
, pp. 155-161
-
-
Rapado, I.1
Grande, S.2
Albizua, E.3
Ayala, R.4
Hernandez, J.A.5
Gallardo, M.6
Gilsanz, F.7
Martinez-Lopez, J.8
-
22
-
-
77749245998
-
Interlaboratory development and validation of a HRM method applied to the detection of JAK2 exon 12 mutations in polycythemia vera patients
-
V. Ugo, S. Tondeur, M.L. Menot et al., Interlaboratory development and validation of a HRM method applied to the detection of JAK2 exon 12 mutations in polycythemia vera patients, Plos 5 (2010), 8893-8901.
-
(2010)
Plos
, vol.5
, pp. 8893-8901
-
-
Ugo, V.1
Tondeur, S.2
Menot, M.L.3
-
23
-
-
3242742969
-
Closed-tube genotyping with unlabeled oligonucleotide probes and a saturating DNA dye
-
DOI 10.1373/clinchem.2004.034322
-
L. Zhou, A.N. Myers, J.G. Vandersteen, L. Wang and C.T. Wit-twer, Closed-tube genotyping with unlabeled oligonucleotide probes and a saturating DNA dye, Clin Chem 50 (2004), 1328-1335. (Pubitemid 38970639)
-
(2004)
Clinical Chemistry
, vol.50
, Issue.8
, pp. 1328-1335
-
-
Zhou, L.1
Myers, A.N.2
Vandersteen, J.G.3
Wang, L.4
Wittwer, C.T.5
-
24
-
-
61849100599
-
Determining the effectivness of high resolution melting analysis for SNP genotyping and mutation scanning at the TP53 locus
-
S. Garritano, F. Gemignani, S.V. Tavtigian et al., Determining the effectivness of high resolution melting analysis for SNP genotyping and mutation scanning at the TP53 locus, BMC Genetics 10 (2009), 5-36.
-
(2009)
BMC Genetics
, vol.10
, pp. 5-36
-
-
Garritano, S.1
Gemignani, F.2
Tavtigian, S.V.3
-
25
-
-
1442276973
-
Transmission of CARD15 (NOD2) Variants Within Families of Patients with Inflammatory Bowel Disease
-
DOI 10.1111/j.1572-0241.2004.04040.x
-
N. Esters, M. Pierik, K. van Steen, S. Vermeire et al., Transmission of CARD15 (NOD2) variants within families of patients with inflammatory bowel disease, Am J Gastroenterol 99 (2004), 299-305. (Pubitemid 38279873)
-
(2004)
American Journal of Gastroenterology
, vol.99
, Issue.2
, pp. 299-305
-
-
Esters, N.1
Pierik, M.2
Van Steen, K.3
Vermeire, S.4
Claessens, G.5
Joossens, S.6
Vlietinck, R.7
Rutgeerts, P.8
-
26
-
-
33745843677
-
NOD2/CARD15 mutations in Croatian patients with Crohn's disease: Prevalence and genotype-phenotype relationship
-
DOI 10.1097/00042737-200608000-00016, PII 0004273720060800000016
-
S. Cukovic-Cavka, S. Vermeire, I. Hrstic et al., NOD2/ CARD15 mutations in Croatian patients with Crohn's disease: prevalence and genotype-phenotype relationship, Eur J Gas-troenterol Hepatol 18 (2006), 895-899. (Pubitemid 44034805)
-
(2006)
European Journal of Gastroenterology and Hepatology
, vol.18
, Issue.8
, pp. 895-899
-
-
Cukovic-Cavka, S.1
Vermeire, S.2
Hrstic, I.3
Claessens, G.4
Kolacek, S.5
Jakic-Razumovic, J.6
Krznaric, Z.7
Grubelic, K.8
Radic, D.9
Misak, Z.10
Jadresin, O.11
Rutgeerts, P.12
Vucelic, B.13
-
27
-
-
48449098636
-
Frequency of representative single nucleotide polymorphisms associated with inflammatory bowel disease in the Czech Republic and Slovak Republic
-
J. Hosek, L. Bartosová, P. Gregor et al., Frequency of representative single nucleotide polymorphisms associated with inflammatory bowel disease in the Czech Republic and Slovak Republic, Folia Biol 54 (2008), 88-96.
-
(2008)
Folia Biol
, vol.54
, pp. 88-96
-
-
Hosek, J.1
Bartosová, L.2
Gregor, P.3
-
28
-
-
27144489085
-
NOD2/CARD15 gene polymorphisms in Crohn's disease: A genotype-phenotype analysis in Danish and Portuguese patients and controls
-
DOI 10.1159/000088371
-
I. Vind, A. Vieira, L. Hougs et al., NOD 2/CARD15 gene polymorphisms in Crohn's disease: a genotype-phenotype analysis in Danish and Portugese patients and controls, Digestion 72 (2005), 156-163. (Pubitemid 41507276)
-
(2005)
Digestion
, vol.72
, Issue.2-3
, pp. 156-163
-
-
Vind, I.1
Vieira, A.2
Hougs, L.3
Tavares, L.4
Riis, L.5
Andersen, P.S.6
Locht, H.7
Freitas, J.8
Monteiro, E.9
Christensen, I.J.10
Munkholm, P.11
-
29
-
-
0036202336
-
The molecular classification of the clinical manifestations of Crohn's disease
-
T. Ahmad, A. Armuzzi, M. Bunce et al., The molecular classification of the clinical manifestations of Crohn's disease, Gastroenterology 122 (2002), 854-866. (Pubitemid 34267267)
-
(2002)
Gastroenterology
, vol.122
, Issue.4
, pp. 854-866
-
-
Ahmad, T.1
Armuzzi, A.2
Bunce, M.3
MulcahyHawes, K.4
Marshall, S.E.5
Orchard, T.R.6
Crawshaw, J.7
Large, O.8
De Silva, A.9
Cook, J.T.10
Barnardo, M.11
Cullen, S.12
Welsh, K.I.13
Jewell, D.P.14
-
30
-
-
0037379286
-
CARD15/NOD2 gene variants are associated with familially occurring and complicated forms of Crohn's disease
-
DOI 10.1136/gut.52.4.558
-
T. Helio, L. Halme, M. Lappalainen et al., CARD15/NOD2 gene variants are associated with familialy occuring and complicated forms of Crohn's disease, Gut 52 (2003), 558-562. (Pubitemid 36363411)
-
(2003)
Gut
, vol.52
, Issue.4
, pp. 558-562
-
-
Helio, T.1
Halme, L.2
Lappalainen, M.3
Fodstad, H.4
Paavola-Sakki, P.5
Turunen, U.6
Farkkila, M.7
Krusius, T.8
Kontula, K.9
-
31
-
-
3042702408
-
NOD2/CARD15 gene polymorphisms in Crohn's disease: A genotype-phenotype analysis
-
DOI 10.1097/00042737-200401000-00009
-
D. Heresbach, V. Gicquel-Douabin, B. Birebent et al., NOD2 /CARD15 gene polymorphisms in Crohn's disease: a geno-type-phenotype analysis, Eur J Gastroenterol Hepatol 16 (2004), 55-62. (Pubitemid 39043703)
-
(2004)
European Journal of Gastroenterology and Hepatology
, vol.16
, Issue.1
, pp. 55-62
-
-
Heresbach, D.1
Gicquel-Douabin, V.2
Birebent, B.3
D'Halluin, P.-N.4
Berre, N.H.-L.5
Dreano, S.6
Siproudhis, L.7
Dabadie, A.8
Gosselin, M.9
Mosser, J.10
Semana, G.11
Bretagne, J.-F.12
Yaouanq, J.13
-
32
-
-
0037062228
-
Association of NOD2 (CARD 15) genotype with clinical course of Crohn's disease: A cohort study
-
DOI 10.1016/S0140-6736(02)08590-2
-
J. Hampe, J. Grebe, S. Nikolaus, C. Solberg et al., Association of NOD(CARD15) genotype with clinical course of Crohn's disease: a cohort study, Lancet 359 (2002), 1661-1665. (Pubitemid 34518526)
-
(2002)
Lancet
, vol.359
, Issue.9318
, pp. 1661-1665
-
-
Hampe, J.1
Grebe, J.2
Nikolaus, S.3
Solberg, C.4
Croucher, P.J.P.5
Mascheretti, S.6
Jahnsen, J.7
Moum, B.8
Klump, B.9
Krawczak, M.10
Mirza, M.M.11
Foelsch, U.R.12
Vatn, M.13
Schreiber, S.14
-
33
-
-
2542574746
-
Mutations in the NOD2/CARD15 gene in Crohn's disease are associated with ileocecal resection and are a risk factor for reoperation
-
DOI 10.1111/j.1365-2036.2004.01967.x
-
C. Buning, J. Genschel, S. Buhner et al., Mutations in the NOD2/CARD15 gene in Crohn's disease are associated with ileocecal resection and are risk factor for reoperation, Aliment Pharmacol Ther 19 (2004), 1073-1078. (Pubitemid 38703519)
-
(2004)
Alimentary Pharmacology and Therapeutics
, vol.19
, Issue.10
, pp. 1073-1078
-
-
Buning, C.1
Genschel, J.2
Buhner, S.3
Kruger, S.4
Kling, K.5
Dignass, A.6
Baier, P.7
Bochow, B.8
Ockenga, J.9
Schmidt, H.H.-J.10
Lochs, H.11
-
34
-
-
13544276471
-
Association between polymorphisms in the Toll-like receptor 4, CD14, and CARD15/NOD2 and inflammatory bowel disease in the Greek population
-
M. Gazouli, G. Mantzaris, A. Kotsinas et al., Association between polymorphisms in the toll-like receptor 4, CD14, and CARD15/NOD2 and inflammatory bowel disease in the Greek population, World J Gastroenterol 11 (2005), 681-685. (Pubitemid 40220757)
-
(2005)
World Journal of Gastroenterology
, vol.11
, Issue.5
, pp. 681-685
-
-
Gazouli, M.1
Mantzaris, G.2
Kotsinas, A.3
Zacharatos, P.4
Papalambros, E.5
Archimandritis, A.6
Ikonomopoulos, J.7
Gorgoulis, V.G.8
-
35
-
-
12344300288
-
NOD2/CARD15 gene polymorphism in patients with inflammatory bowel disease: Is Hungary different?
-
C. Buning, T. Molnar, F. Nagy, J. Lonovics et al., NOD2 /CARD15 gene polymorphism in patients with inflammatory bowel disease: is Hungary different?, World J Gastroenterol 11 (2005), 407-411. (Pubitemid 40125251)
-
(2005)
World Journal of Gastroenterology
, vol.11
, Issue.3
, pp. 407-411
-
-
Buning, C.1
Molnar, T.2
Nagy, F.3
Lonovics, J.4
Weltrich, R.5
Bochow, B.6
Genschel, J.7
Schmidt, H.8
Lochs, H.9
-
36
-
-
25444505341
-
Crohn's disease is associated with polymorphism of CARD15/NOD2 gene in a Hungarian population
-
DOI 10.1196/annals.1361.045
-
Z. Nagy, O. Karadi, G. Rumi et al., Crohn's disease is associated with polymorphism of Card 15/ NOD2 gene in a Hungarian population, Ann N Y Acad Sci 1051 (2005), 45-51. (Pubitemid 41362731)
-
(2005)
Annals of the New York Academy of Sciences
, vol.1051
, pp. 45-51
-
-
Nagy, Z.1
Karadi, O.2
Rumi, G.3
Rumi Jr., G.4
Par, A.5
Mozsik, G.6
Czirjak, L.7
Suto, G.8
-
37
-
-
0038724272
-
Subclinical intestinal inflammation: An inherited abnormality in Crohn's disease relatives?
-
DOI 10.1016/S0016-5085(03)00383-4
-
B. Thjodleifsson, G. Sigthorsson, N. Cariglia et al., Subclinical intestinal inflammation: an inherited abnormality in Crohn's disease relatives?, Gastroenterology 124 (2003), 1728-1737. (Pubitemid 36666769)
-
(2003)
Gastroenterology
, vol.124
, Issue.7
, pp. 1728-1737
-
-
Thjodleifsson, B.1
Sigthorsson, G.2
Cariglia, N.3
Reynisdottir, I.4
Gudbjartsson, D.F.5
Kristjansson, K.6
Meddings, J.B.7
Gudnason, V.8
Wandall, J.H.9
Andersen, L.P.10
Sherwood, R.11
Kjeld, M.12
Oddsson, E.13
Gudjonsson, H.14
Bjarnason, I.15
-
38
-
-
0242500981
-
Association of NOD2 with Crohn's disease in a hemogenous Irish population
-
DOI 10.1038/sj.ejhg.5200954
-
E. Bairead, D.L. Harmon, A.M. Curtis et al., Association of NOD2 with Crohn's disease in homogenous Irish population, Eur J Hum Genet 11 (2003), 237-244. (Pubitemid 36511862)
-
(2003)
European Journal of Human Genetics
, vol.11
, Issue.3
, pp. 237-244
-
-
Bairead, E.1
Harmon, D.L.2
Curtis, A.M.3
Kelly, Y.4
O'Leary, C.5
Gardner, M.6
Leahy, D.T.7
Vaughan, P.8
Keegan, D.9
O'Morain, C.10
O'Donoghue, D.11
Shanahan, F.12
Parfrey, N.A.13
Quane, K.A.14
-
39
-
-
10844264782
-
Analysis of the CARD15 variants R702W, G908R and L1007fs in Italian IBD patients
-
DOI 10.1038/sj.ejhg.5201130
-
D. Giachino, M.M. Van Duist, S. Regazzo et al., Analysis of the CARD15 variants R702W, G908R and L1007fs in Italian IBD patients, Eur J Hum Genet 12 (2004), 206-212. (Pubitemid 38499979)
-
(2004)
European Journal of Human Genetics
, vol.12
, Issue.3
, pp. 206-212
-
-
Giachino, D.1
Van Duist, M.M.2
Regazzoni, S.3
Gregori, D.4
Bardessono, M.5
Salacone, P.6
Scaglione, N.7
Sostegni, R.8
Sapone, N.9
Bresso, F.10
Sambataro, A.11
Gaia, E.12
Pera, A.13
Astegiano, M.14
De Marchi, M.15
-
40
-
-
12144289474
-
CARD15 mutation analysis in an Italian population: Leu1007fsinsC but neither Arg702Trp nor Gly908Arg mutations are associated with Crohn's disease
-
DOI 10.1097/00054725-200403000-00009
-
P. Vavassori, P. Borgiani, L. Biancone et al., CARD15 mutation analysis in an Italian population: Leu1007fsins C but neither Arg702Trp nor Gly908Arg mutations are associated with Crohn's disease, Inflamm Bowel Dis 10 (2004), 116-121. (Pubitemid 38332171)
-
(2004)
Inflammatory Bowel Diseases
, vol.10
, Issue.2
, pp. 116-121
-
-
Vavassori, P.1
Borgiani, P.2
Biancone, L.3
D'Apice, M.R.4
Del Vecchio Blanco, G.5
Vallo, L.6
De Nigris, F.7
Monteleone, I.8
Monteleone, G.9
Pallone, F.10
Novelli, G.11
-
41
-
-
13744264167
-
Variants of CARD15 are associated with an aggressive clinical course of Crohn's disease - An IG-IBD study
-
DOI 10.1111/j.1572-0241.2005.40705.x
-
V. Annese, G. Lombardi, F. Perri et al., Variants of CARD15 are associated with an aggressive clinical course of Crohn's disease: an IG-IBD study, Am J Gastroenterol 100 (2005), 84-92. (Pubitemid 41623274)
-
(2005)
American Journal of Gastroenterology
, vol.100
, Issue.1
, pp. 84-92
-
-
Annese, V.1
Lombardi, G.2
Perri, F.3
D'Inca, R.4
Ardizzone, S.5
Riegler, G.6
Giaccari, S.7
Vecchi, M.8
Castiglione, F.9
Gionchetti, P.10
Cocchiara, E.11
Vigneri, S.12
Latiano, A.13
Palmieri, O.14
Andriulli, A.15
-
42
-
-
34248203140
-
CARD15 mutations in Dutch familial and sporadic inflammatory bowel disease and an overview of European studies
-
DOI 10.1097/01.meg.0000236887.44214.6a, PII 0004273720070600000003
-
K. van der Linde, P.P.C. Boor, J.J. Houwing-Duistermaat et al., CARD15 mutations in Dutch familial and sporadic inflammatory bowel disease and an overview of European studies, Eur J Gastroenterol Hepatol 19 (2007), 449-459. (Pubitemid 46725750)
-
(2007)
European Journal of Gastroenterology and Hepatology
, vol.19
, Issue.6
, pp. 449-459
-
-
Van Der Linde, K.1
Boor, P.P.C.2
Houwing-Duistermaat, J.J.3
Crusius, B.J.A.4
Wilson, P.J.H.5
Kuipers, E.J.6
De Rooij, F.W.M.7
-
43
-
-
20244373335
-
NOD2/CARD15 and TNFA, but not IL1B and IL1RN, are associated with Crohn's disease
-
DOI 10.1097/01.MIB.0000158153.71579.b4
-
A.C. Ferreira, S. Almeida, M. Tavares et al., NOD2/CARD15 and TNFA, but not IL1B and IL1RN, are associated with Crohn's disease, Inflamm Bowel Dis 11 (2005), 331-339. (Pubitemid 40542264)
-
(2005)
Inflammatory Bowel Diseases
, vol.11
, Issue.4
, pp. 331-339
-
-
Ferreira, A.C.1
Almeida, S.2
Tavares, M.3
Canedo, P.4
Pereira, F.5
Regalo, G.6
Figueiredo, C.7
Trindade, E.8
Seruca, R.9
Carneiro, F.10
Amil, J.11
Machado, J.C.12
Tavarela-Veloso, F.13
-
44
-
-
4344671141
-
NOD2/CARD15, TLR4 and CD14 mutations in Scottish and Irish Crohn's disease patients: Evidence for genetic heterogeneity within Europe?
-
DOI 10.1038/sj.gene.6364111
-
I.D. Arnott, E.R. Nimo, H.E. Drummond et al., NOD2/ CARD15, TLR4 and CD14 mutations in Scottish and Irish Crohn's disease patients: evidence for genetic heterogeneity within Europe? Gennes Immun 5 (2004), 417-425. (Pubitemid 39139770)
-
(2004)
Genes and Immunity
, vol.5
, Issue.5
, pp. 417-425
-
-
Arnott, I.D.R.1
Nimmo, E.R.2
Drummond, H.E.3
Fennell, J.4
Smith, B.R.K.5
MacKinlay, E.6
Morecroft, J.7
Anderson, N.8
Kelleher, D.9
O'Sullivan, M.10
McManus, R.11
Satsangi, J.12
-
45
-
-
75149122830
-
Genove polymorfismy jako predispozicni factor IBD - Jejich vztah ke klinicke man-ifestaci a farmakoterapii onemocneni
-
L. Bartosova, M. Kolorz, J. Hosek, D. Dvorackova, P. Loucka, V. Zboril, M. Batovsky and M. Bartos, Genove polymorfismy jako predispozicni factor IBD - jejich vztah ke klinicke man-ifestaci a farmakoterapii onemocneni, Ces a Slov Gastroent a Hepatol 63 (2009), 265-274.
-
(2009)
Ces A Slov Gastroent A Hepatol
, vol.63
, pp. 265-274
-
-
Bartosova, L.1
Kolorz, M.2
Hosek, J.3
Dvorackova, D.4
Loucka, P.5
Zboril, V.6
Batovsky, M.7
Bartos, M.8
-
46
-
-
1942440375
-
CARD15 Mutations in Patients with Crohn's Disease in a Homogeneous Spanish Population
-
DOI 10.1111/j.1572-0241.2004.04066.x
-
C. Nunez, M. Barreiro, J.E. Dominguez-Munoz et al., CARD15 mutations in patients with Crohn's disease in a homogenous Spanish population, Am J Gastroenterol 99 (2004), 450-456. (Pubitemid 38524122)
-
(2004)
American Journal of Gastroenterology
, vol.99
, Issue.3
, pp. 450-456
-
-
Nunez, C.1
Barreiro, M.2
Dominguez-Munoz, J.E.3
Lorenzo, A.4
Zapata, C.5
Pena, A.S.6
-
47
-
-
53549127562
-
CARD15 genepolymorphisms in Serbian patients with Crohn's disease: Genotype-phenotype analysis
-
M.B. Protic, S.T. Pavlovic, D.Z. Bojic et al., CARD15 genepolymorphisms in Serbian patients with Crohn's disease: genotype-phenotype analysis, Eur J Gastroenterol Hepatol 20 (2008), 978-984.
-
(2008)
Eur J Gastroenterol Hepatol
, vol.20
, pp. 978-984
-
-
Protic, M.B.1
Pavlovic, S.T.2
Bojic, D.Z.3
-
48
-
-
2942661490
-
Detection of the Arg702Trp, Gly908Arg and Leu 1007fsinsC polymorphisms of the NOD2/CARD15 gene by real-time PCR with melting curve analysis
-
DOI 10.1515/CCLM.2004.084
-
C. Ruegg, M. Hersberger, B. Wusk et al., Detection of the Arg702Trp, Gly908Arg, and Leu1007fsins C polymorphisms of the NOD2/CARD15 gene by real-time PCR melting curve analysis, Clin Chem Lab Med 42 (2004), 494-498. (Pubitemid 38779749)
-
(2004)
Clinical Chemistry and Laboratory Medicine
, vol.42
, Issue.5
, pp. 494-498
-
-
Ruegg, C.1
Hersberger, M.2
Wusk, B.3
Rentsch, K.4
Kullak-Ublick, G.A.5
Von Eckardstein, A.6
Maly, F.E.7
-
49
-
-
3843078844
-
15 variants in both sporadic and familial cases of Crohn's disease across Italy. An Italian Group for Inflammatory Bowel Disease study
-
DOI 10.1016/j.dld.2003.10.010
-
V. Annese, O. Palmieri, A. Latiano, S. Ardizzone, F. Cas-tiglione, M. Cottone et al., Frequency of NOD2/CARD15 variants in both sporadic and familial cases of Crohn's disease across Italy. An Italian group for inflammatory bowel disease study, Dig Liver Dis 36 (2004), 121-124. (Pubitemid 41115505)
-
(2004)
Digestive and Liver Disease
, vol.36
, Issue.2
, pp. 121-124
-
-
Annese, V.1
Palmieri, O.2
Latiano, A.3
Ardizzone, S.4
Castiglione, F.5
Cottone, M.6
D'Inca, R.7
Gionchetti, P.8
Papi, C.9
Riegler, G.10
Vecchi, M.11
Andriulli, A.12
-
50
-
-
2142663021
-
Genetic and serological markers to identify phenotypic subgroups in a Dutch Crohn's disease population
-
DOI 10.1016/j.dld.2003.10.001, PII S1590865803006005
-
R.K. Linskens, R.C. Mallant-Hent, L.S. Murillo, B.M. von Blomberg, B.Z. Alizade and A.S. Pena, Genetic and sero-logical markers to identify phenotypic subgroups in a Dutch Crohn's disease population, Dig Liver Dis 36 (2004), 29-34. (Pubitemid 41122222)
-
(2004)
Digestive and Liver Disease
, vol.36
, Issue.1
, pp. 29-34
-
-
Linskens, R.K.1
Mallant-Hent, R.C.2
Murillo, L.S.3
Von Blomberg, B.M.E.4
Alizadeh, B.Z.5
Pena, A.S.6
-
51
-
-
0842321801
-
The frame-shift mutation of the NOD2/CARD15 gene is significantly increased in ulcerative colitis: An IG-IBD study
-
DOI 10.1053/j.gastro.2003.12.027
-
A. Andruilli, V. Annese, A. Latiano, O. Palmieri, P. Forti- na, S. Ardizzone et al., The frame-shift mutation of the NOD2/CARD15 gene is significantly increased in ulcerative colitis: an IG-IBD study, Gastroenterol 126 (2004), 625-627. (Pubitemid 38182322)
-
(2004)
Gastroenterology
, vol.126
, Issue.2
, pp. 625-627
-
-
Andruilli, A.1
Annese, V.2
Latiano, A.3
Palmieri, O.4
Fortina, P.5
Ardizzone, S.6
Cottone, M.7
D'Inca, R.8
Riegler, G.9
-
52
-
-
0036202885
-
The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease
-
A.P. Cuthbert, S.A. Fisher, M.M. Mirza, K. King, J. Hampe, P.J. Croucher et al., The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease, Gastroenterol 122 (2002), 867-874. (Pubitemid 34267268)
-
(2002)
Gastroenterology
, vol.122
, Issue.4
, pp. 867-874
-
-
Cuthbert, A.P.1
Fisher, S.A.2
Mirza, M.M.3
King, K.4
Hampe, J.5
Croucher, P.J.P.6
Mascheretti, S.7
Sanderson, J.8
Forbes, A.9
Mansfield, J.10
Schreiber, S.11
Lewis, C.M.12
Mathew, C.G.13
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