-
1
-
-
33646029727
-
Patent ductus arteriosus: Pathophysiology and management
-
Hermes-DeSantis ER, Clyman RI. Patent ductus arteriosus: pathophysiology and management. J Perinatol. 2006;26(suppl 1):S14-S18
-
(2006)
J Perinatol
, vol.26
, Issue.SUPPL. 1
-
-
Hermes-DeSantis, E.R.1
Clyman, R.I.2
-
2
-
-
33745101632
-
Mechanisms regulating the ductus arteriosus
-
DOI 10.1159/000092870
-
Clyman RI. Mechanisms regulating the ductus arteriosus. Biol Neonate. 2006;89(4):330-335 (Pubitemid 43886949)
-
(2006)
Biology of the Neonate
, vol.89
, Issue.4
, pp. 330-335
-
-
Clyman, R.I.1
-
3
-
-
38048999476
-
Impact of patent ductus arteriosus and subsequent therapy with indomethacin on cerebral oxygenation in preterm infants
-
Lemmers PM, Toet MC, van Bel F. Impact of patent ductus arteriosus and subsequent therapy with indomethacin on cerebral oxygenation in preterm infants. Pediatrics. 2008;121(1):142-147
-
(2008)
Pediatrics
, vol.121
, Issue.1
, pp. 142-147
-
-
Lemmers, P.M.1
Toet, M.C.2
Van Bel, F.3
-
4
-
-
0028901765
-
The Vermont-Oxford Neonatal Network: Integrating research and clinical practice to improve the quality of medical care
-
Horbar JD. The Vermont-Oxford Neonatal Network: integrating research and clinical practice to improve the quality of medical care. Semin Perinatol. 1995;19(2):124-131
-
(1995)
Semin Perinatol
, vol.19
, Issue.2
, pp. 124-131
-
-
Horbar, J.D.1
-
5
-
-
0033564061
-
Char syndrome, an inherited disorder with patent ductus arteriosus, maps to chromosome 6p12-p21
-
Satoda M, Pierpont ME, Diaz GA, Bornemeier RA, Gelb BD. Char syndrome, an inherited disorder with patent ductus arteriosus, maps to chromosome 6p12-p21. Circulation. 1999;99(23):3036-3042 (Pubitemid 29270434)
-
(1999)
Circulation
, vol.99
, Issue.23
, pp. 3036-3042
-
-
Satoda, M.1
Pierpont, M.E.M.2
Diaz, G.A.3
Bornemeier, R.A.4
Gelb, B.D.5
-
6
-
-
0037069385
-
Finding genetic contributions to sporadic disease: A recessive locus at 12q24 commonly contributes to patent ductus arteriosus
-
DOI 10.1073/pnas.192582999
-
Mani A, Meraji SM, Houshyar R, et al. Finding genetic contributions to sporadic disease: a recessive locus at 12q24 commonly contributes to patent ductus arteriosus. Proc Natl Acad Sci U S A. 2002;99(23):15054-15059 (Pubitemid 35334608)
-
(2002)
Proceedings of the National Academy of Sciences of the United States of America
, vol.99
, Issue.23
, pp. 15054-15059
-
-
Mani, A.1
Meraji, S.-M.2
Houshyar, R.3
Radhakrishnan, J.4
Mani, A.5
Ahangar, M.6
Rezaie, T.M.7
Taghavinejad, M.-A.8
Broumand, B.9
Zhao, H.10
Nelson-Williams, C.11
Lifton, R.P.12
-
7
-
-
20044365972
-
Syndromic patent ductus arteriosus: Evidence for haploinsufficient TFAP2B mutations and identification of a linked sleep disorder
-
DOI 10.1073/pnas.0409852102
-
Mani A, Radhakrishnan J, Farhi A, et al. Syndromic patent ductus arteriosus: evidence for haploinsufficient TFAP2B mutations and identification of a linked sleep disorder. Proc Natl Acad Sci U S A. 2005;102(8):2975-2979 (Pubitemid 40299901)
-
(2005)
Proceedings of the National Academy of Sciences of the United States of America
, vol.102
, Issue.8
, pp. 2975-2979
-
-
Mani, A.1
Radhakrishnan, J.2
Farhi, A.3
Carew, K.S.4
Warnes, C.A.5
Nelson-Williams, C.6
Day, R.W.7
Pober, B.8
State, M.W.9
Lifton, R.P.10
-
8
-
-
33644627494
-
Mutations in myosin heavy chain 11 cause a syndrome associating thoracic aortic aneurysm/aortic dissection and patent ductus arteriosus
-
DOI 10.1038/ng1721, PII N1721
-
Zhu L, Vranckx R, Khau Van Kien P, et al. Mutations in myosin heavy chain 11 cause a syndrome associating thoracic aortic aneurysm/aortic dissection and patent ductus arteriosus. Nat Genet. 2006;38(3):343-349 (Pubitemid 43315758)
-
(2006)
Nature Genetics
, vol.38
, Issue.3
, pp. 343-349
-
-
Zhu, L.1
Vranckx, R.2
Van Kien, P.K.3
Lalande, A.4
Boisset, N.5
Mathieu, F.6
Wegman, M.7
Glancy, L.8
Gasc, J.-M.9
Brunotte, F.10
Bruneval, P.11
Wolf, J.-E.12
Michel, J.-B.13
Jeunemaitre, X.14
-
9
-
-
0142148058
-
1166C Polymorphism and Prophylactic Indomethacin Treatment Induced Ductus Arteriosus Closure in Very Low Birth Weight Neonates
-
DOI 10.1203/01.PDR.0000088016.67117.39
-
Treszl A, Szabo M, Dunai G, et al. Angiotensin II type 1 receptor A1166C polymorphism and prophylactic indomethacin treatment induced ductus arteriosus closure in very low birth weight neonates. Pediatr Res. 2003;54(5):753-755 (Pubitemid 37310778)
-
(2003)
Pediatric Research
, vol.54
, Issue.5
, pp. 753-755
-
-
Treszl, A.1
Szabo, M.2
Dunai, G.3
Nobilis, A.4
Kocsis, I.5
Machay, T.6
Tulassay, T.7
Vasarhelyi, B.8
-
10
-
-
38849117244
-
Evaluation of fetal and maternal genetic variation in the progesterone receptor gene for contributions to preterm birth
-
Ehn NL, Cooper ME, Orr K, et al. Evaluation of fetal and maternal genetic variation in the progesterone receptor gene for contributions to preterm birth. Pediatr Res. 2007;62(5):630-635
-
(2007)
Pediatr Res
, vol.62
, Issue.5
, pp. 630-635
-
-
Ehn, N.L.1
Cooper, M.E.2
Orr, K.3
-
11
-
-
35648996954
-
Maternal and fetal variation in genes of cholesterol metabolism is associated with preterm delivery
-
DOI 10.1038/sj.jp.7211806, PII 7211806
-
Steffen KM, Cooper ME, Shi M, et al. Maternal and fetal variation in genes of cholesterol metabolism is associated with preterm delivery. J Perinatol. 2007;27(11):672-680 (Pubitemid 350020346)
-
(2007)
Journal of Perinatology
, vol.27
, Issue.11
, pp. 672-680
-
-
Steffen, K.M.1
Cooper, M.E.2
Shi, M.3
Caprau, D.4
Simhan, H.N.5
Dagle, J.M.6
Marazita, M.L.7
Murray, J.C.8
-
12
-
-
0032231941
-
PedCheck: A program for identification of genotype incompatibilities in linkage analysis
-
DOI 10.1086/301904
-
O'Connell JR, Weeks DE. PedCheck: a program for identification of genotype incompatibilities in linkage analysis. Am J Hum Genet. 1998;63(1):259-266 (Pubitemid 30428342)
-
(1998)
American Journal of Human Genetics
, vol.63
, Issue.1
, pp. 259-266
-
-
O'Connell, J.R.1
Weeks, D.E.2
-
13
-
-
0035055544
-
The family based association test method: Strategies for studying general genotype-phenotype associations
-
DOI 10.1038/sj.ejhg.5200625
-
Horvath S, Xu X, Laird NM. The family based association test method: strategies for studying general genotype-phenotype associations. Eur J Hum Genet. 2001;9(4):301-306 (Pubitemid 32366699)
-
(2001)
European Journal of Human Genetics
, vol.9
, Issue.4
, pp. 301-306
-
-
Horvath, S.1
Xu, X.2
Laird, N.M.3
-
14
-
-
0033814928
-
Implementing a unified approach to family-based tests of association
-
Laird NM, Horvath S, Xu X. Implementing a unified approach to family-based tests of association. Genet Epidemiol. 2000;19(suppl 1):S36-S42
-
(2000)
Genet Epidemiol
, vol.19
, Issue.SUPPL. 1
-
-
Laird, N.M.1
Horvath, S.2
Xu, X.3
-
15
-
-
0034054165
-
A unified approach to adjusting association tests for population admixture with arbitrary pedigree structure and arbitrary missing marker information
-
Rabinowitz D, Laird N. A unified approach to adjusting association tests for population admixture with arbitrary pedigree structure and arbitrary missing marker information. Hum Hered. 2000;50(4):211-223 (Pubitemid 30232624)
-
(2000)
Human Heredity
, vol.50
, Issue.4
, pp. 211-223
-
-
Rabinowitz, D.1
Laird, N.2
-
16
-
-
33745302079
-
Familial and genetic susceptibility to major neonatal morbidities in preterm twins
-
DOI 10.1542/peds.2005-1414
-
Bhandari V, Bizzarro MJ, Shetty A, et al. Familial and genetic susceptibility to major neonatal morbidities in preterm twins. Pediatrics. 2006;117(6):1901-1906 (Pubitemid 46071232)
-
(2006)
Pediatrics
, vol.117
, Issue.6
, pp. 1901-1906
-
-
Bhandari, V.1
Bizzarro, M.J.2
Shetty, A.3
Zhong, X.4
Page, G.P.5
Zhang, H.6
Ment, L.R.7
Gruen, J.R.8
-
17
-
-
33750958906
-
Genetic susceptibility to retinopathy of prematurity
-
DOI 10.1542/peds.2006-1088
-
Bizzarro MJ, Hussain N, Jonsson B, et al. Genetic susceptibility to retinopathy of prematurity. Pediatrics. 2006;118(5):1858-1863 (Pubitemid 46393666)
-
(2006)
Pediatrics
, vol.118
, Issue.5
, pp. 1858-1863
-
-
Bizzarro, M.J.1
Hussain, N.2
Jonsson, B.3
Feng, R.4
Ment, L.R.5
Gruen, J.R.6
Zhang, H.7
Bhandari, V.8
-
18
-
-
33947285368
-
What genome-wide association studies can do for medicine
-
Christensen K, Murray JC. What genome-wide association studies can do for medicine. N Engl J Med. 2007;356(11):1094-1097
-
(2007)
N Engl J Med
, vol.356
, Issue.11
, pp. 1094-1097
-
-
Christensen, K.1
Murray, J.C.2
-
19
-
-
0034736585
-
Regulatory roles of AP-2 transcription factors in vertebrate development, apoptosis and cell-cycle control
-
DOI 10.1016/S0378-1119(00)00454-6, PII S0378111900004546
-
Hilger-Eversheim K, Moser M, Schorle H, Buettner R. Regulatory roles of AP-2 transcription factors in vertebrate development, apoptosis and cell-cycle control. Gene. 2000;260(1-2):1-12 (Pubitemid 32008495)
-
(2000)
Gene
, vol.260
, Issue.1-2
, pp. 1-12
-
-
Hilger-Eversheim, K.1
Moser, M.2
Schorle, H.3
Buettner, R.4
-
20
-
-
15444347159
-
Enhanced apoptotic cell death of renal epithelial cells in mice lacking transcription factor AP-2beta
-
Moser M, Pscherer A, Roth C, et al. Enhanced apoptotic cell death of renal epithelial cells in mice lacking transcription factor AP-2beta. Genes Dev. 1997;11(15):1938-1948 (Pubitemid 27332981)
-
(1997)
Genes and Development
, vol.11
, Issue.15
, pp. 1938-1948
-
-
Moser, M.1
Pscherer, A.2
Roth, C.3
Becker, J.4
Mucher, G.5
Zerres, K.6
Dixkens, C.7
Weis, J.8
Guay-Woodford, L.9
Buettner, R.10
Fassler, R.11
-
21
-
-
0027486692
-
Cardiac neural crest contribution to the pulmonary artery and sixth aortic arch artery complex in chick embryos aged 6 to 18 days
-
DOI 10.1002/ar.1092370312
-
Waldo KL, Kirby ML. Cardiac neural crest contribution to the pulmonary artery and sixth aortic arch artery complex in chick embryos aged 6 to 18 days. Anat Rec. 1993;237(3):385-399 (Pubitemid 23320118)
-
(1993)
Anatomical Record
, vol.237
, Issue.3
, pp. 385-399
-
-
Waldo, K.L.1
Kirby, M.L.2
-
22
-
-
34547138171
-
NF-kappaB2 mutation targets TRAF1 to induce lymphomagenesis
-
Zhang B, Wang Z, Li T, Tsitsikov EN, Ding HF. NF-kappaB2 mutation targets TRAF1 to induce lymphomagenesis. Blood. 2007;110(2):743-751
-
(2007)
Blood
, vol.110
, Issue.2
, pp. 743-751
-
-
Zhang, B.1
Wang, Z.2
Li, T.3
Tsitsikov, E.N.4
Ding, H.F.5
-
23
-
-
33846921621
-
TRAF1 regulates recruitment of lymphocytes and, to a lesser extent, neutrophils, myeloid dendritic cells and monocytes to the lung airways following lipopolysaccharide inhalation
-
DOI 10.1111/j.1365-2567.2006.02499.x
-
Oyoshi MK, Barthel R, Tsitsikov EN. TRAF1 regulates recruitment of lymphocytes and, to a lesser extent, neutrophils, myeloid dendritic cells and monocytes to the lung airways following lipopolysaccharide inhalation. Immunology. 2007;120(3):303-314 (Pubitemid 46232905)
-
(2007)
Immunology
, vol.120
, Issue.3
, pp. 303-314
-
-
Oyoshi, M.K.1
Barthel, R.2
Tsitsikov, E.N.3
-
24
-
-
9244265488
-
A novel human homologue of Drosophila polycomblike gene is up-regulated in multiple cancers
-
DOI 10.1016/j.gene.2004.09.006, PII S0378111904005505
-
Wang S, Robertson GP, Zhu J. A novel human homologue of Drosophila polycomblike gene is up-regulated in multiple cancers. Gene. 2004;343(1):69-78 (Pubitemid 39551030)
-
(2004)
Gene
, vol.343
, Issue.1
, pp. 69-78
-
-
Wang, S.1
Robertson, G.P.2
Zhu, J.3
-
25
-
-
33750574749
-
Patent ductus arteriosus
-
DOI 10.1161/CIRCULATIONAHA.105.592063, PII 0000301720061024000014
-
Schneider DJ, Moore JW. Patent ductus arteriosus. Circulation. 2006;114(17):1873-1882 (Pubitemid 44673363)
-
(2006)
Circulation
, vol.114
, Issue.17
, pp. 1873-1882
-
-
Schneider, D.J.1
Moore, J.W.2
-
27
-
-
33845899137
-
Human catechol-O-methyltransferase haplotypes modulate protein expression by altering mRNA secondary structure
-
DOI 10.1126/science.1131262
-
Nackley AG, Shabalina SA, Tchivileva IE, et al. Human catechol-O-methyltransferase haplotypes modulate protein expression by altering mRNA secondary structure. Science. 2006;314(5807):1930-1933 (Pubitemid 46026115)
-
(2006)
Science
, vol.314
, Issue.5807
, pp. 1930-1933
-
-
Nackley, A.G.1
Shabalina, S.A.2
Tchivileva, I.E.3
Satterfield, K.4
Korchynskyi, O.5
Makarov, S.S.6
Maixner, W.7
Diatchenko, L.8
-
28
-
-
0035713025
-
Factors influencing successful closure with indomethacin of the patent ductus arteriosus in premature infants
-
Kalis NN, Pieper C, van der Merwe PL, Nel ED. Factors influencing successful closure with indomethacin of the patent ductus arteriosus in premature infants. Cardiovasc J S Afr. 2001;12(5):268-272
-
(2001)
Cardiovasc J S Afr
, vol.12
, Issue.5
, pp. 268-272
-
-
Kalis, N.N.1
Pieper, C.2
Van Der Merwe, P.L.3
Nel, E.D.4
-
29
-
-
18744425220
-
Indomethacin tocolysis increases postnatal patent ductus arteriosus severity
-
Available at
-
Hammerman C, Glaser J, Kaplan M, Schimmel MS, Ferber B, Eidelman AI. Indomethacin tocolysis increases postnatal patent ductus arteriosus severity. Pediatrics. 1998;102(5). Available at: www.pediatrics.org/cgi/content/full/102/ 5/e56
-
(1998)
Pediatrics
, vol.102
, Issue.5
-
-
Hammerman, C.1
Glaser, J.2
Kaplan, M.3
Schimmel, M.S.4
Ferber, B.5
Eidelman, A.I.6
-
30
-
-
33744902653
-
Indomethacin prophylaxis, patent ductus arteriosus, and the risk of bronchopulmonary dysplasia: Further analyses from the Trial of Indomethacin Prophylaxis in Preterms (TIPP)
-
DOI 10.1016/j.jpeds.2006.01.047, PII S0022347606000746
-
Schmidt B, Roberts RS, Fanaroff A, et al. Indomethacin prophylaxis, patent ductus arteriosus, and the risk of bronchopulmonary dysplasia: further analyses from the Trial of Indomethacin Prophylaxis in Preterms (TIPP). J Pediatr. 2006;148(6):730-734 (Pubitemid 43870093)
-
(2006)
Journal of Pediatrics
, vol.148
, Issue.6
-
-
Schmidt, B.1
Roberts, R.S.2
Fanaroff, A.3
Davis, P.4
Kirpalani, H.M.5
Nwaesei, C.6
Vincer, M.7
|