-
1
-
-
0035888110
-
Descriptive epidemiology of isolated anal anomalies: a survey of 4.6 million births in Europe
-
Cuscherii A. Descriptive epidemiology of isolated anal anomalies: a survey of 4.6 million births in Europe. Am J Med Genet 103 3 (2001) 207-215
-
(2001)
Am J Med Genet
, vol.103
, Issue.3
, pp. 207-215
-
-
Cuscherii, A.1
-
2
-
-
0024149545
-
Incidence, frequency of types, and etiology of anorectal malformations
-
Smith E.D. Incidence, frequency of types, and etiology of anorectal malformations. Birth Defects Orig Artic Ser 24 4 (1988) 231-246
-
(1988)
Birth Defects Orig Artic Ser
, vol.24
, Issue.4
, pp. 231-246
-
-
Smith, E.D.1
-
3
-
-
0022634255
-
Covered anus with anocutaneous fistula: the muscular sphincters
-
N'Guessan G., and Stephens F.D. Covered anus with anocutaneous fistula: the muscular sphincters. J Pediatr Surg 21 1 (1986) 33-35
-
(1986)
J Pediatr Surg
, vol.21
, Issue.1
, pp. 33-35
-
-
N'Guessan, G.1
Stephens, F.D.2
-
4
-
-
34347327322
-
-
Smith ED, Incidence frequency of types and etiology of anorectal malformations. In: Stephens FD, Smith ED, editor. Anorectal malformations in children. New York: March of Dimes Birth Defects foundation, Alan R Liss; 1988. p.238-40
-
-
-
-
5
-
-
0028918014
-
"Anorectal malformations"
-
Pena A. "Anorectal malformations". Semin Pediatr Surg 4 (1995) 35-47
-
(1995)
Semin Pediatr Surg
, vol.4
, pp. 35-47
-
-
Pena, A.1
-
7
-
-
0036393891
-
Descriptive epidemiology of anal atresia in Hawaii, 1986-1999
-
Forrester M.B., and Merz R.D. Descriptive epidemiology of anal atresia in Hawaii, 1986-1999. Teratology 66 Suppl 1 (2002) S12-S16
-
(2002)
Teratology
, vol.66
, Issue.SUPPL. 1
-
-
Forrester, M.B.1
Merz, R.D.2
-
8
-
-
0023263340
-
Anorectal malformations: familial aspects and associated anomalies
-
Boocock G.R., and Donnai D. Anorectal malformations: familial aspects and associated anomalies. Arch Dis Child 62 (1987) 576-579
-
(1987)
Arch Dis Child
, vol.62
, pp. 576-579
-
-
Boocock, G.R.1
Donnai, D.2
-
9
-
-
0029096482
-
The principles of normal and abnormal hindgut development
-
Kluth D., Hillen M., and Lambrecht W. The principles of normal and abnormal hindgut development. J Pediatr Surg 30 8 (1995) 1143-1147
-
(1995)
J Pediatr Surg
, vol.30
, Issue.8
, pp. 1143-1147
-
-
Kluth, D.1
Hillen, M.2
Lambrecht, W.3
-
11
-
-
3142674819
-
Associated anomalies with anorectal malformation (ARM)
-
Mittal A., Airon R.K., Magu S., et al. Associated anomalies with anorectal malformation (ARM). Indian J Pediatr 71 6 (2004) 509-514
-
(2004)
Indian J Pediatr
, vol.71
, Issue.6
, pp. 509-514
-
-
Mittal, A.1
Airon, R.K.2
Magu, S.3
-
12
-
-
0009819406
-
Anorectal malformations
-
Lister J., and Irving I. (Eds), Butterworths, London
-
Cook R.C.M. Anorectal malformations. In: Lister J., and Irving I. (Eds). Neonatal Surgery (1990), Butterworths, London 547-570
-
(1990)
Neonatal Surgery
, pp. 547-570
-
-
Cook, R.C.M.1
-
13
-
-
0021274031
-
Familial incidence of congenital anorectal anomalies
-
Schwoebel M.G., Hirsig J., Schinzel A., et al. Familial incidence of congenital anorectal anomalies. J Pediatr Surg 19 2 (1984) 179-182
-
(1984)
J Pediatr Surg
, vol.19
, Issue.2
, pp. 179-182
-
-
Schwoebel, M.G.1
Hirsig, J.2
Schinzel, A.3
-
14
-
-
0002509181
-
Family studies of congenital heart disease: a syndrome of hydrometrocolpus, proximal polydactyly and congenital heart disease
-
Kaufman R.L., Hartman A., McAlister W.H., et al. Family studies of congenital heart disease: a syndrome of hydrometrocolpus, proximal polydactyly and congenital heart disease. Birth Defects Orig Artic Ser 8 (1972) 85-87
-
(1972)
Birth Defects Orig Artic Ser
, vol.8
, pp. 85-87
-
-
Kaufman, R.L.1
Hartman, A.2
McAlister, W.H.3
-
15
-
-
0141565568
-
Hirschprung's disease and imperforate anus in Pallister-Hall syndrome: a new association
-
Haynes J.H., and Bagwell C.E. Hirschprung's disease and imperforate anus in Pallister-Hall syndrome: a new association. J Pediatr Surg 38 9 (2003) 1411-1412
-
(2003)
J Pediatr Surg
, vol.38
, Issue.9
, pp. 1411-1412
-
-
Haynes, J.H.1
Bagwell, C.E.2
-
16
-
-
0015383189
-
Hereditary syndrome of imperforate anus with hand foot and ear anomalies
-
Townes P.L., and Brock E.R. Hereditary syndrome of imperforate anus with hand foot and ear anomalies. J Pediatr 81 (1972) 321-326
-
(1972)
J Pediatr
, vol.81
, pp. 321-326
-
-
Townes, P.L.1
Brock, E.R.2
-
17
-
-
0020521122
-
Dominant anorectal malformations, nephritis and nerve deafness: a possible new entity?
-
Lowe J., Kohn G., Cohen O., et al. Dominant anorectal malformations, nephritis and nerve deafness: a possible new entity?. Clin Genet 24 (1972) 191-193
-
(1972)
Clin Genet
, vol.24
, pp. 191-193
-
-
Lowe, J.1
Kohn, G.2
Cohen, O.3
-
18
-
-
0036135482
-
OEIS complex, VATER, and the ongoing difficulties in terminology and delineation
-
Bohring A. OEIS complex, VATER, and the ongoing difficulties in terminology and delineation. Am J Med Genet 107 1 (2002) 72-76
-
(2002)
Am J Med Genet
, vol.107
, Issue.1
, pp. 72-76
-
-
Bohring, A.1
-
19
-
-
0036728438
-
Clarification of the processes that lead to anorectal malformations in the ETU-induced rat model of imperforate anus
-
Qi B.Q., Beasley S.W., and Frizelle F.A. Clarification of the processes that lead to anorectal malformations in the ETU-induced rat model of imperforate anus. J Pediatr Surg 37 9 (2002) 1305-1312
-
(2002)
J Pediatr Surg
, vol.37
, Issue.9
, pp. 1305-1312
-
-
Qi, B.Q.1
Beasley, S.W.2
Frizelle, F.A.3
-
20
-
-
0028225024
-
Currarino triad (anorectal malformation, sacral bony abnormality and presacral mass) with partial trisomy of chromosomes 13q and 20p
-
Nagai T., Katoh R., Hasegawa T., et al. Currarino triad (anorectal malformation, sacral bony abnormality and presacral mass) with partial trisomy of chromosomes 13q and 20p. Clin Genet 45 5 (1994) 272-273
-
(1994)
Clin Genet
, vol.45
, Issue.5
, pp. 272-273
-
-
Nagai, T.1
Katoh, R.2
Hasegawa, T.3
-
21
-
-
0034886738
-
Spectrum of mutations and gentype-phenotype analysis in Currarino syndrome
-
Kochling J., Karbasiyan M., and Reis A. Spectrum of mutations and gentype-phenotype analysis in Currarino syndrome. Eur J Hum Genet 9 (2001) 599-605
-
(2001)
Eur J Hum Genet
, vol.9
, pp. 599-605
-
-
Kochling, J.1
Karbasiyan, M.2
Reis, A.3
-
22
-
-
17344363829
-
A homeobox gene HLXB9 is the major locus for dominantly inherited sacral agenesis
-
Ross A.J., Ruiz-Perez V., Wang Y., et al. A homeobox gene HLXB9 is the major locus for dominantly inherited sacral agenesis. Nat Genet 20 (1998) 358-361
-
(1998)
Nat Genet
, vol.20
, pp. 358-361
-
-
Ross, A.J.1
Ruiz-Perez, V.2
Wang, Y.3
-
23
-
-
0033454061
-
Endothelin and the development of the enteric nervous system
-
Gershon M.D. Endothelin and the development of the enteric nervous system. Clin Exp Pharmacol Physiol 26 12 (1999) 985-988
-
(1999)
Clin Exp Pharmacol Physiol
, vol.26
, Issue.12
, pp. 985-988
-
-
Gershon, M.D.1
-
24
-
-
0038676363
-
Currarino triad associated with Hirschsprung's disease
-
Baltogiannis N., Mavridis G., Soutis M., et al. Currarino triad associated with Hirschsprung's disease. J Pediatr Surg 38 7 (2003) 1086-1089
-
(2003)
J Pediatr Surg
, vol.38
, Issue.7
, pp. 1086-1089
-
-
Baltogiannis, N.1
Mavridis, G.2
Soutis, M.3
-
25
-
-
0035882261
-
Hirschsprung disease in an infant with a contiguous gene syndrome of chromosome 13
-
Shanske A., Ferreira J.C., Leonard J.C., et al. Hirschsprung disease in an infant with a contiguous gene syndrome of chromosome 13. Am J Med Genet 102 3 (2001) 231-236
-
(2001)
Am J Med Genet
, vol.102
, Issue.3
, pp. 231-236
-
-
Shanske, A.1
Ferreira, J.C.2
Leonard, J.C.3
-
26
-
-
0029125760
-
Penoscrotal transposition and associated anomalies: report of five new cases and review of the literature
-
Parida S.K., Hall B.D., Barton L., et al. Penoscrotal transposition and associated anomalies: report of five new cases and review of the literature. Am J Med Genet 59 1 (1995) 68-75
-
(1995)
Am J Med Genet
, vol.59
, Issue.1
, pp. 68-75
-
-
Parida, S.K.1
Hall, B.D.2
Barton, L.3
-
27
-
-
0017148259
-
A general method for isolation of high molecular weight DNA from eukaryotes
-
Blin N., and Stafford D.W. A general method for isolation of high molecular weight DNA from eukaryotes. Nucleic Acids Res 3 (1976) 2303-2308
-
(1976)
Nucleic Acids Res
, vol.3
, pp. 2303-2308
-
-
Blin, N.1
Stafford, D.W.2
-
28
-
-
0024284028
-
A simple salting out procedure for extracting DNA from human nucleated cells
-
Miller S.A., Dykes D.D., and Polesky H.F. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 16 (1988) 1215
-
(1988)
Nucleic Acids Res
, vol.16
, pp. 1215
-
-
Miller, S.A.1
Dykes, D.D.2
Polesky, H.F.3
-
29
-
-
0026331904
-
Poorly differentiated adenocarcinoma with lymphoid stroma (lymphoepithelioma-like carcinomas) of the stomach. Report of three cases with Epstein-Barr virus genome demonstrated by the polymerase chain reaction
-
Min K.W., Holmquist S., Peiper S.C., et al. Poorly differentiated adenocarcinoma with lymphoid stroma (lymphoepithelioma-like carcinomas) of the stomach. Report of three cases with Epstein-Barr virus genome demonstrated by the polymerase chain reaction. Am J Clin Pathol 96 (1991) 219-227
-
(1991)
Am J Clin Pathol
, vol.96
, pp. 219-227
-
-
Min, K.W.1
Holmquist, S.2
Peiper, S.C.3
-
30
-
-
12644284522
-
Endothelin-3 gene mutations in isolated and syndromic Hirschsprung disease
-
Bidaud C., Salomon R., van Camp G., et al. Endothelin-3 gene mutations in isolated and syndromic Hirschsprung disease. Eur J Hum Genet 5 4 (1997) 247-251
-
(1997)
Eur J Hum Genet
, vol.5
, Issue.4
, pp. 247-251
-
-
Bidaud, C.1
Salomon, R.2
van Camp, G.3
-
31
-
-
0029008387
-
Nonradioactive multiplex PCR screening strategy for the simultaneous detection of multiple low-density lipoprotein receptor gene mutations
-
Kotze M., Theart L., Callis M., et al. Nonradioactive multiplex PCR screening strategy for the simultaneous detection of multiple low-density lipoprotein receptor gene mutations. PCR Methods Applic 4 (1995) 352-356
-
(1995)
PCR Methods Applic
, vol.4
, pp. 352-356
-
-
Kotze, M.1
Theart, L.2
Callis, M.3
-
32
-
-
0028069130
-
Identity-by-descent and association mapping of a recessive gene for Hirschsprung disease on human chromosome 13q22
-
Puffenberger E., Kauffman E., Bolk S., et al. Identity-by-descent and association mapping of a recessive gene for Hirschsprung disease on human chromosome 13q22. Hum Mol Genet 3 (1994) 1217-1225
-
(1994)
Hum Mol Genet
, vol.3
, pp. 1217-1225
-
-
Puffenberger, E.1
Kauffman, E.2
Bolk, S.3
-
33
-
-
0024366978
-
Anorectal malformations and Down syndrome
-
Zlotogora J., Abu-Dalu K., Lernau O., et al. Anorectal malformations and Down syndrome. Am J Med Genet 34 3 (1989) 330-331
-
(1989)
Am J Med Genet
, vol.34
, Issue.3
, pp. 330-331
-
-
Zlotogora, J.1
Abu-Dalu, K.2
Lernau, O.3
-
34
-
-
0033009643
-
Analysis of 1,992 patients with anorectal malformations over the past two decades in Japan. Steering Committee of Japanese Study Group of Anorectal Anomalies
-
Endo M., Hayashi A., Ishihara M., et al. Analysis of 1,992 patients with anorectal malformations over the past two decades in Japan. Steering Committee of Japanese Study Group of Anorectal Anomalies. J Pediatr Surg 34 3 (1999) 435-441
-
(1999)
J Pediatr Surg
, vol.34
, Issue.3
, pp. 435-441
-
-
Endo, M.1
Hayashi, A.2
Ishihara, M.3
-
35
-
-
0035025182
-
The VACTERL association: lessons from the sonic hedgehog pathway
-
Kim J., Kim P.C.W., and Hui C.-C. The VACTERL association: lessons from the sonic hedgehog pathway. Clin Genet 59 5 (2001) 306-315
-
(2001)
Clin Genet
, vol.59
, Issue.5
, pp. 306-315
-
-
Kim, J.1
Kim, P.C.W.2
Hui, C.-C.3
-
36
-
-
33745010737
-
N-terminal proteolysis of the endothelin B receptor abolishes its ability to induce EGF receptor transactivation and contractile protein expression in vascular smooth muscle cells
-
[E-Published ahead of Print]
-
Grantcharova E., Reusch H.P., Grossmann S., et al. N-terminal proteolysis of the endothelin B receptor abolishes its ability to induce EGF receptor transactivation and contractile protein expression in vascular smooth muscle cells. Arterioscler Thromb Vasc Biol 26 6 (2006) 1288-1296 [E-Published ahead of Print]
-
(2006)
Arterioscler Thromb Vasc Biol
, vol.26
, Issue.6
, pp. 1288-1296
-
-
Grantcharova, E.1
Reusch, H.P.2
Grossmann, S.3
-
37
-
-
0035376984
-
Gbeta gamma mediate differentiation of vascular smooth muscle cells
-
Reusch H.P., Schaefer M., Plum C., et al. Gbeta gamma mediate differentiation of vascular smooth muscle cells. J Biol Chem 276 22 (2001) 19540-19547
-
(2001)
J Biol Chem
, vol.276
, Issue.22
, pp. 19540-19547
-
-
Reusch, H.P.1
Schaefer, M.2
Plum, C.3
-
38
-
-
33644997214
-
Endothelin-1 regulates proliferative responses, both alone and synergistically with PDGF, in rat tracheal smooth muscle cells
-
Yahiaoui L., Villeneuve A., Valderrama-Carvajal H., et al. Endothelin-1 regulates proliferative responses, both alone and synergistically with PDGF, in rat tracheal smooth muscle cells. Cell Physiol Biochem 17 1-2 (2006) 37-46
-
(2006)
Cell Physiol Biochem
, vol.17
, Issue.1-2
, pp. 37-46
-
-
Yahiaoui, L.1
Villeneuve, A.2
Valderrama-Carvajal, H.3
-
39
-
-
0013543367
-
The human endothelin family: three structurally and pharmacologically distinct isopeptides predicted by three separate genes
-
Inoue A., Yanagisawa M., Kimura S., et al. The human endothelin family: three structurally and pharmacologically distinct isopeptides predicted by three separate genes. Proc Natl Acad Sci 86 8 (1989) 2863-2867
-
(1989)
Proc Natl Acad Sci
, vol.86
, Issue.8
, pp. 2863-2867
-
-
Inoue, A.1
Yanagisawa, M.2
Kimura, S.3
-
40
-
-
0027499701
-
The human endothelin-B receptor gene: structural organisation and chromosomal assignment
-
Arai H., Nakao K., Takaya K., et al. The human endothelin-B receptor gene: structural organisation and chromosomal assignment. J Biol Chem 268 (1993) 3463-3470
-
(1993)
J Biol Chem
, vol.268
, pp. 3463-3470
-
-
Arai, H.1
Nakao, K.2
Takaya, K.3
-
41
-
-
0347708995
-
Age-dependent changes in the postnatal intestinal microcirculation
-
Nankervis C.A., Reber K.M., and Nowicki P.T. Age-dependent changes in the postnatal intestinal microcirculation. Microcirculation 8 6 (2001) 377-387
-
(2001)
Microcirculation
, vol.8
, Issue.6
, pp. 377-387
-
-
Nankervis, C.A.1
Reber, K.M.2
Nowicki, P.T.3
-
42
-
-
0037178638
-
Endothelin B receptor deficiency augments neuronal damage upon exposure to hypoxia-ischemia in vivo
-
Siren A.L., Lewczuk P., Hasselblatt M., et al. Endothelin B receptor deficiency augments neuronal damage upon exposure to hypoxia-ischemia in vivo. Brain Res 945 1 (2002) 144-149
-
(2002)
Brain Res
, vol.945
, Issue.1
, pp. 144-149
-
-
Siren, A.L.1
Lewczuk, P.2
Hasselblatt, M.3
-
43
-
-
10844224604
-
Endothelin receptor B inhibition triggers apoptosis and enhances angiogenesis in melanomas
-
Lahav R., Suva M.L., Rimoldi D., et al. Endothelin receptor B inhibition triggers apoptosis and enhances angiogenesis in melanomas. Cancer Res 64 24 (2004) 8945-8953
-
(2004)
Cancer Res
, vol.64
, Issue.24
, pp. 8945-8953
-
-
Lahav, R.1
Suva, M.L.2
Rimoldi, D.3
-
44
-
-
0037044398
-
Vascular endothelin-B receptor system in vivo plays a favorable inhibitory role in vascular remodeling after injury revealed by endothelin-B receptor-knockout mice
-
Murakoshi N., Miyauchi T., Kakinuma Y., et al. Vascular endothelin-B receptor system in vivo plays a favorable inhibitory role in vascular remodeling after injury revealed by endothelin-B receptor-knockout mice. Circulation 106 15 (2002) 1991-1998
-
(2002)
Circulation
, vol.106
, Issue.15
, pp. 1991-1998
-
-
Murakoshi, N.1
Miyauchi, T.2
Kakinuma, Y.3
-
45
-
-
0027787680
-
Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism
-
Pollak M.R., Brown E.M., Chou Y.H., et al. Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism. Cell 75 7 (1993) 1297-1303
-
(1993)
Cell
, vol.75
, Issue.7
, pp. 1297-1303
-
-
Pollak, M.R.1
Brown, E.M.2
Chou, Y.H.3
|