-
3
-
-
0002105653
-
In situ hybridization with RNA probe: An annotated recipe
-
Valentine KL, et al. editors. New York: Oxford University Press
-
Angerer LM, Stoler MH, Angerer RC. 1987. In situ hybridization with RNA probe: an annotated recipe. In: Valentine KL, et al. editors. In situ hybridization: applications to neurobiology. New York: Oxford University Press, p 42-70.
-
(1987)
In Situ Hybridization: Applications to Neurobiology
, pp. 42-70
-
-
Angerer, L.M.1
Stoler, M.H.2
Angerer, R.C.3
-
4
-
-
0031958833
-
Chicken winged-helix transcription factor cFKH-1 prefigures axial and appendicular skeletal structures during chicken embryo-genesis
-
Buchberger A, Schwarzer M, Brand T, Pabst O, Siedl K, Arnold H-H. 1998. Chicken winged-helix transcription factor cFKH-1 prefigures axial and appendicular skeletal structures during chicken embryo-genesis. Dev Dyn 212:94-101.
-
(1998)
Dev Dyn
, vol.212
, pp. 94-101
-
-
Buchberger, A.1
Schwarzer, M.2
Brand, T.3
Pabst, O.4
Siedl, K.5
Arnold, H.-H.6
-
5
-
-
0030961168
-
Smad4 and FAST-1 in the assembly of activin-responsive factor
-
Chen X, Weisberg E, Fridmacher V, Watanabe M, Naco G, Whitman M. 1997. Smad4 and FAST-1 in the assembly of activin-responsive factor. Nature 389:85-89.
-
(1997)
Nature
, vol.389
, pp. 85-89
-
-
Chen, X.1
Weisberg, E.2
Fridmacher, V.3
Watanabe, M.4
Naco, G.5
Whitman, M.6
-
6
-
-
0021378952
-
Mouse trisomy 16 as an animal model of human trisomy 21 (Down syndrome): Formation of viable trisomy 16〈-〉 diploid mouse chimeras
-
Cox DR, Smith SA, Epstein LB, Epstein CJ. 1984. Mouse trisomy 16 as an animal model of human trisomy 21 (Down syndrome): formation of viable trisomy 16〈-〉 diploid mouse chimeras. Dev Biol 101:416-424.
-
(1984)
Dev Biol
, vol.101
, pp. 416-424
-
-
Cox, D.R.1
Smith, S.A.2
Epstein, L.B.3
Epstein, C.J.4
-
7
-
-
0031942931
-
Role of cardiac neural crest cells in cardiovascular development
-
Creazzo TL, Godt RE, Leatherbury L, Conway SJ, Kirby ML. 1998. Role of cardiac neural crest cells in cardiovascular development. Annu Rev Physiol 60:267-286.
-
(1998)
Annu Rev Physiol
, vol.60
, pp. 267-286
-
-
Creazzo, T.L.1
Godt, R.E.2
Leatherbury, L.3
Conway, S.J.4
Kirby, M.L.5
-
8
-
-
6844251598
-
Familial Axenfeld-Rieger anomaly, atrial septal defect, and sensorineural hearing loss
-
Cunningham JET, Eliott D, Miller NR, Maumenee IH, Green WR. 1998. Familial Axenfeld-Rieger anomaly, atrial septal defect, and sensorineural hearing loss. Arch Ophthalmol 116:78-82.
-
(1998)
Arch Ophthalmol
, vol.116
, pp. 78-82
-
-
Cunningham, J.E.T.1
Eliott, D.2
Miller, N.R.3
Maumenee, I.H.4
Green, W.R.5
-
9
-
-
0024476864
-
Congenital cardiovascular malformations associated with chromosome abnormalities: An epidemiologic study
-
Ferencz C, Neill CA, Boughman JA, Rubin JD, Brenner JI, Perry LW. 1989. Congenital cardiovascular malformations associated with chromosome abnormalities: an epidemiologic study. J Pediatr 114: 79-86.
-
(1989)
J Pediatr
, vol.114
, pp. 79-86
-
-
Ferencz, C.1
Neill, C.A.2
Boughman, J.A.3
Rubin, J.D.4
Brenner, J.I.5
Perry, L.W.6
-
10
-
-
0031960248
-
Expression of the mouse Fkh1/Mf1 and Mfh1 genes in late gestation embryos is restricted to mesoderm derivatives
-
Hiemisch H, Monaghan AP, Schutz G, Kaestner KH. 1998a. Expression of the mouse Fkh1/Mf1 and Mfh1 genes in late gestation embryos is restricted to mesoderm derivatives. Mech Dev 73:129-132.
-
(1998)
Mech Dev
, vol.73
, pp. 129-132
-
-
Hiemisch, H.1
Monaghan, A.P.2
Schutz, G.3
Kaestner, K.H.4
-
11
-
-
0032487374
-
The mouse Fkh1/Mf1 gene: cDNA sequence, chromosomal localization and expression in adult tissues
-
Hiemisch H, Schutz G, Kaestner KH. 1998b. The mouse Fkh1/Mf1 gene: cDNA sequence, chromosomal localization and expression in adult tissues. Gene 20:77-82.
-
(1998)
Gene
, vol.20
, pp. 77-82
-
-
Hiemisch, H.1
Schutz, G.2
Kaestner, K.H.3
-
12
-
-
0030696897
-
Essential roles of the winged helix transcription factor MFH-1 in aortic arch patterning and skeletogenesis
-
Iida K, Koseki H, Kakinuma H, Kato N, Mizutani-Koseki Y, Ohuch H, Yoshioka H, Noji S, Kawamura K, Kataoka Y, Ueno F, Taniguchi M, Yoshida N, Sugiyama T, Miura N. 1997. Essential roles of the winged helix transcription factor MFH-1 in aortic arch patterning and skeletogenesis. Development 124:4627-4638.
-
(1997)
Development
, vol.124
, pp. 4627-4638
-
-
Iida, K.1
Koseki, H.2
Kakinuma, H.3
Kato, N.4
Mizutani-Koseki, Y.5
Ohuch, H.6
Yoshioka, H.7
Noji, S.8
Kawamura, K.9
Kataoka, Y.10
Ueno, F.11
Taniguchi, M.12
Yoshida, N.13
Sugiyama, T.14
Miura, N.15
-
13
-
-
0027328360
-
Six members of the mouse forkhead gene family are developmentally regulated
-
Kaestner KH, Lee K-H, Schlondorff J, Hiemisch H, Monaghan AP, Schutz G. 1993. Six members of the mouse forkhead gene family are developmentally regulated. Proc Natl Acad Sci USA 90:7628-7631.
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 7628-7631
-
-
Kaestner, K.H.1
Lee, K.-H.2
Schlondorff, J.3
Hiemisch, H.4
Monaghan, A.P.5
Schutz, G.6
-
14
-
-
0029999782
-
Clustered arrangement of winged helix genes fkh-6 and FKH-1: Possible implications for mesoderm development
-
Kaestner KH, Bleckmann SC, Monaghan AP, Schlondorff J, Mincheva A, Lichter P, Schutz G. 1996. Clustered arrangement of winged helix genes fkh-6 and FKH-1: possible implications for mesoderm development. Development 122:1751-1758.
-
(1996)
Development
, vol.122
, pp. 1751-1758
-
-
Kaestner, K.H.1
Bleckmann, S.C.2
Monaghan, A.P.3
Schlondorff, J.4
Mincheva, A.5
Lichter, P.6
Schutz, G.7
-
15
-
-
0024390884
-
Neural crest origin of the trabecular mesh-work cells and other structures of the anterior chamber
-
Kaiser-Kupfer MI. 1989. Neural crest origin of the trabecular mesh-work cells and other structures of the anterior chamber. Am J Ophthalmol 107:671-672.
-
(1989)
Am J Ophthalmol
, vol.107
, pp. 671-672
-
-
Kaiser-Kupfer, M.I.1
-
16
-
-
0026353568
-
The neural crest as a possible pathogenic factor in coarctation of the aorta and bicuspid aortic valve
-
Kappetein AP, Gittenberger-de Groot AC, Zwinderman AH, Rohmer J, Poelmann RE, Huysmans HA. 1991. The neural crest as a possible pathogenic factor in coarctation of the aorta and bicuspid aortic valve. J Thorac Cardiovasc Surg 102:830-836.
-
(1991)
J Thorac Cardiovasc Surg
, vol.102
, pp. 830-836
-
-
Kappetein, A.P.1
Gittenberger-De Groot, A.C.2
Zwinderman, A.H.3
Rohmer, J.4
Poelmann, R.E.5
Huysmans, H.A.6
-
17
-
-
17344379513
-
Five years on the wings of fork head
-
Kaufmann E, Knochel W. 1996. Five years on the wings of fork head. Mech Dev 57:3-20.
-
(1996)
Mech Dev
, vol.57
, pp. 3-20
-
-
Kaufmann, E.1
Knochel, W.2
-
18
-
-
0032511231
-
The forkhead/winged helix gene Mf1 is disrupted in the pleiotropic mouse mutation congenital hydrocephalus
-
Kume T, Deng K-Y, Winfrey V, Gould DB, Walter MA, Hogan BLM. 1998. The Forkhead/winged helix gene Mf1 is disrupted in the pleiotropic mouse mutation congenital hydrocephalus. Cell 93:985-996.
-
(1998)
Cell
, vol.93
, pp. 985-996
-
-
Kume, T.1
Deng, K.-Y.2
Winfrey, V.3
Gould, D.B.4
Walter, M.A.5
Hogan, B.L.M.6
-
19
-
-
0018253373
-
New hypothesis of developmental anomalies of the anterior chamber associated with glaucoma
-
Kupfer C, Kaiser-Kupfer MI. 1978. New hypothesis of developmental anomalies of the anterior chamber associated with glaucoma. Trans Ophthalmol Soc 98:213-215.
-
(1978)
Trans Ophthalmol Soc
, vol.98
, pp. 213-215
-
-
Kupfer, C.1
Kaiser-Kupfer, M.I.2
-
20
-
-
0027482831
-
Hepatocyte nuclear factor 3/fork head or "winged helix" proteins: A family of transcription factors of diverse biologic function
-
Lai E, Clark KL, Burley SK, Darnell Jr JE. 1991. Hepatocyte nuclear factor 3/fork head or "winged helix" proteins: a family of transcription factors of diverse biologic function. Proc Natl Acad Sci USA 90:10421-10423.
-
(1991)
Proc Natl Acad Sci USA
, vol.90
, pp. 10421-10423
-
-
Lai, E.1
Clark, K.L.2
Burley, S.K.3
Darnell J.E., Jr.4
-
21
-
-
0031857011
-
Distal 6p deletion syndrome: A report of a case with anterior chamber eye anomaly and review of published reports
-
Law CJ, Fisher AM, Temple IK. 1998. Distal 6p deletion syndrome: a report of a case with anterior chamber eye anomaly and review of published reports. J Med Genet 35:685-689.
-
(1998)
J Med Genet
, vol.35
, pp. 685-689
-
-
Law, C.J.1
Fisher, A.M.2
Temple, I.K.3
-
23
-
-
0025004644
-
Atrioventricular canal in Down syndrome. Prevalence of associated cardiac malformations compared with patient without Down syndrome
-
Marino B, Vairo U, Corno A, Nava S, Guccione P, Calabro R, Marcelletti C. 1990. Atrioventricular canal in Down syndrome. Prevalence of associated cardiac malformations compared with patient without Down syndrome. Am J Dis Child 144:1120-1122.
-
(1990)
Am J Dis Child
, vol.144
, pp. 1120-1122
-
-
Marino, B.1
Vairo, U.2
Corno, A.3
Nava, S.4
Guccione, P.5
Calabro, R.6
Marcelletti, C.7
-
24
-
-
0032231330
-
Mutations of the forkhead/winged-helix gene, FKLH7, in patients with Axenfeld-Rieger anomaly
-
Mears AJ, Jodan T, Mirzayans F, Dubois S, Kume T, Parlee M, Ritch R, Koop B, Kuo W-L, Collins C, Marshall J, Gould DB, Pearce W, Carlsson P, Enerback S, Morisete J, Bhattacharya S, Hogan B, Raymond V, Walter MA. 1998. Mutations of the forkhead/winged-helix gene, FKLH7, in patients with Axenfeld-Rieger Anomaly. Am J Hum Genet 63:1316-1328.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 1316-1328
-
-
Mears, A.J.1
Jodan, T.2
Mirzayans, F.3
Dubois, S.4
Kume, T.5
Parlee, M.6
Ritch, R.7
Koop, B.8
Kuo, W.-L.9
Collins, C.10
Marshall, J.11
Gould, D.B.12
Pearce, W.13
Carlsson, P.14
Enerback, S.15
Morisete, J.16
Bhattacharya, S.17
Hogan, B.18
Raymond, V.19
Walter, M.A.20
more..
-
25
-
-
0027174862
-
MFH-1, a new member of the fork head domain family, is expressed in developing mesenchyme
-
Miura N, Wanaka A, Tohyama M, Tanaka K. 1993. MFH-1, a new member of the fork head domain family, is expressed in developing mesenchyme. FEBS Lett 326:171-176.
-
(1993)
FEBS Lett
, vol.326
, pp. 171-176
-
-
Miura, N.1
Wanaka, A.2
Tohyama, M.3
Tanaka, K.4
-
26
-
-
0024605518
-
Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS)
-
Newton CR, Graham A, Heptinstall LE, Powell SJ, Summers C, Kalsheker N, Smith JC, Markham AF. 1989. Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS). Nucleic Acids Res 17:2503-2516.
-
(1989)
Nucleic Acids Res
, vol.17
, pp. 2503-2516
-
-
Newton, C.R.1
Graham, A.2
Heptinstall, L.E.3
Powell, S.J.4
Summers, C.5
Kalsheker, N.6
Smith, J.C.7
Markham, A.F.8
-
27
-
-
17344368672
-
The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25
-
Nishimura DY, Swiderski RE, Alward WLM, Searby CC, Patil SR, Bennet SR, Kanis AB, Gastier JM, Stone EM, Sheffield VC. 1998 The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25. Nat Genet 19:140-147.
-
(1998)
Nat Genet
, vol.19
, pp. 140-147
-
-
Nishimura, D.Y.1
Swiderski, R.E.2
Alward, W.L.M.3
Searby, C.C.4
Patil, S.R.5
Bennet, S.R.6
Kanis, A.B.7
Gastier, J.M.8
Stone, E.M.9
Sheffield, V.C.10
-
28
-
-
0030659557
-
The forkhead transcription factor DAF-16 transduces insulin-like metabolic and longevity signals in C. elegans
-
Ogg S, Paradis S, Gottlieb S, Patterson G, Lee L, Tissenbaum H, Ruvkun G. 1997. The forkhead transcription factor DAF-16 transduces insulin-like metabolic and longevity signals in C. elegans. Nature 389:994-999.
-
(1997)
Nature
, vol.389
, pp. 994-999
-
-
Ogg, S.1
Paradis, S.2
Gottlieb, S.3
Patterson, G.4
Lee, L.5
Tissenbaum, H.6
Ruvkun, G.7
-
29
-
-
0029762015
-
A second locus for Rieger syndrome maps to chromosome 13q14
-
Phillips JC, Del Bono EA, Haines JL, Pralea AM, Cohen JS, Greff LJ, Wiggs JL. 1996. A second locus for Rieger Syndrome maps to chromosome 13q14. Am J Hum Genet 59:613-619.
-
(1996)
Am J Hum Genet
, vol.59
, pp. 613-619
-
-
Phillips, J.C.1
Del Bono, E.A.2
Haines, J.L.3
Pralea, A.M.4
Cohen, J.S.5
Greff, L.J.6
Wiggs, J.L.7
-
30
-
-
0028046675
-
Cloning and characterization of seven human forkhead proteins: Binding site specificity and DNA bending
-
Pierrou S, Hellqvist M, Samuelsson L, Enerback S, Carlsson P. 1994. Cloning and characterization of seven human forkhead proteins: binding site specificity and DNA bending. EMBO J 13:5002-5012.
-
(1994)
EMBO J
, vol.13
, pp. 5002-5012
-
-
Pierrou, S.1
Hellqvist, M.2
Samuelsson, L.3
Enerback, S.4
Carlsson, P.5
-
31
-
-
0001596112
-
Cardiac malformation in mongolism
-
Rowe RD, Uchida IA. 1961. Cardiac malformation in mongolism. Am J Med 31:726-735.
-
(1961)
Am J Med
, vol.31
, pp. 726-735
-
-
Rowe, R.D.1
Uchida, I.A.2
-
32
-
-
0027318791
-
Differential expression of multiple fork head related genes during gastrulation and axial pattern formation in the mouse embryo
-
Sasaki H, Hogan BLM. 1993. Differential expression of multiple fork head related genes during gastrulation and axial pattern formation in the mouse embryo. Development 118:47-59.
-
(1993)
Development
, vol.118
, pp. 47-59
-
-
Sasaki, H.1
Hogan, B.L.M.2
-
33
-
-
0032479573
-
Congenital heart disease caused by mutations in the transcription factor Nkx2.5
-
Schott J, Benson DW, Basson CT, Pease W, Silberbach GM, Moak JP, Maron BJ, Seidman CE, Seidman JG. 1998. Congenital heart disease caused by mutations in the transcription factor Nkx2.5. Science 281:108-111.
-
(1998)
Science
, vol.281
, pp. 108-111
-
-
Schott, J.1
Benson, D.W.2
Basson, C.T.3
Pease, W.4
Silberbach, G.M.5
Moak, J.P.6
Maron, B.J.7
Seidman, C.E.8
Seidman, J.G.9
-
34
-
-
10544233785
-
Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome
-
Semina EV, Reiter R, Leysens NJ, Alward WL, Small KW, Datson NA, Siegel-Bartelt J, Bierke-Nelson D, Bitoun P, Zabel BU, Carey JC, Murray JC. 1996. Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome. Nat Genet 14:392-399.
-
(1996)
Nat Genet
, vol.14
, pp. 392-399
-
-
Semina, E.V.1
Reiter, R.2
Leysens, N.J.3
Alward, W.L.4
Small, K.W.5
Datson, N.A.6
Siegel-Bartelt, J.7
Bierke-Nelson, D.8
Bitoun, P.9
Zabel, B.U.10
Carey, J.C.11
Murray, J.C.12
-
35
-
-
0031022393
-
Identification of a complex congenital heart defect susceptibility locus by using DNA pooling and shared segment analysis
-
Sheffield VC, Pierpont ME, Nishimura D, Beck JS, Burns TL, Berg MA, Stone EM, Patil SR, Lauer RM. 1997. Identification of a complex congenital heart defect susceptibility locus by using DNA pooling and shared segment analysis. Hum Mol Genet 6:117-121.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 117-121
-
-
Sheffield, V.C.1
Pierpont, M.E.2
Nishimura, D.3
Beck, J.S.4
Burns, T.L.5
Berg, M.A.6
Stone, E.M.7
Patil, S.R.8
Lauer, R.M.9
-
36
-
-
0020971487
-
Axenfeld-Rieger syndrome: A theory of mechanism and distinctions from the iridocorneal endothelial syndrome
-
Shields MB. 1983. Axenfeld-Rieger syndrome: a theory of mechanism and distinctions from the iridocorneal endothelial syndrome. Trans Am Ophthalmol Soc 81:736-784.
-
(1983)
Trans Am Ophthalmol Soc
, vol.81
, pp. 736-784
-
-
Shields, M.B.1
-
38
-
-
14444283397
-
Identification of a gene that causes primary open angle glaucoma
-
Stone EM, Fingert JH, Alward WLM, Nguyen TD, Polansky JR, Sunden SLF, Nishimura D, Clark AF, Nystuen A, Nichols BE, Ritch R, Kalenak JW, Craven ER, Sheffield VC. 1997. Identification of a gene that causes primary open angle glaucoma. Science 275:668-670.
-
(1997)
Science
, vol.275
, pp. 668-670
-
-
Stone, E.M.1
Fingert, J.H.2
Alward, W.L.M.3
Nguyen, T.D.4
Polansky, J.R.5
Sunden, S.L.F.6
Nishimura, D.7
Clark, A.F.8
Nystuen, A.9
Nichols, B.E.10
Ritch, R.11
Kalenak, J.W.12
Craven, E.R.13
Sheffield, V.C.14
-
39
-
-
0029812516
-
Origin of the pulmonary venous orifice in the mouse and its relation to the morphogenesis of the sinus venosus, extracardiac mesenchyme (spina vestibuli), and atrium
-
Tasaka H, Krug EL, Markwald RR. 1996. Origin of the pulmonary venous orifice in the mouse and its relation to the morphogenesis of the sinus venosus, extracardiac mesenchyme (spina vestibuli), and atrium. Anat Rec 246:107-113.
-
(1996)
Anat Rec
, vol.246
, pp. 107-113
-
-
Tasaka, H.1
Krug, E.L.2
Markwald, R.R.3
-
40
-
-
0028142341
-
Cardiac valvular disease and Axenfeld-Rieger syndrome
-
Tsai JC, Grajewski AL. 1994. Cardiac valvular disease and Axenfeld-Rieger syndrome. Am J Ophthalmol 118:255-256.
-
(1994)
Am J Ophthalmol
, vol.118
, pp. 255-256
-
-
Tsai, J.C.1
Grajewski, A.L.2
-
41
-
-
0032522996
-
Cardiac neural crest cells provide new insight into septation of the cardiac outflow tract: Aortic sac to ventricular septal closure
-
Waldo K, Miyagawa-Tomita S, Kumiski D, Kirby ML. 1998. Cardiac neural crest cells provide new insight into septation of the cardiac outflow tract: aortic sac to ventricular septal closure. Dev Biol 196:129-144.
-
(1998)
Dev Biol
, vol.196
, pp. 129-144
-
-
Waldo, K.1
Miyagawa-Tomita, S.2
Kumiski, D.3
Kirby, M.L.4
-
42
-
-
0032489848
-
Formation of the atrioventricular septal structures in the normal mouse
-
Webb S, Brown NA, Anderson RH. 1998. Formation of the atrioventricular septal structures in the normal mouse. Circ Res 82:645-656.
-
(1998)
Circ Res
, vol.82
, pp. 645-656
-
-
Webb, S.1
Brown, N.A.2
Anderson, R.H.3
-
43
-
-
0025029381
-
The fork head domain: A novel DNA binding motif of eukaryotic transcription factors
-
Weigel D, Jackle H. 1990. The fork head domain: a novel DNA binding motif of eukaryotic transcription factors. Cell 63:455-456.
-
(1990)
Cell
, vol.63
, pp. 455-456
-
-
Weigel, D.1
Jackle, H.2
-
44
-
-
0028025566
-
The winged-helix transcription factor HNF-3β is regulated for notochord development in the mouse embryo
-
Weinstein DC, Ruiz i Altaba A, Chen WS, Hoodless P, Prezioso VR, Jessell TM, Darnell Jr JE. 1994. The winged-helix transcription factor HNF-3β is regulated for notochord development in the mouse embryo. Cell 78:575-588.
-
(1994)
Cell
, vol.78
, pp. 575-588
-
-
Weinstein, D.C.1
Ruiz I Altaba, A.2
Chen, W.S.3
Hoodless, P.4
Prezioso, V.R.5
Jessell, T.M.6
Darnell J.E., Jr.7
-
45
-
-
0030991153
-
The winged helix transcription factor MFH1 is required for proliferation and patterning of paraxial mesoderm in the mouse embryo
-
Winnier GE, Hargett L, Hogan BLM. 1997. The winged helix transcription factor MFH1 is required for proliferation and patterning of paraxial mesoderm in the mouse embryo. Genes Dev 11:926-940.
-
(1997)
Genes Dev
, vol.11
, pp. 926-940
-
-
Winnier, G.E.1
Hargett, L.2
Hogan, B.L.M.3
|