-
1
-
-
0028801419
-
Partial deletion of chromosome 6p: Autopsy findings in a premature infant and review of the literature
-
Alashari, M., Chen, E., and Poskanzer, L. (1995). Partial deletion of chromosome 6p: autopsy findings in a premature infant and review of the literature. Pediatr. Pathol. Lab. Med. 15, 941-947.
-
(1995)
Pediatr. Pathol. Lab. Med.
, vol.15
, pp. 941-947
-
-
Alashari, M.1
Chen, E.2
Poskanzer, L.3
-
2
-
-
0028169992
-
HNF-3β is essential for node and notochord formation in mouse development
-
Ang, S.-L., and Rossant, J. (1994). HNF-3β Is Essential for Node and Notochord Formation in Mouse Development. Cell 78, 561-574.
-
(1994)
Cell
, vol.78
, pp. 561-574
-
-
Ang, S.-L.1
Rossant, J.2
-
3
-
-
0027425136
-
The formation and maintenance of the definitive endoderm lineage in the mouse: Involvemeent of HNf3/ forkhead genes
-
Ang, S.-L., Wierda, A., Wong, D., Stevens, K.A., Cascio, S., Rossant, J., and Zaret, K.S. (1993). The formation and maintenance of the definitive endoderm lineage in the mouse: involvemeent of HNF3/ forkhead genes. Development 119, 1301-1315.
-
(1993)
Development
, vol.119
, pp. 1301-1315
-
-
Ang, S.-L.1
Wierda, A.2
Wong, D.3
Stevens, K.A.4
Cascio, S.5
Rossant, J.6
Zaret, K.S.7
-
4
-
-
77049140225
-
Studies on the morphogenesis of the mouse sternum I. Normal embryonic development
-
Chen, J.M. (1952). Studies on the morphogenesis of the mouse sternum I. Normal embryonic development. J. Anat. 86, 373-386.
-
(1952)
J. Anat.
, vol.86
, pp. 373-386
-
-
Chen, J.M.1
-
5
-
-
0030961168
-
Smad4 and FAST-1 in the assembly of activinresponsive factor
-
Chen, X., Weisberg, E., Fridmacher, V., Watanabe, M., Naco, G., and Whitman, M. (1997). Smad4 and FAST-1 in the assembly of activinresponsive 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
-
-
0023265169
-
Ring chromosome 6: Report of a patient and literature review
-
Chitayat, D., Hahm, S.Y., Iqbal, M.A., and Nitowsky, H.M. (1987). Ring chromosome 6: report of a patient and literature review. Am. J. Med. Genet. 26, 145-151.
-
(1987)
Am. J. Med. Genet.
, vol.26
, pp. 145-151
-
-
Chitayat, D.1
Hahm, S.Y.2
Iqbal, M.A.3
Nitowsky, H.M.4
-
7
-
-
0032472365
-
Binding of the winged-helix transcription factor HNF to a linker histone site on the nucleosome
-
Cirillo, L.A., McPherson, C.E., Bossard, P., Stevens, K., Cherian, S., Shim, E.Y., Clark, K.L., Burley, S.K., and Zaret, K.S. (1998). Binding of the winged-helix transcription factor HNF to a linker histone site on the nucleosome. EMBO J. 17, 244-254.
-
(1998)
EMBO J.
, vol.17
, pp. 244-254
-
-
Cirillo, L.A.1
McPherson, C.E.2
Bossard, P.3
Stevens, K.4
Cherian, S.5
Shim, E.Y.6
Clark, K.L.7
Burley, S.K.8
Zaret, K.S.9
-
8
-
-
0027270989
-
Cocrystal structure of the HNF-3/fork head DNA-recognition motif resembles histone H5
-
Clark, K.L., Halay, E.D., Lai, E., and Burley, S.K. (1993). Cocrystal structure of the HNF-3/fork head DNA-recognition motif resembles histone H5. Nature 364, 412-420.
-
(1993)
Nature
, vol.364
, pp. 412-420
-
-
Clark, K.L.1
Halay, E.D.2
Lai, E.3
Burley, S.K.4
-
9
-
-
0030935696
-
TWH regulates the development of subsets of spinal cord neurons
-
Dou, C., Ye, X., Stewart, C., Lai, E., and Li, S. (1997). TWH regulates the development of subsets of spinal cord neurons. Neuron 18, 539-551.
-
(1997)
Neuron
, vol.18
, pp. 539-551
-
-
Dou, C.1
Ye, X.2
Stewart, C.3
Lai, E.4
Li, S.5
-
10
-
-
0028972025
-
15-Deoxy-D12,14-prostaglandin J2 is a ligand for the adipocyte determination factor PPARγ
-
Forman, B.M., Tontonoz, P., Chen, J., Brun, R.P., Spiegelman, B.M., and Evans, R.M. (1995). 15-deoxy-D12,14-prostaglandin J2 is a ligand for the adipocyte determination factor PPARγ. Cell 83, 803-812.
-
(1995)
Cell
, vol.83
, pp. 803-812
-
-
Forman, B.M.1
Tontonoz, P.2
Chen, J.3
Brun, R.P.4
Spiegelman, B.M.5
Evans, R.M.6
-
11
-
-
0030844354
-
Bone morphogenetic proteins as regulators of differentiation and morphogenesis during dorsal forebrain development
-
Furuta, Y., Piston, D.W., and Hogan, B.L.M. (1997). Bone morphogenetic proteins as regulators of differentiation and morphogenesis during dorsal forebrain development. Development 124, 2203-2212.
-
(1997)
Development
, vol.124
, pp. 2203-2212
-
-
Furuta, Y.1
Piston, D.W.2
Hogan, B.L.M.3
-
12
-
-
0030800598
-
Autosomal dominant Axenfeld-Rieger anomaly maps to 6p25
-
Gould, D.B., Mears, A.J., Pearce, W.G., and Walter, M.A. (1997). Autosomal dominant Axenfeld-Rieger anomaly maps to 6p25. Am. J. Hum. Genet. 61, 765-768.
-
(1997)
Am. J. Hum. Genet.
, vol.61
, pp. 765-768
-
-
Gould, D.B.1
Mears, A.J.2
Pearce, W.G.3
Walter, M.A.4
-
13
-
-
0014913510
-
The developmental effects of congenital hydrocephalus (ch) in the mouse
-
Green, M. (1970). The developmental effects of congenital hydrocephalus (ch) in the mouse. Dev. Biol. 23, 585-608.
-
(1970)
Dev. Biol.
, vol.23
, pp. 585-608
-
-
Green, M.1
-
14
-
-
0003290037
-
Congenital hydrocephalus in the mouse, a case of spurious pleitropism
-
Gruneberg, H. (1943). Congenital hydrocephalus in the mouse, a case of spurious pleitropism. J. Genet. 45, 1-21.
-
(1943)
J. Genet.
, vol.45
, pp. 1-21
-
-
Gruneberg, H.1
-
15
-
-
0007676001
-
Genetical studies on the skeleton of the mouse VII
-
Gruneberg, H. (1953). Genetical studies on the skeleton of the mouse VII. Congenital hydrocephalus. J. Genet. 51, 327-358.
-
(1953)
Congenital Hydrocephalus. J. Genet.
, vol.51
, pp. 327-358
-
-
Gruneberg, H.1
-
16
-
-
0015049435
-
Exocrine glands and the Chievitz organ of some mouse mutants
-
Gruneberg, H. (1971). Exocrine glands and the Chievitz organ of some mouse mutants. J. Embryol. Exp. Morph. 25, 247-261.
-
(1971)
J. Embryol. Exp. Morph.
, vol.25
, pp. 247-261
-
-
Gruneberg, H.1
-
17
-
-
0015944912
-
A re-examination of two skeletal mutants of the mouse, vestigial-tail (vt) and congenital hydrocephalus (ch)
-
Gruneberg, H., and Wickramaratne, G.A.D.S. (1974). A re-examination of two skeletal mutants of the mouse, vestigial-tail (vt) and congenital hydrocephalus (ch). J. Embrol. Exp. Morph. 31, 207-222.
-
(1974)
J. Embrol. Exp. Morph.
, vol.31
, pp. 207-222
-
-
Gruneberg, H.1
Wickramaratne, G.A.D.S.2
-
18
-
-
0029767664
-
Hepatic specification of the gut endoderm in vitro: Cell signaling and transcriptional control
-
Gualdi, R., Bossard, P., Zheng, M., Hamada, Y., Coleman, J.R., and Zaret, K.S. (1996). Hepatic specification of the gut endoderm in vitro: cell signaling and transcriptional control. Genes Dev. 10, 1670-1682.
-
(1996)
Genes Dev.
, vol.10
, pp. 1670-1682
-
-
Gualdi, R.1
Bossard, P.2
Zheng, M.3
Hamada, Y.4
Coleman, J.R.5
Zaret, K.S.6
-
19
-
-
0029741093
-
Essential role of stromal mesenchyme in kidney morphogenesis revealed by targeted disruption of Winged helix transcription factor BF-2
-
Hatini, V., Huh, S.O., Herzlinger, D., Soares, V.C., and Lai, E. (1996). Essential role of stromal mesenchyme in kidney morphogenesis revealed by targeted disruption of Winged helix transcription factor BF-2. Genes Dev. 10, 1467-1478.
-
(1996)
Genes Dev.
, vol.10
, pp. 1467-1478
-
-
Hatini, V.1
Huh, S.O.2
Herzlinger, D.3
Soares, V.C.4
Lai, E.5
-
20
-
-
0029861447
-
Developmental expression of murine β-trace in embryos and adult animals suggests a function in maturation and maintenance of blood-tissue barriers
-
Hoffmann, A., Bachner, D., Betat, N., Lauber, J., and Gross, G. (1996). Developmental expression of murine β-trace in embryos and adult animals suggests a function in maturation and maintenance of blood-tissue barriers. Dev. Dyn. 207, 332-343.
-
(1996)
Dev. Dyn.
, vol.207
, pp. 332-343
-
-
Hoffmann, A.1
Bachner, D.2
Betat, N.3
Lauber, J.4
Gross, G.5
-
21
-
-
0003799070
-
-
(Cold Spring Harbor, NY: Cold Spring Harbor Press)
-
Hogan, B., Beddington, R., Costantini, F., and Lacy E. (1994). Manipulating the Mouse Embryo: A Laboratory Manual (Cold Spring Harbor, NY: Cold Spring Harbor Press).
-
(1994)
Manipulating the Mouse Embryo: A Laboratory Manual
-
-
Hogan, B.1
Beddington, R.2
Costantini, F.3
Lacy, E.4
-
22
-
-
4243459140
-
Molecular genetics of hydrocephalus: Fine-structure mapping of the congenital hydrocephalus (ch) mouse mutation
-
Hong, H.-K., and Chakravarti, A. (1995). Molecular genetics of hydrocephalus: fine-structure mapping of the congenital hydrocephalus (ch) mouse mutation. Am. J. Hum. Genet. 57, A134.
-
(1995)
Am. J. Hum. Genet.
, vol.57
-
-
Hong, H.-K.1
Chakravarti, A.2
-
23
-
-
0030940213
-
The fate of the first avian somite
-
Huang, R., Zhi, Q., Ordahl, C.P., and Christ, B. (1997). The fate of the first avian somite. Anat. Embryol. 195, 435-449.
-
(1997)
Anat. Embryol.
, vol.195
, pp. 435-449
-
-
Huang, R.1
Zhi, Q.2
Ordahl, C.P.3
Christ, B.4
-
24
-
-
0030696897
-
Essential roles of the winged helix transcription factor MFH-1 in aortic patterning and skeletogenesis
-
Iida, K., Koseki, H., Kakinuma, H., Kato, N., Mizutani-Koseki, Y., Ohuchi, H., Yoshioka, H., Noji, S., Kawamura, K., Kataoka, Y., et al. (1997). Essential roles of the winged helix transcription factor MFH-1 in aortic 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
Ohuchi, H.6
Yoshioka, H.7
Noji, S.8
Kawamura, K.9
Kataoka, Y.10
-
25
-
-
0030870983
-
Familial glaucoma iridogoniodysplasia maps to a 6p25 region implicated in primary congenital glaucoma and iridogoniodysgenesis anomaly
-
Jordan, T., Ebenezer, N., Manners, R., McGill, J., and Bhattacharya, S. (1997). Familial glaucoma iridogoniodysplasia maps to a 6p25 region implicated in primary congenital glaucoma and iridogoniodysgenesis anomaly. Am. J. Hum. Genet. 61, 882-888.
-
(1997)
Am. J. Hum. Genet.
, vol.61
, pp. 882-888
-
-
Jordan, T.1
Ebenezer, N.2
Manners, R.3
McGill, J.4
Bhattacharya, S.5
-
26
-
-
0029999782
-
Clustered arrangement of winged helix genes fkh-6 and MFH-1: Possible implications for mesoderm development
-
Kaestner, K.H., Bleckman, S.C., Monaghan, A.P., Schlondorff, J., Micheva, A., Lichter, P., and Schutz, G. (1996). Clustered arrangement of winged helix genes fkh-6 and MFH-1: possible implications for mesoderm development. Development 122, 1751-1758.
-
(1996)
Development
, vol.122
, pp. 1751-1758
-
-
Kaestner, K.H.1
Bleckman, S.C.2
Monaghan, A.P.3
Schlondorff, J.4
Micheva, A.5
Lichter, P.6
Schutz, G.7
-
27
-
-
0030907001
-
The mesenchymal winged helix transcription factor Fkh6 is required for the control of gastrointestional proliferation and differentiation
-
Kaestner, K., Silberg, D., Traber, P., and Schutz, G. (1997). The mesenchymal winged helix transcription factor Fkh6 is required for the control of gastrointestional proliferation and differentiation. Genes Dev. 11, 1583-1595.
-
(1997)
Genes Dev.
, vol.11
, pp. 1583-1595
-
-
Kaestner, K.1
Silberg, D.2
Traber, P.3
Schutz, G.4
-
28
-
-
17344379513
-
Five years on the wings of fork head
-
Kaufmann, E., and 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
-
29
-
-
0024418401
-
Tandem Y/6 translocation with partial deletion 6 (p23-pter)
-
Kelly, P.C., Blake, W.W., and Davis, J.R. (1989). Tandem Y/6 translocation with partial deletion 6 (p23-pter). Clin. Genet. 36, 204-207.
-
(1989)
Clin. Genet.
, vol.36
, pp. 204-207
-
-
Kelly, P.C.1
Blake, W.W.2
Davis, J.R.3
-
30
-
-
0026440993
-
The mouse short ear skeletal morphogenesis locus is associated with defects in a bone morphogenetic member of the TGFβ superfamily
-
Kingsley, D.M., Bland, A.E., Grubber, J.M., Marker, P.C., Russell, L.B., Copeland, N.G., and Jenkins, N.A. (1992). The mouse short ear skeletal morphogenesis locus is associated with defects in a bone morphogenetic member of the TGFβ superfamily. Cell 71, 399-410.
-
(1992)
Cell
, vol.71
, pp. 399-410
-
-
Kingsley, D.M.1
Bland, A.E.2
Grubber, J.M.3
Marker, P.C.4
Russell, L.B.5
Copeland, N.G.6
Jenkins, N.A.7
-
31
-
-
0028972026
-
A prostaglandin J2 metabolite binds peroxisome proliferator-activated receptor and promotes adipocyte differentiation
-
Kliewer, S.A., Lenhard, J.M., Willson, T.M., Patel, I., Morris, D.C., and Lehmann, J.M. (1995). A prostaglandin J2 metabolite binds peroxisome proliferator-activated receptor and promotes adipocyte differentiation. Cell 83, 813-819.
-
(1995)
Cell
, vol.83
, pp. 813-819
-
-
Kliewer, S.A.1
Lenhard, J.M.2
Willson, T.M.3
Patel, I.4
Morris, D.C.5
Lehmann, J.M.6
-
32
-
-
0030000906
-
The chromosomal mapping of four genes encoding winged helix proteins expressed early in mouse development
-
Labosky, P.A., Winnier, G.E., Sasaki, H., Blessing, M., and Hogan, B.L.M. (1996). The chromosomal mapping of four genes encoding winged helix proteins expressed early in mouse development. Genomics 34, 241-245.
-
(1996)
Genomics
, vol.34
, pp. 241-245
-
-
Labosky, P.A.1
Winnier, G.E.2
Sasaki, H.3
Blessing, M.4
Hogan, B.L.M.5
-
33
-
-
0030972375
-
The winged helix gene, Mf3, is required for normal development of the diencephalon and midbrain, postnatal growth and milk-ejection reflex
-
Labosky, P.A., Winnier, G.E., Jetton, T.L., Hargett, L., Ryan, A.K., Rosenfeld, M.G., Parlow, A.F., and Hogan, B.L.M. (1997). The winged helix gene, Mf3, is required for normal development of the diencephalon and midbrain, postnatal growth and milk-ejection reflex. Development 124, 1263-1274.
-
(1997)
Development
, vol.124
, pp. 1263-1274
-
-
Labosky, P.A.1
Winnier, G.E.2
Jetton, T.L.3
Hargett, L.4
Ryan, A.K.5
Rosenfeld, M.G.6
Parlow, A.F.7
Hogan, B.L.M.8
-
34
-
-
0029572447
-
Chromosomal localization of six human forkhead genes, freac-1 (FKHL5), -3 (FKHL7), -4 (FKHL8), -5 (FKHL9), -6 (FKHL10) and -8 (FKHL12)
-
Larsson, C., Hellqvist, M., Pierrou, S., White, I., Enerback, S., and Carlsson, P. (1995). Chromosomal localization of six human forkhead genes, freac-1 (FKHL5), -3 (FKHL7), -4 (FKHL8), -5 (FKHL9), -6 (FKHL10) and -8 (FKHL12). Genomics 10, 464-469.
-
(1995)
Genomics
, vol.10
, pp. 464-469
-
-
Larsson, C.1
Hellqvist, M.2
Pierrou, S.3
White, I.4
Enerback, S.5
Carlsson, P.6
-
35
-
-
0028960753
-
Colocalization of BMP 7 and BMP 2 RNAs suggest that these factors cooperatively mediate tissue interactions during murine development
-
Lyons, K.M., Hogan, B.L.M., and Robertson, E.J. (1995). Colocalization of BMP 7 and BMP 2 RNAs suggest that these factors cooperatively mediate tissue interactions during murine development. Mech. Dev. 50, 71-83.
-
(1995)
Mech. Dev.
, vol.50
, pp. 71-83
-
-
Lyons, K.M.1
Hogan, B.L.M.2
Robertson, E.J.3
-
36
-
-
0016662831
-
Developmental morphology of the subarachnoid space and contiguous structures in the mouse
-
McLone, D.G., and Bondareff, W. (1975). Developmental morphology of the subarachnoid space and contiguous structures in the mouse. Am. J. Anat. 142, 273-294.
-
(1975)
Am. J. Anat.
, vol.142
, pp. 273-294
-
-
McLone, D.G.1
Bondareff, W.2
-
37
-
-
0027507894
-
An active tissue-specific enhancer and bound transcription factors existing in a precisely positioned nucleosomal array
-
McPherson, C.E., Shim, E.-Y., Friedman, D.S., and Zaret, K.S. (1993). An active tissue-specific enhancer and bound transcription factors existing in a precisely positioned nucleosomal array. Cell 75, 387-398.
-
(1993)
Cell
, vol.75
, pp. 387-398
-
-
McPherson, C.E.1
Shim, E.-Y.2
Friedman, D.S.3
Zaret, K.S.4
-
38
-
-
0029807866
-
Autosomal dominant iridogoniodysgenesis anomaly maps to 6p25
-
Mears, A.J., Mirzayans, F., Gould, D.B., Pearce, W.G., and Walter, M.A. (1996). Autosomal dominant iridogoniodysgenesis anomaly maps to 6p25. Am. J. Hum. Genet. 59, 1321-1327.
-
(1996)
Am. J. Hum. Genet.
, vol.59
, pp. 1321-1327
-
-
Mears, A.J.1
Mirzayans, F.2
Gould, D.B.3
Pearce, W.G.4
Walter, M.A.5
-
39
-
-
0029551439
-
Divide, accumulate, differentiate: Cell condensation in skeletal development revisited
-
Miyake, T., and Hall, B.K. (1995). Divide, accumulate, differentiate: cell condensation in skeletal development revisited. Int. J. Dev. Biol. 39, 881-893.
-
(1995)
Int. J. Dev. Biol.
, vol.39
, pp. 881-893
-
-
Miyake, T.1
Hall, B.K.2
-
40
-
-
0028000121
-
New member of the winged-helix protein family disrupted in mouse and rat nude mutations
-
Nehls, M., Pfeifer, D., Schropp, M., Hedrich, H., and Boehm, T. (1994). New member of the winged-helix protein family disrupted in mouse and rat nude mutations. Nature 372, 103-107.
-
(1994)
Nature
, vol.372
, pp. 103-107
-
-
Nehls, M.1
Pfeifer, D.2
Schropp, M.3
Hedrich, H.4
Boehm, T.5
-
41
-
-
0023811391
-
Interactions and fates of avian craniofacial mesenchyme
-
Noden, D.M. (1988). Interactions and fates of avian craniofacial mesenchyme. Dev. Suppl. 103, 121-140.
-
(1988)
Dev. Suppl.
, vol.103
, pp. 121-140
-
-
Noden, D.M.1
-
42
-
-
0021154002
-
Ultrastructure of the mouse leptomeninx
-
Oda, Y., and Nakanishi, I. (1984). Ultrastructure of the mouse leptomeninx. J. Comp. Neurol. 225, 448-457.
-
(1984)
J. Comp. Neurol.
, vol.225
, pp. 448-457
-
-
Oda, Y.1
Nakanishi, I.2
-
43
-
-
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., and 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
-
44
-
-
0029821431
-
Cultured leptomeningeal cells secrete cerebrospinal fluid proteins
-
Ohe, Y., Ishikawa, K., Itoh, Z., and Tatemoto, K. (1996). Cultured leptomeningeal cells secrete cerebrospinal fluid proteins. J. Neurochem. 67, 964-971.
-
(1996)
J. Neurochem.
, vol.67
, pp. 964-971
-
-
Ohe, Y.1
Ishikawa, K.2
Itoh, Z.3
Tatemoto, K.4
-
45
-
-
0028046675
-
Cloning and charcterization of seven human forkhead proteins: Binding site specificity and DNA bending
-
Pierrou, S., Hellqvist, M., Samuelsson, L., Enerback, S., and Carlsson, P. (1994). Cloning and charcterization 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
-
46
-
-
0028920898
-
Analysis of heptocyte nuclear factor-3β protein domains required for transcriptional activation and nuclear targeting
-
Qian, X., and Costa, R.H. (1995). Analysis of heptocyte nuclear factor-3β protein domains required for transcriptional activation and nuclear targeting. Nucleic Acids Res. 23, 1184-1191.
-
(1995)
Nucleic Acids Res.
, vol.23
, pp. 1184-1191
-
-
Qian, X.1
Costa, R.H.2
-
47
-
-
0027318791
-
Differential expression of multiple fork head related genes during gastrulation and axial pattern formation in the mouse embryo
-
Sasaki, H., and Hogan, B.L.M. (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
-
48
-
-
10544233785
-
Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in rieger syndrome
-
Semina, E.V., Reiter, R., Leysens, N.J., Alward, W.L.M., Small, K.W., Datson, N.A., Siegel-Bartelt, J., Bierke-Nelson, D., Bitoun, P., Zabel, B.U., et al. (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.M.4
Small, K.W.5
Datson, N.A.6
Siegel-Bartelt, J.7
Bierke-Nelson, D.8
Bitoun, P.9
Zabel, B.U.10
-
49
-
-
0031803414
-
Mice lacking BMP6 function
-
in press
-
Solloway, M.J., Dudley, A.T., Bikoff, E.K., Lyons, K.M., Hogan, B.L.M., and Robertson, E.J. (1998). Mice lacking BMP6 function. Dev. Genet., in press.
-
(1998)
Dev. Genet.
-
-
Solloway, M.J.1
Dudley, A.T.2
Bikoff, E.K.3
Lyons, K.M.4
Hogan, B.L.M.5
Robertson, E.J.6
-
50
-
-
0030824599
-
Somatic linker histones cause loss of mesodermal competence in Xenopus
-
Steinbach, O.C., Wolffe, A.P., and Rupp, R.A.W. (1997). Somatic linker histones cause loss of mesodermal competence in Xenopus. Nature 389, 395-398.
-
(1997)
Nature
, vol.389
, pp. 395-398
-
-
Steinbach, O.C.1
Wolffe, A.P.2
Rupp, R.A.W.3
-
51
-
-
0030481707
-
Joint patterning defects caused by single and double mutations in members of the bone morphogenetic protein (BMP) family
-
Storm, E.E., and Kingsley, D.M. (1996). Joint patterning defects caused by single and double mutations in members of the bone morphogenetic protein (BMP) family. Development 122, 3969-3979.
-
(1996)
Development
, vol.122
, pp. 3969-3979
-
-
Storm, E.E.1
Kingsley, D.M.2
-
52
-
-
0028232724
-
Limb alterations in brachypodism mice due to mutations in a new member of the TGFβ-superfamily
-
Storm, E.E., Huynh, T.V., Copeland, N.G., Jenkins, N.A., Kingsley, D.M., and Lee, S.-J. (1994). Limb alterations in brachypodism mice due to mutations in a new member of the TGFβ-superfamily. Nature 368, 639-643.
-
(1994)
Nature
, vol.368
, pp. 639-643
-
-
Storm, E.E.1
Huynh, T.V.2
Copeland, N.G.3
Jenkins, N.A.4
Kingsley, D.M.5
Lee, S.-J.6
-
53
-
-
0030953217
-
Lipocalin-type prostaglandin D synthase (β-trace) is a newly recognized type of retinoid transporter
-
Tanaka, T., Urade, Y., Kimura, H., Eguchi, N., Nishikawa, A., and Hayaishi, O. (1997). Lipocalin-type prostaglandin D synthase (β-trace) is a newly recognized type of retinoid transporter. J. Biol. Chem. 272, 15789-15795.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 15789-15795
-
-
Tanaka, T.1
Urade, Y.2
Kimura, H.3
Eguchi, N.4
Nishikawa, A.5
Hayaishi, O.6
-
54
-
-
0010512261
-
Deletion 6(p25.1) in a child with mild dysmorphic features and absence of major eye malformations: Implications for the localization of genes involved in ocular development
-
Tepperberg, J.H., Rao, K.W., Albright, S.G., Kaiser-Rogers, K., and Powell, C.M. (1994). Deletion 6(p25.1) in a child with mild dysmorphic features and absence of major eye malformations: implications for the localization of genes involved in ocular development. Am. J. Hum. Genet. 55, Supplement A119.
-
(1994)
Am. J. Hum. Genet.
, vol.55
, Issue.SUPPL. A119
-
-
Tepperberg, J.H.1
Rao, K.W.2
Albright, S.G.3
Kaiser-Rogers, K.4
Powell, C.M.5
-
55
-
-
0009938051
-
Neural tube defects and other congenital malformations of the central nervous system
-
D.L. Rimoin, J.M. Connor, and R.E. Pyeritz, eds. (New York: Churchill Livingstone)
-
Tolmie, J. (1997). Neural tube defects and other congenital malformations of the central nervous system. In Emery and Rimoin's Principles and Practice of Medical Genetics, D.L. Rimoin, J.M. Connor, and R.E. Pyeritz, eds. (New York: Churchill Livingstone), pp. 2145-2176.
-
(1997)
Emery and Rimoin's Principles and Practice of Medical Genetics
, pp. 2145-2176
-
-
Tolmie, J.1
-
56
-
-
0029852490
-
Autosomal-dominant iridogoniodysgenesis and Axenfeld-Rieger syndrome are genetically distinct
-
Walter, M.A., Mirzayans, F., Mears, A.J., Hickey, K., and Pearce, W.G. (1996). Autosomal-dominant iridogoniodysgenesis and Axenfeld-Rieger syndrome are genetically distinct. Opthalmology 103, 1907-1915.
-
(1996)
Opthalmology
, vol.103
, pp. 1907-1915
-
-
Walter, M.A.1
Mirzayans, F.2
Mears, A.J.3
Hickey, K.4
Pearce, W.G.5
-
57
-
-
0024973841
-
The homeotic gene fork head encodes a nuclear protein and is expressed in the terminal regions of the Drosophila embryo
-
Weigel, D., Jurgens, G., Kuttner, F., Seifert, E., and Jackle, H. (1989). The homeotic gene fork head encodes a nuclear protein and is expressed in the terminal regions of the Drosophila embryo. Cell 57, 645-658.
-
(1989)
Cell
, vol.57
, pp. 645-658
-
-
Weigel, D.1
Jurgens, G.2
Kuttner, F.3
Seifert, E.4
Jackle, H.5
-
58
-
-
0028025566
-
The winged-helix transcription factor HNF-3β is required for notochord development in the mouse embryo
-
Weinstein, D.C., Altaba, A.R.i., Chen, W.S., Hoodless, P., Preziosos, V.R., Jessell, T.M., and Darnell, J.E., Jr. (1994). The winged-helix transcription factor HNF-3β is required for notochord development in the mouse embryo. Cell 78, 575-588.
-
(1994)
Cell
, vol.78
, pp. 575-588
-
-
Weinstein, D.C.1
Altaba, A.R.I.2
Chen, W.S.3
Hoodless, P.4
Preziosos, V.R.5
Jessell, T.M.6
Darnell, J.E.7
-
59
-
-
0030991153
-
The winged helix transcription factor, MFH1, is required for proliferation and patterning of the paraxial mesoderm in the mouse embryo
-
Winnier, G.E., Hargett, L., and Hogan, B.L.M. (1997). The winged helix transcription factor, MFH1, is required for proliferation and patterning of the 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
-
60
-
-
0031906176
-
Mouse mesenchyme forkhead 2 (Mf2): Expression, DNA binding and induction by sonic hedgehog during somitogenesis
-
Wu, S.C.-Y., Grindley, J., Winnier, G.E., Hargett, L., and Hogan, B.L.M. (1998). Mouse mesenchyme forkhead 2 (Mf2): expression, DNA binding and induction by sonic hedgehog during somitogenesis. Mech. Dev. 70, 3-13.
-
(1998)
Mech. Dev.
, vol.70
, pp. 3-13
-
-
Wu, S.C.-Y.1
Grindley, J.2
Winnier, G.E.3
Hargett, L.4
Hogan, B.L.M.5
-
61
-
-
0029009621
-
Winged helix transcription factor BF-1 is essential for the development of the cerebral hemispheres
-
Xuan, S., Baptista, C.A., Balas, G., Tao, W., Soares, V.C., and Lai, E. (1995). Winged helix transcription factor BF-1 is essential for the development of the cerebral hemispheres. Neuron 14, 1141-1152.
-
(1995)
Neuron
, vol.14
, pp. 1141-1152
-
-
Xuan, S.1
Baptista, C.A.2
Balas, G.3
Tao, W.4
Soares, V.C.5
Lai, E.6
-
62
-
-
0025058418
-
Distal deletion of the short arm of chromosome
-
Zurcher, V.L., Golden, W.L., and Zinn, A.B. (1990). Distal deletion of the short arm of chromosome. Am. J. Med. Genet. 6, 261-265.
-
(1990)
Am. J. Med. Genet.
, vol.6
, pp. 261-265
-
-
Zurcher, V.L.1
Golden, W.L.2
Zinn, A.B.3
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