-
1
-
-
0036021289
-
Trisomy 4q syndrome: presentation of a new case and review of the literature
-
Lundin, C., Zech, L., Sjörs, K., Wadelius, C. and Annerén, G. (2002) Trisomy 4q syndrome: presentation of a new case and review of the literature. Ann. Genet., 45, 53-57.
-
(2002)
Ann. Genet.
, vol.45
, pp. 53-57
-
-
Lundin, C.1
Zech, L.2
Sjörs, K.3
Wadelius, C.4
Annerén, G.5
-
2
-
-
0037487191
-
Cytogenetic and molecular characterization of a de novo 4q24qter duplication and correlation to the associated phenotype
-
Rinaldi, R., De Bernardo, C., Assumma, M., Grammatico, B., Buffone, E., Poscente, M. and Grammatico, P. (2003) Cytogenetic and molecular characterization of a de novo 4q24qter duplication and correlation to the associated phenotype. Am. J. Med. Genet. A., 118A, 122-126.
-
(2003)
Am. J. Med. Genet. A.
, vol.118 A
, pp. 122-126
-
-
Rinaldi, R.1
De Bernardo, C.2
Assumma, M.3
Grammatico, B.4
Buffone, E.5
Poscente, M.6
Grammatico, P.7
-
3
-
-
16344365687
-
Duplication of chromosome 4q: renal pathology of two siblings
-
Otsuka, T., Fujinaka, H., Imamura, M., Tanaka, Y., Hayakawa, H. and Tomizawa, S. (2005) Duplication of chromosome 4q: renal pathology of two siblings. Am. J. Med. Genet. A., 134A, 330-333.
-
(2005)
Am. J. Med. Genet. A.
, vol.134 A
, pp. 330-333
-
-
Otsuka, T.1
Fujinaka, H.2
Imamura, M.3
Tanaka, Y.4
Hayakawa, H.5
Tomizawa, S.6
-
4
-
-
16344395194
-
Karyotype/ phenotype correlations in duplication 4q: evidence for a critical region within 4q27-28 for preaxial defects
-
Battaglia, A., Chen, Z., Brothman, A.R., Morelli, S., Palumbos, J.C., Carey, J.C., Hudgins, L. and Disteche, C. (2005) Karyotype/ phenotype correlations in duplication 4q: evidence for a critical region within 4q27-28 for preaxial defects. Am. J. Med. Genet. A., 134A, 334-337.
-
(2005)
Am. J. Med. Genet. A.
, vol.134 A
, pp. 334-337
-
-
Battaglia, A.1
Chen, Z.2
Brothman, A.R.3
Morelli, S.4
Palumbos, J.C.5
Carey, J.C.6
Hudgins, L.7
Disteche, C.8
-
5
-
-
25644460076
-
Partial trisomy 4q and preaxial limb defects
-
Lurie, I.W. (2005) Partial trisomy 4q and preaxial limb defects. Am. J. Med. Genet. A., 138A, 304-305.
-
(2005)
Am. J. Med. Genet. A.
, vol.138 A
, pp. 304-305
-
-
Lurie, I.W.1
-
6
-
-
0016856980
-
Phenotypic variation in partial trisomy 4q
-
Vogel, W., Siebers, J.W. and Gunkel, J. (1975) Phenotypic variation in partial trisomy 4q. Humangenetik, 28, 103-112.
-
(1975)
Humangenetik
, vol.28
, pp. 103-112
-
-
Vogel, W.1
Siebers, J.W.2
Gunkel, J.3
-
7
-
-
0017681828
-
Partial trisomy 4q
-
Yunis, E., Giraldo, A., Zuniga, R., Egel, H. and Ramirez, E. (1977) Partial trisomy 4q. Ann. Genet., 20, 243-248.
-
(1977)
Ann. Genet.
, vol.20
, pp. 243-248
-
-
Yunis, E.1
Giraldo, A.2
Zuniga, R.3
Egel, H.4
Ramirez, E.5
-
8
-
-
0018879212
-
Partial duplication of the long arm of chromosome 4
-
Fryns, J.P. and van den Berghe, H. (1980) Partial duplication of the long arm of chromosome 4. Ann. Genet., 23, 52-53.
-
(1980)
Ann. Genet.
, vol.23
, pp. 52-53
-
-
Fryns, J.P.1
Den Berghe, V.H.2
-
9
-
-
0027453083
-
Cytogenetic and molecular identification of a de novo direct duplication of the long arm of chromosome 4(q21.3-q31.3)
-
Jeziorowska, A., Ciesla, W., Houck, G.E. Jr, Yao, X.L., Harris, M.S., Truszczak, B., Skorski, M., Jakubowski, L., Jenkins, E.C. and Kaluzewski, B. (1993) Cytogenetic and molecular identification of a de novo direct duplication of the long arm of chromosome 4(q21.3-q31.3). Am. J. Med. Genet., 46, 83-87.
-
(1993)
Am. J. Med. Genet.
, vol.46
, pp. 83-87
-
-
Jeziorowska, A.1
Ciesla, W.2
Houck Jr., G.E.3
Yao, X.L.4
Harris, M.S.5
Truszczak, B.6
Skorski, M.7
Jakubowski, L.8
Jenkins, E.C.9
Kaluzewski, B.10
-
10
-
-
0033836156
-
Duplication of chromosome region 4q28.3-qter in monozygotic twins with discordant phenotypes.
-
Celle, L., Lee, L., Rintoul, N., Savani, R.C., Long, W., Mennuti, M.T. and Krantz, I.D. (2000) Duplication of chromosome region 4q28.3-qter in monozygotic twins with discordant phenotypes. Am. J. Med. Genet., 94, 125-140.
-
(2000)
Am. J. Med. Genet.
, vol.94
, pp. 125-140
-
-
Celle, L.1
Lee, L.2
Rintoul, N.3
Savani, R.C.4
Long, W.5
Mennuti, M.T.6
Krantz, I.D.7
-
11
-
-
33748266871
-
Partial trisomy of long arm of chromosome 4 as a result of dir dup (4)(q27q31.3) de novo
-
Hubert, E., Sawicka, A., Wasilewska, E. and Midro, A.T. (2006) Partial trisomy of long arm of chromosome 4 as a result of dir dup (4)(q27q31.3) de novo. Genet. Couns., 17, 211-218.
-
(2006)
Genet. Couns.
, vol.17
, pp. 211-218
-
-
Hubert, E.1
Sawicka, A.2
Wasilewska, E.3
Midro, A.T.4
-
12
-
-
1242330479
-
Behavioral characterization of mouse models for Smith-Magenis syndrome and dup (17)(p11.2p11.2)
-
Walz, K., Spencer, C., Kaasik, K., Lee, C.C., Lupski, J.R. and Paylor, R. (2004) Behavioral characterization of mouse models for Smith-Magenis syndrome and dup(17)(p11.2p11.2). Hum. Mol. Genet., 13, 367-378.
-
(2004)
Hum. Mol. Genet.
, vol.13
, pp. 367-378
-
-
Walz, K.1
Spencer, C.2
Kaasik, K.3
Lee, C.C.4
Lupski, J.R.5
Paylor, R.6
-
13
-
-
7444231620
-
A chromosome 21 critical region does not cause specific Down syndrome phenotypes
-
Olson, L.E., Richtsmeier, J.T., Leszl, J. and Reeves, R.H. (2004) A chromosome 21 critical region does not cause specific Down syndrome phenotypes. Science, 306, 687-690.
-
(2004)
Science
, vol.306
, pp. 687-690
-
-
Olson, L.E.1
Richtsmeier, J.T.2
Leszl, J.3
Reeves, R.H.4
-
14
-
-
25444442381
-
An aneuploid mouse strain carrying human chromosome 21 with Down syndrome phenotypes
-
O'Doherty, A., Ruf, S., Mulligan, C., Hildreth, V., Errington, M.L., Cooke, S., Sesay, A., Modino, S., Vanes, L., Hernandez, D. et al. (2005) An aneuploid mouse strain carrying human chromosome 21 with Down syndrome phenotypes. Science, 309, 2033-2037.
-
(2005)
Science
, vol.309
, pp. 2033-2037
-
-
O'doherty, A.1
Ruf, S.2
Mulligan, C.3
Hildreth, V.4
Errington, M.L.5
Cooke, S.6
Sesay, A.7
Modino, S.8
Vanes, L.9
Hernandez, D.10
-
15
-
-
67549083336
-
Abnormal behavior in a chromosome-engineered mouse model for human 15q11-13 duplication seen in autism
-
Nakatani, J., Tamada, K., Hatanaka, F., Ise, S., Ohta, H., Inoue, K., Tomonaga, S., Watanabe, Y., Chung, Y.J., Banerjee, R. et al. (2009) Abnormal behavior in a chromosome-engineered mouse model for human 15q11-13 duplication seen in autism. Cell, 137, 1235-1246.
-
(2009)
Cell
, vol.137
, pp. 1235-1246
-
-
Nakatani, J.1
Tamada, K.2
Hatanaka, F.3
Ise, S.4
Ohta, H.5
Inoue, K.6
Tomonaga, S.7
Watanabe, Y.8
Chung, Y.J.9
Banerjee, R.10
-
16
-
-
0029117749
-
A duplicated zone of polarizing activity in polydactylous mouse mutants
-
Masuya, H., Sagai, T., Wakana, S., Moriwaki, K. and Shiroishi, T. (1995) A duplicated zone of polarizing activity in polydactylous mouse mutants. Genes. Dev., 9, 1645-1653.
-
(1995)
Genes. Dev.
, vol.9
, pp. 1645-1653
-
-
Masuya, H.1
Sagai, T.2
Wakana, S.3
Moriwaki, K.4
Shiroishi, T.5
-
17
-
-
0030903857
-
Regulation of cardiac mesodermal and neural crest development by the bHLH transcription factor, dHAND
-
Srivastava, D., Thomas, T., Lin, Q., Kirby, M.L., Brown, D. and Olson, E.N. (1997) Regulation of cardiac mesodermal and neural crest development by the bHLH transcription factor, dHAND. Nat. Genet., 16, 154-160.
-
(1997)
Nat. Genet.
, vol.16
, pp. 154-160
-
-
Srivastava, D.1
Thomas, T.2
Lin, Q.3
Kirby, M.L.4
Brown, D.5
Olson, E.N.6
-
18
-
-
0036340168
-
Misexpression of dHAND induces ectopic digits in the developing limb bud in the absence of direct DNA binding
-
McFadden, D.G., McAnally, J., Richardson, J.A., Charite, J. and Olson, E.N. (2002) Misexpression of dHAND induces ectopic digits in the developing limb bud in the absence of direct DNA binding. Development, 129, 3077-3088.
-
(2002)
Development
, vol.129
, pp. 3077-3088
-
-
Mcfadden, D.G.1
Mcanally, J.2
Richardson, J.A.3
Charite, J.4
Olson, E.N.5
-
19
-
-
40449090767
-
Mouse inter-subspecific consomic strains for genetic dissection of quantitative complex traits
-
Takada, T., Mita, A., Maeno, A., Sakai, T., Shitara, H., Kikkawa, Y., Moriwaki, K., Yonekawa, H. and Shiroishi, T. (2008) Mouse inter-subspecific consomic strains for genetic dissection of quantitative complex traits. Genome Res., 18, 500-508.
-
(2008)
Genome Res.
, vol.18
, pp. 500-508
-
-
Takada, T.1
Mita, A.2
Maeno, A.3
Sakai, T.4
Shitara, H.5
Kikkawa, Y.6
Moriwaki, K.7
Yonekawa, H.8
Shiroishi, T.9
-
20
-
-
16844376635
-
Altered Twist1 and Hand2 dimerization is associated with Saethre-Chotzen syndrome and limb abnormalities
-
Firulli, B.A., Krawchuk, D., Centonze, V.E., Vargesson, N., Virshup, D.M., Conway, S.J., Cserjesi, P., Laufer, E. and Firulli, A.B. (2005) Altered Twist1 and Hand2 dimerization is associated with Saethre-Chotzen syndrome and limb abnormalities. Nat. Genet., 37, 373-381.
-
(2005)
Nat. Genet.
, vol.37
, pp. 373-381
-
-
Firulli, B.A.1
Krawchuk, D.2
Centonze, V.E.3
Vargesson, N.4
Virshup, D.M.5
Conway, S.J.6
Cserjesi, P.7
Laufer, E.8
Firulli, A.B.9
-
21
-
-
70449805406
-
Vertebrate limb bud development: moving towards integrative analysis of organogenesis
-
Zeller, R., López-Ríos, J. and Zuniga, A. (2009) Vertebrate limb bud development: moving towards integrative analysis of organogenesis. Nat. Rev. Genet., 10, 845-858.
-
(2009)
Nat. Rev. Genet.
, vol.10
, pp. 845-858
-
-
Zeller, R.1
López-ríos, J.2
Zuniga, A.3
-
22
-
-
0018100745
-
A case of distal 4q trisomy due to familial (4;5)(q31;p15) translocation
-
Oka, S., Nakagome, Y., Honda, T. and Arima, M. (1978) A case of distal 4q trisomy due to familial (4;5)(q31;p15) translocation. Jpn. J. Hum. Genet. (Jinrui Idengaku Zasshi), 23, 167-172.
-
(1978)
Jpn. J. Hum. Genet. (Jinrui Idengaku Zasshi)
, vol.23
, pp. 167-172
-
-
Oka, S.1
Nakagome, Y.2
Honda, T.3
Arima, M.4
-
23
-
-
0028029689
-
De novo translocation involving chromosomes 1 and 4 resulting in partial duplication of 4q and partial deletion of 1p
-
Legare, J.M., Sekhon, G.S. and Laxova, R. (1994) De novo translocation involving chromosomes 1 and 4 resulting in partial duplication of 4q and partial deletion of 1p. Am. J. Med. Genet., 53, 216-221.
-
(1994)
Am. J. Med. Genet.
, vol.53
, pp. 216-221
-
-
Legare, J.M.1
Sekhon, G.S.2
Laxova, R.3
-
24
-
-
0034650311
-
Cardiac expression of the ventricle-specific homeobox gene Irx4 is modulated by Nkx2.5 and dHand.
-
Bruneau, B.G., Bao, Z.Z., Tanaka, M., Schott, J.J., Izumo, S., Cepko, C.L., Seidman, J.G. and Seidman, C.E. (2000) Cardiac expression of the ventricle-specific homeobox gene Irx4 is modulated by Nkx2.5 and dHand. Dev. Biol., 217, 266-277.
-
(2000)
Dev. Biol.
, vol.217
, pp. 266-277
-
-
Bruneau, B.G.1
Bao, Z.Z.2
Tanaka, M.3
Schott, J.J.4
Izumo, S.5
Cepko, C.L.6
Seidman, J.G.7
Seidman, C.E.8
-
25
-
-
0034523355
-
A GATA-dependent right ventricular enhancer controls dHAND transcription in the developing heart
-
McFadden, D.G., Charité, J., Richardson, J.A., Srivastava, D., Firulli, A.B. and Olson, E.N. (2000) A GATA-dependent right ventricular enhancer controls dHAND transcription in the developing heart. Development, 127, 5331-5341.
-
(2000)
Development
, vol.127
, pp. 5331-5341
-
-
Mcfadden, D.G.1
Charité, J.2
Richardson, J.A.3
Srivastava, D.4
Firulli, A.B.5
Olson, E.N.6
-
26
-
-
0032523101
-
The bHLH factors, dHAND and eHAND, specify pulmonary and systemic cardiac ventricles independent of left-right sidedness
-
Thomas, T., Yamagishi, H., Overbeek, P.A., Olson, E.N. and Srivastava, D. (1998) The bHLH factors, dHAND and eHAND, specify pulmonary and systemic cardiac ventricles independent of left-right sidedness. Dev. Biol., 196, 228-236.
-
(1998)
Dev. Biol.
, vol.196
, pp. 228-236
-
-
Thomas, T.1
Yamagishi, H.2
Overbeek, P.A.3
Olson, E.N.4
Srivastava, D.5
-
27
-
-
0029987879
-
De novo interstitial tandem duplication of chromosome 4(q21-q28)
-
Navarro, E.G., Romero, M.C., Expósito, I.L., Velasco, C.M., Llamas, J.G., Ramón, F.J. and Jimenez, R.D. (1996) De novo interstitial tandem duplication of chromosome 4(q21-q28). Am. J. Med. Genet., 62, 297-299.
-
(1996)
Am. J. Med. Genet.
, vol.62
, pp. 297-299
-
-
Navarro, E.G.1
Romero, M.C.2
Expósito, I.L.3
Velasco, C.M.4
Llamas, J.G.5
Ramón, F.J.6
Jimenez, R.D.7
-
28
-
-
0031021336
-
Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome
-
Howard, T.D., Paznekas, W.A., Green, E.D., Chiang, L.C., Ma, N., Ortiz De Luna, R.I., Delgado, C.G., Gonzalez-Ramos, M., Kline, A.D. and Jabs, E.W. (1997) Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome. Nat. Genet., 15, 36-41.
-
(1997)
Nat. Genet.
, vol.15
, pp. 36-41
-
-
Howard, T.D.1
Paznekas, W.A.2
Green, E.D.3
Chiang, L.C.4
Ma, N.5
De Luna, O.R.I.6
Delgado, C.G.7
Gonzalez-ramos, M.8
Kline, A.D.9
Jabs, E.W.10
-
29
-
-
0031012353
-
Mutations of the TWIST gene in the Saethre-Chotzen syndrome
-
El Ghouzzi, V., Le Merrer, M., Perrin-Schmitt, F., Lajeunie, E., Benit, P., Renier, D., Bourgeois, P., Bolcato-Bellemin, A.L., Munnich, A. and Bonaventure, J. (1997) Mutations of the TWIST gene in the Saethre-Chotzen syndrome. Nat. Genet., 15, 42-46.
-
(1997)
Nat. Genet.
, vol.15
, pp. 42-46
-
-
El Ghouzzi, V.1
Le Merrer, M.2
Perrin-schmitt, F.3
Lajeunie, E.4
Benit, P.5
Renier, D.6
Bourgeois, P.7
Bolcato-bellemin, A.L.8
Munnich, A.9
Bonaventure, J.10
-
30
-
-
0036435318
-
The mouse polydactylous mutation, luxate (lx), causes anterior shift of the anteroposterior border in the developing hind limb bud
-
Yada, Y., Makino, S., Chigusa-Ishiwa, S. and Shiroishi, T. (2002) The mouse polydactylous mutation, luxate (lx), causes anterior shift of the anteroposterior border in the developing hind limb bud. Int. J. Dev. Biol., 46, 975-982.
-
(2002)
Int. J. Dev. Biol.
, vol.46
, pp. 975-982
-
-
Yada, Y.1
Makino, S.2
Chigusa-ishiwa, S.3
Shiroishi, T.4
-
31
-
-
0030952445
-
Unbalanced t(4;11)(q32;q23) in a 34-year-old man with manifestations of distal monosomy 11q and trisomy 4q syndromes
-
Byatt, S.A., Baker, E., Richards, R.I., Roberts, C. and Smith, A. (1997) Unbalanced t(4;11)(q32;q23) in a 34-year-old man with manifestations of distal monosomy 11q and trisomy 4q syndromes. Am. J. Med. Genet., 70, 357-360.
-
(1997)
Am. J. Med. Genet.
, vol.70
, pp. 357-360
-
-
Byatt, S.A.1
Baker, E.2
Richards, R.I.3
Roberts, C.4
Smith, A.5
-
32
-
-
0027056330
-
Translocation/ duplication of 9p onto a duplicated 4q
-
Rivera, H., Figuera, L.E. and Vasquez, A.I. (1992) Translocation/ duplication of 9p onto a duplicated 4q. Genet. Couns., 3, 201-203.
-
(1992)
Genet. Couns.
, vol.3
, pp. 201-203
-
-
Rivera, H.1
Figuera, L.E.2
Vasquez, A.I.3
-
33
-
-
67349211156
-
Hand2 is required in the epithelium for palatogenesis in mice
-
Xiong, W., He, F., Morikawa, Y., Yu, X., Zhang, Z., Lan, Y., Jiang, R., Cserjesi, P. and Chen, Y. (2009) Hand2 is required in the epithelium for palatogenesis in mice. Dev. Biol., 330, 131-141.
-
(2009)
Dev. Biol.
, vol.330
, pp. 131-141
-
-
Xiong, W.1
He, F.2
Morikawa, Y.3
Yu, X.4
Zhang, Z.5
Lan, Y.6
Jiang, R.7
Cserjesi, P.8
Chen, Y.9
-
34
-
-
34147153781
-
Dysregulation of cardiogenesis, cardiac conduction, and cell cycle in mice lacking miRNA-1-2
-
Zhao, Y., Ransom, J.F., Li, A., Vedantham, V., von Drehle, M., Muth, A.N., Tsuchihashi, T., McManus, M.T., Schwartz, R.J. and Srivastava, D. (2007) Dysregulation of cardiogenesis, cardiac conduction, and cell cycle in mice lacking miRNA-1-2. Cell, 129, 303-317.
-
(2007)
Cell
, vol.129
, pp. 303-317
-
-
Zhao, Y.1
Ransom, J.F.2
Li, A.3
Vedantham, V.4
Von Drehle, M.5
Muth, A.N.6
Tsuchihashi, T.7
Mcmanus, M.T.8
Schwartz, R.J.9
Srivastava, D.10
-
35
-
-
63949084807
-
Lymphatic vessels develop during tubulointerstitial fibrosis
-
Sakamoto, I., Ito, Y., Mizuno, M., Suzuki, Y., Sawai, A., Tanaka, A., Maruyama, S., Takei, Y., Yuzawa, Y. and Matsuo, S. (2009) Lymphatic vessels develop during tubulointerstitial fibrosis. Kidney Int., 75, 828-838.
-
(2009)
Kidney Int.
, vol.75
, pp. 828-838
-
-
Sakamoto, I.1
Ito, Y.2
Mizuno, M.3
Suzuki, Y.4
Sawai, A.5
Tanaka, A.6
Maruyama, S.7
Takei, Y.8
Yuzawa, Y.9
Matsuo, S.10
-
36
-
-
77952350426
-
Distinct roles of Hand2 in initiating polarity and posterior Shh expression during the onset of mouse limb bud development
-
Galli, A., Robay, D., Osterwalder, M., Bao, X., Be'nazet, J.D., Tariq, M., Paro, R., Mackem, S. and Zeller, R. (2010) Distinct roles of Hand2 in initiating polarity and posterior Shh expression during the onset of mouse limb bud development. PLoS Genet., 6, e1000901.
-
(2010)
PLoS Genet.
, vol.6
-
-
Galli, A.1
Robay, D.2
Osterwalder, M.3
Bao, X.4
Be'nazet, J.D.5
Tariq, M.6
Paro, R.7
Mackem, S.8
Zeller, R.9
-
37
-
-
34247217928
-
Members of a novel gene family, Gsdm, are expressed exclusively in the epithelium of the skin and gastrointestinal tract in a highly tissue-specific manner
-
Tamura, M., Tanaka, S., Fujii, T., Aoki, A., Komiyama, H., Ezawa, K., Sumiyama, K., Sagai, T. and Shiroishi, T. (2007) Members of a novel gene family, Gsdm, are expressed exclusively in the epithelium of the skin and gastrointestinal tract in a highly tissue-specific manner. Genomics, 89, 618-629.
-
(2007)
Genomics
, vol.89
, pp. 618-629
-
-
Tamura, M.1
Tanaka, S.2
Fujii, T.3
Aoki, A.4
Komiyama, H.5
Ezawa, K.6
Sumiyama, K.7
Sagai, T.8
Shiroishi, T.9
-
38
-
-
0035710746
-
Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method
-
Livak, K.J. and Schmittgen, T.D. (2001) Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. Methods, 25, 402-408.
-
(2001)
Methods
, vol.25
, pp. 402-408
-
-
Livak, K.J.1
Schmittgen, T.D.2
-
39
-
-
58149463874
-
Chromosomal dynamics at the Shh locus: limb bud-specific differential regulation of competence and active transcription
-
Amano, T., Sagai, T., Tanabe, H., Mizushina, Y., Nakazawa, H. and Shiroishi, T. (2009) Chromosomal dynamics at the Shh locus: limb bud-specific differential regulation of competence and active transcription. Dev. Cell, 16, 47-57.
-
(2009)
Dev. Cell
, vol.16
, pp. 47-57
-
-
Amano, T.1
Sagai, T.2
Tanabe, H.3
Mizushina, Y.4
Nakazawa, H.5
Shiroishi, T.6
-
40
-
-
77953648269
-
Rapid 3D phenotyping of cardiovascular development in mouse embryos by micro-CT with iodine staining
-
Degenhardt, K., Wright, A.C., Horng, D., Padmanabhan, A. and Epstein, J.A. (2010) Rapid 3D phenotyping of cardiovascular development in mouse embryos by micro-CT with iodine staining. Circ. Cardiovasc. Imaging, 3, 314-322.
-
(2010)
Circ. Cardiovasc. Imaging
, vol.3
, pp. 314-322
-
-
Degenhardt, K.1
Wright, A.C.2
Horng, D.3
Padmanabhan, A.4
Epstein, J.A.5
-
41
-
-
0034612342
-
One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products
-
Datsenko, K.A. and Wanner, B.L. (2000) One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products. Proc. Natl. Acad. Sci. USA, 97, 6640-6645.
-
(2000)
Proc. Natl. Acad. Sci. USA
, vol.97
, pp. 6640-6645
-
-
Datsenko, K.A.1
Wanner, B.L.2
-
42
-
-
34250753983
-
A new Gsdma3 mutation affecting anagen phase of first hair cycle
-
Tanaka, S., Tamura, M., Aoki, A., Fujii, T., Komiyama, H., Sagai, T. and Shiroishi, T. (2007) A new Gsdma3 mutation affecting anagen phase of first hair cycle. Biochem. Biophys. Res. Commun., 359, 902-907.
-
(2007)
Biochem. Biophys. Res. Commun.
, vol.359
, pp. 902-907
-
-
Tanaka, S.1
Tamura, M.2
Aoki, A.3
Fujii, T.4
Komiyama, H.5
Sagai, T.6
Shiroishi, T.7
-
43
-
-
49149092804
-
Identification of the bHLH factor Math6 as a novel component of the embryonic pancreas transcriptional network
-
Lynn, F.C., Sanchez, L., Gomis, R., German, M.S. and Gasa, R. (2008) Identification of the bHLH factor Math6 as a novel component of the embryonic pancreas transcriptional network. PLoS One, 3, e2430.
-
(2008)
PLoS One
, vol.3
-
-
Lynn, F.C.1
Sanchez, L.2
Gomis, R.3
German, M.S.4
Gasa, R.5
-
44
-
-
0020468768
-
Familial occurrence of partial trisomy 4q and probable monosomy 5p due to 4q/5p translocation
-
Gencik, A., Gencikova, A. and Pa'lova, A. (1982) Familial occurrence of partial trisomy 4q and probable monosomy 5p due to 4q/5p translocation. Acta. Paediatr. Acad. Sci. Hung., 23, 291-298.
-
(1982)
Acta. Paediatr. Acad. Sci. Hung.
, vol.23
, pp. 291-298
-
-
Gencik, A.1
Gencikova, A.2
Pa'lova, A.3
-
45
-
-
0017077334
-
Partial trisomy 4q due to familial 2/4 translocation
-
Biederman, B. and Bowen, P. (1976) Partial trisomy 4q due to familial 2/4 translocation. Hum. Genet., 33, 147-153.
-
(1976)
Hum. Genet.
, vol.33
, pp. 147-153
-
-
Biederman, B.1
Bowen, P.2
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