-
1
-
-
27444439377
-
Members of the Plag gene family are expressed in complementary and overlapping regions in the developing murine nervous system
-
Alam, S., D. Zinyk, L. Ma, and C. Schuurmans, 2005 Members of the Plag gene family are expressed in complementary and overlapping regions in the developing murine nervous system. Dev. Dyn. 234: 772-782.
-
(2005)
Dev. Dyn
, vol.234
, pp. 772-782
-
-
Alam, S.1
Zinyk, D.2
Ma, L.3
Schuurmans, C.4
-
2
-
-
84864136574
-
Clinical utility gene card for: Leri-Weill dyschondrosteosis (LWD) and Langer mesomelic dysplasia (LMD)
-
PMC3400739
-
Albuisson, J., S. Schmitt, S. Baron, S. Bezieau, S. Benito-Sanz et al., 2012 Clinical utility gene card for: Leri-Weill dyschondrosteosis (LWD) and Langer mesomelic dysplasia (LMD). Eur. J. Hum. Genet. 20: PMC3400739.
-
(2012)
Eur. J. Hum. Genet
, vol.20
-
-
Albuisson, J.1
Schmitt, S.2
Baron, S.3
Bezieau, S.4
Benito-Sanz, S.5
-
3
-
-
84878754528
-
A switch between topological domains underlies HoxD genes collinearity in mouse limbs
-
Andrey, G., T. Montavon, B. Mascrez, F. Gonzalez, D. Noordermeer et al., 2013 A switch between topological domains underlies HoxD genes collinearity in mouse limbs. Science 340: 1234167.
-
(2013)
Science
, vol.340
-
-
Andrey, G.1
Montavon, T.2
Mascrez, B.3
Gonzalez, F.4
Noordermeer, D.5
-
4
-
-
0026544785
-
Cloning of the human and mouse type X collagen genes and mapping of the mouse type X collagen gene to chromosome 10
-
Apte, S. S., M. F. Seldin, M. Hayashi, and B. R. Olsen, 1992 Cloning of the human and mouse type X collagen genes and mapping of the mouse type X collagen gene to chromosome 10. Eur. J. Biochem. 206: 217-224.
-
(1992)
Eur. J. Biochem
, vol.206
, pp. 217-224
-
-
Apte, S.S.1
Seldin, M.F.2
Hayashi, M.3
Olsen, B.R.4
-
5
-
-
17344363774
-
SHOX mutations in dyschondrosteosis (Leri-Weill syndrome)
-
Belin, V., V. Cusin, G. Viot, D. Girlich, A. Toutain et al., 1998 SHOX mutations in dyschondrosteosis (Leri-Weill syndrome). Nat. Genet. 19: 67-69.
-
(1998)
Nat. Genet
, vol.19
, pp. 67-69
-
-
Belin, V.1
Cusin, V.2
Viot, G.3
Girlich, D.4
Toutain, A.5
-
6
-
-
84875608868
-
Shox2 regulates progression through chondrogenesis in the mouse proximal limb
-
Bobick, B. E., and J. Cobb, 2012 Shox2 regulates progression through chondrogenesis in the mouse proximal limb. J. Cell Sci. 125: 6071-6083.
-
(2012)
J. Cell Sci
, vol.125
, pp. 6071-6083
-
-
Bobick, B.E.1
Cobb, J.2
-
7
-
-
0842344616
-
Multiple roles of Hoxa11 and Hoxd11 in the formation of the mammalian forelimb zeugopod
-
Boulet, A. M., and M. R. Capecchi, 2004 Multiple roles of Hoxa11 and Hoxd11 in the formation of the mammalian forelimb zeugopod. Development 131: 299-309.
-
(2004)
Development
, vol.131
, pp. 299-309
-
-
Boulet, A.M.1
Capecchi, M.R.2
-
8
-
-
17144464108
-
The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome
-
Clement-Jones, M., S. Schiller, E. Rao, R. J. Blaschke, A. Zuniga et al., 2000 The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome. Hum. Mol. Genet. 9: 695-702.
-
(2000)
Hum. Mol. Genet
, vol.9
, pp. 695-702
-
-
Clement-Jones, M.1
Schiller, S.2
Rao, E.3
Blaschke, R.J.4
Zuniga, A.5
-
9
-
-
23144464156
-
Comparative analysis of genes downstream of the Hoxd cluster in developing digits and external genitalia
-
Cobb, J., and D. Duboule, 2005 Comparative analysis of genes downstream of the Hoxd cluster in developing digits and external genitalia. Development 132: 3055-3067.
-
(2005)
Development
, vol.132
, pp. 3055-3067
-
-
Cobb, J.1
Duboule, D.2
-
10
-
-
33645211529
-
A mouse model for human short-stature syndromes identifies Shox2 as an upstream regulator of Runx2 during long-bone development
-
Cobb, J., A. Dierich, Y. Huss-Garcia, and D. Duboule, 2006 A mouse model for human short-stature syndromes identifies Shox2 as an upstream regulator of Runx2 during long-bone development. Proc. Natl. Acad. Sci. USA 103: 4511-4515.
-
(2006)
Proc. Natl. Acad. Sci. USA
, vol.103
, pp. 4511-4515
-
-
Cobb, J.1
Dierich, A.2
Huss-Garcia, Y.3
Duboule, D.4
-
11
-
-
0029026767
-
Absence of radius and ulna in mice lacking hoxa-11 and hoxd-11
-
Davis, A. P., D. P. Witte, H. M. Hsieh-Li, S. S. Potter, and M. R. Capecchi, 1995 Absence of radius and ulna in mice lacking hoxa-11 and hoxd-11. Nature 375: 791-795.
-
(1995)
Nature
, vol.375
, pp. 791-795
-
-
Davis, A.P.1
Witte, D.P.2
Hsieh-Li, H.M.3
Potter, S.S.4
Capecchi, M.R.5
-
12
-
-
0026326323
-
The Hox-4.8 gene is localized at the 59 extremity of the Hox-4 complex and is expressed in the most posterior parts of the body during development
-
Dolle, P., J. C. Izpisua-Belmonte, E. Boncinelli, and D. Duboule, 1991 The Hox-4.8 gene is localized at the 59 extremity of the Hox-4 complex and is expressed in the most posterior parts of the body during development. Mech. Dev. 36: 3-13.
-
(1991)
Mech. Dev
, vol.36
, pp. 3-13
-
-
Dolle, P.1
Izpisua-Belmonte, J.C.2
Boncinelli, E.3
Duboule, D.4
-
13
-
-
84875532638
-
Height matters-from monogenic disorders to normal variation
-
Durand, C., and G. A. Rappold, 2013 Height matters-from monogenic disorders to normal variation. Nat. Rev. Endocrinol. 9: 171-177.
-
(2013)
Nat. Rev. Endocrinol
, vol.9
, pp. 171-177
-
-
Durand, C.1
Rappold, G.A.2
-
14
-
-
0030040552
-
Specific and redundant functions of the paralogous Hoxa-9 and Hoxd-9 genes in forelimb and axial skeleton patterning
-
Fromental-Ramain, C., X. Warot, S. Lakkaraju, B. Favier, H. Haack et al., 1996a Specific and redundant functions of the paralogous Hoxa-9 and Hoxd-9 genes in forelimb and axial skeleton patterning. Development 122: 461-472.
-
(1996)
Development
, vol.122
, pp. 461-472
-
-
Fromental-Ramain, C.1
Warot, X.2
Lakkaraju, S.3
Favier, B.4
Haack, H.5
-
15
-
-
0029851376
-
Hoxa-13 and Hoxd-13 play a crucial role in the patterning of the limb autopod
-
Fromental-Ramain, C., X. Warot, N. Messadecq, M. Lemeur, P. Dolle et al., 1996b Hoxa-13 and Hoxd-13 play a crucial role in the patterning of the limb autopod. Development 122: 2997-3011.
-
(1996)
Development
, vol.122
, pp. 2997-3011
-
-
Fromental-Ramain, C.1
Warot, X.2
Messadecq, N.3
Lemeur, M.4
Dolle, P.5
-
16
-
-
0035212127
-
Differential divergence of three human pseudoautosomal genes and their mouse homologs: Implications for sex chromosome evolution
-
Gianfrancesco, F., R. Sanges, T. Esposito, S. Tempesta, E. Rao et al., 2001 Differential divergence of three human pseudoautosomal genes and their mouse homologs: implications for sex chromosome evolution. Genome Res. 11: 2095-2100.
-
(2001)
Genome Res
, vol.11
, pp. 2095-2100
-
-
Gianfrancesco, F.1
Sanges, R.2
Esposito, T.3
Tempesta, S.4
Rao, E.5
-
17
-
-
84904391423
-
Long bone development requires a threshold of Hox function
-
Gonzalez-Martin, M. C., M. Mallo, and M. A. Ros, 2014 Long bone development requires a threshold of Hox function. Dev. Biol. 392: 454-465.
-
(2014)
Dev. Biol
, vol.392
, pp. 454-465
-
-
Gonzalez-Martin, M.C.1
Mallo, M.2
Ros, M.A.3
-
18
-
-
84865173746
-
Hoxa11 and Hoxd11 regulate chondrocyte differentiation upstream of Runx2 and Shox2 in mice
-
Gross, S., Y. Krause, M. Wuelling, and A. Vortkamp, 2012 Hoxa11 and Hoxd11 regulate chondrocyte differentiation upstream of Runx2 and Shox2 in mice. PLoS ONE 7: e43553.
-
(2012)
PLoS ONE
, vol.7
-
-
Gross, S.1
Krause, Y.2
Wuelling, M.3
Vortkamp, A.4
-
19
-
-
49849092907
-
Simultaneous inference in general parametric models
-
Hothorn, T., F. Bretz, and P. Westfall, 2008 Simultaneous inference in general parametric models. Biom. J. 50: 346-363.
-
(2008)
Biom. J
, vol.50
, pp. 346-363
-
-
Hothorn, T.1
Bretz, F.2
Westfall, P.3
-
21
-
-
0036225281
-
Reaching a genetic and molecular understanding of skeletal development
-
Karsenty, G., and E. F. Wagner, 2002 Reaching a genetic and molecular understanding of skeletal development. Dev. Cell 2: 389-406.
-
(2002)
Dev. Cell
, vol.2
, pp. 389-406
-
-
Karsenty, G.1
Wagner, E.F.2
-
22
-
-
0037079049
-
Serial deletions and duplications suggest a mechanism for the collinearity of Hoxd genes in limbs
-
Kmita, M., N. Fraudeau, Y. Herault, and D. Duboule, 2002 Serial deletions and duplications suggest a mechanism for the collinearity of Hoxd genes in limbs. Nature 420: 145-150.
-
(2002)
Nature
, vol.420
, pp. 145-150
-
-
Kmita, M.1
Fraudeau, N.2
Herault, Y.3
Duboule, D.4
-
23
-
-
21344455343
-
Early developmental arrest of mammalian limbs lacking HoxA/HoxD gene function
-
Kmita, M., B. Tarchini, J. Zakany, M. Logan, C. J. Tabin et al., 2005 Early developmental arrest of mammalian limbs lacking HoxA/HoxD gene function. Nature 435: 1113-1116.
-
(2005)
Nature
, vol.435
, pp. 1113-1116
-
-
Kmita, M.1
Tarchini, B.2
Zakany, J.3
Logan, M.4
Tabin, C.J.5
-
24
-
-
37249040479
-
The role of the perichondrium in fetal bone development
-
Kronenberg, H. M., 2007 The role of the perichondrium in fetal bone development. Ann. N. Y. Acad. Sci. 1116: 59-64.
-
(2007)
Ann. N. Y. Acad. Sci
, vol.1116
, pp. 59-64
-
-
Kronenberg, H.M.1
-
25
-
-
79955751499
-
Functional redundancy between human SHOX and mouse Shox2 genes in the regulation of sinoatrial node formation and pacemaking function
-
Liu, H., C. H. Chen, R. A. Espinoza-Lewis, Z. Jiao, I. Sheu et al., 2011 Functional redundancy between human SHOX and mouse Shox2 genes in the regulation of sinoatrial node formation and pacemaking function. J. Biol. Chem. 286: 17029-17038.
-
(2011)
J. Biol. Chem
, vol.286
, pp. 17029-17038
-
-
Liu, H.1
Chen, C.H.2
Espinoza-Lewis, R.A.3
Jiao, Z.4
Sheu, I.5
-
26
-
-
0036076389
-
Expression of Cre Recombinase in the developing mouse limb bud driven by a Prxl enhancer
-
Logan, M., J. F. Martin, A. Nagy, C. Lobe, E. N. Olson et al., 2002 Expression of Cre Recombinase in the developing mouse limb bud driven by a Prxl enhancer. Genesis 33: 77-80.
-
(2002)
Genesis
, vol.33
, pp. 77-80
-
-
Logan, M.1
Martin, J.F.2
Nagy, A.3
Lobe, C.4
Olson, E.N.5
-
27
-
-
0025863378
-
Specific hybridization probes for mouse type I, II, III and IX collagen mRNAs
-
Metsaranta, M., D. Toman, B. De Crombrugghe, and E. Vuorio, 1991 Specific hybridization probes for mouse type I, II, III and IX collagen mRNAs. Biochim. Biophys. Acta 1089: 241-243.
-
(1991)
Biochim. Biophys. Acta
, vol.1089
, pp. 241-243
-
-
Metsaranta, M.1
Toman, D.2
De Crombrugghe, B.3
Vuorio, E.4
-
28
-
-
0028792229
-
Aromatase deficiency in male and female siblings caused by a novel mutation and the physiological role of estrogens
-
Morishima, A., M. M. Grumbach, E. R. Simpson, C. Fisher, and K. Qin, 1995 Aromatase deficiency in male and female siblings caused by a novel mutation and the physiological role of estrogens. J. Clin. Endocrinol. Metab. 80: 3689-3698.
-
(1995)
J. Clin. Endocrinol. Metab
, vol.80
, pp. 3689-3698
-
-
Morishima, A.1
Grumbach, M.M.2
Simpson, E.R.3
Fisher, C.4
Qin, K.5
-
29
-
-
15844372073
-
Analysis of Hox gene expression in the chick limb bud
-
Nelson, C. E., B. A. Morgan, A. C. Burke, E. Laufer, E. Dimambro et al., 1996 Analysis of Hox gene expression in the chick limb bud. Development 122: 1449-1466.
-
(1996)
Development
, vol.122
, pp. 1449-1466
-
-
Nelson, C.E.1
Morgan, B.A.2
Burke, A.C.3
Laufer, E.4
Dimambro, E.5
-
30
-
-
84882569681
-
MRNA fluorescence in situ hybridization to determine overlapping gene expression in whole-mount mouse embryos
-
Neufeld, S. J., X. Zhou, P. D. Vize, and J. Cobb, 2013 MRNA fluorescence in situ hybridization to determine overlapping gene expression in whole-mount mouse embryos. Dev. Dyn. 242: 1094-1100.
-
(2013)
Dev. Dyn
, vol.242
, pp. 1094-1100
-
-
Neufeld, S.J.1
Zhou, X.2
Vize, P.D.3
Cobb, J.4
-
31
-
-
0034456564
-
Short stature homeobox-containing gene duplication on the der(X) chromosome in a female with 45,X/46,X, der(X), gonadal dysgenesis, and tall stature
-
Ogata, T., T. Kosho, K. Wakui, Y. Fukushima, M. Yoshimoto et al., 2000 Short stature homeobox-containing gene duplication on the der(X) chromosome in a female with 45,X/46,X, der(X), gonadal dysgenesis, and tall stature. J. Clin. Endocrinol. Metab. 85: 2927-2930.
-
(2000)
J. Clin. Endocrinol. Metab
, vol.85
, pp. 2927-2930
-
-
Ogata, T.1
Kosho, T.2
Wakui, K.3
Fukushima, Y.4
Yoshimoto, M.5
-
32
-
-
77951758776
-
Increased number of sex chromosomes affects height in a nonlinear fashion: A study of 305 patients with sex chromosome aneuploidy
-
Ottesen, A. M., L. Aksglaede, I. Garn, N. Tartaglia, F. Tassone et al., 2010 Increased number of sex chromosomes affects height in a nonlinear fashion: a study of 305 patients with sex chromosome aneuploidy. Am. J. Med. Genet. A. 152A: 1206-1212.
-
(2010)
Am. J. Med. Genet. A
, vol.152A
, pp. 1206-1212
-
-
Ottesen, A.M.1
Aksglaede, L.2
Garn, I.3
Tartaglia, N.4
Tassone, F.5
-
33
-
-
0030666372
-
Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone development
-
Otto, F., A. P. Thornell, T. Crompton, A. Denzel, K. C. Gilmour et al., 1997 Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone development. Cell 89: 765-771.
-
(1997)
Cell
, vol.89
, pp. 765-771
-
-
Otto, F.1
Thornell, A.P.2
Crompton, T.3
Denzel, A.4
Gilmour, K.C.5
-
34
-
-
54149088214
-
Epistasis-the essential role of gene interactions in the structure and evolution of genetic systems
-
Phillips, P. C., 2008 Epistasis-the essential role of gene interactions in the structure and evolution of genetic systems. Nat. Rev. Genet. 9: 855-867.
-
(2008)
Nat. Rev. Genet
, vol.9
, pp. 855-867
-
-
Phillips, P.C.1
-
35
-
-
79955553860
-
SHH propagates distal limb bud development by enhancing CYP26B1-mediated retinoic acid clearance via AER- FGF signalling
-
Probst, S., C. Kraemer, P. Demougin, R. Sheth, G. R. Martin et al., 2011 SHH propagates distal limb bud development by enhancing CYP26B1-mediated retinoic acid clearance via AER- FGF signalling. Development 138: 1913-1923.
-
(2011)
Development
, vol.138
, pp. 1913-1923
-
-
Probst, S.1
Kraemer, C.2
Demougin, P.3
Sheth, R.4
Martin, G.R.5
-
36
-
-
84855199947
-
-
R Core Team, R Foundation for Statistical Computing, Vienna. Available at
-
R Core Team, 2013 A Language and Environment for Statistical Computing. R Foundation for Statistical Computing, Vienna. Available at: http://www.R-project.org/.
-
(2013)
A Language and Environment for Statistical Computing
-
-
-
37
-
-
0030940217
-
Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome
-
Rao, E., B. Weiss, M. Fukami, A. Rump, B. Niesler et al., 1997 Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome. Nat. Genet. 16: 54-63.
-
(1997)
Nat. Genet
, vol.16
, pp. 54-63
-
-
Rao, E.1
Weiss, B.2
Fukami, M.3
Rump, A.4
Niesler, B.5
-
38
-
-
0026524350
-
Comparison of mouse and human HOX- 4 complexes defines conserved sequences involved in the regulation of Hox-4.4
-
Renucci, A., V. Zappavigna, J. Zakany, J. C. Izpisua-Belmonte, K. Burki et al., 1992 Comparison of mouse and human HOX- 4 complexes defines conserved sequences involved in the regulation of Hox-4.4. EMBO J. 11: 1459-1468.
-
(1992)
EMBO J
, vol.11
, pp. 1459-1468
-
-
Renucci, A.1
Zappavigna, V.2
Zakany, J.3
Izpisua-Belmonte, J.C.4
Burki, K.5
-
39
-
-
0033994671
-
Phenotypic variation and genetic heterogeneity in Leri- Weill syndrome
-
Schiller, S., S. Spranger, B. Schechinger, M. Fukami, S. Merker et al., 2000 Phenotypic variation and genetic heterogeneity in Leri- Weill syndrome. Eur. J. Hum. Genet. 8: 54-62.
-
(2000)
Eur. J. Hum. Genet
, vol.8
, pp. 54-62
-
-
Schiller, S.1
Spranger, S.2
Schechinger, B.3
Fukami, M.4
Merker, S.5
-
40
-
-
79955770171
-
Transcription factor short stature homeobox 2 is required for proper development of tropomyosin-related kinase B-expressing mechanosensory neurons
-
Scott, A., H. Hasegawa, K. Sakurai, A. Yaron, J. Cobb et al., 2011 Transcription factor short stature homeobox 2 is required for proper development of tropomyosin-related kinase B-expressing mechanosensory neurons. J. Neurosci. 31: 6741-6749.
-
(2011)
J. Neurosci
, vol.31
, pp. 6741-6749
-
-
Scott, A.1
Hasegawa, H.2
Sakurai, K.3
Yaron, A.4
Cobb, J.5
-
41
-
-
0031747158
-
Mutation and deletion of the pseudoautosomal gene SHOX cause Leri-Weill dyschondrosteosis
-
Shears, D. J., H. J. Vassal, F. R. Goodman, R. W. Palmer, W. Reardon et al., 1998 Mutation and deletion of the pseudoautosomal gene SHOX cause Leri-Weill dyschondrosteosis. Nat. Genet. 19: 70-73.
-
(1998)
Nat. Genet
, vol.19
, pp. 70-73
-
-
Shears, D.J.1
Vassal, H.J.2
Goodman, F.R.3
Palmer, R.W.4
Reardon, W.5
-
42
-
-
0028143234
-
Estrogen resistance caused by a mutation in the estrogen- receptor gene in a man
-
Smith, E. P., J. Boyd, G. R. Frank, H. Takahashi, R. M. Cohen et al., 1994 Estrogen resistance caused by a mutation in the estrogen- receptor gene in a man. N. Engl. J. Med. 331: 1056-1061.
-
(1994)
N. Engl. J. Med
, vol.331
, pp. 1056-1061
-
-
Smith, E.P.1
Boyd, J.2
Frank, G.R.3
Takahashi, H.4
Cohen, R.M.5
-
43
-
-
0029027342
-
Hox gene expression in teleost fins and the origin of vertebrate digits
-
Sordino, P., F. Van Der Hoeven, and D. Duboule, 1995 Hox gene expression in teleost fins and the origin of vertebrate digits. Nature 375: 678-681.
-
(1995)
Nature
, vol.375
, pp. 678-681
-
-
Sordino, P.1
Van Der Hoeven, F.2
Duboule, D.3
-
44
-
-
0035448880
-
Large scale transgenic and cluster deletion analysis of the HoxD complex separate an ancestral regulatory module from evolutionary innovations
-
Spitz, F., F. Gonzalez, C. Peichel, T. F. Vogt, D. Duboule et al., 2001 Large scale transgenic and cluster deletion analysis of the HoxD complex separate an ancestral regulatory module from evolutionary innovations. Genes Dev. 15: 2209-2214.
-
(2001)
Genes Dev
, vol.15
, pp. 2209-2214
-
-
Spitz, F.1
Gonzalez, F.2
Peichel, C.3
Vogt, T.F.4
Duboule, D.5
-
45
-
-
84880701815
-
Generation of Shox2-Cre allele for tissue specific manipulation of genes in the developing heart, palate, and limb
-
Sun, C., T. Zhang, C. Liu, S. Gu, and Y. Chen, 2013 Generation of Shox2-Cre allele for tissue specific manipulation of genes in the developing heart, palate, and limb. Genesis 51: 515-522.
-
(2013)
Genesis
, vol.51
, pp. 515-522
-
-
Sun, C.1
Zhang, T.2
Liu, C.3
Gu, S.4
Chen, Y.5
-
46
-
-
84887130567
-
Hox11 genes are required for regional patterning and integration of muscle, tendon and bone
-
Swinehart, I. T., A. J. Schlientz, C. A. Quintanilla, D. P. Mortlock, and D. M. Wellik, 2013 Hox11 genes are required for regional patterning and integration of muscle, tendon and bone. Development 140: 4574-4582.
-
(2013)
Development
, vol.140
, pp. 4574-4582
-
-
Swinehart, I.T.1
Schlientz, A.J.2
Quintanilla, C.A.3
Mortlock, D.P.4
Wellik, D.M.5
-
47
-
-
29744447562
-
Control of Hoxd genes’ collinearity during early limb development
-
Tarchini, B., and D. Duboule, 2006 Control of Hoxd genes’ collinearity during early limb development. Dev. Cell 10: 93-103.
-
(2006)
Dev. Cell
, vol.10
, pp. 93-103
-
-
Tarchini, B.1
Duboule, D.2
-
49
-
-
0033662329
-
A megakaryocytic thrombocytopenia and radio-ulnar synostosis are associated with HOXA11 mutation
-
Thompson, A. A., and L. T. Nguyen, 2000 A megakaryocytic thrombocytopenia and radio-ulnar synostosis are associated with HOXA11 mutation. Nat. Genet. 26: 397-398.
-
(2000)
Nat. Genet
, vol.26
, pp. 397-398
-
-
Thompson, A.A.1
Nguyen, L.T.2
-
50
-
-
33748967708
-
Expression of the short stature homeobox gene Shox is restricted by proximal and distal signals in chick limb buds and affects the length of skeletal elements
-
Tiecke, E., F. Bangs, R. Blaschke, E. R. Farrell, G. Rappold et al., 2006 Expression of the short stature homeobox gene Shox is restricted by proximal and distal signals in chick limb buds and affects the length of skeletal elements. Dev. Biol. 298: 585-596.
-
(2006)
Dev. Biol
, vol.298
, pp. 585-596
-
-
Tiecke, E.1
Bangs, F.2
Blaschke, R.3
Farrell, E.R.4
Rappold, G.5
-
51
-
-
77953191249
-
Homeobox genes d11-d13 and a13 control mouse autopod cortical bone and joint formation
-
Villavicencio-Lorini, P., P. Kuss, J. Friedrich, J. Haupt, M. Farooq et al., 2010 Homeobox genes d11-d13 and a13 control mouse autopod cortical bone and joint formation. J. Clin. Invest. 120: 1994-2004.
-
(2010)
J. Clin. Invest
, vol.120
, pp. 1994-2004
-
-
Villavicencio-Lorini, P.1
Kuss, P.2
Friedrich, J.3
Haupt, J.4
Farooq, M.5
-
52
-
-
0031466723
-
Gene dosage-dependent effects of the Hoxa- 13 and Hoxd-13 mutations on morphogenesis of the terminal parts of the digestive and urogenital tracts
-
Warot, X., C. Fromental-Ramain, V. Fraulob, P. Chambon, and P. Dolle, 1997 Gene dosage-dependent effects of the Hoxa- 13 and Hoxd-13 mutations on morphogenesis of the terminal parts of the digestive and urogenital tracts. Development 124: 4781-4791.
-
(1997)
Development
, vol.124
, pp. 4781-4791
-
-
Warot, X.1
Fromental-Ramain, C.2
Fraulob, V.3
Chambon, P.4
Dolle, P.5
-
53
-
-
0038299546
-
Hox10 and Hox11 genes are required to globally pattern the mammalian skeleton
-
Wellik, D. M., and M. R. Capecchi, 2003 Hox10 and Hox11 genes are required to globally pattern the mammalian skeleton. Science 301: 363-367.
-
(2003)
Science
, vol.301
, pp. 363-367
-
-
Wellik, D.M.1
Capecchi, M.R.2
-
54
-
-
84893777034
-
Conservation and divergence of regulatory strategies at Hox loci and the origin of tetrapod digits
-
Woltering, J. M., D. Noordermeer, M. Leleu, and D. Duboule, 2014 Conservation and divergence of regulatory strategies at Hox loci and the origin of tetrapod digits. PLoS Biol. 12: e1001773.
-
(2014)
PLoS Biol
, vol.12
-
-
Woltering, J.M.1
Noordermeer, D.2
Leleu, M.3
Duboule, D.4
-
55
-
-
11144354938
-
Runx2 and Runx3 are essential for chondrocyte maturation, and Runx2 regulates limb growth through induction of Indian hedgehog
-
Yoshida, C. A., H. Yamamoto, T. Fujita, T. Furuichi, K. Ito et al., 2004 Runx2 and Runx3 are essential for chondrocyte maturation, and Runx2 regulates limb growth through induction of Indian hedgehog. Genes Dev. 18: 952-963.
-
(2004)
Genes Dev
, vol.18
, pp. 952-963
-
-
Yoshida, C.A.1
Yamamoto, H.2
Fujita, T.3
Furuichi, T.4
Ito, K.5
-
56
-
-
34249911762
-
Shox2 is required for chondrocyte proliferation and maturation in proximal limb skeleton
-
Yu, L., H. Liu, M. Yan, J. Yang, F. Long et al., 2007 Shox2 is required for chondrocyte proliferation and maturation in proximal limb skeleton. Dev. Biol. 306: 549-559.
-
(2007)
Dev. Biol
, vol.306
, pp. 549-559
-
-
Yu, L.1
Liu, H.2
Yan, M.3
Yang, J.4
Long, F.5
-
57
-
-
84901645732
-
GxGxE for lifespan in Drosophila: Mitochondrial, nuclear, and dietary interactions that modify longevity
-
Zhu, C. T., P. Ingelmo, and D. M. Rand, 2014 GxGxE for lifespan in Drosophila: mitochondrial, nuclear, and dietary interactions that modify longevity. PLoS Genet. 10: e1004354.
-
(2014)
PLoS Genet
, vol.10
-
-
Zhu, C.T.1
Ingelmo, P.2
Rand, D.M.3
-
58
-
-
0037097345
-
Complete SHOX deficiency causes Langer mesomelic dysplasia
-
Zinn, A. R., F. Wei, L. Zhang, F. F. Elder, C. I. Scott, Jr. et al., 2002 Complete SHOX deficiency causes Langer mesomelic dysplasia. Am. J. Med. Genet. 110: 158-163.
-
(2002)
Am. J. Med. Genet
, vol.110
, pp. 158-163
-
-
Zinn, A.R.1
Wei, F.2
Zhang, L.3
Elder, F.F.4
Scott, C.I.5
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