-
2
-
-
0024554568
-
Origin of luteinizing hormone-releasing hormone neurons
-
Schwanzel-Fukuda M, Pfaff DW: Origin of luteinizing hormone-releasing hormone neurons. Nature 1989, 338:161-164.
-
(1989)
Nature
, vol.338
, pp. 161-164
-
-
Schwanzel-Fukuda, M.1
Pfaff, D.W.2
-
3
-
-
0000678016
-
Evidence that cells expressing luteinizing hormone-releasing hormone mRNA in the mouse are derived from progenitor cells in the olfactory placode
-
Wray S, Grant P, Gainer H: Evidence that cells expressing luteinizing hormone-releasing hormone mRNA in the mouse are derived from progenitor cells in the olfactory placode. Proc Natl Acad Sci USA 1989, 86:8132-8136.
-
(1989)
Proc Natl Acad Sci USA
, vol.86
, pp. 8132-8136
-
-
Wray, S.1
Grant, P.2
Gainer, H.3
-
4
-
-
0032953341
-
Anosmin-1 is a regionally restricted component of basement membranes and interstitial matrices during organogenesis: Implications for the developmental anomalies of X chromosome-linked Kallmann syndrome
-
Hardelin JP, Julliard AK, Moniot B, Soussi-Yanicostas N, Verney C, Schwanzel-Fukuda M, Ayer-Le Lievre C, Petit C: Anosmin-1 is a regionally restricted component of basement membranes and interstitial matrices during organogenesis: implications for the developmental anomalies of X chromosome-linked Kallmann syndrome. Dev Dyn 1999, 215:26-44.
-
(1999)
Dev Dyn
, vol.215
, pp. 26-44
-
-
Hardelin, J.P.1
Julliard, A.K.2
Moniot, B.3
Soussi-Yanicostas, N.4
Verney, C.5
Schwanzel-Fukuda, M.6
Ayer-Le Lievre, C.7
Petit, C.8
-
5
-
-
0033525624
-
X-linked Kallmann syndrome and renal agenesis occurring together and independently in a large Australian family
-
Colquhoun-Kerr JS, Gu WX, Jameson JL, Withers S, Bode HH: X-linked Kallmann syndrome and renal agenesis occurring together and independently in a large Australian family. Am J Med Genet 1999, 83:23-27.
-
(1999)
Am J Med Genet
, vol.83
, pp. 23-27
-
-
Colquhoun-Kerr, J.S.1
Gu, W.X.2
Jameson, J.L.3
Withers, S.4
Bode, H.H.5
-
6
-
-
0022256144
-
Heterogeneity of Kallmann's syndrome
-
Hermanussen M, Sippell WJ: Heterogeneity of Kallmann's syndrome. Clin Genet 1985, 28:106-111.
-
(1985)
Clin Genet
, vol.28
, pp. 106-111
-
-
Hermanussen, M.1
Sippell, W.J.2
-
7
-
-
0016740866
-
Familial Kallmann syndrome with unilateral renal aplasia
-
Wegenke JD, Uehling DT, Wear JB Jr, Gordon ES, Bargman JG, Deacon JS, Herrmann JP, Opitz JM: Familial Kallmann syndrome with unilateral renal aplasia. Clin Genet 1975, 7:368-381.
-
(1975)
Clin Genet
, vol.7
, pp. 368-381
-
-
Wegenke, J.D.1
Uehling, D.T.2
Wear Jr., J.B.3
Gordon, E.S.4
Bargman, J.G.5
Deacon, J.S.6
Herrmann, J.P.7
Opitz, J.M.8
-
8
-
-
0025938481
-
A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules
-
Franco B, Guioli S, Pragliola A, Incerti B, Bardoni B, Tonlorenzi R, Carrozzo R, Maestrini E, Pieretti M, Taillon-Miller P, Brown CJ, Willard HF, Lawrence C, Persico MG, Camerino G, Ballabio A: A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules. Nature 1991, 353:529-536.
-
(1991)
Nature
, vol.353
, pp. 529-536
-
-
Franco, B.1
Guioli, S.2
Pragliola, A.3
Incerti, B.4
Bardoni, B.5
Tonlorenzi, R.6
Carrozzo, R.7
Maestrini, E.8
Pieretti, M.9
Taillon-Miller, P.10
Brown, C.J.11
Willard, H.F.12
Lawrence, C.13
Persico, M.G.14
Camerino, G.15
Ballabio, A.16
-
9
-
-
0025940669
-
The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules
-
Legouis R, Hardelin JP, Levilliers J, Claverie JM, Compain S, Wunderle V, Millasseau P, Le Paslier D, Cohen D, Caterina D, Bougueleret L, Delemarre-Van de Waal H, Lutfalla G, Weissenbach J, Petit C: The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules. Cell 1991, 67:423-435.
-
(1991)
Cell
, vol.67
, pp. 423-435
-
-
Legouis, R.1
Hardelin, J.P.2
Levilliers, J.3
Claverie, J.M.4
Compain, S.5
Wunderle, V.6
Millasseau, P.7
Le Paslier, D.8
Cohen, D.9
Caterina, D.10
Bougueleret, L.11
Delemarre-Van de Waal, H.12
Lutfalla, G.13
Weissenbach, J.14
Petit, C.15
-
10
-
-
20244366799
-
Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome
-
Dode C, Levilliers J, Dupont JM, De Paepe A, Le Du N, Soussi-Yanicostas N, Coimbra RS, Delmaghani S, Compain-Nouaille S, Baverel F, Pecheux C, Le Tessier D, Cruaud C, Delpech M, Speleman F, Vermeulen S, Amalfitano A, Bachelot Y, Bouchard P, Cabrol S, Carel JC, Delemarre-van de Waal H, Goulet-Salmon B, Kottler ML, Richard O, Sanchez-Franco F, Saura R, Young J, Petit C, Hardelin JP: Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome. Nat Genet 2003, 33:463-465.
-
(2003)
Nat Genet
, vol.33
, pp. 463-465
-
-
Dode, C.1
Levilliers, J.2
Dupont, J.M.3
De Paepe, A.4
Le Du, N.5
Soussi-Yanicostas, N.6
Coimbra, R.S.7
Delmaghani, S.8
Compain-Nouaille, S.9
Baverel, F.10
Pecheux, C.11
Le Tessier, D.12
Cruaud, C.13
Delpech, M.14
Speleman, F.15
Vermeulen, S.16
Amalfitano, A.17
Bachelot, Y.18
Bouchard, P.19
Cabrol, S.20
Carel, J.C.21
Delemarre-van de Waal, H.22
Goulet-Salmon, B.23
Kottler, M.L.24
Richard, O.25
Sanchez-Franco, F.26
Saura, R.27
Young, J.28
Petit, C.29
Hardelin, J.P.30
more..
-
11
-
-
0036336826
-
The Kallmann syndrome gene homolog in C. elegans is involved in epidermal morphogenesis and neurite branching
-
Rugarli EI, Di Schiavi E, Hilliard MA, Arbucci S, Ghezzi C, Facciolli A, Coppola G, Ballabio A, Bazzicalupo P: The Kallmann syndrome gene homolog in C. elegans is involved in epidermal morphogenesis and neurite branching. Development 2002, 129:1283-1294.
-
(2002)
Development
, vol.129
, pp. 1283-1294
-
-
Rugarli, E.I.1
Di Schiavi, E.2
Hilliard, M.A.3
Arbucci, S.4
Ghezzi, C.5
Facciolli, A.6
Coppola, G.7
Ballabio, A.8
Bazzicalupo, P.9
-
12
-
-
0037197904
-
Heparan sulfate proteoglycan-dependent induction of axon branching and axon misrouting by the Kallmann syndrome gene kal-1
-
Bülow HE, Berry KL, Topper LH, Peles E, Hobert O: Heparan sulfate proteoglycan-dependent induction of axon branching and axon misrouting by the Kallmann syndrome gene kal-1. Proc Natl Acad Sci USA 2002, 99:6346-6351.
-
(2002)
Proc Natl Acad Sci USA
, vol.99
, pp. 6346-6351
-
-
Bülow, H.E.1
Berry, K.L.2
Topper, L.H.3
Peles, E.4
Hobert, O.5
-
13
-
-
8844228221
-
Embryonic expression pattern of the Drosophila Kallmann syndrome gene kal-1
-
Andrenacci D, Le Bras S, Grimaldi MR, Rugarli EI, Graziani F: Embryonic expression pattern of the Drosophila Kallmann syndrome gene kal-1. Gene Expr Patterns 2004, 5:67-73.
-
(2004)
Gene Expr Patterns
, vol.5
, pp. 67-73
-
-
Andrenacci, D.1
Le Bras, S.2
Grimaldi, M.R.3
Rugarli, E.I.4
Graziani, F.5
-
14
-
-
0027478174
-
Expression of the KAL gene in multiple neuronal sites during chicken development
-
Legouis R, Lievre CA, Leibovici M, Lapointe F, Petit C: Expression of the KAL gene in multiple neuronal sites during chicken development. Proc Natl Acad Sci USA 1993, 90:2461-2465.
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 2461-2465
-
-
Legouis, R.1
Lievre, C.A.2
Leibovici, M.3
Lapointe, F.4
Petit, C.5
-
15
-
-
0027278607
-
Expression pattern of the Kallmann syndrome gene in the olfactory system suggests a role in neuronal targeting
-
Rugarli EI, Lutz B, Kuratani SC, Wawersik S, Borsani G, Ballabio A, Eichele G: Expression pattern of the Kallmann syndrome gene in the olfactory system suggests a role in neuronal targeting. Nat Genet 1993, 4:19-26.
-
(1993)
Nat Genet
, vol.4
, pp. 19-26
-
-
Rugarli, E.I.1
Lutz, B.2
Kuratani, S.C.3
Wawersik, S.4
Borsani, G.5
Ballabio, A.6
Eichele, G.7
-
16
-
-
0028137132
-
Expression of the Kallmann syndrome gene in human fetal brain and in the manipulated chick embryo
-
Lutz B, Kuratani S, Rugarli EI, Wawersik S, Wong C, Bieber FR, Ballabio A, Eichele G: Expression of the Kallmann syndrome gene in human fetal brain and in the manipulated chick embryo. Hum Mol Genet 1994, 3:1717-1723.
-
(1994)
Hum Mol Genet
, vol.3
, pp. 1717-1723
-
-
Lutz, B.1
Kuratani, S.2
Rugarli, E.I.3
Wawersik, S.4
Wong, C.5
Bieber, F.R.6
Ballabio, A.7
Eichele, G.8
-
17
-
-
0031787628
-
Anosmin-1 underlying the X chromosome-linked Kallmann syndrome is an adhesion molecule that can modulate neurite growth in a cell-type specific manner
-
Soussi-Yanicostas N, Faivre-Sarrailh C, Hardelin JP, Levilliers J, Rougon G, Petit C: Anosmin-1 underlying the X chromosome-linked Kallmann syndrome is an adhesion molecule that can modulate neurite growth in a cell-type specific manner. J Cell Sci 1998, 111:2953-2965.
-
(1998)
J Cell Sci
, vol.111
, pp. 2953-2965
-
-
Soussi-Yanicostas, N.1
Faivre-Sarrailh, C.2
Hardelin, J.P.3
Levilliers, J.4
Rougon, G.5
Petit, C.6
-
18
-
-
0037133961
-
Anosmin-1, defective in the X-linked form of Kallmann syndrome, promotes axonal branch formation from olfactory bulb output neurons
-
Soussi-Yanicostas N, De Castro F, Julliard AK, Perfettini I, Chedotal A, Petit C: Anosmin-1, defective in the X-linked form of Kallmann syndrome, promotes axonal branch formation from olfactory bulb output neurons. Cell 2002, 109:217-228.
-
(2002)
Cell
, vol.109
, pp. 217-228
-
-
Soussi-Yanicostas, N.1
De Castro, F.2
Julliard, A.K.3
Perfettini, I.4
Chedotal, A.5
Petit, C.6
-
19
-
-
9444238033
-
The product of X-linked Kallmann's syndrome gene (KAL1) affects the migratory activity of gonadotropin-releasing hormone (GnRH)-producing neurons
-
Cariboni A, Pimpinelli F, Colamarino S, Zaninetti R, Piccolella M, Rumio C, Piva F, Rugarli EI, Maggi R: The product of X-linked Kallmann's syndrome gene (KAL1) affects the migratory activity of gonadotropin-releasing hormone (GnRH)-producing neurons. Hum Mol Genet 2004, 13:2781-2791.
-
(2004)
Hum Mol Genet
, vol.13
, pp. 2781-2791
-
-
Cariboni, A.1
Pimpinelli, F.2
Colamarino, S.3
Zaninetti, R.4
Piccolella, M.5
Rumio, C.6
Piva, F.7
Rugarli, E.I.8
Maggi, R.9
-
20
-
-
0027477310
-
Heterogeneity in the mutations responsible for X chromosome-linked Kallmann syndrome
-
Hardelin JP, Levilliers J, Blanchard S, Carel JC, Leutenegger M, Pinard-Bertelletto JP, Bouloux P, Petit C: Heterogeneity in the mutations responsible for X chromosome-linked Kallmann syndrome. Hum Mol Genet 1993, 2:373-377.
-
(1993)
Hum Mol Genet
, vol.2
, pp. 373-377
-
-
Hardelin, J.P.1
Levilliers, J.2
Blanchard, S.3
Carel, J.C.4
Leutenegger, M.5
Pinard-Bertelletto, J.P.6
Bouloux, P.7
Petit, C.8
-
21
-
-
0037198705
-
Kallmann syndrome: Adhesion, afferents, and anosmia
-
Maccoll G, Bouloux P, Quinton R: Kallmann syndrome: adhesion, afferents, and anosmia. Neuron 2002, 34:675-678.
-
(2002)
Neuron
, vol.34
, pp. 675-678
-
-
Maccoll, G.1
Bouloux, P.2
Quinton, R.3
-
22
-
-
0041941641
-
Sex-specific apoptosis regulates sexual dimorphism in the Drosophila embryonic gonad
-
DeFalco TJ, Verney G, Jenkins AB, McCaffery JM, Russell S, Van Doren M: Sex-specific apoptosis regulates sexual dimorphism in the Drosophila embryonic gonad. Dev Cell 2003, 5:205-216.
-
(2003)
Dev Cell
, vol.5
, pp. 205-216
-
-
DeFalco, T.J.1
Verney, G.2
Jenkins, A.B.3
McCaffery, J.M.4
Russell, S.5
Van Doren, M.6
-
23
-
-
0028795364
-
Control of Drosophila head segment identity by the bZIP homeotic gene cnc
-
Mohler J, Mahaffey JW, Deutsch E, Vani K: Control of Drosophila head segment identity by the bZIP homeotic gene cnc. Development 1995, 121:237-247.
-
(1995)
Development
, vol.121
, pp. 237-247
-
-
Mohler, J.1
Mahaffey, J.W.2
Deutsch, E.3
Vani, K.4
-
24
-
-
0027160708
-
Targeted gene expression as a means of altering cell fates and generating dominant phenotypes
-
Brand AH, Perrimon N: Targeted gene expression as a means of altering cell fates and generating dominant phenotypes. Development 1993, 118:401-415.
-
(1993)
Development
, vol.118
, pp. 401-415
-
-
Brand, A.H.1
Perrimon, N.2
-
25
-
-
0031002430
-
GAL4 enhancer traps expressed in the embryo, larval brain, imaginal discs, and ovary of Drosophila
-
Manseau L, Baradaran A, Brower D, Budhu A, Elefant F, Phan H, Philp AV, Yang M, Glover D, Kaiser K, Palter K, Selleck S: GAL4 enhancer traps expressed in the embryo, larval brain, imaginal discs, and ovary of Drosophila. Dev Dynamics 1997, 209:310-322.
-
(1997)
Dev Dynamics
, vol.209
, pp. 310-322
-
-
Manseau, L.1
Baradaran, A.2
Brower, D.3
Budhu, A.4
Elefant, F.5
Phan, H.6
Philp, A.V.7
Yang, M.8
Glover, D.9
Kaiser, K.10
Palter, K.11
Selleck, S.12
-
26
-
-
0034525271
-
The EGF and FGF receptors mediate neuroglian function to control growth cone decisions during sensory axon guidance in Drosophila
-
Garcia-Alonso L, Romani S, Jimenez F: The EGF and FGF receptors mediate neuroglian function to control growth cone decisions during sensory axon guidance in Drosophila. Neuron 2000, 28:741-752.
-
(2000)
Neuron
, vol.28
, pp. 741-752
-
-
Garcia-Alonso, L.1
Romani, S.2
Jimenez, F.3
-
27
-
-
0032006909
-
Glycosaminoglycan-protein interactions: Definition of consensus sites in glycosaminoglycan binding proteins
-
Hileman RE, Fromm JR, Weiler JM, Linhardt RJ: Glycosaminoglycan-protein interactions: definition of consensus sites in glycosaminoglycan binding proteins. Bioessays 1998, 20:156-167.
-
(1998)
Bioessays
, vol.20
, pp. 156-167
-
-
Hileman, R.E.1
Fromm, J.R.2
Weiler, J.M.3
Linhardt, R.J.4
-
28
-
-
12144288744
-
Clinical assessment and mutation analysis of Kallmann syndrome 1 (KAL1) and fibroblast growth factor receptor 1 (FGFR1, or AL2) in five families and 18 sporadic patients
-
Sato N, Katsumata N, Kagami M, Hasegawa T, Hori N, Kawakita S, Minowada S, Shimotsuka A, Shishiba Y, Yokozawa M, Yasuda T, Nagasaki K, Hasegawa D, Hasegawa Y, Tachibana K, Naiki Y, Horikawa R, Tanaka T, Ogata T: Clinical assessment and mutation analysis of Kallmann syndrome 1 (KAL1) and fibroblast growth factor receptor 1 (FGFR1, or AL2) in five families and 18 sporadic patients. J Clin Endocrinol Metab 2004, 89:1079-1088.
-
(2004)
J Clin Endocrinol Metab
, vol.89
, pp. 1079-1088
-
-
Sato, N.1
Katsumata, N.2
Kagami, M.3
Hasegawa, T.4
Hori, N.5
Kawakita, S.6
Minowada, S.7
Shimotsuka, A.8
Shishiba, Y.9
Yokozawa, M.10
Yasuda, T.11
Nagasaki, K.12
Hasegawa, D.13
Hasegawa, Y.14
Tachibana, K.15
Naiki, Y.16
Horikawa, R.17
Tanaka, T.18
Ogata, T.19
-
29
-
-
0027983638
-
Targeted expression of the signaling molecule decapentaplegic induces pattern duplications and growth alterations in Drosophila wings
-
Capdevila J, Guerrero I: Targeted expression of the signaling molecule decapentaplegic induces pattern duplications and growth alterations in Drosophila wings. EMBO J 1994, 13:4459-4468.
-
(1994)
EMBO J
, vol.13
, pp. 4459-4468
-
-
Capdevila, J.1
Guerrero, I.2
-
30
-
-
9244231594
-
Cross-talk of anosmin-1, the protein implicated in X-linked Kallmann's syndrome, with heparan sulphate and urokinase-type plasminogen activator
-
Hu Y, Gonzalez-Martinez D, Kim SH, Bouloux PM: Cross-talk of anosmin-1, the protein implicated in X-linked Kallmann's syndrome, with heparan sulphate and urokinase-type plasminogen activator. Biochem J 2004, 384:495-505.
-
(2004)
Biochem J
, vol.384
, pp. 495-505
-
-
Hu, Y.1
Gonzalez-Martinez, D.2
Kim, S.H.3
Bouloux, P.M.4
-
31
-
-
16244399678
-
Kallmann syndrome: 14 novel mutations in KAL1 and FGFR1 (KAL2)
-
Albuisson J, Pecheux C, Carel JC, Lacombe D, Leheup B, Lapuzina P, Bouchard P, Legius E, Matthijs G, Wasniewska M, Delpech M, Young J, Hardelin JP, Dode C: Kallmann syndrome: 14 novel mutations in KAL1 and FGFR1 (KAL2). Hum Mutat 2005, 25:98-99.
-
(2005)
Hum Mutat
, vol.25
, pp. 98-99
-
-
Albuisson, J.1
Pecheux, C.2
Carel, J.C.3
Lacombe, D.4
Leheup, B.5
Lapuzina, P.6
Bouchard, P.7
Legius, E.8
Matthijs, G.9
Wasniewska, M.10
Delpech, M.11
Young, J.12
Hardelin, J.P.13
Dode, C.14
-
32
-
-
21444451432
-
Kallmann's syndrome with a novel missense mutation in the KAL1 gene that modifies the major cell adhesion site of the anosmin-1 protein
-
Loidi L, Castro-Feijoo L, Barreiro J, Quinteiro C, Cabanas P, Varela R, Alonso A, Dominguez F, Pombo M: Kallmann's syndrome with a novel missense mutation in the KAL1 gene that modifies the major cell adhesion site of the anosmin-1 protein. J Pediatr Endocrinol Metab 2005, 18:545-8.
-
(2005)
J Pediatr Endocrinol Metab
, vol.18
, pp. 545-548
-
-
Loidi, L.1
Castro-Feijoo, L.2
Barreiro, J.3
Quinteiro, C.4
Cabanas, P.5
Varela, R.6
Alonso, A.7
Dominguez, F.8
Pombo, M.9
-
33
-
-
0019945644
-
Genetic transformation of Drosophila with transposable element vectors
-
Rubin GM, Spradling AC: Genetic transformation of Drosophila with transposable element vectors. Science 1982, 218:348-35.
-
(1982)
Science
, vol.218
, pp. 348-435
-
-
Rubin, G.M.1
Spradling, A.C.2
-
34
-
-
0035030742
-
Direct regulation of the muscle-identity gene apterous by a Hox protein in the somatic mesoderm
-
Capovilla M, Kambris Z, Botas J: Direct regulation of the muscle-identity gene apterous by a Hox protein in the somatic mesoderm. Development 2001, 128:1221-1230.
-
(2001)
Development
, vol.128
, pp. 1221-1230
-
-
Capovilla, M.1
Kambris, Z.2
Botas, J.3
-
35
-
-
0029797416
-
The Kallmann syndrome gene product expressed in COS cells is cleaved on the cell surface to yield a diffusible component
-
Rugarli EI, Ghezzi C, Valsecchi V, Ballabio A: The Kallmann syndrome gene product expressed in COS cells is cleaved on the cell surface to yield a diffusible component. Hum Mol Genet 1996, 5:1109-1115.
-
(1996)
Hum Mol Genet
, vol.5
, pp. 1109-1115
-
-
Rugarli, E.I.1
Ghezzi, C.2
Valsecchi, V.3
Ballabio, A.4
-
37
-
-
0034212674
-
Cell behaviour of Drosophila fat cadherin mutations in wing development
-
Garoia F, Guerra D, Pezzoli MC, Lopez-Varea A, Cavicchi S, Garcia-Bellido A: Cell behaviour of Drosophila fat cadherin mutations in wing development. Mech Dev 2000, 94:95-109.
-
(2000)
Mech Dev
, vol.94
, pp. 95-109
-
-
Garoia, F.1
Guerra, D.2
Pezzoli, M.C.3
Lopez-Varea, A.4
Cavicchi, S.5
Garcia-Bellido, A.6
|