-
1
-
-
0029118115
-
Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure
-
Aittomaki K, Lucena JLD, Pakarinen P, Sistonen P, Tapanainen J, Gromoll J, Kaskikari R, et al (1995) Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure. Cell 82:959-968
-
(1995)
Cell
, vol.82
, pp. 959-968
-
-
Aittomaki, K.1
Lucena, J.L.D.2
Pakarinen, P.3
Sistonen, P.4
Tapanainen, J.5
Gromoll, J.6
Kaskikari, R.7
-
2
-
-
9044223283
-
Identification and mapping of human cDNAs homologous to Drosophila mutant genes through EST database searching
-
Banfi S, Borsani G, Rossi E, Bernard L, Guffanti A, Rubboli F, Marchitiello A, et al (1996) Identification and mapping of human cDNAs homologous to Drosophila mutant genes through EST database searching. Nat Genet 13:167-174
-
(1996)
Nat Genet
, vol.13
, pp. 167-174
-
-
Banfi, S.1
Borsani, G.2
Rossi, E.3
Bernard, L.4
Guffanti, A.5
Rubboli, F.6
Marchitiello, A.7
-
3
-
-
0027985787
-
Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy
-
Bione S, Maestrini E, Rivella S, Mancini M, Regis S, Romeo G, Toniolo D (1994) Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy. Nat Genet 8:323-327
-
(1994)
Nat Genet
, vol.8
, pp. 323-327
-
-
Bione, S.1
Maestrini, E.2
Rivella, S.3
Mancini, M.4
Regis, S.5
Romeo, G.6
Toniolo, D.7
-
4
-
-
0027524597
-
Transcriptional organization of a 450-kb region of the human X chromosome in Xq28
-
Bione S, Tamanini F, Maestrini E, Tribioli C, Poustka A, Torri G, Rivella S, et al (1993) Transcriptional organization of a 450-kb region of the human X chromosome in Xq28. Proc Natl Acad Sci USA 90:10977-10981
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 10977-10981
-
-
Bione, S.1
Tamanini, F.2
Maestrini, E.3
Tribioli, C.4
Poustka, A.5
Torri, G.6
Rivella, S.7
-
5
-
-
0028053435
-
Diaphanous is required for cytokinesis in Drosophila and shares domains of similarity with the products of the limb deformity gene
-
Castrillon DH, Wasserman SA (1994) diaphanous is required for cytokinesis in Drosophila and shares domains of similarity with the products of the limb deformity gene. Development 120:3367-3377
-
(1994)
Development
, vol.120
, pp. 3367-3377
-
-
Castrillon, D.H.1
Wasserman, S.A.2
-
6
-
-
0029833287
-
Genetic evidence that formins function within the nucleus
-
Chan DC, Leder P (1996) Genetic evidence that formins function within the nucleus. J Biol Chem 271:23472-23477
-
(1996)
J Biol Chem
, vol.271
, pp. 23472-23477
-
-
Chan, D.C.1
Leder, P.2
-
7
-
-
0030958087
-
cdc12p, a protein required for cytokinesis in fission yeast, is a component of the cell division ring and interacts with profilin
-
Chang F, Drubin D, Nurse P (1997) cdc12p, a protein required for cytokinesis in fission yeast, is a component of the cell division ring and interacts with profilin. J Cell Biol 137: 169-182
-
(1997)
J Cell Biol
, vol.137
, pp. 169-182
-
-
Chang, F.1
Drubin, D.2
Nurse, P.3
-
8
-
-
0020359680
-
Premature gonadal failure
-
Coulam CB (1982) Premature gonadal failure. Fertil Steril 38: 645-655
-
(1982)
Fertil Steril
, vol.38
, pp. 645-655
-
-
Coulam, C.B.1
-
9
-
-
0028973402
-
Cappuccino, a Drosophila maternal effect gene required for polarity of the egg and embryo, is related to the vertebrate limb deformity locus
-
Emmons S, Phan H, Galley J, Chen W, James B, Manseau L (1995) cappuccino, a Drosophila maternal effect gene required for polarity of the egg and embryo, is related to the vertebrate limb deformity locus. Genes Dev 9:2482-2494
-
(1995)
Genes Dev
, vol.9
, pp. 2482-2494
-
-
Emmons, S.1
Phan, H.2
Galley, J.3
Chen, W.4
James, B.5
Manseau, L.6
-
10
-
-
0030932405
-
Bni1p, a yeast formin linking Cdc42p and the actin cytoskeleton during polarized morphogenesis
-
Evangelista M, Blundell K, Longtine MS, Chow CJ, Adames N, Pringle JR, Peter M, et al (1997) Bni1p, a yeast formin linking Cdc42p and the actin cytoskeleton during polarized morphogenesis. Science 276:118-122
-
(1997)
Science
, vol.276
, pp. 118-122
-
-
Evangelista, M.1
Blundell, K.2
Longtine, M.S.3
Chow, C.J.4
Adames, N.5
Pringle, J.R.6
Peter, M.7
-
11
-
-
0030927282
-
The Aspergillus nidulans sepA gene encodes an FH1/2 protein involved in cytokinesis and the maintenance of cellular polarity
-
Harris SD, Hamer L, Sharpless KE, Hamer JE (1997) The Aspergillus nidulans sepA gene encodes an FH1/2 protein involved in cytokinesis and the maintenance of cellular polarity. EMBO J 16:3474-3483
-
(1997)
EMBO J
, vol.16
, pp. 3474-3483
-
-
Harris, S.D.1
Hamer, L.2
Sharpless, K.E.3
Hamer, J.E.4
-
12
-
-
0030927327
-
Bnilp and Bnrlp: Downstream targets of the Rho family small G-proteins which interact with profilin and regulate actin cytoskeleton in Saccharomyces cerevisiae
-
Imamura H, Tanaka K, Hihara T, Umikawa M, Kamei T, Takahashi K, Sasaki T, et al (1997) Bnilp and Bnrlp: downstream targets of the Rho family small G-proteins which interact with profilin and regulate actin cytoskeleton in Saccharomyces cerevisiae. EMBO J 16:2745-2755
-
(1997)
EMBO J
, vol.16
, pp. 2745-2755
-
-
Imamura, H.1
Tanaka, K.2
Hihara, T.3
Umikawa, M.4
Kamei, T.5
Takahashi, K.6
Sasaki, T.7
-
13
-
-
10544228528
-
Bnilp implicated in cytoskeletal control is a putative target of Rho1p small GTP binding protein in Saccharomyces cerevisiae
-
Kohno H, Tanaka K, Mino A, Umikawa M, Imamura H, Fujiwara T, Fujita Y, et al (1996) Bnilp implicated in cytoskeletal control is a putative target of Rho1p small GTP binding protein in Saccharomyces cerevisiae. EMBO J 15: 6060-6068
-
(1996)
EMBO J
, vol.15
, pp. 6060-6068
-
-
Kohno, H.1
Tanaka, K.2
Mino, A.3
Umikawa, M.4
Imamura, H.5
Fujiwara, T.6
Fujita, Y.7
-
14
-
-
0030707797
-
Nonsyndromic deafness DFNA1 associated with mutation of a human homolog of the Drosophila gene diaphanous
-
Lynch ED, Lee MK, Morrow JE, Welcsh PL, Leon PE, King M-C (1997) Nonsyndromic deafness DFNA1 associated with mutation of a human homolog of the Drosophila gene diaphanous. Science 278:1315-1318
-
(1997)
Science
, vol.278
, pp. 1315-1318
-
-
Lynch, E.D.1
Lee, M.K.2
Morrow, J.E.3
Welcsh, P.L.4
Leon, P.E.5
King, M.-C.6
-
15
-
-
0025035808
-
Disruption of formin-encoding transcripts in two mutant limb deformity alleles
-
Maas RL, Zeller R, Woychik RP, Vogt TF, Leder P (1990) Disruption of formin-encoding transcripts in two mutant limb deformity alleles. Nature 346:853-855
-
(1990)
Nature
, vol.346
, pp. 853-855
-
-
Maas, R.L.1
Zeller, R.2
Woychik, R.P.3
Vogt, T.F.4
Leder, P.5
-
16
-
-
0024444395
-
Choroideremia and deafness with stapes fixation: A contiguous gene deletion syndrome in Xq21
-
Merry DE, Lesko JG, Sosnoski DM, Lewis RA, Lubinsky M, Trask B, van den Engh G, et al (1989) Choroideremia and deafness with stapes fixation: a contiguous gene deletion syndrome in Xq21. Am J Med Genet 45:530-540
-
(1989)
Am J Med Genet
, vol.45
, pp. 530-540
-
-
Merry, D.E.1
Lesko, J.G.2
Sosnoski, D.M.3
Lewis, R.A.4
Lubinsky, M.5
Trask, B.6
Van Den Engh, G.7
-
17
-
-
0029019950
-
Characterization of fus1 of Schizosaccharomyces pombe: A developmentally controlled function needed for conjugation
-
Petersen J, Weilguny D, Egel R, Nielsen O (1995) Characterization of fus1 of Schizosaccharomyces pombe: a developmentally controlled function needed for conjugation. Mol Cell Biol 15:3697-3707
-
(1995)
Mol Cell Biol
, vol.15
, pp. 3697-3707
-
-
Petersen, J.1
Weilguny, D.2
Egel, R.3
Nielsen, O.4
-
18
-
-
0027283764
-
Physical mapping of DNA markers in the q13-q22 region of the human X chromosome
-
Philippe C, Cremers FPM, Chery M, Bach I, Abbadi N, Ropers HH, Gilgenkrantz S (1993) Physical mapping of DNA markers in the q13-q22 region of the human X chromosome. Genomics 17:147-152
-
(1993)
Genomics
, vol.17
, pp. 147-152
-
-
Philippe, C.1
Cremers, F.P.M.2
Chery, M.3
Bach, I.4
Abbadi, N.5
Ropers, H.H.6
Gilgenkrantz, S.7
-
19
-
-
0028087750
-
Molecular and cytogenetic studies of an X;autosome translocation in a patient with premature ovarian failure and review of the literature
-
Powell CM, Taggart RT, Drumheller TC, Wangsa D, Qian C, Nelson LM, White BJ (1994) Molecular and cytogenetic studies of an X;autosome translocation in a patient with premature ovarian failure and review of the literature. Am J Med Genet 52:19-26
-
(1994)
Am J Med Genet
, vol.52
, pp. 19-26
-
-
Powell, C.M.1
Taggart, R.T.2
Drumheller, T.C.3
Wangsa, D.4
Qian, C.5
Nelson, L.M.6
White, B.J.7
-
20
-
-
0028081303
-
Order of six loci at 2q24-q13 and orientation of the HOXD locus
-
Rossi E, Faiella A, Zeviani M, Labeit S, Florida S, Brunelli S, Cammarata M, et al (1994) Order of six loci at 2q24-q13 and orientation of the HOXD locus. Genomics 24:34-40
-
(1994)
Genomics
, vol.24
, pp. 34-40
-
-
Rossi, E.1
Faiella, A.2
Zeviani, M.3
Labeit, S.4
Florida, S.5
Brunelli, S.6
Cammarata, M.7
-
21
-
-
0031568876
-
Eleven X chromosome breakpoints associated with premature ovarian failure (POF) map to a 15-Mb YAC contig spanning Xq21
-
Sala C, Arrigo G, Torri G, Martinazzi F, Riva P, Larizza L, Philippe C, et al (1997) Eleven X chromosome breakpoints associated with premature ovarian failure (POF) map to a 15-Mb YAC contig spanning Xq21. Genomics 40:123-131
-
(1997)
Genomics
, vol.40
, pp. 123-131
-
-
Sala, C.1
Arrigo, G.2
Torri, G.3
Martinazzi, F.4
Riva, P.5
Larizza, L.6
Philippe, C.7
-
23
-
-
0025092789
-
The critical region on the human Xq
-
Therman E, Laxova R, Susman B (1990) The critical region on the human Xq. Hum Genet 85:455-461
-
(1990)
Hum Genet
, vol.85
, pp. 455-461
-
-
Therman, E.1
Laxova, R.2
Susman, B.3
-
24
-
-
0029111481
-
Yeast artificial chromosome cloning of the Xq13.3-q21.31 region and fine mapping of a deletion associated with choroideremia and nonspecific mental retardation
-
van der Maarel SM, Scholten IHJM, Maat-Kievit JA, Huber I, de Kok YJM, de Wijs I, van de Pol TJR, et al (1995) Yeast artificial chromosome cloning of the Xq13.3-q21.31 region and fine mapping of a deletion associated with choroideremia and nonspecific mental retardation. Eur J Hum Genet 3:207-218
-
(1995)
Eur J Hum Genet
, vol.3
, pp. 207-218
-
-
Van Der Maarel, S.M.1
Scholten, I.H.J.M.2
Maat-Kievit, J.A.3
Huber, I.4
De Kok, Y.J.M.5
De Wijs, I.6
Van De Pol, T.J.R.7
-
25
-
-
0029297889
-
Awakening dormant mRNAs
-
Vassalli JD, Stutz A (1995) Awakening dormant mRNAs. Curr Biol 5:476-479
-
(1995)
Curr Biol
, vol.5
, pp. 476-479
-
-
Vassalli, J.D.1
Stutz, A.2
-
26
-
-
0030911424
-
p140mDia, a mammalian homolog of Drosophila diaphanous, is a target protein for Rho small GTPase and is a ligand for profilin
-
Watanabe N, Madaule P, Reid T, Ishizaki T, Watanabe G, Kakizuka A, Saito Y, et al (1997) p140mDia, a mammalian homolog of Drosophila diaphanous, is a target protein for Rho small GTPase and is a ligand for profilin. EMBO J 16: 3044-3056
-
(1997)
EMBO J
, vol.16
, pp. 3044-3056
-
-
Watanabe, N.1
Madaule, P.2
Reid, T.3
Ishizaki, T.4
Watanabe, G.5
Kakizuka, A.6
Saito, Y.7
-
27
-
-
0025007616
-
"Formins": Proteins deduced from the alternative transcripts of the limb deformity gene
-
Woychik RP, Maas RL, Zeller R, Vogt TF, Leder P (1990) "Formins": proteins deduced from the alternative transcripts of the limb deformity gene. Nature 346:850-853
-
(1990)
Nature
, vol.346
, pp. 850-853
-
-
Woychik, R.P.1
Maas, R.L.2
Zeller, R.3
Vogt, T.F.4
Leder, P.5
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