AAAAAA

   
Results: 1-25 | 26-31
Results: 1-25/31
A 11.7-kb deletion triggers intersexuality and polledness in goats
Authors: Pailhoux, E Vigier, B Chaffaux, S Servel, N Taourit, S Furet, JP Fellous, M Grosclaude, F Cribiu, EP Cotinot, C Vaiman, D
Citation: E. Pailhoux et al., A 11.7-kb deletion triggers intersexuality and polledness in goats, NAT GENET, 29(4), 2001, pp. 453-458
Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype-phenotype correlation
Authors: De Baere, E Dixon, MJ Small, KW Jabs, EW Leroy, BP Devriendt, K Gillerot, Y Mortier, G Meire, F Van Maldergem, L Courtens, W Hjalgrim, H Huang, S Liebaers, I Van Regemorter, N Touraine, P Praphanphoj, V Verloes, A Udar, N Yellore, V Chalukya, M Yelchits, S De Paepe, A Kuttenn, F Fellous, M Veitia, R Messiaen, L
Citation: E. De Baere et al., Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype-phenotype correlation, HUM MOL GEN, 10(15), 2001, pp. 1591-1600
NSPc1, a novel mammalian Polycomb gene, is expressed in neural crest-derived structures of the peripheral nervous system
Authors: Nunes, M Blanc, I Maes, J Fellous, M Robert, B McElreavey, K
Citation: M. Nunes et al., NSPc1, a novel mammalian Polycomb gene, is expressed in neural crest-derived structures of the peripheral nervous system, MECH DEVEL, 102(1-2), 2001, pp. 219-222
Transduction of the human gene FAM8A1 by endogenous retrovirus during primate evolution
Authors: Jamain, S Girondot, M Leroy, P Clergue, M Quach, H Fellous, M Bourgeron, T
Citation: S. Jamain et al., Transduction of the human gene FAM8A1 by endogenous retrovirus during primate evolution, GENOMICS, 78(1-2), 2001, pp. 38-45
Identification of the human KIF13A gene homologous to Drosophila kinesin-73 and candidate for schizophrenia
Authors: Jamain, S Quach, H Fellous, M Bourgeron, T
Citation: S. Jamain et al., Identification of the human KIF13A gene homologous to Drosophila kinesin-73 and candidate for schizophrenia, GENOMICS, 74(1), 2001, pp. 36-44
The origin and evolution of mammalian sex chromosomes.
Authors: Quintana-Murci, T Jamain, S Fellous, M
Citation: T. Quintana-murci et al., The origin and evolution of mammalian sex chromosomes., CR AC S III, 324(1), 2001, pp. 1-11
Testis determination in mammals: more questions than answers
Authors: Veitia, RA Salas-Cortes, L Ottolenghi, C Pailhoux, E Cotinot, C Fellous, M
Citation: Ra. Veitia et al., Testis determination in mammals: more questions than answers, MOL C ENDOC, 179(1-2), 2001, pp. 3-16
Uncoordinated HLA-D gene expression in a RFXANK-defective patient with MHCclass II deficiency
Authors: Lennon-Dumenil, AM Barbouche, MR Vedrenne, J Prod'Homme, T Bejaoui, M Ghariani, S Charron, D Fellous, M Dellagi, K Alcaide-Loridan, C
Citation: Am. Lennon-dumenil et al., Uncoordinated HLA-D gene expression in a RFXANK-defective patient with MHCclass II deficiency, J IMMUNOL, 166(9), 2001, pp. 5681-5687
Contribution of domestic animals to the identification of new genes involved in sex determination
Authors: Pailhoux, E Vigier, B Vaiman, D Schibler, L Vaiman, A Cribiu, E Nezer, C Georges, M Sundstrom, J Pelliniemi, LJ Fellous, M Cotinot, C
Citation: E. Pailhoux et al., Contribution of domestic animals to the identification of new genes involved in sex determination, J EXP ZOOL, 290(7), 2001, pp. 700-708
Expression of the human SRY protein during development in normal male gonadal and sex-reversed tissues
Authors: Salas-Cortes, L Jaubert, F Bono, MR Fellous, M Rosemblatt, M
Citation: L. Salas-cortes et al., Expression of the human SRY protein during development in normal male gonadal and sex-reversed tissues, J EXP ZOOL, 290(6), 2001, pp. 607-615
Absence of mutations involving the lim homeobox domain gene LHX9 in 46,XY gonadal agenesis and dysgenesis
Authors: Ottolenghi, C Moreira, C Mendonca, BB Barbieri, M Fellous, M Berkovitz, GD McElreavey, K
Citation: C. Ottolenghi et al., Absence of mutations involving the lim homeobox domain gene LHX9 in 46,XY gonadal agenesis and dysgenesis, J CLIN END, 86(6), 2001, pp. 2465-2469
Y chromosome microsatellite variation in three populations of Jerba Island(Tunisia)
Authors: El Khil, HK Marrakchi, RT Loueslati, BY Langaney, A Fellous, M Elgaaied, AB
Citation: Hk. El Khil et al., Y chromosome microsatellite variation in three populations of Jerba Island(Tunisia), ANN HUM GEN, 65, 2001, pp. 263-270
Absence of mutations involving the INSL3 gene in human idiopathic cryptorchidism
Authors: Krausz, C Quintana-Murci, L Fellous, M Siffroi, JP McElreavey, K
Citation: C. Krausz et al., Absence of mutations involving the INSL3 gene in human idiopathic cryptorchidism, MOL HUM REP, 6(4), 2000, pp. 298-302
The region on 9p associated with 46,XY sex reversal contains several transcripts expressed in the urogenital system and a novel doublesex-related domain
Authors: Ottolenghi, C Veitia, R Quintana-Murci, L Torchard, D Scapoli, L Souleyreau-Therville, N Beckmann, J Fellous, M McElreavey, K
Citation: C. Ottolenghi et al., The region on 9p associated with 46,XY sex reversal contains several transcripts expressed in the urogenital system and a novel doublesex-related domain, GENOMICS, 64(2), 2000, pp. 170-178
The human doublesex-related gene, DMRT2 is homologous to a gene involved in somitogenesis and encodes a potential bicistronic transcript
Authors: Ottolenghi, C Veitia, R Barbieri, M Fellous, M McElreavey, K
Citation: C. Ottolenghi et al., The human doublesex-related gene, DMRT2 is homologous to a gene involved in somitogenesis and encodes a potential bicistronic transcript, GENOMICS, 64(2), 2000, pp. 179-186
Male infertility: molecular pathologies and new therapeutic approaches
Authors: Siffroi, JP Le Bourhis, C Krausz, C Dadoune, JP Fellous, M
Citation: Jp. Siffroi et al., Male infertility: molecular pathologies and new therapeutic approaches, M S-MED SCI, 16(3), 2000, pp. 307-315
SRY protein is expressed in ovotestis and streak gonads from human sex-reversal
Authors: Salas-Cortes, L Jaubert, F Nihoul-Fekete, C Brauner, R Rosemblatt, M Fellous, M
Citation: L. Salas-cortes et al., SRY protein is expressed in ovotestis and streak gonads from human sex-reversal, CYTOG C GEN, 91(1-4), 2000, pp. 212-216
Sex chromosome mosaicism in males carrying Y chromosome long arm deletions
Authors: Siffroi, JP Le Bourhis, C Krausz, C Barbaux, S Quintana-Murci, L Kanafani, S Rouba, H Bujan, L Bourrouillou, G Seifer, I Boucher, D Fellous, M McElreavey, K Dadoune, JP
Citation: Jp. Siffroi et al., Sex chromosome mosaicism in males carrying Y chromosome long arm deletions, HUM REPR, 15(12), 2000, pp. 2559-2562
WT1 splice-site mutations are rarely associated with primary steroid-resistant focal and segmental glomerulosclerosis
Authors: Denamur, E Bocquet, N Baudouin, V Da Silva, F Veitia, R Peuchmaur, M Elion, J Gubler, MC Fellous, M Niaudet, P Loirat, C
Citation: E. Denamur et al., WT1 splice-site mutations are rarely associated with primary steroid-resistant focal and segmental glomerulosclerosis, KIDNEY INT, 57(5), 2000, pp. 1868-1872
sY116, a human Y-linked polymorphic STS
Authors: Saifi, GM Veitia, R El Khil, HK Barbaux, S Tilak, P Thomas, IM Fellous, M
Citation: Gm. Saifi et al., sY116, a human Y-linked polymorphic STS, J GENETICS, 79(1), 2000, pp. 17-20
A study of the coregulation and tissue specificity of XG and MIC2 gene expression in eukaryotic cells
Authors: Fouchet, C Gane, P Huet, M Fellous, M Rouger, P Banting, G Cartron, JP Lopez, C
Citation: C. Fouchet et al., A study of the coregulation and tissue specificity of XG and MIC2 gene expression in eukaryotic cells, BLOOD, 95(5), 2000, pp. 1819-1826
A tribute to Donald Pious (1930-1998)
Authors: Fellous, M
Citation: M. Fellous, A tribute to Donald Pious (1930-1998), MICROBES IN, 1(11), 1999, pp. 837-837
Differential expression of MHC class II isotype chains
Authors: Alcaide-Loridan, C Lennon, AM Bono, MR Barbouche, R Dellagi, K Fellous, M
Citation: C. Alcaide-loridan et al., Differential expression of MHC class II isotype chains, MICROBES IN, 1(11), 1999, pp. 929-934
The same mutation affecting the splicing of WT1 gene is present on Frasiersyndrome patients with or without Wilms' tumor
Authors: Barbosa, AS Hadjiathanasiou, CG Theodoridis, C Papathanasiou, A Tar, A Merksz, M Gyorvari, B Sultan, C Dumas, R Jaubert, F Niaudet, P Moreira, CA Cotinot, C Fellous, M
Citation: As. Barbosa et al., The same mutation affecting the splicing of WT1 gene is present on Frasiersyndrome patients with or without Wilms' tumor, HUM MUTAT, 13(2), 1999, pp. 146-153
High-resolution human/goat comparative map of the goat polled/intersex syndrome (PIS): The human homologue is contained in a human YAC from HSA3q23
Authors: Vaiman, D Schibler, L Oustry-Vaiman, A Pailhoux, E Goldammer, T Stevanovic, M Furet, JP Schwerin, M Cotinot, C Fellous, M Cribiu, EP
Citation: D. Vaiman et al., High-resolution human/goat comparative map of the goat polled/intersex syndrome (PIS): The human homologue is contained in a human YAC from HSA3q23, GENOMICS, 56(1), 1999, pp. 31-39
Risultati: 1-25 | 26-31