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Results: 1-25 | 26-30
Results: 1-25/30
X-Y translocations and sex differentiation
Authors: McElreavey, K Cortes, LS
Citation: K. Mcelreavey et Ls. Cortes, X-Y translocations and sex differentiation, SEMIN REP M, 19(2), 2001, pp. 133-139
Identification of a Y chromosome haplogroup associated with reduced sperm counts
Authors: Krausz, C Quintana-Murci, L Rajpert-De Meyts, E Jorgensen, N Jobling, MA Rosser, ZH Skakkebaek, NE McElreavey, K
Citation: C. Krausz et al., Identification of a Y chromosome haplogroup associated with reduced sperm counts, HUM MOL GEN, 10(18), 2001, pp. 1873-1877
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
The human Y chromosome: function, evolution and disease
Authors: Quintana-Murci, L Krausz, C McElreavey, K
Citation: L. Quintana-murci et al., The human Y chromosome: function, evolution and disease, FOREN SCI I, 118(2-3), 2001, pp. 169-181
The relationship between Y chromosome DNA haplotypes and Y chromosome deletions leading to male infertility
Authors: Quintana-Murci, L Krausz, C Heyer, E Gromoll, J Seifer, I Barton, DE Barrett, T Skakkebaek, NE Rajpert-De Meyts, E Mitchell, M Lee, AC Jobling, MA McElreavey, K
Citation: L. Quintana-murci et al., The relationship between Y chromosome DNA haplotypes and Y chromosome deletions leading to male infertility, HUM GENET, 108(1), 2001, pp. 55-58
Y chromosome microdeletions in 'fertile' males
Authors: Krausz, C McElreavey, K
Citation: C. Krausz et K. Mcelreavey, Y chromosome microdeletions in 'fertile' males, HUM REPR, 16(6), 2001, pp. 1306-1307
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
Double-blind Y chromosome microdeletion analysis in men with known sperm parameters and reproductive hormone profiles: Microdeletions are specific for spermatogenic failure
Authors: Krausz, C Rajpert-De Meyts, E Frydelund-Larsen, L Quintana-Murci, L McElreavey, K Skakkebaek, NE
Citation: C. Krausz et al., Double-blind Y chromosome microdeletion analysis in men with known sperm parameters and reproductive hormone profiles: Microdeletions are specific for spermatogenic failure, J CLIN END, 86(6), 2001, pp. 2638-2642
Y-chromosome lineages trace diffusion of people and languages in southwestern Asia
Authors: Quintana-Murci, L Krausz, C Zerjal, T Sayar, SH Hammer, MF Mehdi, SQ Ayub, Q Qamar, R Mohyuddin, A Radhakrishna, U Jobling, MA Tyler-Smith, C McElreavey, K
Citation: L. Quintana-murci et al., Y-chromosome lineages trace diffusion of people and languages in southwestern Asia, AM J HU GEN, 68(2), 2001, pp. 537-542
Y chromosome microdeletions and germinal mosaicism in infertile males
Authors: Le Bourhis, C Siffroi, JP McElreavey, K Dadoune, JP
Citation: C. Le Bourhis et al., Y chromosome microdeletions and germinal mosaicism in infertile males, MOL HUM REP, 6(8), 2000, pp. 688-693
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
Deletions of 9p and the quest for a conserved mechanism of sex determination
Authors: Ottolenghi, C McElreavey, K
Citation: C. Ottolenghi et K. Mcelreavey, Deletions of 9p and the quest for a conserved mechanism of sex determination, MOL GEN MET, 71(1-2), 2000, pp. 397-404
SRY, SOX9, and DAX1 expression patterns during human sex determination andgonadal development
Authors: Hanley, NA Hagan, DM Clement-Jones, M Ball, SG Strachan, T Salas-Cortes, L McElreavey, K Lindsay, S Robson, S Bullen, P Ostrer, H Wilson, DI
Citation: Na. Hanley et al., SRY, SOX9, and DAX1 expression patterns during human sex determination andgonadal development, MECH DEVEL, 91(1-2), 2000, pp. 403-407
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
Prognostic value of Y deletion analysis - What is the clinical prognostic value of Y chromosome microdeletion analysis?
Authors: Krausz, C Quintana-Murci, L McElreavey, K
Citation: C. Krausz et al., Prognostic value of Y deletion analysis - What is the clinical prognostic value of Y chromosome microdeletion analysis?, HUM REPR, 15(7), 2000, pp. 1431-1434
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
Y-chromosomal diversity in Europe is clinal and influenced primarily by geography, rather than by language
Authors: Rosser, ZH Zerjal, T Hurles, ME Adojaan, M Alavantic, D Amorim, A Amos, W Armenteros, M Arroyo, E Barbujani, G Beckman, G Beckman, L Bertranpetit, J Bosch, E Bradley, DG Brede, G Cooper, G Corte-Real, HBSM de Knijff, P Decorte, R Dubrova, YE Evgrafov, O Gilissen, A Glisic, S Golge, M Hill, EW Jeziorowska, A Kalaydjieva, L Kayser, M Kivisild, T Kravchenko, SA Krumina, A Kucinskas, V Lavinha, J Livshits, LA Malaspina, P Maria, S McElreavey, K Meitinger, TA Mikelsaar, AV Mitchell, RJ Nafa, K Nicholson, J Norby, S Pandya, A Parik, J Patsalis, PC Pereira, L Peterlin, B Pielberg, G Prata, ML Previdere, C Roewer, L Rootsi, S Rubinsztein, DC Saillard, J Santos, FR Stefanescu, G Sykes, BC Tolun, A Villems, R Tyler-Smith, C Jobling, MA
Citation: Zh. Rosser et al., Y-chromosomal diversity in Europe is clinal and influenced primarily by geography, rather than by language, AM J HU GEN, 67(6), 2000, pp. 1526-1543
Genetic evidence of an early exit of Homo sapiens sapiens from Africa through eastern Africa
Authors: Quintana-Murci, L Semino, O Bandelt, HJ Passarino, G McElreavey, K Santachiara-Benerecetti, AS
Citation: L. Quintana-murci et al., Genetic evidence of an early exit of Homo sapiens sapiens from Africa through eastern Africa, NAT GENET, 23(4), 1999, pp. 437-441
Frasier syndrome: A cause of focal segmental glomerulosclerosis in a 46,XXfemale
Authors: Demmer, L Primack, W Loik, V Brown, R Therville, N McElreavey, K
Citation: L. Demmer et al., Frasier syndrome: A cause of focal segmental glomerulosclerosis in a 46,XXfemale, J AM S NEPH, 10(10), 1999, pp. 2215-2218
Mitochondrial DNA, Y chromosome and human population history
Authors: Quintana-Murci, L Veitia, R Santachiara-Benerecetti, S McElreavey, K Fellous, M Bourgeron, T
Citation: L. Quintana-murci et al., Mitochondrial DNA, Y chromosome and human population history, M S-MED SCI, 15(8-9), 1999, pp. 974-982
Ullrich-Turner syndrome: Relevance of searching for Y chromosome fragments
Authors: Damiani, D Guedes, DR Fellous, M Barbaux, S McElreavey, K Kalil, J Goldberg, ACK Moreira, CA Barbosa, A Manna, TD Dichtchekenian, V Setian, N
Citation: D. Damiani et al., Ullrich-Turner syndrome: Relevance of searching for Y chromosome fragments, J PED END M, 12(6), 1999, pp. 827-831
Screening for microdeletions of Y chromosome genes in patients undergoing intracytoplasmic sperm injection
Authors: Krausz, C Bussani-Mastellone, C Granchi, S McElreavey, K Scarselli, G Forti, G
Citation: C. Krausz et al., Screening for microdeletions of Y chromosome genes in patients undergoing intracytoplasmic sperm injection, HUM REPR, 14(7), 1999, pp. 1717-1721
The human SRY protein is present in fetal and adult Sertoli cells and germcells
Authors: Salas-Cortes, L Jaubert, F Barbaux, S Nessmann, C Bono, MR Fellous, M McElreavey, K Rosemblatt, M
Citation: L. Salas-cortes et al., The human SRY protein is present in fetal and adult Sertoli cells and germcells, INT J DEV B, 43(2), 1999, pp. 135-140
Sex determination and the Y chromosome
Authors: McElreavey, K Fellous, M
Citation: K. Mcelreavey et M. Fellous, Sex determination and the Y chromosome, AM J MED G, 89(4), 1999, pp. 176-185
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