-
1
-
-
0032130368
-
Dynamics of meiotic prophase I during spermatogenesis: From pairing to division
-
Cobb, J., and Handel, M. A. (1998) Dynamics of meiotic prophase I during spermatogenesis: from pairing to division. Semin. Cell Dev. Biol. 9, 440-450
-
(1998)
Semin. Cell Dev. Biol.
, vol.9
, pp. 440-450
-
-
Cobb, J.1
Handel, M.A.2
-
2
-
-
0032076484
-
Zip2, a meiosis-specific protein required for the initiation of chromosome synapsis
-
Chua, P. R., and Roeder, G. S. (1998) Zip2, a meiosis-specific protein required for the initiation of chromosome synapsis. Cell 93, 349-359
-
(1998)
Cell
, vol.93
, pp. 349-359
-
-
Chua, P.R.1
Roeder, G.S.2
-
3
-
-
0032493878
-
Meiotic recombination in C. Elegans initiates by a conserved mechanism and is dispensable for homologous chromosome synapsis
-
Dernburg, A. F., McDonald, K., Moulder, G., Barstead, R., Dresser, M., and Villeneuve, A. M. (1998) Meiotic recombination in C. elegans initiates by a conserved mechanism and is dispensable for homologous chromosome synapsis. Cell 94, 387-398
-
(1998)
Cell
, vol.94
, pp. 387-398
-
-
Dernburg, A.F.1
McDonald, K.2
Moulder, G.3
Barstead, R.4
Dresser, M.5
Villeneuve, A.M.6
-
4
-
-
0032493921
-
The meiosis-specific Hop2 protein of S. Cerevisiae ensures synapsis between homologous chromosomes
-
Leu, J.-Y., Chua, P. R., and Roeder, G. S. (1998) The meiosis-specific Hop2 protein of S. cerevisiae ensures synapsis between homologous chromosomes. Cell 94, 375-386
-
(1998)
Cell
, vol.94
, pp. 375-386
-
-
Leu, J.-Y.1
Chua, P.R.2
Roeder, G.S.3
-
5
-
-
0032535037
-
Maintenance of sister-chromatid cohesion at the centromere by the Drosophila MEI-s332 protein
-
Tang, T. T.-L., Bickel, S. E., Young, L. M., and Orr-Weaver, T. L. (1998) Maintenance of sister-chromatid cohesion at the centromere by the Drosophila MEI-S332 protein. Genes Dev. 12, 3843-3856
-
(1998)
Genes Dev.
, vol.12
, pp. 3843-3856
-
-
Tang, T.T.-L.1
Bickel, S.E.2
Young, L.M.3
Orr-Weaver, T.L.4
-
6
-
-
0030748778
-
SA-1, a nuclear protein encoded by one member of a novel gene family molecular cloning and detection in hemopoietic organs
-
Carramolino, L., Lee, B. C., Zaballos, A., Peled, A., Barthelemy, I., Shav-Tal, Y., Prieto, I., Carmi, P., Gothelf, Y., González de Buitrago, G., Aracil, M., Márquez, G., Barbero, J. L., and Zipori, D. (1997) SA-1, a nuclear protein encoded by one member of a novel gene family molecular cloning and detection in hemopoietic organs. Gene 195, 151-159
-
(1997)
Gene
, vol.195
, pp. 151-159
-
-
Carramolino, L.1
Lee, B.C.2
Zaballos, A.3
Peled, A.4
Barthelemy, I.5
Shav-Tal, Y.6
Prieto, I.7
Carmi, P.8
Gothelf, Y.9
González De Buitrago, G.10
Aracil, M.11
Márquez, G.12
Barbero, J.L.13
Zipori, D.14
-
7
-
-
0031815480
-
Molecular cloning and expression of stromalin protein from drosophila melanogaster: Homologous to mammalian stromalin family of nuclear proteins
-
Valdeolmillos, A., Villares, R., Buesa, J. M., González-Crespo, S., Martínez-A., C., and Barbero, J. L. (1998) Molecular cloning and expression of stromalin protein from Drosophila melanogaster: homologous to mammalian stromalin family of nuclear proteins. DNA Cell Biol. 17, 699-706
-
(1998)
DNA Cell Biol.
, vol.17
, pp. 699-706
-
-
Valdeolmillos, A.1
Villares, R.2
Buesa, J.M.3
González-Crespo, S.4
And Barbero, J.L.5
-
8
-
-
0028295681
-
2.2 Mb of contiguous nucleotide sequence from chromosome III of C. Elegans
-
Wilson, R., Ainscough, R., Anderson, K., Baynes, C., Berks, M., Bonfield, J., Burton, J., Connell, M., Copsev, T., Cooper, J., Coulson, A., Craxton, M., Dear, S., Du, Z., Durbin, R., Favelio, A., Fulton, L., Gardner, A., Green, P., Hawkins, T., Miller, L., Jier, M., Johnston, L., Jones, M., Kershae, J., Kirsten, J., Laister, N., Latreille, P., Lightning, J., Lloyd, C., McMurrary, A., Mortimore, B., O'Callaghan, M., Parsons, J., Percy, C., Rilken, L., Roopra, A., Saunders, D., Shownkeen, R., Smaldon, N., Smith, A., Sonnhammer, F., Staden, R., Sulston, J., Thierry-Mieg, J., Thomas, K., Vaudin, M., Vaughan, K., Waterston, R., Watson, A., Weinstock, L., Wilkinson-Sproat, J., and Wohldman, P. (1994) 2.2 Mb of contiguous nucleotide sequence from chromosome III of C. elegans. Nature (London) 368, 32-38
-
(1994)
Nature (London)
, vol.368
, pp. 32-38
-
-
Wilson, R.1
Ainscough, R.2
Anderson, K.3
Baynes, C.4
Berks, M.5
Bonfield, J.6
Burton, J.7
Connell, M.8
Copsev, T.9
Cooper, J.10
Coulson, A.11
Craxton, M.12
Dear, S.13
Du, Z.14
Durbin, R.15
Favelio, A.16
Fulton, L.17
Gardner, A.18
Green, P.19
Hawkins, T.20
Miller, L.21
Jier, M.22
Johnston, L.23
Jones, M.24
Kershae, J.25
Kirsten, J.26
Laister, N.27
Latreille, P.28
Lightning, J.29
Lloyd, C.30
McMurrary, A.31
Mortimore, B.32
O'Callaghan, M.33
Parsons, J.34
Percy, C.35
Rilken, L.36
Roopra, A.37
Saunders, D.38
Shownkeen, R.39
Smaldon, N.40
Smith, A.41
Sonnhammer, F.42
Staden, R.43
Sulston, J.44
Thierry-Mieg, J.45
Thomas, K.46
Vaudin, M.47
Vaughan, K.48
Waterston, R.49
Watson, A.50
Weinstock, L.51
Wilkinson-Sproat, J.52
Wohldman, P.53
more..
-
9
-
-
0029074430
-
A new essential gene located on saccharomyces cerevisiase chromosome IX
-
Kurlandzka, A., Rytka, J., Gromadka, R., and Murawski, M. (1995) A new essential gene located on Saccharomyces cerevisiase chromosome IX. Yeast 11, 885-890
-
(1995)
Yeast
, vol.11
, pp. 885-890
-
-
Kurlandzka, A.1
Rytka, J.2
Gromadka, R.3
Murawski, M.4
-
10
-
-
0033083727
-
Yeast cohesin complex requires a conserved protein, Ecolp(Ctf7), to establish cohesion between sister chromatids during DNA replication
-
Töth, A. Ciosk, R., Uhlmann, F., Galova, M., Schleilfer, A., and Nasmyth, K. (1999) Yeast cohesin complex requires a conserved protein, Ecolp(Ctf7), to establish cohesion between sister chromatids during DNA replication, genes Dev. 13, 320-333
-
(1999)
Genes Dev.
, vol.13
, pp. 320-333
-
-
Töth, A.1
Ciosk, R.2
Uhlmann, F.3
Galova, M.4
Schleilfer, A.5
Nasmyth, K.6
-
11
-
-
0022521057
-
Williams syndrome
-
Burn, J. (1986) Williams syndrome. J. Med. Genet. 23, 389-395
-
(1986)
J. Med. Genet.
, vol.23
, pp. 389-395
-
-
Burn, J.1
-
12
-
-
0023688145
-
The natural history of Williams syndrome: Physical characteristics
-
Morris, C. A., Demsey, S. A., Leonard, C. O., Dilts, C., and Blackburn, B. L. (1988) The natural history of Williams syndrome: physical characteristics. J. Pedtatr. 113, 318-326
-
(1988)
J. Pedtatr.
, vol.113
, pp. 318-326
-
-
Morris, C.A.1
Demsey, S.A.2
Leonard, C.O.3
Dilts, C.4
Blackburn, B.L.5
-
13
-
-
0025070995
-
Williams syndrome professional symposim
-
Greenberg, F. (1991) Williams syndrome professional symposim. Am. J. Med. Genet. (Suppl.) 6, 85-88
-
(1991)
Am. J. Med. Genet. (Suppl.)
, vol.6
, pp. 85-88
-
-
Greenberg, F.1
-
14
-
-
0027185655
-
Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome
-
Ewart, A. K., Morris, C. A., Atkinson, D., Jin, W., Sternes, K., Spallone, P., Stock, A. D., Leppert, M., and Keating, M. T. (1993) Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome. Nat. Genet. 5, 11-16
-
(1993)
Nat. Genet.
, vol.5
, pp. 11-16
-
-
Ewart, A.K.1
Morris, C.A.2
Atkinson, D.3
Jin, W.4
Sternes, K.5
Spallone, P.6
Stock, A.D.7
Leppert, M.8
Keating, M.T.9
-
15
-
-
0002391264
-
Molecular definition of the chromosome 7 deletion in Williams syndrome and parent-of-origin effects on growth
-
Pèrez Jurado, L.A., Peoples, R., Wang, Y.-K., Kaplan, P., Hamel, B. C. M., and Francke, U. (1996) Molecular definition of the chromosome 7 deletion in Williams syndrome and parent-of-origin effects on growth. Am. J. Hum. Genet. 59, 781-792
-
(1996)
Am. J. Hum. Genet.
, vol.59
, pp. 781-792
-
-
Pèrez Jurado, L.A.1
Peoples, R.2
Wang, Y.-K.3
Kaplan, P.4
Hamel, B.C.M.5
Francke, U.6
-
16
-
-
0031811718
-
Delineation of the common critical region in williams syndrome and clinical correlation of growth, heart defects, ethnicity and parental origin
-
Wu, Y. Q., Sutton, V. R., Nickerson, E., Lupski, J. R., Potocki, L., Korenberg, J. R., Greenberg, F., Tassabehji, M., and Shaffer, L. G. (1998) Delineation of the common critical region in Williams syndrome and clinical correlation of growth, heart defects, ethnicity and parental origin. Am. J. Med. Genet. 78, 82-89
-
(1998)
Am. J. Med. Genet.
, vol.78
, pp. 82-89
-
-
Wu, Y.Q.1
Sutton, V.R.2
Nickerson, E.3
Lupski, J.R.4
Potocki, L.5
Korenberg, J.R.6
Greenberg, F.7
Tassabehji, M.8
Shaffer, L.G.9
-
17
-
-
0029798778
-
7q11.23 deletions in Williams syndrome arise as a consequence of unequal meiotic crossing over
-
Urbán, Z., Helms, C., Fekete, G., Csiszar, K., Bonnet, D., Munich, A., Donnis-Keller, H., and Boyd, C. (1996) 7q11.23 deletions in Williams syndrome arise as a consequence of unequal meiotic crossing over. Am. J. Hum. Genet. 59, 958-962
-
(1996)
Am. J. Hum. Genet.
, vol.59
, pp. 958-962
-
-
Urbán, Z.1
Helms, C.2
Fekete, G.3
Csiszar, K.4
Bonnet, D.5
Munich, A.6
Donnis-Keller, H.7
Boyd, C.8
-
18
-
-
0029831686
-
Unequal interchromosomal rearrangements may result in elastin gene deletions causing the Williams-Beuren syndrome
-
Dutly, F., and Schinzel, A. (1996) Unequal interchromosomal rearrangements may result in elastin gene deletions causing the Williams-Beuren syndrome. Hum. Mol. Genet. 5, 1893-1898
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 1893-1898
-
-
Dutly, F.1
Schinzel, A.2
-
19
-
-
0031886974
-
A duplicate gene in the breakpoint regions of the Williams-Beuren syndrome deletion encodes the initiator binding protein TFII-I and BAP-135, a phosphorylation target of BTK
-
Pérez Jurado, L. A., Wang, Y.-K., Peoples, R., Coloma, A., Cruces, J., and Francke, U. (1998) A duplicate gene in the breakpoint regions of the Williams-Beuren syndrome deletion encodes the initiator binding protein TFII-I and BAP-135, a phosphorylation target of BTK. Hum. Mol. Genet. 7, 325-334
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 325-334
-
-
Pérez Jurado, L.A.1
Wang, Y.-K.2
Peoples, R.3
Coloma, A.4
Cruces, J.5
Francke, U.6
-
20
-
-
0029891886
-
Delineation of 7q11.2 deletions associated with Williams-Beuren syndrome and maping of a repetitive sequence to within and to either side of the common deletion
-
Robinson, W. P., Waslynka, J., Bernasconi, F., Wang, M., Clark, S., Kotzot, D., and Schinzel, A. (1996) Delineation of 7q11.2 deletions associated with Williams-Beuren syndrome and maping of a repetitive sequence to within and to either side of the common deletion. Genomics 34, 17-23
-
(1996)
Genomics
, vol.34
, pp. 17-23
-
-
Robinson, W.P.1
Waslynka, J.2
Bernasconi, F.3
Wang, M.4
Clark, S.5
Kotzot, D.6
Schinzel, A.7
-
21
-
-
17144434420
-
A high-resolution microsatellite map of the mouse genome
-
Rhodes, M., Straw, R., Fernando, S., Evans, A., Lacey, T., Dearlove, A., Greystrong, J., Walker, J., Watson, P., Weston, P., Kelly, M., Taylor, D., Gibson, K., Mundy, C., Bourgade, F., Poirier, C., Simon, D., Brunialti, A. L., Montagutelli, X., Guenet, J. L., Haynes, A., and Brown, S. D. (1998) A high-resolution microsatellite map of the mouse genome. Genome Res. 8, 531-542
-
(1998)
Genome Res.
, vol.8
, pp. 531-542
-
-
Rhodes, M.1
Straw, R.2
Fernando, S.3
Evans, A.4
Lacey, T.5
Dearlove, A.6
Greystrong, J.7
Walker, J.8
Watson, P.9
Weston, P.10
Kelly, M.11
Taylor, D.12
Gibson, K.13
Mundy, C.14
Bourgade, F.15
Poirier, C.16
Simon, D.17
Brunialti, A.L.18
Montagutelli, X.19
Guenet, J.L.20
Haynes, A.21
Brown, S.D.22
more..
-
22
-
-
0002587852
-
-
Cold Spring Harbor Laboratory, Cold Spring Harbor, New York
-
Sambrook, J., Fritsch, E. F., and Maniatis, T. (1989) Molecular Cloning: A Laboratory Manual, 2nd Ed, pp. 846-855, Cold Spring Harbor Laboratory, Cold Spring Harbor, New York
-
(1989)
Molecular Cloning: A Laboratory Manual, 2nd Ed
, pp. 846-855
-
-
Sambrook, J.1
Fritsch, E.F.2
Maniatis, T.3
-
23
-
-
0021760092
-
A comprehensive set of sequence analysis programs for the VAX
-
Devereux, J., Hacherli, P., and Smithies, O. (1984) A comprehensive set of sequence analysis programs for the VAX. Nucleic Acids Res. 12, 387-395
-
(1984)
Nucleic Acids Res.
, vol.12
, pp. 387-395
-
-
Devereux, J.1
Hacherli, P.2
Smithies, O.3
-
24
-
-
0019877801
-
Affinity purification of antibodies from diazotized paper blots of heterogeneous protein samples
-
Olmsted, J. B. (1981) Affinity purification of antibodies from diazotized paper blots of heterogeneous protein samples. J. Biol. Chem. 256, 11955-11957
-
(1981)
J. Biol. Chem.
, vol.256
, pp. 11955-11957
-
-
Olmsted, J.B.1
-
25
-
-
0028882412
-
Preparation of spermatogonia, spermatocytes and round spermatids for analysis of gene expression using fluorescent-activated cell sorting
-
Mays-Hoopes, L., Bolen, J., Riggs, A. D., and Sam, J. S. (1995) Preparation of spermatogonia, spermatocytes and round spermatids for analysis of gene expression using fluorescent-activated cell sorting. Biol. Reprod. 53, 1003-1011
-
(1995)
Biol. Reprod.
, vol.53
, pp. 1003-1011
-
-
Mays-Hoopes, L.1
Bolen, J.2
Riggs, A.D.3
Sam, J.S.4
-
26
-
-
0022872822
-
Centromere pattern in different mouse seminiferous tubule cells
-
del Mazo, J., Martín-Sempere, M. J., Kremer, L., and Avila, J. (1986) Centromere pattern in different mouse seminiferous tubule cells. Cytogenet. Cell Genet. 43, 201-206
-
(1986)
Cytogenet. Cell Genet.
, vol.43
, pp. 201-206
-
-
Del Mazo, J.1
Martín-Sempere, M.J.2
Kremer, L.3
Avila, J.4
-
27
-
-
0026567977
-
Microtubule-associated proteins during mouse spermatogenesis: Localization of a protein immunologically related to brain MAP1B protein in the synaptonemal complex
-
Gil-Alberdi, L., and del Mazo, J. (1992) Microtubule-associated proteins during mouse spermatogenesis: localization of a protein immunologically related to brain MAP1B protein in the synaptonemal complex. Cytogenet. Cell Genet. 59, 1-5
-
(1992)
Cytogenet. Cell Genet.
, vol.59
, pp. 1-5
-
-
Gil-Alberdi, L.1
Del Mazo, J.2
-
28
-
-
0029100814
-
Analysis of the 5′ region of PMS2 reveals heterogeneous transcripts and a novel overlapping gene
-
Nicolaides, N. C., Kinzler, K. W., and Vogelstein, B. (1995) Analysis of the 5′ region of PMS2 reveals heterogeneous transcripts and a novel overlapping gene. Genomics 29, 329-334
-
(1995)
Genomics
, vol.29
, pp. 329-334
-
-
Nicolaides, N.C.1
Kinzler, K.W.2
Vogelstein, B.3
-
29
-
-
0030667669
-
PMS2-related genes flank the rearrangement breakpoints associated with Williams syndrome and other diseases on human chromosome 7
-
Osborne, L. R., Herbrick, J.-A., Greavette, T., Heng, H. H. Q., Tsui, L.-C., and Scherer, S. W. (1997) PMS2-related genes flank the rearrangement breakpoints associated with Williams syndrome and other diseases on human chromosome 7. Genomics 45, 402-406
-
(1997)
Genomics
, vol.45
, pp. 402-406
-
-
Osborne, L.R.1
Herbrick, J.-A.2
Greavette, T.3
Heng, H.H.Q.4
Tsui, L.-C.5
Scherer, S.W.6
-
30
-
-
0040945789
-
A p47-phox pseudogene carries the most common mutation causing p47-phox-deficient chronic granulomatous disease
-
Gorlach, A., Lee, P. L., Roesler, J., Hopkins, P. J., Christensen, B., Green, E. D., Chanock, S. J., and Curnutte, J. T. (1997) A p47-phox pseudogene carries the most common mutation causing p47-phox-deficient chronic granulomatous disease. J. Clin. Invest. 100, 1907-1918
-
(1997)
J. Clin. Invest.
, vol.100
, pp. 1907-1918
-
-
Gorlach, A.1
Lee, P.L.2
Roesler, J.3
Hopkins, P.J.4
Christensen, B.5
Green, E.D.6
Chanock, S.J.7
Curnutte, J.T.8
-
31
-
-
0027091588
-
A coiled-coil related protein specific for synapsed regions of meiotic prophase chromosomes
-
Meuwissen, R. L. J., Offenberg, H. H., Dietrich, A. J. J., Riesewijk, A., Van Iersel, M., and Heyting, C. (1992) A coiled-coil related protein specific for synapsed regions of meiotic prophase chromosomes. EMBO J. 11, 5091-5100
-
(1992)
EMBO J.
, vol.11
, pp. 5091-5100
-
-
Meuwissen, R.L.J.1
Offenberg, H.H.2
Dietrich, A.J.J.3
Riesewijk, A.4
Van Iersel, M.5
Heyting, C.6
-
32
-
-
0027958447
-
The gene encoding a major component of synaptonemal complexes of the rat is related to X-linked lymphocyte-regulated genes
-
Lammers, J. H. M., Offenberg, H. H., Van Aalderen, M., Vink, A. C. G., Dietrich, A. J. J., and Heyting, C. (1994) The gene encoding a major component of synaptonemal complexes of the rat is related to X-linked lymphocyte-regulated genes. Mol. Cell. Biol. 14, 1137-1146
-
(1994)
Mol. Cell. Biol.
, vol.14
, pp. 1137-1146
-
-
Lammers, J.H.M.1
Offenberg, H.H.2
Van Aalderen, M.3
Vink, A.C.G.4
Dietrich, A.J.J.5
Heyting, C.6
-
33
-
-
0029099989
-
Male mice defective in the DNA mismatch repair gene PMS 2 exhibit abnormal chromosome synapsis in meiosis
-
Baker, S. M., Bronner, C. E., Zhang, L., Plug, A. W., Robatzek, M., Warren, G., Elliot, E. A., Yu, J., Ashley, T., Arnheim, N., Flavell, R. A., and Liskay, R. M. (1995) Male mice defective in the DNA mismatch repair gene PMS 2 exhibit abnormal chromosome synapsis in meiosis. Cell 82, 309-319
-
(1995)
Cell
, vol.82
, pp. 309-319
-
-
Baker, S.M.1
Bronner, C.E.2
Zhang, L.3
Plug, A.W.4
Robatzek, M.5
Warren, G.6
Elliot, E.A.7
Yu, J.8
Ashley, T.9
Arnheim, N.10
Flavell, R.A.11
Liskay, R.M.12
-
34
-
-
15844367099
-
Meiotic pachytene arrest in MLHI-deficient mice
-
Edelmann, W. Cohen, P. E., Kane, M., Lau, K., Morrow, B., Bennett, S., Umar, A., Kunkel, T., Cattoretti, G., Chaganti, R., Pollard, W., Kolodner, R. D., and Kucherlapati, R. (1996) Meiotic pachytene arrest in MLHI-deficient mice. Cell 85, 1125-1134
-
(1996)
Cell
, vol.85
, pp. 1125-1134
-
-
Edelmann, W.1
Cohen, P.E.2
Kane, M.3
Lau, K.4
Morrow, B.5
Bennett, S.6
Umar, A.7
Kunkel, T.8
Cattoretti, G.9
Chaganti, R.10
Pollard, W.11
Kolodner, R.D.12
Kucherlapati, R.13
-
35
-
-
0032900534
-
Mammalian MutS homologue 5 is required for chromosome pairing in meiosis
-
Edelmann, W., Cohen, P. E., Kneitz, B., Winand, N., Lia, M., Heyer, J., Kolodner, R., Pollard, J. W., and Kucherlapati, R. (1999) Mammalian MutS homologue 5 is required for chromosome pairing in meiosis. Nature Genet. 21, 123-127
-
(1999)
Nature Genet.
, vol.21
, pp. 123-127
-
-
Edelmann, W.1
Cohen, P.E.2
Kneitz, B.3
Winand, N.4
Lia, M.5
Heyer, J.6
Kolodner, R.7
Pollard, J.W.8
Kucherlapati, R.9
-
36
-
-
0030818573
-
Distribution of the Rad51 recombinase in human and mouse spermatocytes
-
Barlow, A. Benson, F. E., West, S. C., and Hulten, M. A. (1997) Distribution of the Rad51 recombinase in human and mouse spermatocytes. EMBO J. 16, 5207-5215
-
(1997)
EMBO J.
, vol.16
, pp. 5207-5215
-
-
Barlow, A.1
Benson, F.E.2
West, S.C.3
Hulten, M.A.4
-
37
-
-
0032127940
-
Identification of Xenopus SMC protein complexes required for sister chromatid cohesion
-
Losada, A., Hirano, M., and Hirano, T. (1998) Identification of Xenopus SMC protein complexes required for sister chromatid cohesion. Genes Dev. 12, 1986-1997
-
(1998)
Genes Dev.
, vol.12
, pp. 1986-1997
-
-
Losada, A.1
Hirano, M.2
Hirano, T.3
-
38
-
-
0032564457
-
Identification of more (microorchidia), a mutation that results in arrest of spermatogenesis at an early meiotic stage in the mouse
-
Watson, M. L., Zinn, A. R., Inoue, N., Hess, K. D., Cobb, J., Handel, M. A., Halaban, R., Duchene, C. C., Albright, G. M., and Moreadith, R. W. (1998) Identification of more (microorchidia), a mutation that results in arrest of spermatogenesis at an early meiotic stage in the mouse. Proc. Natl. Acad. Sci. USA 95, 14361-14366
-
(1998)
Proc. Natl. Acad. Sci. USA
, vol.95
, pp. 14361-14366
-
-
Watson, M.L.1
Zinn, A.R.2
Inoue, N.3
Hess, K.D.4
Cobb, J.5
Handel, M.A.6
Halaban, R.7
Duchene, C.C.8
Albright, G.M.9
Moreadith, R.W.10
-
39
-
-
0028128358
-
Case control study of whether subfertility in men is familial
-
Lilford, R., Jones, A. M., Bishop, D. T., Thorton, J., and Mueller, R. (1994) Case control study of whether subfertility in men is familial. Br. Med. J. 309, 570-573
-
(1994)
Br. Med. J.
, vol.309
, pp. 570-573
-
-
Lilford, R.1
Jones, A.M.2
Bishop, D.T.3
Thorton, J.4
Mueller, R.5
-
40
-
-
0029088061
-
Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene
-
Reijo, R., Lee, T.-Y., Sato, P., Alagappan, R., Brown, L. G., Rosenberg, M., Rozen, S., Jaffe, T., Strauss, D., Hovatta, O., de la Chapelle, A., Silber, S., and Page, D. C. (1995) Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene. Nat. Genet. 10, 383-393
-
(1995)
Nat. Genet.
, vol.10
, pp. 383-393
-
-
Reijo, R.1
Lee, T.-Y.2
Sato, P.3
Alagappan, R.4
Brown, L.G.5
Rosenberg, M.6
Rozen, S.7
Jaffe, T.8
Strauss, D.9
Hovatta, O.10
De La Chapelle, A.11
Silber, S.12
Page, D.C.13
-
41
-
-
0019180851
-
Genetically determined asynapsis, spermatogenic degenration and infertility in men
-
Chaganti, R. S. K., Jhanwar, S. C., Ehrenbard, L. T., Kourides, I.. A., and Williams, J. J. (1980) Genetically determined asynapsis, spermatogenic degenration and infertility in men. Am. J. Hum. Genet 32, 833-848
-
(1980)
Am. J. Hum. Genet
, vol.32
, pp. 833-848
-
-
Chaganti, R.S.K.1
Jhanwar, S.C.2
Ehrenbard, L.T.3
Kourides, I.A.4
Williams, J.J.5
-
42
-
-
0029842285
-
The human autosomal gene DAZLA: Testis specificity and a candidate for male infertility
-
Yen, P. H., Chai, N. N., and Salido, E. C. (1996) The human autosomal gene DAZLA: testis specificity and a candidate for male infertility. Hum. Mol. Genet. 5, 2013-2017
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 2013-2017
-
-
Yen, P.H.1
Chai, N.N.2
Salido, E.C.3
-
43
-
-
0019815370
-
Meiotic arrest at first spermatocyte level: A new inherited infertility disorder
-
Cantu, J. M., Rivas, F., Hernandez-Jauregui, P., Diaz, M., Cortes-Gallego, V., Vaca, G., Velazquez, A., and Ibarra, B. (1981) Meiotic arrest at first spermatocyte level: a new inherited infertility disorder. Hum. Genet. 59, 380-385
-
(1981)
Hum. Genet.
, vol.59
, pp. 380-385
-
-
Cantu, J.M.1
Rivas, F.2
Hernandez-Jauregui, P.3
Diaz, M.4
Cortes-Gallego, V.5
Vaca, G.6
Velazquez, A.7
Ibarra, B.8
-
44
-
-
0031945026
-
High level of unequal meiotic crossovers at the origin of the 22q11.1 and 7q11.23 deletions
-
Baumer, A., Dutly, F., Balmer, D., Riegel, M., Tukel, T., Krajewska-Walsek, M., and Schinzel, A. A. (1998) High level of unequal meiotic crossovers at the origin of the 22q11.1 and 7q11.23 deletions. Hum. Mol. Genet. 7, 887-894
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 887-894
-
-
Baumer, A.1
Dutly, F.2
Balmer, D.3
Riegel, M.4
Tukel, T.5
Krajewska-Walsek, M.6
Schinzel, A.A.7
-
45
-
-
0031008697
-
Two discrete regions of deletion at 7q in uterine leiomyomas
-
Ishwad, C. S., Ferrell, R. E., Hanley, K., Davare, J., Meloni, A. M., Sandberg, A. A., and Surti, U. (1997) Two discrete regions of deletion at 7q in uterine leiomyomas. Genes Chromosomes Cancer 19, 156-160
-
(1997)
Genes Chromosomes Cancer
, vol.19
, pp. 156-160
-
-
Ishwad, C.S.1
Ferrell, R.E.2
Hanley, K.3
Davare, J.4
Meloni, A.M.5
Sandberg, A.A.6
Surti, U.7
-
46
-
-
0027275670
-
Heterogeneity in the phosphorylation of microtubule-associated protein MAP1B during rat brain development
-
Ulloa, L., Avila, J., and Diaz-Nido, J. (1993) Heterogeneity in the phosphorylation of microtubule-associated protein MAP1B during rat brain development. J. Neurochem. 61, 961-972
-
(1993)
J. Neurochem.
, vol.61
, pp. 961-972
-
-
Ulloa, L.1
Avila, J.2
Diaz-Nido, J.3
|