Science 5 January 1990: Vol. 247. no. 4938, pp. 64 - 69 DOI: 10.1126/science.2294592

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Articles

Tracking the complex flow of chromosome rearrangements from the Hominoidea Ancestor to extant Hylobates and Nomascus Gibbons by high-resolution synteny mapping.

D. Misceo, O. Capozzi, R. Roberto, M. P. Dell'Oglio, M. Rocchi, R. Stanyon, and N. Archidiacono (2008)
Genome Res. 18, 1530-1537
 |  Abstract »  |  Full Text »  |  PDF »

DNA replication timing of the human {beta}-globin domain is controlled by histone modification at the origin.

A. Goren, A. Tabib, M. Hecht, and H. Cedar (2008)
Genes & Dev. 22, 1319-1324
 |  Abstract »  |  Full Text »  |  PDF »

Characterization and evolution of the novel gene family FAM90A in primates originated by multiple duplication and rearrangement events.

N. Bosch, M. Caceres, M. F. Cardone, A. Carreras, E. Ballana, M. Rocchi, L. Armengol, and X. Estivill (2007)
Hum. Mol. Genet. 16, 2572-2582
 |  Abstract »  |  Full Text »  |  PDF »

3q26 Amplification and Polysomy of Chromosome 3 in Squamous Cell Lesions of the Lung: A Fluorescence In situ Hybridization Study.

G. Pelosi, B. Del Curto, M. Trubia, A. G. Nicholson, M. Manzotti, G. Veronesi, L. Spaggiari, P. Maisonneuve, F. Pasini, A. Terzi, et al. (2007)
Clin. Cancer Res. 13, 1995-2004
 |  Abstract »  |  Full Text »  |  PDF »

Molecular and genomic characterisation of cryptic chromosomal alterations leading to paternal duplication of the 11p15.5 Beckwith-Wiedemann region..

S Russo, P Finelli, M P Recalcati, S Ferraiuolo, F Cogliati, B Dalla Bernardina, M G Tibiletti, M Agosti, M Sala, M T Bonati, et al. (2006)
J. Med. Genet. 43, e39
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Innate Immune Responses in NF-{kappa}B-Repressing Factor-Deficient Mice.

N. Froese, M. Schwarzer, I. Niedick, U. Frischmann, M. Koster, A. Kroger, P. P. Mueller, M. Nourbakhsh, B. Pasche, J. Reimann, et al. (2006)
Mol. Cell. Biol. 26, 293-302
 |  Abstract »  |  Full Text »  |  PDF »

High-mobility group A2 gene expression is frequently induced in non-functioning pituitary adenomas (NFPAs), even in the absence of chromosome 12 polysomy.

G. M. Pierantoni, P. Finelli, E. Valtorta, D. Giardino, O. Rodeschini, F. Esposito, M. Losa, A. Fusco, and L. Larizza (2005)
Endocr. Relat. Cancer 12, 867-874
 |  Abstract »  |  Full Text »  |  PDF »

Ultrastructural studies of spermatozoa from infertile males with Robertsonian translocations and 18, X, Y aneuploidies.

B. Baccetti, G. Collodel, R. Marzella, E. Moretti, P. Piomboni, G. Scapigliati, and F. Serafini (2005)
Hum. Reprod. 20, 2295-2300
 |  Abstract »  |  Full Text »  |  PDF »

Transdifferentiation of corneal epithelium into epidermis occurs by means of a multistep process triggered by dermal developmental signals.

D. J. Pearton, Y. Yang, and D. Dhouailly (2005)
PNAS 102, 3714-3719
 |  Abstract »  |  Full Text »  |  PDF »

Human cytomegalovirus cell-to-cell spread in the absence of an essential assembly protein.

M. C. Silva, J. Schroer, and T. Shenk (2005)
PNAS 102, 2081-2086
 |  Abstract »  |  Full Text »  |  PDF »

Evolutionary History of Chromosome 20.

D. Misceo, M. F. Cardone, L. Carbone, P. D'Addabbo, P. J. de Jong, M. Rocchi, and N. Archidiacono (2005)
Mol. Biol. Evol. 22, 360-366
 |  Abstract »  |  Full Text »  |  PDF »

Human Cytomegalovirus TRS1 Protein Is Required for Efficient Assembly of DNA-Containing Capsids.

J. E. Adamo, J. Schroer, and T. Shenk (2004)
J. Virol. 78, 10221-10229
 |  Abstract »  |  Full Text »  |  PDF »

FISH characterisation of an identical (16)(p11.2p12.2) tandem duplication in two unrelated patients with autistic behaviour.

P Finelli, F Natacci, M T Bonati, G Gottardi, J J M Engelen, C E M de Die-Smulders, M Sala, D Giardino, and L Larizza (2004)
J. Med. Genet. 41, e90
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Analysis of Segmental Duplications and Genome Assembly in the Mouse.

J. A. Bailey, D. M. Church, M. Ventura, M. Rocchi, and E. E. Eichler (2004)
Genome Res. 14, 789-801
 |  Abstract »  |  Full Text »  |  PDF »

Sister chromatid separation at human telomeric regions.

M. Yalon, S. Gal, Y. Segev, S. Selig, and K. L. Skorecki (2004)
J. Cell Sci. 117, 1961-1970
 |  Abstract »  |  Full Text »  |  PDF »

A palindrome-mediated mechanism distinguishes translocations involving LCR-B of chromosome 22q11.2.

A. L. Gotter, T. H. Shaikh, M. L. Budarf, C. H. Rhodes, and B. S. Emanuel (2004)
Hum. Mol. Genet. 13, 103-115
 |  Abstract »  |  Full Text »  |  PDF »

10, 15 reciprocal translocation in an infertile man: ultrastructural and fluorescence in-situ hybridization sperm study: Case report.

B. Baccetti, E. Bruni, G. Collodel, L. Gambera, E. Moretti, R. Marzella, and P. Piomboni (2003)
Hum. Reprod. 18, 2302-2308
 |  Abstract »  |  Full Text »  |  PDF »

A novel sequence-based approach to localize translocation breakpoints identifies the molecular basis of a t(4;22).

M. A. Nimmakayalu, A. L. Gotter, T. H. Shaikh, and B. S. Emanuel (2003)
Hum. Mol. Genet. 12, 2817-2825
 |  Abstract »  |  Full Text »  |  PDF »

Neocentromeres in 15q24-26 Map to Duplicons Which Flanked an Ancestral Centromere in 15q25.

M. Ventura, J. M. Mudge, V. Palumbo, S. Burn, E. Blennow, M. Pierluigi, R. Giorda, O. Zuffardi, N. Archidiacono, M. S. Jackson, et al. (2003)
Genome Res. 13, 2059-2068
 |  Abstract »  |  Full Text »  |  PDF »

Chromosome 6 Phylogeny in Primates and Centromere Repositioning.

V. Eder, M. Ventura, M. Ianigro, M. Teti, M. Rocchi, and N. Archidiacono (2003)
Mol. Biol. Evol. 20, 1506-1512
 |  Abstract »  |  Full Text »  |  PDF »

Incorporation of reporter molecule-labeled nucleotides by DNA polymerases. I. Chemical synthesis of various reporter group-labeled 2'-deoxyribonucleoside-5'-triphosphates.

G. Giller, T. Tasara, B. Angerer, K. Muhlegger, M. Amacker, and H. Winter (2003)
Nucleic Acids Res. 31, 2630-2635
 |  Abstract »  |  Full Text »  |  PDF »

Epigenetic abnormalities associated with a chromosome 18(q21-q22) inversion and a Gilles de la Tourette syndrome phenotype.

M. W. State, J. M. Greally, A. Cuker, P. N. Bowers, O. Henegariu, T. M. Morgan, M. Gunel, M. DiLuna, R. A. King, C. Nelson, et al. (2003)
PNAS 100, 4684-4689
 |  Abstract »  |  Full Text »  |  PDF »

Large-Scale Variation Among Human and Great Ape Genomes Determined by Array Comparative Genomic Hybridization.

D. P. Locke, R. Segraves, L. Carbone, N. Archidiacono, D. G. Albertson, D. Pinkel, and E. E. Eichler (2003)
Genome Res. 13, 347-357
 |  Abstract »  |  Full Text »  |  PDF »

Complex Events in the Evolution of the Human Pseudoautosomal Region 2 (PAR2).

F. J. Charchar, M. Svartman, N. El-Mogharbel, M. Ventura, P. Kirby, M. R. Matarazzo, A. Ciccodicola, M. Rocchi, M. D'Esposito, and J. A. M. Graves (2003)
Genome Res. 13, 281-286
 |  Abstract »  |  Full Text »  |  PDF »

Genetic analysis of de novo CD5+ diffuse large B-cell lymphomas suggests an origin from a somatically mutated CD5+ progenitor B cell.

T. Katzenberger, A. Lohr, S. Schwarz, M. Dreyling, J. Schoof, C. Nickenig, S. Stilgenbauer, J. Kalla, M. M. Ott, H. K. Muller-Hermelink, et al. (2003)
Blood 101, 699-702
 |  Abstract »  |  Full Text »  |  PDF »

HIP14, a novel ankyrin domain-containing protein, links huntingtin to intracellular trafficking and endocytosis.

R. R. Singaraja, S. Hadano, M. Metzler, S. Givan, C. L. Wellington, S. Warby, A. Yanai, C.-A. Gutekunst, B. R. Leavitt, H. Yi, et al. (2002)
Hum. Mol. Genet. 11, 2815-2828
 |  Abstract »  |  Full Text »  |  PDF »

A 76-kb duplicon maps close to the BCR gene on chromosome 22 and the ABL gene on chromosome 9: Possible involvement in the genesis of the Philadelphia chromosome translocation.

G. Saglio, C. T. Storlazzi, E. Giugliano, C. Surace, L. Anelli, G. Rege-Cambrin, A. Zagaria, A. J. Velasco, A. Heiniger, P. Scaravaglio, et al. (2002)
PNAS 99, 9882-9887
 |  Abstract »  |  Full Text »  |  PDF »

Alport syndrome and mental retardation: clinical and genetic dissection of the contiguous gene deletion syndrome in Xq22.3 (ATS-MR).

I Meloni, F Vitelli, L Pucci, R B Lowry, R Tonlorenzi, E Rossi, M Ventura, G Rizzoni, C E Kashtan, B Pober, et al. (2002)
J. Med. Genet. 39, 359-365
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The High Mobility Group A2 Gene Is Amplified and Overexpressed in Human Prolactinomas.

P. Finelli, G. M. Pierantoni, D. Giardino, M. Losa, O. Rodeschini, M. Fedele, E. Valtorta, P. Mortini, C. M. Croce, L. Larizza, et al. (2002)
Cancer Res. 62, 2398-2405
 |  Abstract »  |  Full Text »  |  PDF »

AIbZIP, a Novel bZIP Gene Located on Chromosome 1q21.3 That Is Highly Expressed in Prostate Tumors and of Which the Expression Is Up-Regulated by Androgens in LNCaP Human Prostate Cancer Cells.

H. Qi, C. Fillion, Y. Labrie, J. Grenier, A. Fournier, L. Berger, M. El-Alfy, and C. Labrie (2002)
Cancer Res. 62, 721-733
 |  Abstract »  |  Full Text »  |  PDF »

Human Paralogs of KIAA0187 Were Created through Independent Pericentromeric-Directed and Chromosome-Specific Duplication Mechanisms.

M. Crosier, L. Viggiano, J. Guy, D. Misceo, R. Stones, W. Wei, T. Hearn, M. Ventura, N. Archidiacono, M. Rocchi, et al. (2002)
Genome Res. 12, 67-80
 |  Abstract »  |  Full Text »  |  PDF »

Divergent Origins and Concerted Expansion of Two Segmental Duplications on Chromosome 16.

E. E. Eichler, M. E. Johnson, C. Alkan, E. Tuzun, C. Sahinalp, D. Misceo, N. Archidiacono, and M. Rocchi (2001)
J. Hered. 92, 462-468
 |  Abstract »  |  Full Text »  |  PDF »

Loss-of-function mutations in SIP1 Smad interacting protein 1 result in a syndromic Hirschsprung disease.

V. Cacheux, F. Dastot-Le Moal, H. Kaariainen, N. Bondurand, R. Rintala, B. Boissier, M. Wilson, D. Mowat, and M. Goossens (2001)
Hum. Mol. Genet. 10, 1503-1510
 |  Abstract »  |  Full Text »  |  PDF »

Cloning of the human MCCA and MCCB genes and mutations therein reveal the molecular cause of 3-methylcrotonyl-CoA: carboxylase deficiency.

A. Holzinger, W. Roschinger, F. Lagler, P. U. Mayerhofer, P. Lichtner, T. Kattenfeld, L. P. Thuy, W. L. Nyhan, H. G. Koch, A. C. Muntau, et al. (2001)
Hum. Mol. Genet. 10, 1299-1306
 |  Abstract »  |  Full Text »  |  PDF »

Characterization of Mouse Carboxypeptidase N Small Active Subunit Gene Structure.

K. W. Matthews and R. A. Wetsel (2001)
J. Immunol. 166, 6196-6202
 |  Abstract »  |  Full Text »  |  PDF »

Identification and characterization of a novel human vanilloid receptor-like protein, VRL-2.

N. S. DELANY, M. HURLE, P. FACER, T. ALNADAF, C. PLUMPTON, I. KINGHORN, C. G. SEE, M. COSTIGAN, P. ANAND, C. J. WOOLF, et al. (2001)
Physiol Genomics 4, 165-174
 |  Abstract »  |  Full Text »  |  PDF »

Unexpected high frequency of de novo unbalanced translocations in patients with Wolf-Hirschhorn syndrome (WHS).

D. WIECZOREK, M. KRAUSE, F. MAJEWSKI, B. ALBRECHT, P. MEINECKE, O. RIESS, and G. GILLESSEN-KAESBACH (2000)
J. Med. Genet. 37, 798-804
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Sequence Similarities between a Novel Putative G Protein-Coupled Receptor and Na+/Ca2+ Exchangers Define a Cation Binding Domain.

H. Nikkila, D. R. McMillan, B. S. Nunez, L. Pascoe, K. M. Curnow, and P. C. White (2000)
Mol. Endocrinol. 14, 1351-1364
 |  Abstract »  |  Full Text »

Immunohistochemical Analysis of Cyclin D1 Shows Deregulated Expression in Multiple Myeloma with the t(11;14).

G. Pruneri, S. Fabris, L. Baldini, N. Carboni, S. Zagano, M. A. Colombi, G. Ciceri, L. Lombardi, M. Rocchi, R. Buffa, et al. (2000)
Am. J. Pathol. 156, 1505-1513
 |  Abstract »  |  Full Text »  |  PDF »

ERO1-L, a Human Protein That Favors Disulfide Bond Formation in the Endoplasmic Reticulum.

A. Cabibbo, M. Pagani, M. Fabbri, M. Rocchi, M. R. Farmery, N. J. Bulleid, and R. Sitia (2000)
J. Biol. Chem. 275, 4827-4833
 |  Abstract »  |  Full Text »  |  PDF »

Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal region.

A. Ciccodicola, M. D'Esposito, T. Esposito, F. Gianfrancesco, C. Migliaccio, M. G. Miano, M. R. Matarazzo, M. Vacca, A. Franze, M. Cuccurese, et al. (2000)
Hum. Mol. Genet. 9, 395-401
 |  Abstract »  |  Full Text »  |  PDF »

Molecular structure and evolution of an alpha satellite/non-alpha satellite junction at 16p11.

J. E. Horvath, L. Viggiano, B. J. Loftus, M. D. Adams, N. Archidiacono, M. Rocchi, and E. E. Eichler (2000)
Hum. Mol. Genet. 9, 113-123
 |  Abstract »  |  Full Text »  |  PDF »

Centromere Repositioning.

G. Montefalcone, S. Tempesta, M. Rocchi, and N. Archidiacono (1999)
Genome Res. 9, 1184-1188
 |  Abstract »  |  Full Text »

Leigh syndrome transmitted by uniparental disomy of chromosome 9.

V. TIRANTI, E. LAMANTEA, G. UZIEL, M. ZEVIANI, P. GASPARINI, R. MARZELLA, M. ROCCHI, and M. FRIED (1999)
J. Med. Genet. 36, 927-928
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CAGGG Repeats and the Pericentromeric Duplication of the Hominoid Genome.

E. E. Eichler, N. Archidiacono, and M. Rocchi (1999)
Genome Res. 9, 1048-1058
 |  Abstract »  |  Full Text »

Melusin Is a New Muscle-specific Interactor for beta 1 Integrin Cytoplasmic Domain.

M. Brancaccio, S. Guazzone, N. Menini, E. Sibona, E. Hirsch, M. De Andrea, M. Rocchi, F. Altruda, G. Tarone, and L. Silengo (1999)
J. Biol. Chem. 274, 29282-29288
 |  Abstract »  |  Full Text »  |  PDF »

Position effect of human telomeric repeats on replication timing.

R. Ofir, A. C. C. Wong, H. E. McDermid, K. L. Skorecki, and S. Selig (1999)
PNAS 96, 11434-11439
 |  Abstract »  |  Full Text »  |  PDF »

Microdeletion 22q11.2: clinical data and deletion size.

W S KERSTJENS-FREDERIKSE, H KURAHASHI, D A DRISCOLL, M L BUDARF, B S EMANUEL, B BEATTY, T SCHEIDL, J SIEGEL-BARTELT, K HENDERSON, C CYTRYNBAUM, et al. (1999)
J. Med. Genet. 36, 721-723
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Spleen-specific Expression of the Malaria-inducible Intronless Mouse Gene imap38.

J. Krucken, O. Stamm, H.-P. Schmitt-Wrede, A. Mincheva, P. Lichter, and F. Wunderlich (1999)
J. Biol. Chem. 274, 24383-24391
 |  Abstract »  |  Full Text »  |  PDF »

Molecular characterization of a slowly gating human hyperpolarization-activated channel predominantly expressed in thalamus, heart, and testis.

R. Seifert, A. Scholten, R. Gauss, A. Mincheva, P. Lichter, and U. B. Kaupp (1999)
PNAS 96, 9391-9396
 |  Abstract »  |  Full Text »  |  PDF »

Detection of t(4;14)(p16.3;q32) Chromosomal Translocation in Multiple Myeloma by Double-Color Fluorescent In Situ Hybridization.

P. Finelli, S. Fabris, S. Zagano, L. Baldini, D. Intini, L. Nobili, L. Lombardi, A. T. Maiolo, and A. Neri (1999)
Blood 94, 724-732
 |  Abstract »  |  Full Text »  |  PDF »

Applications of comparative genomic hybridisation in constitutional chromosome studies.

C. J Breen, L. Barton, A. Carey, A. Dunlop, M. Glancy, K. Hall, A. M. Hegarty, M T. Khokhar, M. Power, K. Ryan, et al. (1999)
J. Med. Genet. 36, 511-517
 |  Abstract »  |  Full Text »

Localization of Single- and Low-Copy Sequences on Tomato Synaptonemal Complex Spreads Using Fluorescence in Situ Hybridization (FISH).

D. G. Peterson, N. L. V. Lapitan, and S. M. Stack (1999)
Genetics 152, 427-439
 |  Abstract »  |  Full Text »

Cloning and Characterization of a Lymphoid-Specific, Inducible Human Protein Tyrosine Phosphatase, Lyp.

S. Cohen, H. Dadi, E. Shaoul, N. Sharfe, and C. M. Roifman (1999)
Blood 93, 2013-2024
 |  Abstract »  |  Full Text »  |  PDF »

De novo deletion (14)(q11.2q13) including PAX9: clinical and molecular findings.

S. Schuffenhauer, H.-J. Leifheit, P. Lichtner, H. Peters, J. Murken, and P Emmerich (1999)
J. Med. Genet. 36, 233-236
 |  Abstract »  |  Full Text »

Human Ligands of the Notch Receptor.

G. E. Gray, R. S. Mann, E. Mitsiadis, D. Henrique, M.-L. Carcangiu, A. Banks, J. Leiman, D. Ward, D. Ish-Horowitz, and S. Artavanis-Tsakonas (1999)
Am. J. Pathol. 154, 785-794
 |  Abstract »  |  Full Text »  |  PDF »

Molecular Analysis of 11q13 Breakpoints in Multiple Myeloma.

D. Ronchetti, P. Finelli, R. Richelda, L. Baldini, M. Rocchi, L. Viggiano, A. Cuneo, S. Bogni, S. Fabris, L. Lombardi, et al. (1999)
Blood 93, 1330-1337
 |  Abstract »  |  Full Text »  |  PDF »

Insertion of Foreign DNA into an Established Mammalian Genome Can Alter the Methylation of Cellular DNA Sequences.

R. Remus, C. Kämmer, H. Heller, B. Schmitz, G. Schell, and W. Doerfler (1999)
J. Virol. 73, 1010-1022
 |  Abstract »  |  Full Text »

Mapping ESTs by Fiber-FISH.

N. Horelli-Kuitunen, J. Aaltonen, M.-L. Yaspo, M. Eeva, M. Wessman, L. Peltonen, and A. Palotie (1999)
Genome Res. 9, 62-71
 |  Abstract »  |  Full Text »

Molecular Cytogenetic Characterization of a Critical Region in Bands 7q35-q36 Commonly Deleted in Malignant Myeloid Disorders.

K. Dohner, J. Brown, U. Hehmann, C. Hetzel, J. Stewart, G. Lowther, C. Scholl, S. Frohling, A. Cuneo, L. C. Tsui, et al. (1998)
Blood 92, 4031-4035
 |  Abstract »  |  Full Text »  |  PDF »

New 5'-(CGG)n-3' Repeats in the Human Genome.

L. Mangel, T. Ternes, B. Schmitz, and W. Doerfler (1998)
J. Biol. Chem. 273, 30466-30471
 |  Abstract »  |  Full Text »  |  PDF »

Subtracted, Unique-Sequence, In Situ Hybridization : Experimental and Diagnostic Applications.

J. M. Davison, T. W. Morgan, B.-L. Hsi, S. Xiao, and J. A. Fletcher (1998)
Am. J. Pathol. 153, 1401-1409
 |  Abstract »  |  Full Text »  |  PDF »

The Locus Control Region Is Necessary for Gene Expression in the Human beta -Globin Locus but Not the Maintenance of an Open Chromatin Structure in Erythroid Cells.

A. Reik, A. Telling, G. Zitnik, D. Cimbora, E. Epner, and M. Groudine (1998)
Mol. Cell. Biol. 18, 5992-6000
 |  Abstract »  |  Full Text »

Genomic Organization and Expression of a Human Gene for Myc-associated Zinc Finger Protein (MAZ).

J. Song, H. Murakami, H. Tsutsui, X. Tang, M. Matsumura, K. Itakura, I. Kanazawa, K. Sun, and K. K. Yokoyama (1998)
J. Biol. Chem. 273, 20603-20614
 |  Abstract »  |  Full Text »  |  PDF »

The Human Glycine Receptor Subunit alpha 3. GLRA3 GENE STRUCTURE, CHROMOSOMAL LOCALIZATION, AND FUNCTIONAL CHARACTERIZATION OF ALTERNATIVE TRANSCRIPTS.

Z. Nikolic, B. Laube, R. G. Weber, P. Lichter, P. Kioschis, A. Poustka, C. Mulhardt, and C.-M. Becker (1998)
J. Biol. Chem. 273, 19708-19714
 |  Abstract »  |  Full Text »  |  PDF »

Gene Structure, Promoter Characterization, and Basis for Alternative mRNA Splicing of the Human CD58 Gene.

R. Wallich, C. Brenner, Y. Brand, M. Roux, M. Reister, and S. Meuer (1998)
J. Immunol. 160, 2862-2871
 |  Abstract »  |  Full Text »  |  PDF »

Cloning and Characterization of the Human Homolog of Mouse Jak2.

I. Dalal, E. Arpaia, H. Dadi, S. Kulkarni, J. Squire, and C. M. Roifman (1998)
Blood 91, 844-851
 |  Abstract »  |  Full Text »  |  PDF »

Establishment of a Reproducible Model of Chronic-Phase Chronic Myeloid Leukemia in NOD/SCID Mice Using Blood-Derived Mononuclear or CD34+ Cells.

I. D. Lewis, L. A. McDiarmid, L. M. Samels, L. Bik To, and T. P. Hughes (1998)
Blood 91, 630-640
 |  Abstract »  |  Full Text »  |  PDF »

Identification of an interchromosomal compartment by polymerization of nuclear-targeted vimentin.

J. Bridger, H Herrmann, C Munkel, and P Lichter (1998)
J. Cell Sci. 111, 1241-1253
 |  Abstract »  |  PDF »

Inhibition of Granulocyte-Macrophage Colony-Stimulating Factor Prevents Dissemination and Induces Remission of Juvenile Myelomonocytic Leukemia in Engrafted Immunodeficient Mice.

P. O. Iversen, I. D. Lewis, S. Turczynowicz, H. Hasle, C. Niemeyer, K. Schmiegelow, S. Bastiras, A. Biondi, T. P. Hughes, and A. F. Lopez (1997)
Blood 90, 4910-4917
 |  Abstract »  |  Full Text »  |  PDF »

beta -Dystrobrevin, a New Member of the Dystrophin Family. IDENTIFICATION, CLONING, AND PROTEIN ASSOCIATIONS.

M. F. Peters, K. F. O'Brien, H. M. Sadoulet-Puccio, L. M. Kunkel, M. E. Adams, and S. C. Froehner (1997)
J. Biol. Chem. 272, 31561-31569
 |  Abstract »  |  Full Text »  |  PDF »

A Novel Chromosomal Translocation t(4; 14)(p16.3; q32) in Multiple Myeloma Involves the Fibroblast Growth-Factor Receptor 3 Gene.

R. Richelda, D. Ronchetti, L. Baldini, L. Cro, L. Viggiano, R. Marzella, M. Rocchi, T. Otsuki, L. Lombardi, A. T. Maiolo, et al. (1997)
Blood 90, 4062-4070
 |  Abstract »  |  Full Text »  |  PDF »

A 3-Mb Contig from D11S987 to MLK3, a Gene-Rich Region in 11q13.

C. M. Smith, N. S. Ma, N. J. Nowak, T. B. Shows, and D. S. Gerhard (1997)
Genome Res. 7, 835-842
 |  Abstract »  |  Full Text »  |  PDF »

Mammalian Homolog of Drosophila retinal degeneration B Rescues the Mutant Fly Phenotype.

J. T. Chang, S. Milligan, Y. Li, C. E. Chew, J. Wiggs, N. G. Copeland, N. A. Jenkins, P. A. Campochiaro, D. R. Hyde, and D. J. Zack (1997)
J. Neurosci. 17, 5881-5890
 |  Abstract »  |  Full Text »  |  PDF »

Enhanced apoptotic cell death of renal epithelial cells in mice lacking transcription factor AP-2beta.

M. Moser, A. Pscherer, C. Roth, J. Becker, G. Mucher, K. Zerres, C. Dixkens, J. Weis, L. Guay-Woodford, R. Buettner, et al. (1997)
Genes & Dev. 11, 1938-1948
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11q Deletions Identify a New Subset of B-Cell Chronic Lymphocytic Leukemia Characterized by Extensive Nodal Involvement and Inferior Prognosis.

H. Dohner, S. Stilgenbauer, M. R. James, A. Benner, T. Weilguni, M. Bentz, K. Fischer, W. Hunstein, and P. Lichter (1997)
Blood 89, 2516-2522
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Molecular Cytogenetic Delineation of Deletions and Translocations Involving Chromosome Band 7q22 in Myeloid Leukemias.

K. Fischer, S. Frohling, S. W. Scherer, J. McAllister Brown, C. Scholl, S. Stilgenbauer, L.-C. Tsui, P. Lichter, and H. Dohner (1997)
Blood 89, 2036-2041
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Foreign (M13) DNA ingested by mice reaches peripheral leukocytes, spleen, and liver via the intestinal wall mucosa and can be covalently linked to mouse DNA.

R. Schubbert, D. Renz, B. Schmitz, and W. Doerfler (1997)
PNAS 94, 961-966
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The centrosomal protein centrosomin A and the nuclear protein centrosomin B derive from one gene by post-transcriptional processes involving RNA editing.

C Petzelt, G Joswig, A Mincheva, P Lichter, H Stammer, and D Werner (1997)
J. Cell Sci. 110, 2573-2578
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Statistical methods for gene map construction by fluorescence in situ hybridization..

S W Guo and W L Flejter (1996)
Genome Res. 6, 1133-1148
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Isolation and Characterization of the Human Cytochrome P450 CYP1B1 Gene.

Y. M. Tang, Y.-Y. P. Wo, J. Stewart, A. L. Hawkins, C. A. Griffin, T. R. Sutter, and W. F. Greenlee (1996)
J. Biol. Chem. 271, 28324-28330
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Juvenile chronic myelogenous leukemia multilineage CD34+ cells: aberrant growth and differentiation properties.

M. Freedman, J. Hitzler, N Bunin, T Grunberger, and J Squire (1996)
Stem Cells 14, 690-701
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Utilization of FISH in positional cloning: an example on 13q22..

M Laan, J Isosomppi, T Klockars, L Peltonen, and A Palotie (1996)
Genome Res. 6, 1002-1012
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Huntingtin Is Ubiquitinated and Interacts with a Specific Ubiquitin-conjugating Enzyme.

M. A. Kalchman, R. K. Graham, G. Xia, H. B. Koide, J. G. Hodgson, K. C. Graham, Y. P. Goldberg, R. D. Gietz, C. M. Pickart, and M. R. Hayden (1996)
J. Biol. Chem. 271, 19385-19394
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A palindromic structure in the pericentromeric region of various human chromosomes..

G Wohr, T Fink, and G Assum (1996)
Genome Res. 6, 267-279
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The Three Human Syntrophin Genes Are Expressed in Diverse Tissues, Have Distinct Chromosomal Locations, and Each Bind to Dystrophin and Its Relatives.

A. H. Ahn, C. A. Freener, E. Gussoni, M. Yoshida, E. Ozawa, and L. M. Kunkel (1996)
J. Biol. Chem. 271, 2724-2730
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Clustered arrangement of winged helix genes fkh-6 and MFH-1: possible implications for mesoderm development.

K. Kaestner, S. Bleckmann, A. Monaghan, J Schlondorff, A Mincheva, P Lichter, and G Schutz (1996)
Development 122, 1751-1758
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The Mouse fkh-2 Gene.

K. H. Kaestner, A. P. Monaghan, H. Kern, S.-L. Ang, S. Weitz, P. Lichter, and Gün. Schütz (1995)
J. Biol. Chem. 270, 30029-30035
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