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1

Molecular analysis of chromosome 20q deletions associated with myeloproliferative disorders and myelodysplastic syndromes -н FA Asimakopoulos, NJ White, Elisabeth P. Nacheva, AR Green

Хэвлэсэн 1994

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Artigo

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2

Genetic Control of Enzyme Induction in the β-Ketoadipate Pathway of Pseudomonas putida: Deletion Mapping of cat Mutations -н Mark L. Wheelis, L. Nicholas Ornston

Хэвлэсэн 1972

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Artigo

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3

Isolation and behavior of Escherichia coli deletion mutants lacking chemotaxis functions -н John S. Parkinson, Susan E. Houts

Хэвлэсэн 1982

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Artigo

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4

CHARACTERIZATION OF A RECOMBINANT MOUSE t HAPLOTYPE THAT EXPRESSES A DOMINANT LETHAL MATERNAL EFFECT -н Heinz Winking, Lee M. Silver

Хэвлэсэн 1984

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Artigo

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5

Molecular genetics of the Caenorhabditis elegans heterochronic gene lin-14. -н Gary Ruvkun, Victor Ambros, Alan Coulson, R Waterston, John Sulston, H. Robert Horvitz

Хэвлэсэн 1989

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Artigo

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6

Detailed Molecular Delineation of 13q14.3 Loss in B-Cell Chronic Lymphocytic Leukemia -н Martin Corcoran, Omid Rasool, Yie Liu, Arati Iyengar, Dan Grandér, Rachel Ibbotson, Mats Merup, Xiushan Wu, V. M. Brodyansky, Anne Gardiner, Gunnar Juliusson, Robert M. Chapman, Ganka Ivanova, Mary Tiller, Gösta Gahrton, N. K. Yankovsky, Eugene R. Zabarovsky, David Oscier, Stefan Einhorn

Хэвлэсэн 1998

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Artigo

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7

GENETIC ANALYSIS OF THE ACTIVE SITES OF lac REPRESSOR -н Magnus Pfahl, Christel Stockter, Bruno Gronenborn

Хэвлэсэн 1974

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Artigo

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8

A combined genetic and physical map of the Streptomyces coelicolor A3(2) chromosome -н Helen M. Kieser, Tobias Kieser, David A. Hopwood

Хэвлэсэн 1992

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9

The mechanisms involved in formation of deletions and duplications of 15q11-q13. -н Wendy P. Robinson, Fabrizio Dutly, Robert D. Nicholls, Fosco Bernasconi, María S. Peñaherrera, Ron C. Michaelis, Dvorah Abeliovich, Albert Schinzel

Хэвлэсэн 1998

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10

A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2-36.3. -н Peter S. White, John M. Maris, Christian Beltinger, Erik P. Sulman, Helen Marshall, Maiko Fujimori, Bruce A. Kaufman, Jaclyn A. Biegel, C. Allen, Colette Hilliard

Хэвлэсэн 1995

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11

Array comparative genomic hybridization (aCGH) analysis in Prader–Willi syndrome -н Merlin G. Butler, Will Fischer, Nataliya Kibiryeva, Douglas C. Bittel

Хэвлэсэн 2008

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12

McpandFab-7: molecular analysis of putative boundaries of cis-regulatory domains in the bithorax complex ofDrosophila melanogaster -н François Karch, Mireille Galloni, László Sípos, János Gausz, Henrik Gyurkovics, Paul Sched

Хэвлэсэн 1994

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Artigo

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13

Localization of the Congenital Dyserythropoietic Anemia II Locus to Chromosome 20q11.2 by Genomewide Search -н Paolo Gasparini, Emanuele Miraglia del Giudice, J. Delaunay, Antonio Totaro, Matteo Granatiero, Salvatore Melchionda, L. Zelante, Achille Iolascon

Хэвлэсэн 1997

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14

Association of somatotrophinomas with loss of alleles on chromosome 11 and with gsp mutations. -н Rajesh V. Thakker, Mark A. Pook, C Wooding, Marco Boscaro, M Scanarini, Richard N. Clayton

Хэвлэсэн 1993

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Artigo

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15

Physical Mapping of Chromosome 8p22 Markers and Their Homozygous Deletion in a Metastatic Prostate Cancer -н G. Steven Bova, Donal MacGrogan, Alina Levy, Sokhom S. Pin, Robert Bookstein, William B. Isaacs

Хэвлэсэн 1996

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16

Mapping Drosophila mutations with molecularly defined P element insertions -н R. Grace Zhai, P. Robin Hiesinger, Tong‐Wey Koh, Patrik Verstreken, Karen L. Schulze, Yu Cao, Hamed Jafar‐Nejad, Koen Norga, Hongling Pan, Vafa Bayat, Michael P. Greenbaum, Hugo J. Bellen

Хэвлэсэн 2003

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17

NF1 Microdeletion Syndrome: Refined FISH Characterization of Sporadic and Familial Deletions with Locus-Specific Probes -н Paola Riva, Lucia Corrado, Federica Natacci, Pierangela Castorina, Bai-Li Wu, Gretchen Schneider, Maurizio Clementi, Romano Tenconi, Bruce R. Korf, Lidia Larizza

Хэвлэсэн 2000

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18

High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGH -н Carl E.G. Bruder, Carina Hirvelä, Isabel Tapia‐Páez, Ingegerd Fransson, Richard Segraves, Greg Hamilton, Xiao Zhang, D. Gareth Evans, Andrew Wallace, Michael E. Baser, Jessica Zucman‐Rossi, Martin Hergersberg, Eugene Boltshauser, Laura Papi, Guy A. Rouleau, G. Poptodorov, Albena Jordanova, Helge Rask‐Andersen, Lan Kluwe, Victor Mautner, Markku Sainio, Gene Hung, Tiit Mathiesen, Claes Möller, Stefan M. Pulst, Henrik Harder, Arvid Heiberg, Mariko Honda, Michihito Niimura, Sigrid Sahlén, Elisabeth Blennow, Donna G. Albertson, Daniel Pinkel, Jan P. Dumanski

Хэвлэсэн 2001

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19

Central 22q11.2 deletions -н Patrick Rump, Nicole de Leeuw, Anthonie J. van Essen, Corien C. Verschuuren‐Bemelmans, Hermine E. Veenstra‐Knol, Mariëlle E.M. Swinkels, Wilma Oostdijk, Claudia Ruivenkamp, William Reardon, Sonja de Munnik, Mariken Ruiter, Ayala Frumkin, Dorit Lev, Christina Evers, Birgit Sikkema‐Raddatz, Trijnie Dijkhuizen, Conny M.A. van Ravenswaaij‐Arts

Хэвлэсэн 2014

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20

Fine-structure deletion map and complementation analysis of the glnA-glnL-glnG region in Escherichia coli -н Tanya MacNeil, Douglas J. MacNeil, B Tyler

Хэвлэсэн 1982

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Artigo

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Molecular analysis of chromosome 20q deletions associated with myeloproliferative disorders and myelodysplastic syndromes -н FA Asimakopoulos, NJ White, Elisabeth P. Nacheva, AR Green

Genetic Control of Enzyme Induction in the β-Ketoadipate Pathway of <i>Pseudomonas putida:</i> Deletion Mapping of <i>cat</i> Mutations -н Mark L. Wheelis, L. Nicholas Ornston

Isolation and behavior of Escherichia coli deletion mutants lacking chemotaxis functions -н John S. Parkinson, Susan E. Houts

CHARACTERIZATION OF A RECOMBINANT MOUSE <i>t</i> HAPLOTYPE THAT EXPRESSES A DOMINANT LETHAL MATERNAL EFFECT -н Heinz Winking, Lee M. Silver

Molecular genetics of the Caenorhabditis elegans heterochronic gene lin-14. -н Gary Ruvkun, Victor Ambros, Alan Coulson, R Waterston, John Sulston, H. Robert Horvitz

GENETIC ANALYSIS OF THE ACTIVE SITES OF <i>lac</i> REPRESSOR -н Magnus Pfahl, Christel Stockter, Bruno Gronenborn

A combined genetic and physical map of the Streptomyces coelicolor A3(2) chromosome -н Helen M. Kieser, Tobias Kieser, David A. Hopwood

The mechanisms involved in formation of deletions and duplications of 15q11-q13. -н Wendy P. Robinson, Fabrizio Dutly, Robert D. Nicholls, Fosco Bernasconi, María S. Peñaherrera, Ron C. Michaelis, Dvorah Abeliovich, Albert Schinzel

A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2-36.3. -н Peter S. White, John M. Maris, Christian Beltinger, Erik P. Sulman, Helen Marshall, Maiko Fujimori, Bruce A. Kaufman, Jaclyn A. Biegel, C. Allen, Colette Hilliard

Array comparative genomic hybridization (aCGH) analysis in Prader–Willi syndrome -н Merlin G. Butler, Will Fischer, Nataliya Kibiryeva, Douglas C. Bittel

<i>Mcp</i>and<i>Fab</i>-7: molecular analysis of putative boundaries of cis-regulatory domains in the bithorax complex of<i>Drosophila melanogaster</i> -н François Karch, Mireille Galloni, László Sípos, János Gausz, Henrik Gyurkovics, Paul Sched

Localization of the Congenital Dyserythropoietic Anemia II Locus to Chromosome 20q11.2 by Genomewide Search -н Paolo Gasparini, Emanuele Miraglia del Giudice, J. Delaunay, Antonio Totaro, Matteo Granatiero, Salvatore Melchionda, L. Zelante, Achille Iolascon

Association of somatotrophinomas with loss of alleles on chromosome 11 and with gsp mutations. -н Rajesh V. Thakker, Mark A. Pook, C Wooding, Marco Boscaro, M Scanarini, Richard N. Clayton

Physical Mapping of Chromosome 8p22 Markers and Their Homozygous Deletion in a Metastatic Prostate Cancer -н G. Steven Bova, Donal MacGrogan, Alina Levy, Sokhom S. Pin, Robert Bookstein, William B. Isaacs

Mapping <i>Drosophila</i> mutations with molecularly defined <i>P</i> element insertions -н R. Grace Zhai, P. Robin Hiesinger, Tong‐Wey Koh, Patrik Verstreken, Karen L. Schulze, Yu Cao, Hamed Jafar‐Nejad, Koen Norga, Hongling Pan, Vafa Bayat, Michael P. Greenbaum, Hugo J. Bellen

NF1 Microdeletion Syndrome: Refined FISH Characterization of Sporadic and Familial Deletions with Locus-Specific Probes -н Paola Riva, Lucia Corrado, Federica Natacci, Pierangela Castorina, Bai-Li Wu, Gretchen Schneider, Maurizio Clementi, Romano Tenconi, Bruce R. Korf, Lidia Larizza

Fine-structure deletion map and complementation analysis of the glnA-glnL-glnG region in Escherichia coli -н Tanya MacNeil, Douglas J. MacNeil, B Tyler

Хайлтын үр дүнгүүд

Molecular analysis of chromosome 20q deletions associated with myeloproliferative disorders and myelodysplastic syndromes -н FA Asimakopoulos, NJ White, Elisabeth P. Nacheva, AR Green

Genetic Control of Enzyme Induction in the β-Ketoadipate Pathway of <i>Pseudomonas putida:</i> Deletion Mapping of <i>cat</i> Mutations -н Mark L. Wheelis, L. Nicholas Ornston

Isolation and behavior of Escherichia coli deletion mutants lacking chemotaxis functions -н John S. Parkinson, Susan E. Houts

CHARACTERIZATION OF A RECOMBINANT MOUSE <i>t</i> HAPLOTYPE THAT EXPRESSES A DOMINANT LETHAL MATERNAL EFFECT -н Heinz Winking, Lee M. Silver

Molecular genetics of the Caenorhabditis elegans heterochronic gene lin-14. -н Gary Ruvkun, Victor Ambros, Alan Coulson, R Waterston, John Sulston, H. Robert Horvitz

GENETIC ANALYSIS OF THE ACTIVE SITES OF <i>lac</i> REPRESSOR -н Magnus Pfahl, Christel Stockter, Bruno Gronenborn

A combined genetic and physical map of the Streptomyces coelicolor A3(2) chromosome -н Helen M. Kieser, Tobias Kieser, David A. Hopwood

The mechanisms involved in formation of deletions and duplications of 15q11-q13. -н Wendy P. Robinson, Fabrizio Dutly, Robert D. Nicholls, Fosco Bernasconi, María S. Peñaherrera, Ron C. Michaelis, Dvorah Abeliovich, Albert Schinzel

A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2-36.3. -н Peter S. White, John M. Maris, Christian Beltinger, Erik P. Sulman, Helen Marshall, Maiko Fujimori, Bruce A. Kaufman, Jaclyn A. Biegel, C. Allen, Colette Hilliard

Array comparative genomic hybridization (aCGH) analysis in Prader–Willi syndrome -н Merlin G. Butler, Will Fischer, Nataliya Kibiryeva, Douglas C. Bittel

<i>Mcp</i>and<i>Fab</i>-7: molecular analysis of putative boundaries of cis-regulatory domains in the bithorax complex of<i>Drosophila melanogaster</i> -н François Karch, Mireille Galloni, László Sípos, János Gausz, Henrik Gyurkovics, Paul Sched

Localization of the Congenital Dyserythropoietic Anemia II Locus to Chromosome 20q11.2 by Genomewide Search -н Paolo Gasparini, Emanuele Miraglia del Giudice, J. Delaunay, Antonio Totaro, Matteo Granatiero, Salvatore Melchionda, L. Zelante, Achille Iolascon

Association of somatotrophinomas with loss of alleles on chromosome 11 and with gsp mutations. -н Rajesh V. Thakker, Mark A. Pook, C Wooding, Marco Boscaro, M Scanarini, Richard N. Clayton

Physical Mapping of Chromosome 8p22 Markers and Their Homozygous Deletion in a Metastatic Prostate Cancer -н G. Steven Bova, Donal MacGrogan, Alina Levy, Sokhom S. Pin, Robert Bookstein, William B. Isaacs

Mapping <i>Drosophila</i> mutations with molecularly defined <i>P</i> element insertions -н R. Grace Zhai, P. Robin Hiesinger, Tong‐Wey Koh, Patrik Verstreken, Karen L. Schulze, Yu Cao, Hamed Jafar‐Nejad, Koen Norga, Hongling Pan, Vafa Bayat, Michael P. Greenbaum, Hugo J. Bellen

NF1 Microdeletion Syndrome: Refined FISH Characterization of Sporadic and Familial Deletions with Locus-Specific Probes -н Paola Riva, Lucia Corrado, Federica Natacci, Pierangela Castorina, Bai-Li Wu, Gretchen Schneider, Maurizio Clementi, Romano Tenconi, Bruce R. Korf, Lidia Larizza

Fine-structure deletion map and complementation analysis of the glnA-glnL-glnG region in Escherichia coli -н Tanya MacNeil, Douglas J. MacNeil, B Tyler

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