Works matching IS 09646906 AND DT 1998 AND VI 7 AND IP 12

Results: 36

Erratum.

Published in:: 1998
Publication type:: Correction Notice

Chromatin Conformation of the H19 Epigenetic Mark.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 12, p. 1979, doi. 10.1093/hmg/7.12.1979

By:

Hark, Amy T.;
Tilghman, Shirley M.

Publication type:

Article

The Distribution of SMN Protein Complex in Human Fetal Tissues and Its Alteration in Spinal Muscular Atrophy.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 12, p. 1927, doi. 10.1093/hmg/7.12.1927

By:

Burlet, P.;
Huber, C.;
Bertrandy, S.;
Ludosky, M. A.;
Zwaenepoel, I.;
Clermont, O.;
Roume, J.;
Delezoide, A. L.;
Cartaud, J.;
Munnich, A.;
Lefebvre, S.

Publication type:

Article

Localization of Myotonic Dystrophy Protein Kinase in Human and Rabbit Tissues using a new Panel of Monoclonal Antibodies.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 12, p. 1957, doi. 10.1093/hmg/7.12.1957

By:

Pham, Y. C. N.;
thi Man, Nguyen;
Thanh Lam, Le;
Morris, G. E.

Publication type:

Article

Genetic Association of an (α2-Macroglobulin (Val1000lle) Polymorphism and Alzheimer's Disease.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 12, p. 1953, doi. 10.1093/hmg/7.12.1953

By:

Liao, A.;
Nitsch, R. M.;
Greenberg, S. M.;
Finckh, U.;
Blacker, D.;
Albert, M.;
Rebeck, G. W.;
Gomez-Isla, T.;
Clatworthy, A.;
Binetti, G.;
Hock, C.;
Mueller-Thomsen, T.;
Mann, U.;
Zuchowski, K.;
Beisiegel, U.;
Staehelin, H.;
Growdon, J. H.;
Tanzi, R. E.;
Hyman, B. T.

Publication type:

Article

Encapsidated Adenovirus Mini-Chromosome-Mediated Delivery of Genes to the Retina: Application to the Rescue of Photoreceptor Degeneration.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 12, p. 1893, doi. 10.1093/hmg/7.12.1893

By:

Kumar-Singh, Rajendra;
Farber, Debora B.

Publication type:

Article

The Treacher Collins Syndrome (TCOF1) Gene Product, Treacle, is Targeted to the Nucleolus by Signals in Its C-Terminus.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 12, p. 1947, doi. 10.1093/hmg/7.12.1947

By:

Winokur, Sara T.;
Shiang, Rita

Publication type:

Article

Genome-Wide Mapping of Unselected Transcripts From Extraembryonic Tissue of 7.5-Day Mouse Embryos Reveals Enrichment in the t-Complex and Under-Representation on the X Chromosome.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 12, p. 1967

By:

Ko, Minoru S. H.;
Threat, Tracy A.;
Wang, Xueqian;
Horton, Joseph H.;
Cui, Yushun;
Wang, Xiaohong;
Pryor, Eric;
Paris, Jason;
Wells-Smith, Jeannine;
Kitchen, John R.;
Rowe, Lucy B.;
Eppig, Janan;
Satoh, Toshihiko;
Brant, Larry;
Fujiwara, Hiroyuki;
Yotsumoto, Shinichi;
Nakashima, Hiroshi

Publication type:

Article

Targeted Replacement of Normal and Mutant CFTR Sequences in Human Airway Epithelial Cells Using DNA Fragments.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 12, p. 1913, doi. 10.1093/hmg/7.12.1913

By:

Goncz, Kaarin K.;
Kunzelmann, Karl;
Xu, Zhidong;
Gruenert, Dieter C.

Publication type:

Article

Mutations in DPC4 (SMAD4) Cause Juvenile Polyposis Syndrome, But Only Account for a Minority of Cases.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 12, p. 1907, doi. 10.1093/hmg/7.12.1907

By:

Houlston, Richard;
Bevan, Stephen;
Williams, Andrew;
Young, Joanne;
Dunlop, Malcolm;
Rozen, Paul;
Eng, Charis;
Markie, David;
Woodford-Richens, Kelly;
Rodriguez-Bigas, Miguel A.;
Leggett, Barbara;
Neale, Kay;
Phillips, Robin;
Sheridan, Eamon;
Hodgson, Shirley;
Iwama, Takeo;
Eccles, Diana;
Bodmer, Walter;
Tomlinson, Ian

Publication type:

Article

Parental Gender, Age at Birth and Expansion Length Influence GAA Repeat Intergenerational Instability in the X25 Gene: Pedigree Studies and Analysis of Sperm from Patients with Friedreich's Ataxia.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 12, p. 1901, doi. 10.1093/hmg/7.12.1901

By:

De Michele, Giuseppe;
Cavalcanti, Francesca;
Criscuolo, Chiara;
Pianese, Luigi;
Monticelli, Antonella;
Filla, Alessandro;
Cocozza, Sergio

Publication type:

Article

Re-Examination of Factors Associated with Expansion of CGG Repeats Using a Single Nucleotide Polymorphism in FMR1.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 12, p. 1935, doi. 10.1093/hmg/7.12.1935

By:

Gunter, Chris;
Paradee, William;
Crawford, Dana C.;
Meadows, Kellen A.;
Newman, James;
Kunst, Catherine B.;
Nelson, David L.;
Schwartz, Charles;
Murray, Anna;
Macpherson, James N.;
Sherman, Stephanie L.;
Warren, Stephen T.

Publication type:

Article

Risk for Alzheimer's Disease Correlates with Transcriptional Activity of the APOE Gene.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 12, p. 1887, doi. 10.1093/hmg/7.12.1887

By:

Artiga, M. J.;
Bullido, M. J.;
Frank, A.;
Sastre, I.;
Recuero, M.;
García, M. A.;
Lendon, C. L.;
Han, S. W.;
Morris, J. C.;
Vázquez, J.;
Goate, A.;
Valdivieso, F.

Publication type:

Article

Analysis of the Human GDNF Gene Reveals an Inducible Promoter, Three Exons, a Triplet Repeat Within the 3′-UTR and Alternative Splice Products.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 12, p. 1873, doi. 10.1093/hmg/7.12.1873

By:

Grimm, Lena;
Holinski-Feder, Elke;
Teodoridis, Jens;
Scheffer, Beatrix;
Schindelhauer, Dirk;
Meitinger, Thomas;
Ueffing, Marius

Publication type:

Article

Novel Immunogenic Antigen Homologous to Hyaluronidase in Meningioma.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 12, p. 1859, doi. 10.1093/hmg/7.12.1859

By:

Heckel, Dirk;
Comtesse, Nicole;
Brass, Nicole;
Blin, Nikolaus;
Zang, Klaus D.;
Meese, Eckart

Publication type:

Article

Multilocus Linkage Identifies Two New Loci for a Mendelian Form of Stroke, Cerebral Cavernous Malformation, at 7p15–13 and 3q25.2–27.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 12, p. 1851, doi. 10.1093/hmg/7.12.1851

By:

Craig, Holly D.;
Günel, Murat;
Cepeda, Obed;
Johnson, Eric W.;
Ptacek, Louis;
Steinberg, Gary K.;
Ogilvy, Christopher S.;
Berg, Michael J.;
Crawford, Stephen C.;
Scott, R. Michael;
Steichen-Gersdorf, Elizabeth;
Sabroe, Ruth;
Kennedy, C. T. C.;
Mettler, Gabrielle;
Beis, M. Jill;
Fryer, Alan;
Awad, Issam A.;
Lifton, Richard P.

Publication type:

Article

Goosecoid-like (GSCL), a Candidate Gene for Velocardiofacial Syndrome, Is Not Essential for Normal Mouse Development.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 12, p. 1841, doi. 10.1093/hmg/7.12.1841

By:

Saint-Jore, Bruno;
Puech, Anne;
Heyer, Jörg;
Lin, Qingcong;
Raine, Cedric;
Kucherlapati, Raju;
Skoultchi, Arthur I.

Publication type:

Article

Functional Analysis of Gscl in the Pathogenesis of the DiGeorge and Velocardiofacial Syndromes.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 12, p. 1835, doi. 10.1093/hmg/7.12.1835

By:

Wakamiya, Maki;
Lindsay, Elizabeth A.;
Rivera-Pérez, Jaime A.;
Baldini, Antonio;
Behringer, Richard R.

Publication type:

Article

Targeted replacement of normal and mutant CFTR sequences in human airway epithelial cells using DNA fragments.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 12, p. 1913, doi. 10.1093/hmg/7.12.1913

By:

Goncz, Kaarin K.;
Kunzelmann, Karl;
Xu, Zhidong;
Gruenert, Dieter C.

Publication type:

Article

The Treacher Collins syndrome (TCOF1) gene product, treacle, is targeted to the nucleolus by signals in its C-terminus.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 12, p. 1947, doi. 10.1093/hmg/7.12.1947

By:

Winokur, Sara T.;
Shiang, Rita

Publication type:

Article

Multilocus linkage identifies two new loci for a Mendelian form of stroke, cerebral cavernous malformation, at 7p15-13 and 3q25.2-27.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 12, p. 1851, doi. 10.1093/hmg/7.12.1851

By:

Craig, Holly D.;
Günel, Murat;
Cepeda, Obed;
Johnson, Eric W.;
Ptacek, Louis;
Steinberg, Gary K.;
Ogilvy, Christopher S.;
Berg, Michael J.;
Crawford, Stephen C.;
Scott, R. Michael;
Steichen‐Gersdorf, Elizabeth;
Sabroe, Ruth;
Kennedy, C. T. C.;
Mettler, Gabrielle;
Beis, M. Jill;
Fryer, Alan;
Awad, Issam A.;
Lifton, Richard P.

Publication type:

Article

Functional analysis of Gscl in the pathogenesis of the DiGeorge and velocardiofacial syndromes.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 12, p. 1835, doi. 10.1093/hmg/7.12.1835

By:

Wakamiya, Maki;
Lindsay, Elizabeth A.;
Rivera‐Pérez, Jaime A.;
Baldini, Antonio;
Behringer, Richard R.

Publication type:

Article

Encapsidated adenovirus mini-chromosome-mediated delivery of genes to the retina: application to the rescue of photoreceptor degeneration.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 12, p. 1893

By:

Kumar‐Singh, Rajendra;
Farber, Debora B.

Publication type:

Article

Parental gender, age at birth and expansion length influence GAA repeat intergenerational instability in the X25 gene: pedigree studies and analysis of sperm from patients with Friedreich's ataxia.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 12, p. 1901, doi. 10.1093/hmg/7.12.1901

By:

De Michele, Giuseppe;
Cavalcanti, Francesca;
Criscuolo, Chiara;
Pianese, Luigi;
Monticelli, Antonella;
Filla, Alessandro;
Cocozza, Sergio

Publication type:

Article

Localization of myotonic dystrophy protein kinase in human and rabbit tissues using a new panel of monoclonal antibodies.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 12, p. 1957, doi. 10.1093/hmg/7.12.1957

By:

Pham, Y. C. N.;
Man, Nguyen thi;
Lam, Le Thanh;
Morris, G. E.

Publication type:

Article

Analysis of the human GDNF gene reveals an inducible promoter, three exons, a triplet repeat within the 3′-UTR and alternative splice products.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 12, p. 1873, doi. 10.1093/hmg/7.12.1873

By:

Grimm, Lena;
Holinski‐Feder, Elke;
Teodoridis, Jens;
Scheffer, Beatrix;
Schindelhauer, Dirk;
Meitinger, Thomas;
Ueffing, Marius

Publication type:

Article

Mutations in DPC4 (SMAD4) cause juvenile polyposis syndrome, but only account for a minority of cases.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 12, p. 1907, doi. 10.1093/hmg/7.12.1907

By:

Houlston, Richard;
Bevan, Stephen;
Williams, Andrew;
Young, Joanne;
Dunlop, Malcolm;
Rozen, Paul;
Eng, Charis;
Markie, David;
Woodford‐Richens, Kelly;
Rodriguez‐Bigas, Miguel A.;
Leggett, Barbara;
Neale, Kay;
Phillips, Robin;
Sheridan, Eamon;
Hodgson, Shirley;
Iwama, Takeo;
Eccles, Diana;
Bodmer, Walter;
Tomlinson, Ian

Publication type:

Article

The distribution of SMN protein complex in human fetal tissues and its alteration in spinal muscular atrophy.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 12, p. 1927, doi. 10.1093/hmg/7.12.1927

By:

Burlet, P.;
Huber, C.;
Bertrandy, S.;
Ludosky, M. A.;
Zwaenepoel, I.;
Clermont, O.;
Roume, J.;
Delezoide, A. L.;
Cartaud, J.;
Munnich, A.;
Lefebvre, S.

Publication type:

Article

Risk for Alzheimer's disease correlates with transcriptional activity of the APOE gene.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 12, p. 1887, doi. 10.1093/hmg/7.12.1887

By:

Artiga, M. J.;
Bullido, M. J.;
Frank, A.;
Sastre, I.;
Recuero, M.;
García, M. A.;
Lendon, C. L.;
Han, S. W.;
Morris, J. C.;
Vázquez, J.;
Goate, A.;
Valdivieso, F.

Publication type:

Article

Novel immunogenic antigen homologous to hyaluronidase in meningioma.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 12, p. 1859, doi. 10.1093/hmg/7.12.1859

By:

Heckel, Dirk;
Comtesse, Nicole;
Brass, Nicole;
Blin, Nikolaus;
Zang, Klaus D.;
Meese, Eckart

Publication type:

Article

Molecular characterization of homozygous variegate porphyria.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 12, p. 1921, doi. 10.1093/hmg/7.12.1921

By:

Roberts, Andrew G.;
Puy, Hervé;
Dailey, Tamara A.;
Morgan, Rhian R.;
Whatley, Sharon D.;
Dailey, Harry A.;
Martasek, Pavel;
Nordmann, Yves;
Deybach, Jean‐Charles;
Elder, George H.

Publication type:

Article

Goosecoid-like ( Gscl ), a candidate gene for velocardiofacial syndrome, is not essential for normal mouse development.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 12, p. 1841

By:

Saint‐Jore, Bruno;
Puech, Anne;
Heyer, Jörg;
Lin, Qingcong;
Raine, Cedric;
Kucherlapati, Raju;
Skoultchi, Arthur I.

Publication type:

Article

Chromatin conformation of the H19 epigenetic mark.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 12, p. 1979, doi. 10.1093/hmg/7.12.1979

By:

Hark, Amy T.;
Tilghman, Shirley M.

Publication type:

Article

Genome-wide mapping of unselected transcripts from extraembryonic tissue of 7.5-day mouse embryos reveals enrichment in the t -complex and under-representation on the X chromosome.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 12, p. 1967

By:

Ko, Minoru S. H.;
Threat, Tracy A.;
Wang, Xueqian;
Horton, Joseph H.;
Cui, Yushun;
Wang, Xiaohong;
Pryor, Eric;
Paris, Jason;
Wells‐Smith, Jeannine;
Kitchen, John R.;
Rowe, Lucy B.;
Eppig, Janan;
Satoh, Toshihiko;
Brant, Larry;
Fujiwara, Hiroyuki;
Yotsumoto, Shinichi;
Nakashima, Hiroshi

Publication type:

Article

Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 12, p. 1935, doi. 10.1093/hmg/7.12.1935

By:

Gunter, Chris;
Paradee, William;
Crawford, Dana C.;
Meadows, Kellen A.;
Newman, James;
Kunst, Catherine B.;
Nelson, David L.;
Schwartz, Charles;
Murray, Anna;
Macpherson, James N.;
Sherman, Stephanie L.;
Warren, Stephen T.

Publication type:

Article

Genetic association of an α2-macroglobulin (Val1000Ile) polymorphism and Alzheimer's disease.

Published in:

Human Molecular Genetics, 1998, v. 7, n. 12, p. 1953, doi. 10.1093/hmg/7.12.1953

By:

Liao, A.;
Nitsch, R. M.;
Greenberg, S. M.;
Finckh, U.;
Blacker, D.;
Albert, M.;
Rebeck, G. W.;
Gomez‐Isla, T.;
Clatworthy, A.;
Binetti, G.;
Hock, C.;
Mueller‐Thomsen, T.;
Mann, U.;
Zuchowski, K.;
Beisiegel, U.;
Staehelin, H.;
Growdon, J. H.;
Tanzi, R. E.;
Hyman, B. T.

Publication type:

Article