Works matching IS 10614036 AND DT 1999 AND VI 22 AND IP 4

Results: 25

Gene therapy for rare diseases.

Published in:: Nature Genetics, 1999, v. 22, n. 4, p. 313, doi. 10.1038/11875
Publication type:: Article

Of ancient tales and hairless tails.

Published in:

Nature Genetics, 1999, v. 22, n. 4, p. 315, doi. 10.1038/11876

By:

Barsh, Gregory

Publication type:

Article

The ABCs of cholesterol efflux.

Published in:

Nature Genetics, 1999, v. 22, n. 4, p. 316, doi. 10.1038/11878

By:

Young, Stephen G;
Fielding, Christopher J

Publication type:

Article

Having a go at the hepatitis B virus.

Published in:

Nature Genetics, 1999, v. 22, n. 4, p. 318, doi. 10.1038/11880

By:

Phimister, Bette

Publication type:

Article

Gene dosage in mice?BAC to the future.

Published in:

Nature Genetics, 1999, v. 22, n. 4, p. 319, doi. 10.1038/11882

By:

Magdaleno, Susan M;
Curran, Tom

Publication type:

Article

TOUCHINGbase.

Published in:

Nature Genetics, 1999, v. 22, n. 4, p. 321

By:

Cahill, Dan

Publication type:

Article

Conditional deletion of Xist disrupts histone macroH2A localization but not maintenance of X inactivation.

Published in:

Nature Genetics, 1999, v. 22, n. 4, p. 323, doi. 10.1038/11887

By:

Csankovszki, Györgyi;
Panning, Barbara;
Bates, Brian;
Pehrson, John R.;
Jaenisch, Rudolf

Publication type:

Article

Transmission ratio distortion at the INS-IGF2 VNTR.

Published in:

Nature Genetics, 1999, v. 22, n. 4, p. 324, doi. 10.1038/11890

By:

Eaves, Iain A.;
Bennett, Simon T.;
Forster, Peter;
Ferber, Karin M.;
Ehrmann, David;
Wilson, Amanda J.;
Bhattacharyya, Sumit;
Ziegler, Anette-G.;
Brinkmann, Bernd;
Todd, John A.

Publication type:

Article

Polymorphism in intron 4 of HFE may cause overestimation of C282Y homozygote prevalence in haemochromatosis.

Published in:

Nature Genetics, 1999, v. 22, n. 4, p. 325, doi. 10.1038/11892

By:

Jeffrey, Gary P.;
Chakrabarti, Subrata;
Hegele, Robert A.;
Adams, Paul C.

Publication type:

Article

FDA comments on phase I clinical trials without vector biodistribution data.

Published in:

Nature Genetics, 1999, v. 22, n. 4, p. 326, doi. 10.1038/11895

By:

Epstein, Suzanne;
Bauer, Steven;
Miller, Andra;
Pilaro, Anne;
Noguchi, Philip

Publication type:

Article

BAC-mediated gene-dosage analysis reveals a role for Zipro1 (Ru49/Zfp38) in progenitor cell proliferation in cerebellum and skin.

Published in:

Nature Genetics, 1999, v. 22, n. 4, p. 327, doi. 10.1038/11896

By:

Yang, Xiangdong W.;
Wynder, Christopher;
Doughty, Martin L.;
Heintz, Nathaniel

Publication type:

Article

Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency.

Published in:

Nature Genetics, 1999, v. 22, n. 4, p. 336, doi. 10.1038/11905

By:

Brooks-Wilson, Angela;
Marcil, Michel;
Clee, Susanne M.;
Zhang, Lin-Hua;
Roomp, Kirsten;
van Dam, Marjel;
Yu, Lu;
Brewer, Carl;
Collins, Jennifer A.;
Molhuizen, Henri O.F.;
Loubser, Odell;
Ouelette, B.F. Francis;
Fichter, Keith;
Ashbourne-Excoffon, Katherine J.D.;
Sensen, Christoph W.;
Scherer, Stephen;
Mott, Stephanie;
Denis, Maxime;
Martindale, Duane

Publication type:

Article

The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier disease.

Published in:

Nature Genetics, 1999, v. 22, n. 4, p. 347, doi. 10.1038/11914

By:

Bodzioch, Marek;
Orsó, Evelyn;
Klucken, Jochen;
Langmann, Thomas;
Böttcher, Alfred;
Diederich, Wendy;
Drobnik, Wolfgang;
Barlage, Stefan;
Büchler, Christa;
Porsch-Özcürümez, Mustafa;
Kaminski, Wolfgang E.;
Hahmann, Harry W.;
Oette, Kurt;
Rothe, Gregor;
Aslanidis, Charalampos;
Lackner, Karl J.;
Schmitz, Gerd

Publication type:

Article

Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1.

Published in:

Nature Genetics, 1999, v. 22, n. 4, p. 352, doi. 10.1038/11921

By:

Rust, Stephan;
Rosier, Marie;
Funke, Harald;
Real, José;
Amoura, Zahir;
Piette, Jean-Charles;
Deleuze, Jean-Francois;
Brewer, H. Bryan;
Duverger, Nicolas;
Denèfle, Patrice;
Assmann, Gerd

Publication type:

Article

Klf4 is a transcription factor required for establishing the barrier function of the skin.

Published in:

Nature Genetics, 1999, v. 22, n. 4, p. 356, doi. 10.1038/11926

By:

Segre, Julia A.;
Bauer, Christoph;
Fuchs, Elaine

Publication type:

Article

Requirement for Wnt3 in vertebrate axis formation.

Published in:

Nature Genetics, 1999, v. 22, n. 4, p. 361, doi. 10.1038/11932

By:

Liu, Pentao;
Wakamiya, Maki;
Shea, Martin J.;
Albrecht, Urs;
Behringer, Richard R.;
Bradley, Allan

Publication type:

Article

Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia.

Published in:

Nature Genetics, 1999, v. 22, n. 4, p. 366, doi. 10.1038/11937

By:

Monreal, Alex W.;
Ferguson, Betsy M.;
Headon, Denis J.;
Street, Summer L.;
Overbeek, Paul A.;
Zonana, Jonathan

Publication type:

Article

Involvement of a novel Tnf receptor homologue in hair follicle induction.

Published in:

Nature Genetics, 1999, v. 22, n. 4, p. 370, doi. 10.1038/11943

By:

Headon, Denis J.;
Overbeek, Paul A.

Publication type:

Article

Engineering a mouse balancer chromosome.

Published in:

Nature Genetics, 1999, v. 22, n. 4, p. 375, doi. 10.1038/11949

By:

Zheng, Binhai;
Sage, Marijke;
Cai, Wei-Wen;
Thompson, Debrah M.;
Tavsanli, Beril C.;
Cheah, Yin-Chai;
Bradley, Allan

Publication type:

Article

Spontaneous functional correction of homozygous Fanconi anaemia alleles reveals novel mechanistic basis for reverse mosaicism.

Published in:

Nature Genetics, 1999, v. 22, n. 4, p. 379, doi. 10.1038/11956

By:

Waisfisz, Quinten;
Morgan, Neil V.;
Savino, Maria;
de Winter, Johan P.;
van Berkel, Carola G.M.;
Hoatlin, Maureen E.;
Ianzano, Leonarda;
Gibson, Rachel A.;
Arwert, Fre;
Savoia, Anna;
Mathew, Christopher G.;
Pronk, Jan C.;
Joenje, Hans

Publication type:

Article

Radiation hybrid map of the mouse genome.

Published in:

Nature Genetics, 1999, v. 22, n. 4, p. 384, doi. 10.1038/11962

By:

Van Etten, William J.;
Steen, Robert G.;
Nguyen, Huy;
Castle, Andrew B.;
Slonim, Donna K.;
Ge, Bing;
Nusbaum, Chad;
Schuler, Greg D.;
Lander, Eric S.;
Hudson, Thomas J.

Publication type:

Article

A YAC-based physical map of the mouse genome.

Published in:

Nature Genetics, 1999, v. 22, n. 4, p. 388, doi. 10.1038/11967

By:

Nusbaum, Chad;
Slonim, Donna K.;
Harris, Katrina L.;
Birren, Bruce W.;
Steen, Robert G.;
Stein, Lincoln D.;
Miller, Joyce;
Dietrich, William F.;
Nahf, Robert;
Wang, Victoria;
Merport, Olga;
Castle, Andrew B.;
Husain, Zeeshan;
Farino, Gail;
Gray, Delphine;
Anderson, Mechele O.;
Devine, Richard;
Horton, Lloyd T.;
Ye, Wenjuan

Publication type:

Article

RLIM inhibits functional activity of LIM homeodomain transcription factors via recruitment of the histone deacetylase complex.

Published in:

Nature Genetics, 1999, v. 22, n. 4, p. 394, doi. 10.1038/11970

By:

Bach, Ingolf;
Rodriguez-Esteban, Concepción;
Carrière, Catherine;
Bhushan, Anil;
Krones, Anna;
Rose, David W.;
Glass, Christopher K.;
Andersen, Bogi;
Belmonte, Juan Carlos Izpisúa;
Rosenfeld, Michael G.

Publication type:

Article

Identification of the gene (SEDL) causing X-linked spondyloepiphyseal dysplasia tarda.

Published in:

Nature Genetics, 1999, v. 22, n. 4, p. 400, doi. 10.1038/11976

By:

Gedeon, Ági K.;
Colley, Alison;
Jamieson, Robyn;
Thompson, Elizabeth M.;
Rogers, John;
Sillence, David;
Tiller, George E.;
Mulley, John C.;
Gécz, Jozef

Publication type:

Article

Sry requires a CAG repeat domain for male sex determination in Mus musculus.

Published in:

Nature Genetics, 1999, v. 22, n. 4, p. 405, doi. 10.1038/11981

By:

Bowles, Josephine;
Cooper, Leanne;
Berkman, Jennifer;
Koopman, Peter

Publication type:

Article