GENEALOGY-DNA-L Archives

From: "Dale E. Reddick" <>
Subject: Nature Genetics Contents: August 2005 Volume 37 pp 783 - 911
Date: Mon, 01 Aug 2005 16:10:12 -0400

Hi Folks,

I hope someone sees something interesting amongst the contents of this
issue of Nature Genetics.

Dale

________________________________


August 2005, Volume 37 No 8

Editorial

WayStation to HUGOBase p783

doi: 10.1038/ng0805-783

Correspondence

Microdeletion and IGF2 loss of imprinting in a cascade causing
Beckwith-Wiedemann syndrome with Wilms' tumor pp785 - 786

Dirk Prawitt, Thorsten Enklaar, Barbara Gartner-Rupprecht, Christian
Spangenberg, Ekkehart Lausch, Dirk Reutzel, Stephan Fees, Maria Korzon,
Izabela Brozek, Janusz Limon, David E Housman, Jerry Pelletier &
Bernhard Zabel

doi: 10.1038/ng0805-785

Reply to "Microdeletion and IGF2 loss of imprinting in a cascade causing
Beckwith-Wiedemann syndrome with Wilms' tumor" pp786 - 787

Flavia Cerrato, Angela Sparago, Lucia Farina, Giovanni Battista Ferrero,
Margherita Cirillo Silengo & Andrea Riccio

doi: 10.1038/ng0805-786

Meeting Report

Are we making progress in the debate over racial and ethnic categories
in biomedical research? pp789 - 790

Susan M Wolf

doi: 10.1038/ng0805-789

Book Review

Evo-devo for the general reader p791

Reviewed by: Adam S Wilkins

doi: 10.1038/ng0805-791

News and Views

Unraveling TACIt functions pp793 - 794

Flavius Martin & Vishva M Dixit

doi: 10.1038/ng0805-793


See also: Article by Salzer et al. | Article by Castigli et al.
Pharmacogenetics goes 3D pp794 - 795

Howard L McLeod & Sharon Marsh

doi: 10.1038/ng0805-794


See also: Letter by Cheng et al.
Splicing on the brain pp796 - 797

Benjamin J Blencowe

doi: 10.1038/ng0805-796


See also: Article by Ule et al.
Touching base p799

doi: 10.1038/ng0805-799

Research Highlights p801

doi: 10.1038/ng0805-801

Brief Communications

A deletion in the gene encoding sphingomyelin phosphodiesterase 3
(Smpd3) results in osteogenesis and dentinogenesis imperfecta in the
mouse pp803 - 805

Isabelle Aubin, Carolyn P Adams, Sibylle Opsahl, Dominique Septier,
Colin E Bishop, Nathalie Auge, Robert Salvayre, Anne Negre-Salvayre,
Michel Goldberg, Jean-Louis Guenet & Christophe Poirier

doi: 10.1038/ng1603

Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in
frontotemporal dementia pp806 - 808

Gaia Skibinski, Nicholas J Parkinson, Jeremy M Brown, Lisa Chakrabarti,
Sarah L Lloyd, Holger Hummerich, Jorgen E Nielsen, John R Hodges, Maria
Grazia Spillantini, Tove Thusgaard, Sebastian Brandner, Arne Brun,
Martin N Rossor, Anders Gade, Peter Johannsen, Sven Asger Sorensen,
Susanne Gydesen, Elizabeth MC Fisher & John Collinge

doi: 10.1038/ng1609

Articles

Comprehensive analysis of heterochromatin- and RNAi-mediated epigenetic
control of the fission yeast genome pp809 - 819

Hugh P Cam, Tomoyasu Sugiyama, Ee Sin Chen, Xi Chen, Peter C FitzGerald
& Shiv I S Grewal

doi: 10.1038/ng1602

Mutations in TNFRSF13B encoding TACI are associated with common variable
immunodeficiency in humans pp820 - 828

U Salzer, H M Chapel, A D B Webster, Q Pan-Hammarstrom, A
Schmitt-Graeff, M Schlesier, H H Peter, J K Rockstroh, P Schneider, A A
Schaffer, L Hammarstrom & B Grimbacher

doi: 10.1038/ng1600


See also: News and Views by Martin and Dixit
TACI is mutant in common variable immunodeficiency and IgA deficiency
pp829 - 834

Emanuela Castigli, Stephen A Wilson, Lilit Garibyan, Rima Rachid,
Francisco Bonilla, Lynda Schneider & Raif S Geha

doi: 10.1038/ng1601


See also: News and Views by Martin and Dixit
Complement factor 5 is a quantitative trait gene that modifies liver
fibrogenesis in mice and humans pp835 - 843

Sonja Hillebrandt, Hermann E Wasmuth, Ralf Weiskirchen, Claus
Hellerbrand, Hildegard Keppeler, Alexa Werth, Ramin Schirin-Sokhan,
Gabriele Wilkens, Andreas Geier, Johann Lorenzen, Jorg Kohl, Axel M
Gressner, Siegfried Matern & Frank Lammert

doi: 10.1038/ng1599

Nova regulates brain-specific splicing to shape the synapse pp844 - 852

Jernej Ule, Aljaz Ule, Joanna Spencer, Alan Williams, Jing-Shan Hu,
Melissa Cline, Hui Wang, Tyson Clark, Claire Fraser, Matteo Ruggiu,
Barry R Zeeberg, David Kane, John N Weinstein, John Blume & Robert B Darnell

doi: 10.1038/ng1610

See also: News and Views by Blencowe
Chromosome-wide and promoter-specific analyses identify sites of
differential DNA methylation in normal and transformed human cells pp853
- 862

Michael Weber, Jonathan J Davies, David Wittig, Edward J Oakeley,
Michael Haase, Wan L Lam & Dirk Schubeler

doi: 10.1038/ng1598

Letters

Variants of ENPP1 are associated with childhood and adult obesity and
increase the risk of glucose intolerance and type 2 diabetes pp863 - 867

David Meyre, Nabila Bouatia-Naji, Agnes Tounian, Chantal Samson, Cecile
Lecoeur, Vincent Vatin, Maya Ghoussaini, Christophe Wachter, Serge
Hercberg, Guillaume Charpentier, Wolfgang Patsch, Francois Pattou,
Marie-Aline Charles, Patrick Tounian, Karine Clement, Beatrice Jouret,
Jacques Weill, Betty A Maddux, Ira D Goldfine, Andrew Walley, Philippe
Boutin, Christian Dina & Philippe Froguel

doi: 10.1038/ng1604

Demonstrating stratification in a European American population pp868 - 872

Catarina D Campbell, Elizabeth L Ogburn, Kathryn L Lunetta, Helen N
Lyon, Matthew L Freedman, Leif C Groop, David Altshuler, Kristin G
Ardlie & Joel N Hirschhorn

doi: 10.1038/ng1607

Recombination of mitochondrial DNA in skeletal muscle of individuals
with multiple mitochondrial DNA heteroplasmy pp873 - 877

Gabor Zsurka, Yevgenia Kraytsberg, Tatiana Kudina, Cornelia Kornblum,
Christian E Elger, Konstantin Khrapko & Wolfram S Kunz

doi: 10.1038/ng1606

Karyotypic abnormalities create discordance of germline genotype and
cancer cell phenotypes pp878 - 882

Qing Cheng, WenJian Yang, Susana C Raimondi, Ching-Hon Pui, Mary V
Relling & William E Evans

doi: 10.1038/ng1612


See also: News and Views by McLeod and Marsh
Plk4 haploinsufficiency causes mitotic infidelity and carcinogenesis
pp883 - 888

Michael A Ko, Carla O Rosario, John W Hudson, Sarang Kulkarni, Aaron
Pollett, James W Dennis & Carol J Swallow

doi: 10.1038/ng1605

Inversion-induced disruption of the Hoxd cluster leads to the partition
of regulatory landscapes pp889 - 893

Francois Spitz, Carole Herkenne, Michael A Morris & Denis Duboule

doi: 10.1038/ng1597

A stress-sensitive reporter predicts longevity in isogenic populations
of Caenorhabditis elegans pp894 - 898

Shane L Rea, Deqing Wu, James R Cypser, James W Vaupel & Thomas E Johnson

doi: 10.1038/ng1608

Distinct epigenetic changes in the stromal cells of breast cancers pp899
- 905

Min Hu, Jun Yao, Li Cai, Kurt E Bachman, Frederic van den Brule, Victor
Velculescu & Kornelia Polyak

doi: 10.1038/ng1596

Short double-stranded RNA induces transcriptional gene silencing in
human cancer cells in the absence of DNA methylation pp906 - 910

Angela H Ting, Kornel E Schuebel, James G Herman & Stephen B Baylin

doi: 10.1038/ng1611

Corrigenda

Corrigendum: Table of contents p911

doi: 10.1038/ng0805-911a

Corrigendum: An adaptive radiation model for the origin of new gene
functions p911

M P Francino

doi: 10.1038/ng0805-911b

This thread:

• Nature Genetics Contents: August 2005 Volume 37 pp 783 - 911 by "Dale E. Reddick" <>