From: LARRY KLAES (ljk4_at_msn.com)
Date: Thu Apr 03 2003 - 10:46:33 PST
----- Original Message -----
From: Nature Genetics
Sent: Thursday, April 03, 2003 1:29 PM
To: ljk4_at_msn.com
Subject: Nature Genetics Contents: April 2003 Volume 33 pp. 431 - 533
NATURE GENETICS CONTENTS
April 2003 Volume 33 Number 4, pp 431 - 533
(c) Copyright 2003 Nature Publishing Group
Now available at http://www.nature.com/naturegenetics/
Visit Nature Genetics online to browse the content of the current
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NATURE ENCYCLOPEDIA OF THE HUMAN GENOME
Publishing in June in 5 printed volumes, Nature EHG is the only major
reference source devoted to the scientific basis of human genetics
and genomics research and its ethical, philosophical, and commercial
ramifications.
Complete list of contents with sample material at
http://www.ehgonline.net/.
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Brief Communications
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Mutant dynactin in motor neuron disease
I PULS, C JONNAKUTY, B H LAMONTE, E L F HOLZBAUR, M TOKITO, E MANN, M K FLOETER, K BIDUS, D DRAYNA, S J OH, R H BROWN, C L LUDLOW & K H FISCHBECK
http://www.nature.com/nglink/v33/n4/abs/ng1123.html
Quality and completeness of SNP databases
D E REICH, S B GABRIEL & D ALTSHULER
http://www.nature.com/nglink/v33/n4/abs/ng1133.html
Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome
J AMIEL, B LAUDIER, T ATTII-BITACH, H TRANG, L DE PONTUAL, B GENER, D TROCHET, H ETCHEVERS, P RAY, M SIMONNEAU, M VEKEMANS, A MUNNICH, C GAULTIER & S LYONNET
http://www.nature.com/nglink/v33/n4/abs/ng1130.html
Mutations in SOX2 cause anophthalmia
J FANTES, N K RAGGE, S -A LYNCH, N I MCGILL, J R O COLLIN, P N HOWARD-PEEBLES, C HAYWARD, A J VIVIAN, K WILLIAMSON, V VAN HEYNINGEN & D R FITZPATRICK
http://www.nature.com/nglink/v33/n4/abs/ng1120.html
Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome
C DODI, J LEVILLIERS, J -M DUPONT, A DE PAEPE, N LE D[, N SOUSSI-YANICOSTAS, R S COIMBRA, S DELMAGHANI, S COMPAIN-NOUAILLE, F BAVEREL, C PJCHEUX, D LE TESSIER, C CRUAUD, M DELPECH, F SPELEMAN, S VERMEULEN, A AMALFITANO, Y BACHELOT, P BOUCHARD, S CABROL, J -C CAREL, H DELEMARRE-VAN DE WAAL, B GOULET-SALMON, M -L KOTTLER, O RICHARD, F SANCHEZ-FRANCO, R SAURA, J YOUNG, C PETIT & J -P HARDELIN
http://www.nature.com/nglink/v33/n4/abs/ng1122.html
Mutations in RAI1 associated with Smith--Magenis syndrome
R E SLAGER, T L NEWTON, C N VLANGOS, B FINUCANE & S H ELSEA
http://www.nature.com/nglink/v33/n4/abs/ng1126.html
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New Technology
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In vivo characterization of regulatory polymorphisms by allele-specific quantification of RNA polymerase loading
J C KNIGHT, B J KEATING, K A ROCKETT & D P KWIATKOWSKI
http://www.nature.com/nglink/v33/n4/abs/ng1124.html
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Article
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Loss of neuropathy target esterase in mice links organophosphate exposure to hyperactivity
C J WINROW, M L HEMMING, D M ALLEN, G B QUISTAD, J E CASIDA & C BARLOW
http://www.nature.com/nglink/v33/n4/abs/ng1131.html
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Letters
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Localized mutations in the gene encoding the cytoskeletal protein filamin A cause diverse malformations in humans
S P ROBERTSON, S R F TWIGG, A J SUTHERLAND-SMITH, V BIANCALANA, R J GORLIN, D HORN, S J KENWRICK, C A KIM, E MORAVA, R NEWBURY-ECOB, K H XRSTAVIK, O W J QUARRELL, C E SCHWARTZ, D J SHEARS, M SURI, J KENDRICK-JONES, A O M WILKIE, C BACINO, K BECKER, J CLAYTON-SMITH, M GIOVANNUCCI-UZIELLI, D GOH, D GRANGE, M KRAJEWSKA-WELASEK, D LACOMBE, C MORRIS, S ODENT, R SAVARIRAYAN, R STRATTON, A SUPERTI-FURGA, A VERLOES, J VIGNERON, W WILCOX, R WINTER & K YOUNG
http://www.nature.com/nglink/v33/n4/abs/ng1119.html
Erosion of the telomeric single-strand overhang at replicative senescence
S A STEWART, I BEN-PORATH, V J CAREY, B F O'CONNOR, W C HAHN & R A WEINBERG
http://www.nature.com/nglink/v33/n4/abs/ng1127.html
A splicing mutation affecting expression of ataxia--telangiectasia and Rad3--related protein (ATR) results in Seckel syndrome
M O'DRISCOLL, V L RUIZ-PEREZ, C G WOODS, P A JEGGO & J A GOODSHIP
http://www.nature.com/nglink/v33/n4/abs/ng1129.html
Genome imprinting regulated by the mouse Polycomb group protein Eed
J MAGER, N D MONTGOMERY, F P -M DE VILLENA & T MAGNUSON
http://www.nature.com/nglink/v33/n4/abs/ng1125.html
A defective response to Hedgehog signaling in disorders of cholesterol biosynthesis
M K COOPER, C A WASSIF, P A KRAKOWIAK, J TAIPALE, R GONG, R I KELLEY, F D PORTER & P A BEACHY
http://www.nature.com/nglink/v33/n4/abs/ng1134.html
Transcription-associated mutational asymmetry in mammalian evolution
P GREEN, B EWING, W MILLER, P J THOMAS, NISC Comparative Sequencing Program & E D GREEN
http://www.nature.com/nglink/v33/n4/abs/ng1103.html
Additional SNPs and linkage-disequilibrium analyses are necessary for whole-genome association studies in humans
C S CARLSON, M A EBERLE, M J RIEDER, J D SMITH, L KRUGLYAK & D A NICKERSON
http://www.nature.com/nglink/v33/n4/abs/ng1128.html
Sir3p phosphorylation by the Slt2p pathway effects redistribution of silencing function and shortened lifespan
A RAY, R E HECTOR, N ROY, J -H SONG, K L BERKNER & K W RUNGE
http://www.nature.com/nglink/v33/n4/abs/ng1132.html
Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies
K HAUG, M WARNSTEDT, A K ALEKOV, T SANDER, A RAMMREZ, B POSER, S MALJEVIC, S HEBEISEN, C KUBISCH, J REBSTOCK, S HORVATH, K HALLMANN, J S DULLINGER, B RAU, F HAVERKAMP, S BEYENBURG, H SCHULZ, D JANZ, B GIESE, G M\LLER-NEWEN, P PROPPING, C E ELGER, C FAHLKE, H LERCHE & A HEILS
http://www.nature.com/nglink/v33/n4/abs/ng1121.html
****************************************************************************
The content listing below is accessible only through a subscription.
To purchase a subscription, please visit:
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---------------------
Editorial
---------------------
Genetical implications
---------------------
News & Views
---------------------
The need for Eed
A C FERGUSON-SMITH & W REIK
Classifying humans
F CALAFELL
Neurotoxic esterase: not so toxic?
J P O'CALLAGHAN
Wanted: regulatory SNPs
T J HUDSON
A clinician's plea
J G HALL
The smoking gun of gene transfer
W MARTIN
---------------------
News & Views {Touching Base}
---------------------
TOUCHINGbase
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Book Review
---------------------
DNA: The Secret of Life
by JAMES D. WATSON & ANDREW BERRY
Reviewed by G WEISSMANN
The Common Thread: A Story of Science, Politics, Ethics, and the Human Genome
by JOHN SULSTON & GEORGINA FERRY
Reviewed by J R LUPSKI
---------------------
Commentary
---------------------
Was there life before 1953?
J F CROW
Just before Watson and Crick
L B SLOBODKIN
DNA and the meaning of life
S MAWER
---------------------
Corrigenda
---------------------
Corrigendum: Mice deficient in protein tyrosine phosphatase receptor type Z are resistant to gastric ulcer induction by VacA of Helicobacter pylori
A FUJIKAWA, D SHIRASAKA, S YAMAMOTO, H OTA, K YAHIRO, M FUKADA, T SHINTANI, A WADA, N AOYAMA, T HIRAYAMA, H FUKAMACHI & M NODA
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