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| Frank S. Zollmann: LITE: GENOMICS Contents, Volume 27, Number 3, June 10, 1995 | ||||||||||||||||
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To: Multiple recipients of list HUM-MOLGEN <HUM-MOLGEN@NIC.SURFNET.NL> Subject: LITE: GENOMICS Contents, Volume 27, Number 3, June 10, 1995 From: "Frank S. Zollmann" <zollmann.1@osu.edu> Date: Thu, 8 Jun 1995 02:53:15 -0400
GENOMICS
International Journal for Analyses of the Human and Other Genomes
Editors-in-Chief
Victor A. McKusick
The Johns Hopkins University, Baltimore, Maryland
Raju S. Kucherlapati
Albert Einstein College of Medicine, Bronx, New York
Frank H. Ruddle
Yale University, New Haven, Connecticut
GENOMICS emphasizes the integration of basic and applied research
in human and comparative gene mapping, molecular cloning,
large-scale restriction mapping, and DNA sequencing and
computational analysis. The journal provides a common meeting
ground for those involved in molecular biology and genetics.
Technologic and methodologic advances in genomic analysis and
interpretation are described, and analyses of the human genome in
hereditary and neoplastic diseases are reported. Full-length
articles, short communications, brief reports, and reviews are
included. In addition, GENOMICS promotes efficient communication
with the major genetic databases.
Research Areas Include: Chromosomal assignments of genes and DNA
fragments by Mendelian and physical mapping approaches; Reports of
nucleic acid sequences of cloned genes and other interesting
portions of a genome; Descriptions of distributions of gene
families and genes that share nucleic acid or amino acid sequence
domains; Comparative analyses of genomes to yield structural,
functional, or evolutionary insights;
Patterns of genome organization that provide insights into gene
regulation and development; Methods for large-scale genomic
cloning, restriction mapping, and DNA sequencing; Computational
methods and descriptions of algorithms for the manipulation of DNA
and protein sequence data; Analyses of genetic linkage data in
pursuit of information on inherited disorders; Development of
experimental, computational, and database management techniques of
broad applicability in genome research.
Database coverage includes Biological Abstracts (BIOSIS), Current
Contents/Life Sciences, Genetics Abstracts, Index Medicus
(MEDLINE), and Science Citation Index.
CONTENTS FROM A FORTHCOMING ISSUE:
Volume 27, Number 3, June 10, 1995
NEW TECHNOLOGY AND RESOURCES
D Smith; Y Zhu; J Zhang; J Cheng; E Rubin
Construction of a Panel of Transgenic Mice Containing a Contiguous 2-Mb
Set of YAC/P1 Clones from Human Chromosome 21q22.2
GENE STRUCTURE AND GENE ORGANIZATION
H Chen; I Thalmann; J Adams; K Avraham, N Copeland; N Jenkins; D Beier;
D Corey; R Thalmann, G Duyk
cDNA Cloning, Tissue Distribution, and Chromosomal Localization of
Ocp2, a Gene Encoding a Putative Transcription-Associated Factor
Predominantly Expressed in the Auditory Organs
M Bozza; L Kolakowski Jr; N Jenkins, D Gilbert; N Copeland, J David, C
Gerard
Structural Characterization and Chromosomal Location of the Mouse
Macrophage Migration Inhibitory Factor Gene and Pseudogenes
S Chakravarti; R Stallings; N SundarRaj; P Cornuet; J Hassell
Primary Structure of Human Lumican (Keratan Sulfate Proteoglycan) and
Localization of the Gene (LUM) to Chromosome 12q21.3-q22
M Saijo; Y Sakai; T Kishino; N Niikawa; Y Matsuura; K Morino; K Tamai;
Y Taya
Molecular Cloning of a Human Protein That Binds to the Retinoblastoma
Protein and Chromosomal Mapping
M El-Maghrabi; A Lange; W Jiang; K Yamagata; M Stoffel; J Takeda; A
Fernald; M Le Beau; G Bell; L Baker; S Pilkis
Human Fructose-1,6-Bisphosphatase Gene (FBP1): Exon-Intron
Organization, Localization to Chromosome Bands 9q22.2-q22.3, and
Mutation Screening in Subjects with Fructose-1,6-Bisphosphatase
Deficiency
K Bloch; J Wolfram; D Brown; J Roberts, Jr; D Zapol; J Lepore; G
Filippov, J Thomas; H Jacob; D Bloch
Short Communication: Three Members of the Nitric Oxide Synthase II
Gene Family (NOS2A, NOS2B, and NOS2C) Colocalize to Human Chromosome 17
L Erikson; N Maeda
Short Communication: A New Family of Retroviral Long Terminal Repeat
Elements in the Human Genome Identified by Their Homologies to an
Element 5' to the Spider Monkey Haptoglobin Gene
I Yulug; A Yulug; E Fisher
Short Communication: The Frequency and Position of Alu Repeats in
cDNAs, as Determined by Database Searching
K Harder; J Saw; N Miki; F Jirik
Brief Report: Coexisting Amplifications of the Chromosome 1p32 Genes
(PTPRF and MYCL1) Encoding Protein Tyrosine Phosphatase LAR and L-myc
in a Small Cell Lung Cancer Line
GENE STRUCTURE/FUNCTION RELATIONSHIPS
L Xu; C Sterner; M Maheshwar; P Wilson; M Nellist; P Short; J Haines; J
Sampson; V Ramesh
Alternative Splicing of the Tuberous Sclerosis 2 (TSC2) Gene in Human
and Mouse Tissues
D Hunt; J Cowing; R Patel; B Appukuttan; J Bowmaker; J Mollon
Short Communication: Sequence and Evolution of the Blue Cone Pigment
Gene in Old and New World Primates
LINKAGE AND GENETIC MAPS
S Miyazaki; C Kozak; A Marchetti; F Buttitta; D Gallahan; R Callahan
The Chomosomal Location of the Mouse Mammary Tumor Gene Int6 and
Related Pseudogenes in the Mouse Genome
A Scalzo; P Lyons; N Fitzgerald; C Forbes; W Yokoyama; G Shellam
Genetic Mapping of Cmv1 in the Region of Mouse Chromosome 6 Encoding
the NK Gene Complex-Associated Loci LY49 and musNKR-P1
J Suh;l T Yamanishi; K Matsui; K Tanaka; K Wada
Short Communication: Mapping of the Gracile Axonal Dystropohy (gad)
Gene to a Region between D5Mit197 and D5Mit113 on Proximal Mouse
Chromosome 5
PHYSICAL MAPS
L Hawthorne; J Cowell
Integration of the Physical and Genetic Linkage Map for Human
Chromosome 13
B Holdener; J Thomas; A Schumacher; M Potter; E Rinchik; S Sharan; T
Magnuson
Physical Localization of eed: A Region of Mouse Chromosome 7 Required
for Gastrulation
N Pollet; S Dhorne-Pollet; J Deleueze; C Boccaccio; C Driancourt; N
Raynaud; D Paslier; M Hadchouel; M Meunier-Rotival
Construction of a 3.7-Mb Physical Map within Human Chromosome 20p12
Ordering 18 Markers in the Alagille Syndrome Locus
S Washington; J Farr; B Thiel; T Matise; J Weissenbach; A Chakaravarti;
C Richard III
A Radiation Hybrid Map of 95 STSs Spanning Human Chromosome 13q
C Philippe; C Arnould; F Sloan; H van Bokhoven; S van der Velde-Visser;
M Chery; H Hilger Ropers; S Gilgenkrantz; A Monaco; F Cremers
Short Communication: A High-Resolution Interval Map of the q21 Region
of the Human X Chromosome
E Raimondi; M Romanelli; D Moralli; C Gamberi; M Russo; C Morandi
Brief Report: Assignment of the Human Gene Encoding Heterogeneous
Nuclear RNA Ribonucleoprotein I (PTB) to Chromosome 14q23-q24.1
V Tiranti; E Rossi; M Rocchi; S DiDonato; O Zuffardi; M Zeviani
Brief Report: The Gene (NFE2L1) for Human NRF-1, an Activator Involved
in Nuclear-Mitochondrial Interactions, Maps to 7q32
A van der Wijngaard; D Weghuis; C Boersma; E van Zoelen; A van Kessel;
W Olijve
Brief Report: Fine Mapping of the Human Bone Morphogenetic Protein-4
Gene (BMP4) to Chromosome 14q22-q23 by in Situ Hybridization
GENE DISCOVERY AND DISEASE GENES
D FitzPatrick; E Germain-Lee; D Valle
Isolation and Characterization of Rat and Human cDNAs Encoding a Novel
Putative Peroxisomal EnoylCoA Hydratase
P Radice; D Perotti; V De Bendetti; P Mondini; M Radice; S Pilotti; R
Luksch; F Bellani; M Pierotti
Allelotyping in Wilms Tumors Identifies a Putative Third Tumor
Suppressor Gene on Chromosome 11
DISEASE MUTATIONS
F Del Gatto; R Breathnach
Brief Report: A Crouzon Syndrome Synonymous Mutation Activates a 5'
Splice Site within the IIIC Exon of the FGFR2 Gene
COMPARATIVE GENOMICS
C Kozak; M Adamson; C Buckler; L Segovia; V Paralkar; G Wistow
Genomic Cloning of Mouse MIF (Macrophage Inhibitory Factor) and Genetic
Mapping of the Human and Mouse Expressed Gene and Nine Mouse
Pseudogenes
G Elgar; F Rattray; J Greystrong; S Brenner
Genomic Structure and Nucleotide Sequence of the p55 Gene of the Puffer
Fish Fugu rubripes
S Solinas-Toldo; C Lengauer; R Fries
Comparative Genome Map of Human and Cattle
AUTHOR INDEX FOR VOLUME 27
NOTICE
The Subject Index for Volume 27 will appear in the December 10, 1995
issue as part of a cumulative index for the year 1995.
FROM ACADEMIC PRESS JOURNALS:
GENOMICS: International Journal for Analyses of the Human and Other
Genomes
PUBLICATION INFORMATION
Volumes 25-30 (1995), 18 issues (including annual subject index)
RATES
Annual Subscription Rates
In the U.S.A. and Canada
Institutional: $698.00
Personal: $231.00
All other countries
Institutional: $760.00
Personal: $275.00
Academic Press U.S.A.
ISSN 0888-7543
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For more information about new book titles from Academic Press, please
see file: ACADEMIC PRESS/BOOKS.
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