Workshop 1999 schedule

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CHROMOSOME 1 WORKSHOP

1999 PROGRAM

PROGRAM

WORKSHOP ABSTRACTS

MEETING PARTICIPANTS

WORKSHOP REPORT

Thursday 5th August

16.00 - 18.00 Registration & Poster set-up

18.30 - 19.30 Reception

19.30 - Dinner

Friday 6th August

08.30 - 9.00 Introduction Jeff Vance

10.30 - 11.00 POSTERS / Coffee

12.30 - 13.30 Lunch

15.00 - 15.30 POSTERS / Coffee

17.00 - 17.30 POSTERS/Coffee

17.30 - 19.00 IT Session (II)

White - CompView

Tutors from Compview/GDB/Webace on hand

20.00 Conference Dinner

Saturday 7th August

10.30 - 11.00 POSTERS/Coffee

12.30 - 13.00 POSTERS/Coffee

13.00 - 14.30 Lunch (BBQ)

14.30 - 15.30 Workshop Report Meeting

15.30 - 17.00 IT Session (III)

17.00 - 17.30 POSTERS/Coffee

17.30 - Concluding remarks / Discussion

19.30 - Dinner

Sunday 8th August

Departure

last modified: Thursday, 29-May-2008 20:07:43 EDT

1.	Matise	The Human Chromosome 1 Web Site.
2.	White	Comprehensive Integration and Cataloging of Chromosome 1 using CompView.
3.	McDonald/Bird	Progress of Chromosome 1 Mapping and Sequencing at the Sanger Centre.
4.	Rhodes/Wilming	Gene Discovery Activities on Finished Chromosome 1 Sequences.
5.	Carpten	A Physical and Transcription Map of 1q24.3-q31.1 as a Resource for Identifying Hereditary genes including HPC1.

6.	Porter	Continuation of the Genome Database Project.
	Carol Scott	Webace

7.	Martinsson	Fine Mapping of a Neuroblastoma Tumor Suppressor Candidate Gene Region in 1p36.2-3, and Mutation Analysis of the Cortistatin Gene Localized to the Region.
8.	Spieker	Analysis of a 5Mb Region of 1p36.1 Harbouring a Tumour Supressor Locus involved in MYCN Amplified Neuroblastoma.
9.	Versteeg	Application of SAGE to Generate a Integral 1p35-36 Transcription Map in Neuroblastoma.
10.	Horii	Cloning and Characterisation of Genes at reciprocal t(1;9)(p32.3;p21.2) Translocation Breakpoint in a Patient with Neuroblastoma.

11.	Chadwick	High Resolution Mapping of Chromosome 1p Deletions in Hereditary and Sporadic CRC Cancers by Combining High Density Nucleotide Polymorphisms and Microsatellite Analysis.
12.	Huang	A Minimal Deleted Region in Hepatocellular Carcinoma Maps within Human 1p36.1-36.2.
13.	Wong	Mapping a Novel Amplicon 1q21-25 in Human Hepatocellular Carcinoma by Interphase FISH.
14.	Meza-Zepeda	FISHing cDNAs from a Frequently Amplified Region of Chromosome 1 in Sarcomas.

15.	Vance	Mapping Direct Selection Transcripts in the Charcot-Marie Tooth type 2 (CMT2A) Region of 1p36.
16.	Irrthum	A Gene for Inherited Cutaneous Venous Anomalies ("Glomangiomas") Localizes to Chromosome 1p21-p22.
17.	Zollo	An Effort to Search for the RP18 Responsible Gene in 1q21 Chromosomal Region.
18.	Trembath	Construction of a Physical Map at 1q21-q22 to Aid in the Identification of the Gene Defective in Partial Lipodystrophy.
19.	Shiina	Sequence Determination of Human Chromosome 1q22-q23 which is paralogous to the HLA Region on Chromosome 6p21.3.

20.	Wolford	Linkage Disequilibrium of a Type 2 Diabetes-Linked Region on 1q21-q23.
21.	Stanier	Comparative Mapping of the Mouse and Human Homologous Chromosome 1 Regions Containing the Mouse NTD Mutant Lp Locus.
22.	Labay	Positional Cloning of the TRMA Gene.
23.	Schutte	An 8Kb Deletion/Insert Polymorphism in the Van Der Woude Critical Region at 1q32-q41.
24.	Schutte	A Primary Transcript Map for the Van Der Woude Syndrome (VWS) Critical Region Derived from 900Kb of Genomic Sequence at 11q32-q41.
25.	Parvari	Transcription Map of Chromosome 1q42-q43: Candidate Genes for the Syndrome of Congenital Hypoparathyroidism, Growth, Mental Retardation and Dysmorphism (HRD).