(Q34140923)

31 July 2017

title

Identification, genomic organization and mRNA expression of CRELD1, the founding member of a unique family of matricellular proteins (English)

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31 July 2017

Kent L Thornburg

8

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Cheryl L Maslen

10

object named as

Cheryl L Maslen

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31 July 2017

Paul A Rupp

1

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31 July 2017

Gameil T Fouad

2

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31 July 2017

Carley A Egelston

3

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31 July 2017

Carol A Reifsteck

4

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31 July 2017

Susan B Olson

5

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31 July 2017

Wendy M Knosp

6

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31 July 2017

Robert W Glanville

7

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31 July 2017

Susan W Robinson

9

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31 July 2017

language of work or name

English

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publication date

1 June 2002

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31 July 2017

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31 July 2017

volume

293

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31 July 2017

issue

1-2

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31 July 2017

page(s)

47-57

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Deletion at 3p25.3-p23 is frequently encountered in endocrine pancreatic tumours and is associated with metastatic progression

31 July 2017

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A second locus for Marfan syndrome maps to chromosome 3p24.2-p25.

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A common region of allelic loss on chromosome region 3p25.3-26.3 in nasopharyngeal carcinoma

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7 January 2021

Precise localisation of 3p25 breakpoints in four patients with the 3p-syndrome

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7 January 2021

EGF-like domains in extracellular matrix proteins: localized signals for growth and differentiation?

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7 January 2021

Potential secondary structure at the translational start domain of eukaryotic and prokaryotic mRNAs

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7 January 2021

Detailed mapping of a congenital heart disease gene in chromosome 3p25

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7 January 2021

Fine mapping of the chromosome 3p susceptibility locus in inflammatory bowel disease

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7 January 2021

Localization of the Fanconi anemia complementation group D gene to a 200-kb region on chromosome 3p25.3.

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7 January 2021

The evolution of cell adhesion

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7 January 2021

Mapping of a familial moyamoya disease gene to chromosome 3p24.2-p26.

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7 January 2021

Frequent loss of heterozygosity at 3p25-p26 is associated with invasive oral squamous cell carcinoma

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7 January 2021

Interpreting cDNA sequences: some insights from studies on translation

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7 January 2021

Loss of heterozygosity on the short arm of chromosome 3 in renal cancer

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7 January 2021

High-resolution chromosome 3p allelotyping of breast carcinomas and precursor lesions demonstrates frequent loss of heterozygosity and a discontinuous pattern of allele loss

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7 January 2021

Chromosome 3p allele loss in early invasive breast cancer: detailed mapping and association with clinicopathological features.

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7 January 2021

Molecular genetic analysis of the 3p- syndrome

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7 January 2021

Genetic aspects of atrioventricular septal defects

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https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900696-0

7 January 2021

Two infants with del(3)(p25pter) and a review of previously reported cases

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7 January 2021

The structure of a Ca2+-binding epidermal growth factor-like domain: Its role in protein-protein interactions

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7 January 2021

Ecto-protein kinases: ecto-domain phosphorylation as a novel target for pharmacological manipulation?

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https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900696-0

7 January 2021

Localization of a novel susceptibility gene for familial ovarian cancer to chromosome 3p22-p25

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7 January 2021

Detection of loss of heterozygosity at chromosome 3p25-26 in primary and metastatic ovarian clear-cell carcinoma: utilization of microdissection and polymerase chain reaction in archival tissues

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2802%2900696-0

7 January 2021

Topogenic signals in integral membrane proteins

1 reference

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7 January 2021

10.1016/S0378-1119(02)00696-0

Identifiers

DOI

1 reference

31 July 2017

1 reference