The unexplored 5q13 locus: a role in hematopoietic malignancies.

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Inositide-specific phospholipase c beta1 gene deletion in the progression of myelodysplastic syndrome to acute myeloid leukemia.Reduced levels of DNA polymerase delta induce chromosome fragile site instability in yeast.

P2860

Q38479148-13C47BF0-8A15-4775-BB56-7CDF2BCEB2B3 Q42407123-327C0086-CB61-4519-A44F-143B6D5BAD56

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The unexplored 5q13 locus: a role in hematopoietic malignancies.

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http://www.wikidata.org/entity/Q52531579

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1998 nî lūn-bûn

@nan

1998年の論文

@ja

1998年学术文章

@wuu

1998年学术文章

@zh

1998年学术文章

@zh-cn

1998年学术文章

@zh-hans

1998年学术文章

@zh-my

1998年学术文章

@zh-sg

1998年學術文章

@yue

1998年學術文章

@zh-hant

name

The unexplored 5q13 locus: a role in hematopoietic malignancies.

@en

The unexplored 5q13 locus: a role in hematopoietic malignancies.

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type

Item

label

The unexplored 5q13 locus: a role in hematopoietic malignancies.

@en

The unexplored 5q13 locus: a role in hematopoietic malignancies.

@nl

prefLabel

The unexplored 5q13 locus: a role in hematopoietic malignancies.

@en

The unexplored 5q13 locus: a role in hematopoietic malignancies.

@nl

P1476

The unexplored 5q13 locus: a role in hematopoietic malignancies.

@en

P2093

Castro PD

http://www.w3.org/2001/XMLSchema#string

Fairman J

http://www.w3.org/2001/XMLSchema#string

Nagarajan L

http://www.w3.org/2001/XMLSchema#string

P2860

Regional chromosomal assignments for four members of the MADS domain transcription enhancer factor 2 (MEF2) gene family to human chromosomes 15q26, 19p12, 5q14, and 1q12-q23

Cytogenetic and molecular delineation of the smallest commonly deleted region of chromosome 5 in malignant myeloid diseases

Lessons from hereditary colorectal cancer

Identification of a putative effector for Cdc42Hs with high sequence similarity to the RasGAP-related protein IQGAP1 and a Cdc42Hs binding partner with similarity to IQGAP2

Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2

Physical mapping of the minimal region of loss in 5q- chromosome.

Loss of heterozygosity on chromosome 5q in ovarian cancer is frequently accompanied by TP53 mutation and identifies a tumour suppressor gene locus at 5q13.1-21.

Molecular delineation of the smallest commonly deleted region of chromosome 5 in malignant myeloid diseases to 1-1.5 Mb and preparation of a PAC-based physical map.

The 5q-anomaly.

Genetic analysis of the catalytic domain of the GAP gene in human lung cancer cell lines.

P304

443-448

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scholarly article

P356

10.3109/10428199809057556

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P433

5-6

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P478

http://www.w3.org/2001/XMLSchema#string

P577

1998-08-01T00:00:00Z

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P698

9711906

http://www.w3.org/2001/XMLSchema#string

The unexplored 5q13 locus: a role in hematopoietic malignancies.

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P2860

P2860

The unexplored 5q13 locus: a role in hematopoietic malignancies.

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P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698