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17q

Known as: Chromosome 17 Distal Arm, Chromosome 17 Long Arm 
Distal (long) arm of chromosome 17
National Institutes of Health

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40 relations
17q1117q11-q1217q11-q2117q11-qter

Papers overview

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2013
2013
Molecular mutations are prognostically relevant in AML with intermediate risk cytogenetics and aberrant karyotype
Molecular mutations are prognostically relevant in AML with intermediate risk cytogenetics and aberrant karyotype 
Review
2011
Review
2011
18 or trisomy 18 in lymphoproliferative disorders
Review on +18 or trisomy 18 in lymphoproliferative disorders, with data on clinics, and the genes involved. 
2003
2003
p15 INK4b , p14 ARF , and p16 INK4a Inactivation in Sporadic and Neurofibromatosis Type 1-related Malignant Peripheral Nerve Sheath Tumors 1
Purpose : Malignant peripheral nerve sheath tumor (MPNST) can arise sporadically or in association with neurofibromatosis type 1… 
2003
2003
Molecular and Functional Analysis of PRKAR 1 A and its Locus ( 17 q 22 – 24 ) in Sporadic Adrenocortical Tumors : 17 q Losses , Somatic Mutations , and Protein Kinase A Expression and Activity 1
Germ-line protein kinase A (PKA) regulatory-subunit type-I (RI ; PRKAR1A)-inactivating mutations and loss-of-heterozygosity (LOH… 
2002
2002
Investigation of the GRB2, GRB7, and CSH1 genes as candidates for the Silver-Russell syndrome (SRS) on chromosome 17q
Silver-Russell syndrome (SRS) (MIM 180860) is characterised by intrauterine and postnatal growth restriction, in association with… 
1999
1999
Isochromosome 17 q in Blast Crisis of Chronic Myeloid Leukemia and in Other Hematologic Malignancies Is the Result of Clustered Breakpoints in 17 p 11 and Is Not Associated With Coding TP 53…
An isochromosome of the long arm of chromosome 17, i(17q), is the most frequent genetic abnormality observed during the disease… 
Highly Cited
1993
Highly Cited
1993
Loss of heterozygosity in familial breast carcinomas.
Three loci have been implicated in the etiology of familial breast cancer; the BRCA1 locus on 17q, the p53 gene on 17p, and the… 
1990
1990
Acute nonlymphocytic leukemia (ANLL) with isochromosome i(17q) as the sole chromosomal anomaly: a distinct entity?
Abstract: 3 patients with acute nonlymphocytic leukemia (ANLL) and an isochromosome (17q) as the sole chromosomal defect are… 
1988
1988
Chromosomal localization of the gene for a human thyroid hormone-binding protein.
A cDNA for the gene that encodes for a human cellular thyroid hormone-binding protein (p55) has recently been isolated and… 
Review
1986
Review
1986
Induction of increased salvage pathways of nucleotide synthesis by dosage effect due to chromosome imbalances may be fundamental in carcinogenesis: the example of colorectal carcinoma.
The cytogenetic study of colorectal carcinomas is consistent with the following sequence in the tumor evolution: rearrangement of…