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2p11
A chromosome band present on 2p
National Institutes of Health
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Related topics
Related topics
3 relations
Chromosome 2 Short Arm
Chromosomes
FABP1 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2013
2013
Amplification but not translocation of anaplastic lymphoma kinase is a frequent event in oesophageal cancer.
S. Schoppmann
,
B. Streubel
,
P. Birner
European Journal of Cancer
2013
Corpus ID: 8438332
Highly Cited
2011
Highly Cited
2011
A genome-wide association study of attempted suicide
V. Willour
,
F. Seifuddin
,
+25 authors
J. Potash
Molecular Psychiatry
2011
Corpus ID: 17304945
The heritable component to attempted and completed suicide is partly related to psychiatric disorders and also partly independent…
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Review
2008
Review
2008
Translocation (18;22)(q21;q11) in B-cell lymphomas: a report of 4 cases and review of the literature.
P. Lin
,
Rechna Jetly
,
Patrick A. Lennon
,
L. Abruzzo
,
Sapana Prajapati
,
L. Medeiros
Human Pathology
2008
Corpus ID: 41560483
Highly Cited
2005
Highly Cited
2005
Genome-wide array-based CGH for mantle cell lymphoma: identification of homozygous deletions of the proapoptotic gene BIM
H. Tagawa
,
S. Karnan
,
+6 authors
M. Seto
Oncogene
2005
Corpus ID: 18355603
Mantle cell lymphoma (MCL) is characterized by 11q13 chromosomal translocation and CCND1 overexpression, but additional genomic…
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2004
2004
Fine mapping of the 2p11 dyslexia locus and exclusion of TACR1 as a candidate gene
M. Peyrard-Janvid
,
H. Anthoni
,
+8 authors
J. Kere
Human Genetics
2004
Corpus ID: 26215216
Developmental dyslexia, or reading disability, is a multigenic complex disease for which at least five loci, i.e. DYX1–3 and DYX5…
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Highly Cited
2002
Highly Cited
2002
Genomewide search for type 2 diabetes mellitus susceptibility loci in Finnish families: the Botnia study.
Cecilia M. Lindgren
,
M. Mahtani
,
+14 authors
Eric S. Lander
American Journal of Human Genetics
2002
Corpus ID: 13932895
Type 2 diabetes mellitus is a heterogeneous inherited disorder characterized by chronic hyperglycemia resulting from pancreatic…
Expand
Review
1998
Review
1998
Masquerading repeats: paralogous pitfalls of the human genome.
E. Eichler
Genome Research
1998
Corpus ID: 38998632
In its most simple terms, the human genome consists of two distinct fractions of DNA: repetitive and unique sequence…
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Highly Cited
1993
Highly Cited
1993
Cytogenetic studies in splenic lymphoma with villous lymphocytes
D. Oscier
,
E. Matutes
,
+5 authors
D. Catovsky
British Journal of Haematology
1993
Corpus ID: 25715572
Summary. We report the cytogenetic findings on 31 cases of splenic lymphoma with villous lymphocytes (SLVL). TPA stimulated cells…
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Highly Cited
1988
Highly Cited
1988
The kappa-deleting element. Germline and rearranged, duplicated and dispersed forms
Winfried B. Graninger
,
P. Goldman
,
Cynthia C. Morton
,
Stephen J. O'Brien
,
Stanley J. Korsmeyer
Journal of Experimental Medicine
1988
Corpus ID: 1801091
Human light chain genes are used in a kappa before lambda order. Accompanying this hierarchy is the rearrangement of a kappa…
Expand
Highly Cited
1984
Highly Cited
1984
Chromosome study of Ewing's sarcoma (ES) cell lines. Consistency of a reciprocal translocation t(11;22)(q24;q12).
C. Turc‐Carel
,
Irène Philip
,
M. Berger
,
Thierry Philip
,
Gilbert M. Lenoir
Cancer Genetics and Cytogenetics
1984
Corpus ID: 3397872
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