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2p16
A chromosome band present on 2p
National Institutes of Health
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Related topics
Related topics
4 relations
Chromosome 2 Short Arm
Chromosomes
EFEMP1 wt Allele
MSH6 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2009
Review
2009
Control of fetal hemoglobin: new insights emerging from genomics and clinical implications.
S. Thein
,
S. Menzel
,
M. Lathrop
,
C. Garner
Human Molecular Genetics
2009
Corpus ID: 16440472
Increased levels of fetal hemoglobin (HbF, alpha(2)gamma(2)) are of no consequence in healthy adults, but confer major clinical…
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Highly Cited
2007
Highly Cited
2007
A constitutively active SPTBN1-FLT3 fusion in atypical chronic myeloid leukemia is sensitive to tyrosine kinase inhibitors and immunotherapy.
F. Grand
,
S. Iqbal
,
Lingyan Zhang
,
N. Russell
,
A. Chase
,
N. Cross
Experimental Hematology
2007
Corpus ID: 38549874
Highly Cited
2006
Highly Cited
2006
Gains of the proto-oncogene BCL11A and nuclear accumulation of BCL11AXL protein are frequent in primary mediastinal B-cell lymphoma
M. Weniger
,
K. Pulford
,
+8 authors
T. Barth
Leukemia
2006
Corpus ID: 20573940
Gains of the proto-oncogene BCL11A and nuclear accumulation of BCL11A XL protein are frequent in primary mediastinal B-cell…
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Highly Cited
2006
Highly Cited
2006
The BCL11AXL transcription factor: its distribution in normal and malignant tissues and use as a marker for plasmacytoid dendritic cells
K. Pulford
,
A. Banham
,
+13 authors
M. Dyer
Leukemia
2006
Corpus ID: 34507130
The BCL11A XL transcription factor: its distribution in normal and malignant tissues and use as a marker for plasmacytoid…
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2003
2003
A whole genome screen for association in Polish multiple sclerosis patients
B. Bielecki
,
M. Mycko
,
+6 authors
K. Selmaj
Journal of Neuroimmunology
2003
Corpus ID: 10722909
Highly Cited
2000
Highly Cited
2000
Isolated familial somatotropinomas: establishment of linkage to chromosome 11q13.1-11q13.3 and evidence for a potential second locus at chromosome 2p16-12.
M. Gadelha
,
M. Gadelha
,
+4 authors
L. Frohman
Journal of Clinical Endocrinology and Metabolism
2000
Corpus ID: 30897986
The majority of somatotropinomas are sporadic, although a small number occur with a familial aggregation, either as a component…
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1998
1998
Malattia leventinese: refinement of the genetic locus and phenotypic variability in autosomal dominant macular drusen.
A. Edwards
,
A. Edwards
,
+6 authors
T. Acott
American journal of ophthalmology-glaucoma
1998
Corpus ID: 22617572
Highly Cited
1996
Highly Cited
1996
Linkage of autosomal dominant radial drusen (malattia leventinese) to chromosome 2p16-21.
E. Héon
,
B. Piguet
,
+11 authors
E. Stone
A M A Archives of Ophthalmology
1996
Corpus ID: 23900938
OBJECTIVE To identify the chromosomal location of the gene involved in the pathogenesis of autosomal dominant radial drusen…
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Highly Cited
1996
Highly Cited
1996
The gene responsible for autosomal dominant Doyne's honeycomb retinal dystrophy (DHRD) maps to chromosome 2p16.
C. Gregory
,
K. Evans
,
+6 authors
S. Bhattacharya
Human Molecular Genetics
1996
Corpus ID: 24146812
Degeneration in the macula region of the retina is a feature of a heterogeneous group of inherited, progressive disorders…
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1996
1996
Calcineurin A alpha (PPP3CA), calcineurin A beta (PPP3CB) and calcineurin B (PPP3R1) are located on human chromosomes 4, 10q21-->q22 and 2p16-->p15 respectively.
Mary G. Wang
,
H. Yi
,
D. Guerini
,
C. Klee
,
O. McBride
Cytogenetics and Cell Genetics
1996
Corpus ID: 46784274
Calcineurin (also called protein phosphatase-2B) is a calmodulin-regulated protein phosphatase which plays an important role in…
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