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1p32
A chromosome band present on 1p
National Institutes of Health
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Related topics
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9 relations
CDKN2C wt Allele
Chromosome 1 Short Arm
Chromosomes
EPS15 wt Allele
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2020
Review
2020
TAL1 (1p32) deletion in lymphoid malignancies
L. Mitev
,
Liliya Grahlyova
2020
Corpus ID: 214319396
Review on TAL1 deletion in lymphoid malignancies with data on clinics.
2017
2017
Role of CDKN2C Fluorescence In Situ Hybridization in the Management of Medullary Thyroid Carcinoma
M. El Naofal
,
A. Kim
,
+8 authors
Peter C. Hu
Annals of Clinical and Laboratory Science
2017
Corpus ID: 25097699
&NA; Medullary thyroid carcinoma (MTC), an aggressive form of thyroid cancer, occurs sporadically in approximately 75% of MTCs…
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2014
2014
Spinoza’s Doctrine of the Imitation of Affects and Teaching as the Art of Offering the Right Amount of Resistance
J. Dahlbeck
2014
Corpus ID: 142705567
ECER, European Conference on Educational Research "The Past, Present and Future of Educational Research in Europe", University of…
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2014
2014
Deletion of the 1p32 region is a major independent prognostic factor in young patients with myeloma: the IFM experience on 1195 patients
B. Hébraud
,
X. Leleu
,
+27 authors
H. Avet-Loiseau
Leukemia
2014
Corpus ID: 20519668
2009
2009
A Susceptibility Locus on 1 p 32 – 1 p 34 for Congenital Macrostomia in a Chinese Family and Identification of a Novel PTCH 2 Mutation
Zhipeng Fan
,
Juan Du
,
+6 authors
Songlin Wang
2009
Corpus ID: 42923045
A Susceptibility Locus on 1p32–1p34 for Congenital Macrostomia in a Chinese Family and Identification of a Novel PTCH2 Mutation…
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2008
2008
Genomic profiling of malignant pleural mesothelioma with array-based comparative genomic hybridization shows frequent non-random chromosomal alteration regions including JUN amplification on 1p32
谷口 哲郎
2008
Corpus ID: 83131668
2006
2006
Loss of heterozygosity and microsatellite instability at RAD52 and RAD54 loci in breast cancer.
Maria Nowacka-Zawisza
,
M. Bryś
,
Romanowicz Hanna
,
M. Zadrozny
,
A. Kulig
,
W. Krajewska
Polish journal of pathology : official journal of…
2006
Corpus ID: 43637744
This study was carried out to evaluate the loss of heterozygosity (LOH) and microsatellite instability (MSI) in breast cancer, in…
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2006
2006
Consistent Association of Ip Loss of Heterozygosity with Pheochromocytomas from Patients with Multiple Endocrine Neoplasia Type 2 Syndromes1
J. Moley
,
M. Brother
,
+5 authors
G. Brodeur
2006
Corpus ID: 15345142
Pheochromocytomas and medullary thyroid cancers (MTCs) are neuroendocrine tumors which arise sporadically or as part of the…
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1996
1996
Physical linkage and orientation of the human complement C8α and C8β genes on chromosome 1p32
P. Platteborze
,
M. Hobart
,
J. Sodetz
Human Genetics
1996
Corpus ID: 29891550
Abstract Human C8 is one of five components (C5b, C6, C7, C8, C9) of the cytolytic C5b-9 complex of complement. It consists of…
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1977
1977
Regional assignment of seven genes on chromosome 1 of man by use of man-Chinese hamster somatic cell hybrids. I. Results obtained after hybridization of human cells carrying reciprocal translocations…
A. Jongsma
,
W. Burgerhout
Cytogenetics and Cell Genetics
1977
Corpus ID: 46795240
Regional localization studies of genes coding for human PGD, PPH1, PGM1, UGPP, GuK1, Pep-C, and FH, which have been assigned to…
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