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1q24.2
A chromosome band present on 1q
National Institutes of Health
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4 relations
Chromosomes
MPZL1 wt Allele
SELP wt Allele
chromosome 1q
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
A functional variant near XCL1 gene improves breast cancer survival via promoting cancer immunity
Wen-Cheng Chou
,
Chia-Ni Hsiung
,
+6 authors
Chen-Yang Shen
International Journal of Cancer
2020
Corpus ID: 209893774
Most genome‐wide association studies (GWASs) identify genetic variants for breast cancer occurrence. In contrast, few are for…
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2015
2015
Abstract PD3-1: Evaluation and clinical impact of intra-tumor heterogeneity (ITH) in primary HER2-overexpressing breast cancers (HER2+BC) treated with adjuvant trastuzumab and chemotherapy (CT)
S. Loi
,
P. Savas
,
+12 authors
T. Speed
2015
Corpus ID: 70935290
Background: Despite the success of trastuzumab, when added to CT, for the treatment of women with primary HER2+ BC, diversity in…
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Review
2015
Review
2015
Chromosomal Imbalances in Patients with Congenital Cardiac Defects: A Meta-analysis Reveals Novel Potential Critical Regions Involved in Heart Development.
Thor Thorsson
,
W. W. Russell
,
+12 authors
M. Russell
Congenital Heart Disease
2015
Corpus ID: 872784
OBJECTIVE Congenital cardiac defects represent the most common group of birth defects, affecting an estimated six per 1000 births…
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2012
2012
A genome-wide association study of venous thromboembolism identifies risk variants in chromosomes 1 q 24 . 2 and 9 q
J. Heit
,
Sebastian M. Armasu
,
+4 authors
M. Andrade
2012
Corpus ID: 44459650
John A. Heit, M.D., Sebastian M. Armasu, M.S., Yan W. Asmann, Ph.D., Julie M. Cunningham, Ph.D., Martha E. Matsumoto, B.S., Tanya…
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2011
2011
[Linkage analysis of susceptibility loci in 2 target chromosomes in pedigrees with paranoid schizophrenia and undifferentiated schizophrenia].
Li-ping Zeng
,
Zhengmao Hu
,
+12 authors
K. Xia
Zhonghua yi xue yi chuan xue za zhi = Zhonghua…
2011
Corpus ID: 25677856
OBJECTIVE To investigate the relationship of susceptibility loci in chromosomes 1q21-25 and 6p21-25 and schizophrenia subtypes in…
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2009
2009
[Linkage analysis of a family with familial hypertriglyceridemia].
Xin-zhi Tang
,
Ying Lin
,
Bing Liu
,
Shi Ma
,
Yang Yang
,
Zheng-lin Yang
Zhonghua yi xue yi chuan xue za zhi = Zhonghua…
2009
Corpus ID: 6598675
OBJECTIVE To perform linkage analysis and mutation screening in a Chinese family with familial hpertriglyceridemia (FHTG…
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2007
2007
Untreated growth hormone deficiency with extremely short stature, bone dysplasia, cleft lip--palate and severe mental retardation in a 26-year-old man with a de novo unbalanced translocation t(1;12…
P. Callier
,
L. Faivre
,
+10 authors
F. Mugneret
European Journal of Medical Genetics
2007
Corpus ID: 20079854
2006
2006
Genomic Profiling Reveals Association of Chromosomal Aberrations on 1 q and 16 pwith Histologic and Genetic Subgroups of Invasive Breast Cancer
D. Stange
,
B. Radlwimmer
,
+8 authors
P. Lichter
2006
Corpus ID: 30890577
Purpose: Invasive ductal carcinoma and invasive lobular carcinoma (ILC) represent the major histologic subtypes of invasive…
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2005
2005
Suggestive linkage of familial primary cutaneous amyloidosis to a locus on chromosome 1q23
M. Lin
,
D. Lee
,
+6 authors
S. Tsai
British Journal of Dermatology
2005
Corpus ID: 43634045
Background There is a high incidence of primary cutaneous amyloidosis (PCA) in South America, South‐east Asia and Taiwan. To…
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