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19p13.1
A chromosome band present on 19p
National Institutes of Health
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9 relations
BRD4 wt Allele
Chromosome 19 Short Arm
Chromosomes
ELL wt Allele
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2011
2011
Acquisition of mixed lineage leukemia rearrangement in a chronic myeloid leukemia patient while on imatinib
A. Zámečníkova
Hematology Reports
2011
Corpus ID: 13126578
Chronic myeloid leukemia (CML) is a clonal myeloproliferative disorder with a specific genetic abnormality, the Philadelphia…
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Highly Cited
2004
Highly Cited
2004
Detection of the founder effect in Finnish CADASIL families
K. Mykkänen
,
M. Savontaus
,
+8 authors
M. Pöyhönen
European Journal of Human Genetics
2004
Corpus ID: 33185033
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is an inherited…
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2003
2003
Antisense-mediated loss of calcium homoeostasis endoplasmic reticulum protein (CHERP; ERPROT213-21) impairs Ca2+ mobilization, nuclear factor of activated T-cells (NFAT) activation and cell…
F. O'Rourke
,
J. M. Laplante
,
M. B. Feinstein
Biochemical Journal
2003
Corpus ID: 7270022
We recently discovered a novel gene on chromosome 19p13.1 and its product, an integral endoplasmic reticulum (ER) membrane…
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2003
2003
Association scan of the novel psoriasis susceptibility region on chromosome 19: evidence for both susceptible and protective loci
P. Hensen
,
C. Windemuth
,
+9 authors
André Reis
Experimental Dermatology
2003
Corpus ID: 24152857
Abstract: To follow up the novel psoriasis susceptibility region on chromosome 19 (PSORS6), we performed an association scan for…
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Highly Cited
2002
Highly Cited
2002
Autosomal dominant epilepsy with febrile seizures plus with missense mutations of the (Na+)-channel α1 subunit gene, SCN1A
M. Ito
,
H. Nagafuji
,
+8 authors
S. Kaneko
Epilepsy Research
2002
Corpus ID: 25555020
2001
2001
Characterization of t(11;19)(q23;p13.3) by fluorescence in situ hybridization analysis in a pediatric patient with therapy-related acute myelogenous leukemia.
L. Cheng
,
K. Ramesh
,
E. Radel
,
H. Ratech
,
D. Wei
,
L. Cannizzaro
Cancer Genetics and Cytogenetics
2001
Corpus ID: 44451844
Highly Cited
1999
Highly Cited
1999
The leukemogenic fusion of MLL with ENL creates a novel transcriptional transactivator
S. Schreiner
,
M. García-Cuéllar
,
G. Fey
,
R. Slany
Leukemia
1999
Corpus ID: 25719989
Translocations affecting the chromosomal locus 11q23 are hallmarks of infant leukemias. These events disrupt the MLL gene (also…
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1997
1997
Physical mapping of human myosin-IXB (MYO9B), the human orthologue of the rat myosin myr 5, to chromosome 19p13.1.
M. Bähler
,
I. Kehrer
,
L. Gordon
,
H. E. Stoffler
,
A. Olsen
Genomics
1997
Corpus ID: 21927996
The gene for human myosin-IXB (MYO9B) was mapped to human chromosome 19p13.1 using fluorescence in situ hybridization. The rat…
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1995
1995
Chromosomal localization of the human prostanoid receptor gene family.
Alessandra M.V. Duncan
,
Linda Anderson
,
Colin D. Funk
,
Mark Abramovitz
,
Mohammed Adam
Genomics
1995
Corpus ID: 39619893
1986
1986
Toward early diagnosis of myotonic dystrophy: construction and characterization of a somatic cell hybrid with a single human der(19) chromosome.
T. Hulsebos
,
B. Wieringa
,
+5 authors
H. Ropers
Cytogenetics and Cell Genetics
1986
Corpus ID: 46879299
We have constructed a somatic cell hybrid line, designated 908K1, with a single human der(19) chromosome on a Chinese hamster…
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