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6q22
A chromosome band present on 6q
National Institutes of Health
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Related topics
Related topics
3 relations
Chromosomes
ROS1 gene
ROS1 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Idiopathic Infantile Arterial Calcification : A Case Report
J. Aldandan
,
Aminah Almoghannam
,
Ammar S Alkhars
,
Ghassan A. Shaath
2017
Corpus ID: 28367146
Idiopathic infantile arterial calcification (IIAC) is a rare inherited disorder in an autosomal recessive manner. IIAC has been…
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2015
2015
РОЛЬ ГЕНЕТИЧЕСКИХ ФАКТОРОВ В РАЗВИТИИ ИШЕМИЧЕСКОГО ИНСУЛЬТА
D. Nikulin
,
S. Nikulina
,
V. A. Shulman
,
Irina Mikhailovna Platonova
,
A. A. Chernova
,
S. S. Tretyakova
2015
Corpus ID: 74034244
Cerebral stroke is a multifactorial polygenic disease, predisposition to stroke is determined by the allelic variants of genes…
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2013
2013
Ассоциация полиморфизмов шестой хромосомы с развитием инфаркта миокарда
Мартынова Елена Андреевна
,
Шестерня Павел Анатольевич
,
Никулина Светлана Юрьевна
2013
Corpus ID: 74978037
The analysis of the relationship of nucleotide polymorphisms (SNPs) rs619203 (6q22) gene ROS1 and rs499818 (6p24.1) with…
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2009
2009
Identifying susceptibility genes of IgA nephropathy: research in progress.
M. Barua
,
Y. Pei
Nephrology, Dialysis and Transplantation
2009
Corpus ID: 16556074
Immunoglobulin A nephropathy (IgAN) is the most common primary glomerular disease worldwide and a significant cause of end-stage…
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2008
2008
Sub-microscopic chromosomal imbalances in idiopathic autism spectrum disorder (ASD)
M. Koochek
2008
Corpus ID: 96422642
Autism spectrum disorders (ASDs) are a group of neurodevelopmental conditions characterized by clinical variability, genetic…
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2007
2007
Del(6)(q22) and BCL6 Rearrangements in Primary Central Nervous System Lymphoma (PCNSL) Are Indicators of an Aggressive Clinical Course.
F. Cady
,
M. Law
,
+6 authors
A. Dogan
2007
Corpus ID: 221030198
Purpose: Despite therapeutic advancements, biological markers that predict the natural history of primary central nervous system…
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2005
2005
Genome-wide scan in novel IgA nephropathy model identifies susceptibility locus on murine chromosome 10, in a region syntenic to human IGAN1 on chromosome 6q22-23
鈴木 仁
2005
Corpus ID: 87845999
2001
2001
HIGH AFFINITY HUMAN IFN-7-BINDING CAPACITY I S ENCODED BY A SINGLE RECEPTOR GENE LOCATED IN PROXIMITY TO cros ON HUMAN CHROMOSOME REGION 6 q 16 TO 6 q 22 l
K. Pfizenmaier
,
K. Wiegmann
,
+6 authors
U. Uçer
2001
Corpus ID: 53000312
We have used human-rodent somatic cell hybrids to investigate the regional localization of the IFNyR gene on human chromosome 6…
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1996
1996
Subregional mapping of the human lymphocyte prolyloligopeptidase gane (6q22) to human chromosome
F. Goossens
,
J. Wauters
,
G. Vanhoof
,
P. Bossuyt
,
K. Loens
,
S. Scharpe
1996
Corpus ID: 90479872
Review
1983
Review
1983
Trisomy 6q22 leads to 6qter due to maternal 6;21 translocation. Case report review of the literature.
K. Taysi
,
W. Chao
,
N. Monaghan
,
M. P. Monaco
Annales de Genetique
1983
Corpus ID: 22316227
Partial trisomy for the long arm of chromosome 6, involving 6q22 leads to 6qter, was observed in a 2-month-old male infant. The…
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