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Chromosomes, Human, Pair 22
Known as:
22s chromosome
, 22 chromosome
, chromosome pair 22
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The designation for each member of the smallest human autosomal chromosome pair. Chromosome 22 spans about 49 million base pairs and represents…
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National Institutes of Health
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Related topics
Related topics
21 relations
22q
Chromatin
Chromosome 22 Short Arm
Loss of Chromosome 22q
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Narrower (7)
22q13.3 Deletion Syndrome
Cat eye syndrome
Chromosome 22, microdeletion 22 q11
Chromosome 22, monosome mosaic
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Broader (1)
Chromosomes, Human, 21-22 and Y
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2010
Highly Cited
2010
Association of Trypanolytic ApoL1 Variants with Kidney Disease in African Americans
G. Genovese
,
D. Friedman
,
+15 authors
M. Pollak
Science
2010
Corpus ID: 13784497
Out of Africa Kidney disease is more common in African Americans than in Americans of European descent, and genetics is likely to…
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Highly Cited
2002
Highly Cited
2002
An anthropoid-specific locus of orphan C to U RNA-editing enzymes on chromosome 22.
A. Jarmuz
,
A. Chester
,
+4 authors
N. Navaratnam
Genomics
2002
Corpus ID: 28479633
The cytidine (C) to uridine (U) editing of apolipoprotein (apo) B mRNA is mediated by tissue-specific, RNA-binding cytidine…
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Review
2000
Review
2000
The molecular biology of chronic myeloid leukemia.
M. Deininger
,
J. Goldman
,
J. Melo
Blood
2000
Corpus ID: 1044492
Chronic myeloid leukemia (CML) is probably the most extensively studied human malignancy. The discovery of the Philadelphia (Ph…
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Highly Cited
1999
Highly Cited
1999
The DNA sequence of human chromosome 22
I. Dunham
,
N. Shimizu
,
+214 authors
K. P. O'Brien
Nature
1999
Corpus ID: 4369891
Knowledge of the complete genomic DNA sequence of an organism allows a systematic approach to defining its genetic components…
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Highly Cited
1993
Highly Cited
1993
Alteration in a new gene encoding a putative membrane-organizing protein causes neuro-fibromatosis type 2
G. Rouleau
,
P. Mérel
,
+18 authors
G. Thomas
Nature
1993
Corpus ID: 24532924
Neurofibromatosis type 2 (NF2) is a monogenic dominantly inherited disease predisposing carriers to develop nervous system…
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Highly Cited
1992
Highly Cited
1992
Gene fusion with an ETS DNA-binding domain caused by chromosome translocation in human tumours
O. Delattre
,
J. Zucman
,
+9 authors
G. Thomas
Nature
1992
Corpus ID: 4331584
EWING'S sarcoma and related subtypes of primitive neuroectodermal tumours share a recurrent and specific t(ll;22) (q24;q12…
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Highly Cited
1985
Highly Cited
1985
Fused transcript of abl and bcr genes in chronic myelogenous leukaemia
E. Shtivelman
,
Batia Lifshitz
,
R. Gale
,
E. Canaani
Nature
1985
Corpus ID: 4317691
Human chronic myelogenous leukaemia is characterized by a reciprocal translocation between chromosomes 9 and 22 resulting in an…
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Highly Cited
1985
Highly Cited
1985
Structural organization of the bcr gene and its role in the Ph′ translocation
N. Heisterkamp
,
K. Stam
,
J. Groffen
,
A. Klein
,
G. Grosveld
Nature
1985
Corpus ID: 4343076
The Philadelphia (Ph′) chromosome, an abnormal chromosome 22 (ref. 1), is one of the best-known examples of a specific human…
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Highly Cited
1984
Highly Cited
1984
Philadelphia chromosomal breakpoints are clustered within a limited region, bcr, on chromosome 22
J. Groffen
,
J. Stephenson
,
N. Heisterkamp
,
A. Klein
,
C. Bartram
,
G. Grosveld
Cell
1984
Corpus ID: 9876892
Highly Cited
1973
Highly Cited
1973
A New Consistent Chromosomal Abnormality in Chronic Myelogenous Leukaemia identified by Quinacrine Fluorescence and Giemsa Staining
J. Rowley
Nature
1973
Corpus ID: 26726071
CELLS from nine consecutive patients with chronic myelogenous leukaemia (CML) have been analysed with quinacrine fluorescence and…
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