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Chromosomes, Human, Pair 11

Known as: Chromosome 11 
The designation for each member of the eleventh largest human autosomal chromosome pair. Chromosome 11 spans about 134.5 million base pairs and… 
National Institutes of Health

Related topics

Related topics

50 relations
Adult Kidney Wilms TumorAleukemic Chronic Lymphocytic LeukemiaAnaplastic Kidney Wilms TumorBeckwith-Wiedemann Syndrome

Narrower (2)

Chromosome 11p deletion syndromechromosome 11q duplication syndrome

Broader (2)

Chromosomes, HumanChromosomes, Human, 6-12 and X

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2004
Highly Cited
2004
Late Breaking Science Abstracts
The Late Breaking Science abstracts were originally presented at the 57th American Academy of Neurology Annual Meeting in San… 
Highly Cited
1999
Highly Cited
1999
Mucosal T lymphocyte numbers are selectively reduced in integrin alpha E (CD103)-deficient mice.
The mucosal lymphocyte integrin alpha E(CD103)beta 7 is thought to be important for intraepithelial lymphocyte (IEL) localization… 
Highly Cited
1999
Highly Cited
1999
Alymphoplasia is caused by a point mutation in the mouse gene encoding Nf-κb-inducing kinase
The alymphoplasia (aly) mutation of mouse is autosomal recessive and characterized by the systemic absence of lymph nodes (LN… 
Highly Cited
1996
Highly Cited
1996
Fusion of the nucleoporin gene NUP98 to HOXA9 by the chromosome translocation t(7;11)(p15;p15) in human myeloid leukaemia
Expression of HoxaT and Hoxa9 is activated by proviral integration in BXH2 murine myeloid leukaemias. This result, combined with… 
Highly Cited
1996
Highly Cited
1996
The t(7;11)(p15;p15) translocation in acute myeloid leukaemia fuses the genes for nucleoporin NUP96 and class I homeoprotein HOXA9
The t(7;11)(p15;p15) translocation is a recurrent chromosomal abnormality associated primarily with acute myeloid leukaemia (FAB… 
Highly Cited
1994
Highly Cited
1994
New member of the winged-helix protein family disrupted in mouse and rat nude mutations
Highly Cited
1992
Highly Cited
1992
The gene for the peripheral myelin protein PMP–22 is a candidate for Charcot–Marie–Tooth disease type 1A
Charcot–Marie-–ooth disease type 1A (CMT1A) is an autosomal dominant peripheral neuropathy associated with a large DNA… 
Highly Cited
1992
Highly Cited
1992
Trembler mouse carries a point mutation in a myelin gene
THE autosomal dominant trembler mutation1 (Tr), maps to mouse chromosome 11 (ref. 2) and manifests as a Schwann-cell… 
Highly Cited
1989
Highly Cited
1989
LINKAGE BETWEEN IMMUNOGLOBULIN E RESPONSES UNDERLYING ASTHMA AND RHINITIS AND CHROMOSOME 11q
Highly Cited
1989
Highly Cited
1989
The human dopamine D2 receptor gene is located on chromosome 11 at q22-q23 and identifies a TaqI RFLP.
Human dopaminergic neurons are involved in the control of hormone secretion, voluntary movement, and emotional behavior… 
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