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Interaction between workers during a short time window is required for bacterial symbiont transmission in Acromyrmex leaf-cutting ants

PloS one, 2014-07, Vol.9 (7), p.e103269-e103269

2014

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Mutations in the Cilia Gene ARL13B Lead to the Classical Form of Joubert Syndrome

American journal of human genetics, 2008-08, Vol.83 (2), p.170-179

2008

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AHI1 gene mutations cause specific forms of Joubert syndrome-related disorders

Annals of neurology, 2006-03, Vol.59 (3), p.527-534

2006

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Molar tooth sign of the midbrain-hindbrain junction: Occurrence in multiple distinct syndromes

American journal of medical genetics, 2004-03, Vol.125A (2), p.125-134

2004

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Distinguishing the four genetic causes of jouberts syndrome-related disorders

Annals of neurology, 2005-04, Vol.57 (4), p.513-519

2005

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Mutations in the AHI1 Gene, Encoding Jouberin, Cause Joubert Syndrome with Cortical Polymicrogyria

American journal of human genetics, 2004-12, Vol.75 (6), p.979-987

2004

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Association between Pseudonocardia symbionts and Atta leaf-cutting ants suggested by improved isolation methods

International microbiology, 2013-03, Vol.16 (1), p.17-25

2013

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Linkage Analysis in Families with Joubert Syndrome Plus Oculo-Renal Involvement Identifies the CORS2 Locus on Chromosome 11p12-q13.3

American journal of human genetics, 2003-09, Vol.73 (3), p.656-662

2003

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The genome sequence of the leaf-cutter ant Atta cephalotes reveals insights into its obligate symbiotic lifestyle

PLoS genetics, 2011-02, Vol.7 (2), p.e1002007-e1002007

2011

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Neuroepithelial cysts in a patient with Joubert syndrome plus renal cysts

Journal of child neurology, 2004-03, Vol.19 (3), p.227-231

2004

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The Genome Sequence of the Leaf-Cutter Ant Atta cephalotes Reveals Insights into Its Obligate Symbiotic Lifestyle: e1002007

PLoS genetics, 2011-02, Vol.7 (2)

2011

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Mutations in the Cilia Gene ARL13B Lead to the Classical Form of Joubort Syndrome

American journal of human genetics, 2008-08, Vol.83 (2), p.170

2008

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Morphometric analyses of hearing in two families of pinnipeds

The Journal of the Acoustical Society of America, 2001-11, Vol.110 (5_Supplement), p.2749-2749

2001

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AHI1 gene mutations cause specific forms of Joubert syndrome-related disorders

Annals of neurology, 2006-01, Vol.59 (3), p.527-534

2006

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Protein Complexes Are under Evolutionary Selection to Assemble via Ordered Pathways

Cell, 2013-04, Vol.153 (2), p.461-470

2013

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Donor selection for natural killer cell receptor genes leads to superior survival after unrelated transplantation for acute myelogenous leukemia

Blood, 2010-10, Vol.116 (14), p.2411-2419

2010

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Principles of assembly reveal a periodic table of protein complexes

Science (American Association for the Advancement of Science), 2015-12, Vol.350 (6266), p.1331-1331

2015

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Guidelines for the diagnosis and management of aplastic anaemia

British journal of haematology, 2009-10, Vol.147 (1), p.43-70

2009

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Donor killer cell Ig-like receptor B haplotypes, recipient HLA-C1, and HLA-C mismatch enhance the clinical benefit of unrelated transplantation for acute myelogenous leukemia

The Journal of immunology (1950), 2014-05, Vol.192 (10), p.4592-4600

2014

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A membrane topology model for human interferon inducible transmembrane protein 1

PloS one, 2014-08, Vol.9 (8), p.e104341-e104341

2014

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Donors with group B KIR haplotypes improve relapse-free survival after unrelated hematopoietic cell transplantation for acute myelogenous leukemia

Blood, 2009-01, Vol.113 (3), p.726-732

2009

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Longitudinal dynamics of clonal hematopoiesis identifies gene-specific fitness effects

Nature medicine, 2022-07, Vol.28 (7), p.1439-1446

2022

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Interaction between workers during a short time window is required for bacterial symbiont transmission in Acromyrmex leaf-cutting ants

CEP41 is mutated in Joubert syndrome and is required for tubulin glutamylation at the cilium

Mutations in the Cilia Gene ARL13B Lead to the Classical Form of Joubert Syndrome

AHI1 gene mutations cause specific forms of Joubert syndrome-related disorders

Molar tooth sign of the midbrain-hindbrain junction: Occurrence in multiple distinct syndromes

Distinguishing the four genetic causes of jouberts syndrome-related disorders

Mutations in the AHI1 Gene, Encoding Jouberin, Cause Joubert Syndrome with Cortical Polymicrogyria

CEP290 Mutations Are Frequently Identified in the Oculo-Renal Form of Joubert Syndrome–Related Disorders

Association between Pseudonocardia symbionts and Atta leaf-cutting ants suggested by improved isolation methods

Linkage Analysis in Families with Joubert Syndrome Plus Oculo-Renal Involvement Identifies the CORS2 Locus on Chromosome 11p12-q13.3

The genome sequence of the leaf-cutter ant Atta cephalotes reveals insights into its obligate symbiotic lifestyle

Neuroepithelial cysts in a patient with Joubert syndrome plus renal cysts

The Genome Sequence of the Leaf-Cutter Ant Atta cephalotes Reveals Insights into Its Obligate Symbiotic Lifestyle: e1002007

Mutations in the Cilia Gene ARL13B Lead to the Classical Form of Joubort Syndrome

Morphometric analyses of hearing in two families of pinnipeds

AHI1 gene mutations cause specific forms of Joubert syndrome-related disorders

Protein Complexes Are under Evolutionary Selection to Assemble via Ordered Pathways

Donor selection for natural killer cell receptor genes leads to superior survival after unrelated transplantation for acute myelogenous leukemia

Principles of assembly reveal a periodic table of protein complexes

Guidelines for the diagnosis and management of aplastic anaemia

Donor killer cell Ig-like receptor B haplotypes, recipient HLA-C1, and HLA-C mismatch enhance the clinical benefit of unrelated transplantation for acute myelogenous leukemia

A membrane topology model for human interferon inducible transmembrane protein 1

Exposure of iPSC-derived human microglia to brain substrates enables the generation and manipulation of diverse transcriptional states in vitro

Donors with group B KIR haplotypes improve relapse-free survival after unrelated hematopoietic cell transplantation for acute myelogenous leukemia

Longitudinal dynamics of clonal hematopoiesis identifies gene-specific fitness effects

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