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Requirement for Pbx1 in skeletal patterning and programming chondrocyte proliferation and differentiation

Development (Cambridge), 2001-09, Vol.128 (18), p.3543-3557

2001

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Hox cofactors in vertebrate development

Developmental biology, 2006-03, Vol.291 (2), p.193-206

2006

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A PBX1 transcriptional network controls dopaminergic neuron development and is impaired in Parkinson's disease

The EMBO journal, 2016-09, Vol.35 (18), p.1963-1978

2016

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Face morphogenesis is promoted by Pbx-dependent EMT via regulation of Snail1 during frontonasal prominence fusion

Development (Cambridge), 2018-03, Vol.145 (5), p.dev157628-dev157628

2018

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Disentangling The Heterogeneity Of The Midfacial Epithelium To Elucidate The Pathogenesis Of Cleft Lip/Palate

FASEB JOURNAL, 2020, Vol.34 (S1), p.1-1

2020

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Ribosomal Protein SA Haploinsufficiency in Humans with Isolated Congenital Asplenia

Science (American Association for the Advancement of Science), 2013-05, Vol.340 (6135), p.976-978

2013

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A Pbx1-dependent genetic and transcriptional network regulates spleen ontogeny

Development (Cambridge), 2005-07, Vol.132 (13), p.3113-3126

2005

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Pbx1 is essential for adrenal development and urogenital differentiation

Genesis (New York, N.Y. : 2000), 2003-11, Vol.37 (3), p.123-130

2003

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Abnormalities of caudal pharyngeal pouch development in Pbx1 knockout mice mimic loss of Hox3 paralogs

Developmental biology, 2004-12, Vol.276 (2), p.301-312

2004

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Type 2 autoimmune hepatitis and hepatitis C virus infection

The Lancet (British edition), 1990-02, Vol.335 (8684), p.258-259

1990

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Ectopic Meis1 expression in the mouse limb bud alters P-D patterning in a Pbx1-independent manner

The International journal of developmental biology, 2009, Vol.53 (8-10), p.1483-1494

2009

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The Hox cofactor and proto-oncogene Pbx1 is required for maintenance of definitive hematopoiesis in the fetal liver

Blood, 2001-08, Vol.98 (3), p.618-626

2001

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Pbx1 inactivation disrupts pancreas development and in Ipf1 -deficient mice promotes diabetes mellitus

Nature genetics, 2002-04, Vol.30 (4), p.430-435

2002

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Pbx3 Deficiency Results in Central Hypoventilation

The American journal of pathology, 2004-10, Vol.165 (4), p.1343-1350

2004

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The TALE Homeodomain Protein Pbx2 Is Not Essential for Development and Long-Term Survival

Molecular and Cellular Biology, 2004-06, Vol.24 (12), p.5324-5331

2004

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Abstract 106: Time Course and Gene Expression Analysis of Infant Mouse Model of Re-Synostosis

Plastic and reconstructive surgery (1963), 2012-07, Vol.130, p.77

2012

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Molecular Localization of the t(11;22)(q24;q12) Translocation of Ewing Sarcoma by Chromosomal in situ Suppression Hybridization

Proceedings of the National Academy of Sciences - PNAS, 1991-02, Vol.88 (3), p.887-891

1991

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Structure and linkage of the D2 dopamine receptor and neural cell adhesion molecule genes on human chromosome 11q23

Genomics (San Diego, Calif.), 1992-12, Vol.14 (4), p.1010-1018

1992

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A trithorax-like gene is interrupted by chromosome 11q23 translocations in acute leukaemias

Nature genetics, 1992-10, Vol.2 (2), p.113-118

1992

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Serum autoantibodies and the diagnosis of type-1 autoimmune hepatitis in Italy: a reappraisal at the light of hepatitis C virus infection

Gut, 1992-09, Vol.33 (9), p.1260-1263

1992

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Translocation (11;15)(q23,q14) in three patients with acute non-lymphoblastic leukemia (ANLL) : clinical, cytogenetic and molecular studies

Leukemia, 1995-07, Vol.9 (7), p.1162-1166

1995

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De novo 46,XX, dir dup (11)(q13.3→q14.2) in a patient with mental retardation, congenital cardiopathy and thrombopenia

Clinical genetics, 1996-04, Vol.49 (4), p.206-210

1996

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Isolation and expression of linked zinc finger gene clusters on human chromosome 11q

Genomics (San Diego, Calif.), 1992-12, Vol.14 (4), p.970-978

1992

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A novel zinc finger gene on human chromosome 1qter that is alternatively spliced in human tissues and cell lines

American journal of human genetics, 1993-01, Vol.52 (1), p.192-203

1993

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Yeast Artificial Chromosome Cloning of 3.2 Megabases within Chromosomal Band 11q24 Closely Linking c-ets 1 and Fli-1 and Encompassing the Ewing Sarcoma Breakpoint

Genomics (San Diego, Calif.), 1994-07, Vol.22 (1), p.137-147

1994

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Requirement for Pbx1 in skeletal patterning and programming chondrocyte proliferation and differentiation

Hox cofactors in vertebrate development

A PBX1 transcriptional network controls dopaminergic neuron development and is impaired in Parkinson's disease

Face morphogenesis is promoted by Pbx-dependent EMT via regulation of Snail1 during frontonasal prominence fusion

Disentangling The Heterogeneity Of The Midfacial Epithelium To Elucidate The Pathogenesis Of Cleft Lip/Palate

Ribosomal Protein SA Haploinsufficiency in Humans with Isolated Congenital Asplenia

A Pbx1-dependent genetic and transcriptional network regulates spleen ontogeny

Pbx1 is essential for adrenal development and urogenital differentiation

Abnormalities of caudal pharyngeal pouch development in Pbx1 knockout mice mimic loss of Hox3 paralogs

Type 2 autoimmune hepatitis and hepatitis C virus infection

Ectopic Meis1 expression in the mouse limb bud alters P-D patterning in a Pbx1-independent manner

The Hox cofactor and proto-oncogene Pbx1 is required for maintenance of definitive hematopoiesis in the fetal liver

Pbx1 inactivation disrupts pancreas development and in Ipf1 -deficient mice promotes diabetes mellitus

Pbx3 Deficiency Results in Central Hypoventilation

The TALE Homeodomain Protein Pbx2 Is Not Essential for Development and Long-Term Survival

Abstract 106: Time Course and Gene Expression Analysis of Infant Mouse Model of Re-Synostosis

Molecular Localization of the t(11;22)(q24;q12) Translocation of Ewing Sarcoma by Chromosomal in situ Suppression Hybridization

Structure and linkage of the D2 dopamine receptor and neural cell adhesion molecule genes on human chromosome 11q23

A trithorax-like gene is interrupted by chromosome 11q23 translocations in acute leukaemias

Serum autoantibodies and the diagnosis of type-1 autoimmune hepatitis in Italy: a reappraisal at the light of hepatitis C virus infection

Translocation (11;15)(q23,q14) in three patients with acute non-lymphoblastic leukemia (ANLL) : clinical, cytogenetic and molecular studies

De novo 46,XX, dir dup (11)(q13.3→q14.2) in a patient with mental retardation, congenital cardiopathy and thrombopenia

Isolation and expression of linked zinc finger gene clusters on human chromosome 11q

A novel zinc finger gene on human chromosome 1qter that is alternatively spliced in human tissues and cell lines

Yeast Artificial Chromosome Cloning of 3.2 Megabases within Chromosomal Band 11q24 Closely Linking c-ets 1 and Fli-1 and Encompassing the Ewing Sarcoma Breakpoint

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