List of works - Marina R. Carpinelli

A mutation in the translation initiation codon of Gata-1 disrupts megakaryocyte maturation and causes thrombocytopenia

scientific article

A new mouse model of Canavan leukodystrophy displays hearing impairment due to central nervous system dysmyelination

scientific article

An ethyl-nitrosourea-induced point mutation in phex causes exon skipping, x-linked hypophosphatemia, and rickets.

scientific article published on November 2002

Anomalous megakaryocytopoiesis in mice with mutations in the c-Myb gene

scientific article published on 21 January 2005

Anti-apoptotic gene Bcl2 is required for stapes development and hearing

scientific article

CHD7 deficiency in "Looper", a new mouse model of CHARGE syndrome, results in ossicle malformation, otosclerosis and hearing impairment

scientific article

Critical roles for c-Myb in lymphoid priming and early B-cell development

scientific article

Genetic Modifier Screens in Mice

scientific article published on March 2012

Grainyhead-like Transcription Factors in Craniofacial Development.

scientific article published on July 2017

Inactivation of Zeb1 in GRHL2-deficient mouse embryos rescues mid-gestation viability and secondary palate closure

scientific article published on 31 January 2020

Mice Haploinsufficient for Ets1 and Fli1 Display Middle Ear Abnormalities and Model Aspects of Jacobsen Syndrome

scientific article

Programmed anuclear cell death delimits platelet life span.

scientific article

Regulation of hematopoietic stem cells by their mature progeny

scientific article

Stage-dependent therapeutic efficacy in PI3K/mTOR-driven squamous cell carcinoma of the skin

scientific article published on 13 December 2017

Suppressor screen in Mpl-/- mice: c-Myb mutation causes supraphysiological production of platelets in the absence of thrombopoietin signaling

scientific article

Thrombocytopenia and kidney disease in mice with a mutation in the C1galt1 gene

scientific article

Two ENU-induced alleles of Atp2b2 cause deafness in mice

scientific article

Vitamin D-deficient diet rescues hearing loss in Klotho mice

scientific article published on 16 December 2010

c-Myb is required for progenitor cell homeostasis in colonic crypts.

scholarly article

List of works by Marina R. Carpinelli

A mutation in the translation initiation codon of Gata-1 disrupts megakaryocyte maturation and causes thrombocytopenia

A new mouse model of Canavan leukodystrophy displays hearing impairment due to central nervous system dysmyelination

An ethyl-nitrosourea-induced point mutation in phex causes exon skipping, x-linked hypophosphatemia, and rickets.

Anomalous megakaryocytopoiesis in mice with mutations in the c-Myb gene

Anti-apoptotic gene Bcl2 is required for stapes development and hearing

CHD7 deficiency in "Looper", a new mouse model of CHARGE syndrome, results in ossicle malformation, otosclerosis and hearing impairment

Critical roles for c-Myb in lymphoid priming and early B-cell development

Genetic Modifier Screens in Mice

Grainyhead-like Transcription Factors in Craniofacial Development.

Inactivation of Zeb1 in GRHL2-deficient mouse embryos rescues mid-gestation viability and secondary palate closure

Mice Haploinsufficient for Ets1 and Fli1 Display Middle Ear Abnormalities and Model Aspects of Jacobsen Syndrome

Programmed anuclear cell death delimits platelet life span.

Regulation of hematopoietic stem cells by their mature progeny

Stage-dependent therapeutic efficacy in PI3K/mTOR-driven squamous cell carcinoma of the skin

Suppressor screen in Mpl-/- mice: c-Myb mutation causes supraphysiological production of platelets in the absence of thrombopoietin signaling

Thrombocytopenia and kidney disease in mice with a mutation in the C1galt1 gene

Two ENU-induced alleles of Atp2b2 cause deafness in mice

Vitamin D-deficient diet rescues hearing loss in Klotho mice

c-Myb is required for progenitor cell homeostasis in colonic crypts.