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Influence of intermediate and uninterrupted FMR1 CGG expansions in premature ovarian failure manifestation

Human reproduction (Oxford), 2006-04, Vol.21 (4), p.952-957

2006

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Mutation analysis of two candidate genes for premature ovarian failure, DACH2 and POF1B

Human reproduction (Oxford), 2004-12, Vol.19 (12), p.2759-2766

2004

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La ricerca a fronte della sfida ambientale: materiali del III Seminario OSDOTTA, Lecco, 12-14 settembre 2007

Ginelli, Elisabetta

2008

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Mutation analysis of the inhibin alpha gene in a cohort of Italian women affected by ovarian failure

Human reproduction (Oxford), 2002-07, Vol.17 (7), p.1741-1745

2002

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Mutations in the coding region of the FOXL2 gene are not a major cause of idiopathic premature ovarian failure

Molecular human reproduction, 2004-08, Vol.10 (8), p.555-557

2004

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Evolution of beta satellite DNA sequences: evidence for duplication-mediated repeat amplification and spreading

Molecular biology and evolution, 2004-09, Vol.21 (9), p.1792-1799

2004

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The boundary of macaque rDNA is constituted by low-copy sequences conserved during evolution

Genomics (San Diego, Calif.), 2006-11, Vol.88 (5), p.564-571

2006

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Genomic organization and transcription of the human retinol dehydrogenase 10 (RDH10) gene

FEBS letters, 2003-11, Vol.554 (1-2), p.59-66

2003

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Use of the International Classification of Functioning, Disability and Health Generic-30 Set for the characterization of outpatients: Italian Society of Physical and Rehabilitative Medicine Residents Section Project

European journal of physical and rehabilitation medicine, 2019-04, Vol.55 (2), p.258

2019

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Human genome dispersal and evolution of 4q35 duplications and interspersed LSau repeats

Gene, 2002-08, Vol.296 (1-2), p.21-27

2002

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The structure of duplications on human acrocentric chromosome short arms derived by the analysis of 15p

Human genetics, 2001-06, Vol.108 (6), p.467-477

2001

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Association between idiopathic premature ovarian failure and fragile X premutation

Human reproduction (Oxford), 2000-01, Vol.15 (1), p.197-202

2000

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Molecular structure and evolution of DNA sequences located at the alpha satellite boundary of chromosome 20

Gene, 2000-10, Vol.256 (1), p.43-50

2000

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FRAXA premutations are not a cause of familial premature ovarian failure [Letters to the Editor]

Human reproduction (Oxford), 1999-02, Vol.14 (2), p.573-575

1999

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Molecular definition of Xq common-deleted region in patients affected by premature ovarian failure

Human genetics, 2000-10, Vol.107 (4), p.304-311

2000

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Use of polymerase chain reaction to diagnose bovine leukemia virus infection in calves at birth

American journal of veterinary research, 1993-03, Vol.54 (3), p.373-378

1993

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Repetitive nucleotide sequences in human genome

Pathologica, 1979-05, Vol.71 (1013), p.377

Ginelli, E

1979

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Iron overload and gene expression in HepG2 cells: analysis by differential display

FEBS letters, 2000-03, Vol.469 (2), p.208-212

2000

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Gene expression analysis in interstitial lung edema induced by saline infusion

Biochimica et biophysica acta, 2003-07, Vol.1638 (2), p.149-156

2003

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Identification of a human clustered G + C-rich DNA family of repeats ( Sau3A family)

Journal of molecular biology, 1985-12, Vol.186 (3), p.483-489

1985

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Linkage in human heterochromatin between highly divergent Sau3A repeats and a new family of repeated DNA sequences (HaeIII family)

Journal of molecular biology, 1989-02, Vol.205 (4), p.625-631

1989

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Variations in repetitive DNA and heterochromatin in the genus Artemia

Chromosoma, 1987-03, Vol.95 (1), p.71-75

1987

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Chromosomal location by in situ hybridization of the human Sau3A family of DNA repeats

Human genetics, 1987-04, Vol.75 (4), p.326-332

1987

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Satellite DNA induces unstable expression of the adjacent herpes simplex virus tk gene cotransfected in mouse cells

Molecular and Cellular Biology, 1988-03, Vol.8 (3), p.1336-1344

1988

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C-heterochromatin variation and transposition in tumor progression

Advances in experimental medicine and biology, 1988, Vol.233, p.309

1988

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Influence of intermediate and uninterrupted FMR1 CGG expansions in premature ovarian failure manifestation

Mutation analysis of two candidate genes for premature ovarian failure, DACH2 and POF1B

La ricerca a fronte della sfida ambientale: materiali del III Seminario OSDOTTA, Lecco, 12-14 settembre 2007

Mutation analysis of the inhibin alpha gene in a cohort of Italian women affected by ovarian failure

Mutations in the coding region of the FOXL2 gene are not a major cause of idiopathic premature ovarian failure

Evolution of beta satellite DNA sequences: evidence for duplication-mediated repeat amplification and spreading

The boundary of macaque rDNA is constituted by low-copy sequences conserved during evolution

Genomic organization and transcription of the human retinol dehydrogenase 10 (RDH10) gene

Use of the International Classification of Functioning, Disability and Health Generic-30 Set for the characterization of outpatients: Italian Society of Physical and Rehabilitative Medicine Residents Section Project

Human genome dispersal and evolution of 4q35 duplications and interspersed LSau repeats

The structure of duplications on human acrocentric chromosome short arms derived by the analysis of 15p

Association between idiopathic premature ovarian failure and fragile X premutation

Molecular structure and evolution of DNA sequences located at the alpha satellite boundary of chromosome 20

FRAXA premutations are not a cause of familial premature ovarian failure [Letters to the Editor]

Molecular definition of Xq common-deleted region in patients affected by premature ovarian failure

Use of polymerase chain reaction to diagnose bovine leukemia virus infection in calves at birth

Repetitive nucleotide sequences in human genome

Iron overload and gene expression in HepG2 cells: analysis by differential display

Gene expression analysis in interstitial lung edema induced by saline infusion

Identification of a human clustered G + C-rich DNA family of repeats ( Sau3A family)

Linkage in human heterochromatin between highly divergent Sau3A repeats and a new family of repeated DNA sequences (HaeIII family)

Variations in repetitive DNA and heterochromatin in the genus Artemia

Chromosomal location by in situ hybridization of the human Sau3A family of DNA repeats

Satellite DNA induces unstable expression of the adjacent herpes simplex virus tk gene cotransfected in mouse cells

C-heterochromatin variation and transposition in tumor progression

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