Search Results - "Camprubi, Cristina" :: K.UTB vyhledávací portál | TBU Library Retrieval Portal

Spermatozoa from infertile patients exhibit differences of DNA methylation associated with spermatogenesis-related processes: an array-based analysis

Spermatozoa from infertile patients exhibit differences of DNA methylation associated with spermatogenesis-related processes: an array-based analysis

by Camprubí, Cristina, Salas-Huetos, Albert, Aiese-Cigliano, Riccardo, Godo, Anna, Pons, Maria-Carme, Castellano, Giancarlo, Grossmann, Mark, Sanseverino, Walter, Martin-Subero, José I, Garrido, Nicolás, Blanco, Joan
Published in Reproductive biomedicine online (01.12.2016)

Get full text

Journal Article

Stability of Genomic Imprinting and Gestational-Age Dynamic Methylation in Complicated Pregnancies Conceived Following Assisted Reproductive Technologies

Stability of Genomic Imprinting and Gestational-Age Dynamic Methylation in Complicated Pregnancies Conceived Following Assisted Reproductive Technologies

by CAMPRUBI, Cristina, IGLESIAS-PLATAS, Isabel, MARTIN-TRUJILLO, Alex, SALVADOR-ALARCON, Cristina, RODRIGUEZ, Maria Angeles, BARREDO, Dalia Rodriguez, COURT, Franck, MONK, David
Published in Biology of reproduction (01.09.2013)

Get full text

Journal Article

What the human sperm methylome tells us

What the human sperm methylome tells us

by Camprubí, Cristina, Cigliano, Riccardo Aiese, Salas-Huetos, Albert, Garrido, Nicolas, Blanco, Joan
Published in Epigenomics (01.10.2017)

Get full text

Journal Article

Semen samples showing an increased rate of spermatozoa with imprinting errors have a negligible effect in the outcome of assisted reproduction techniques

Semen samples showing an increased rate of spermatozoa with imprinting errors have a negligible effect in the outcome of assisted reproduction techniques

by Camprubí, Cristina, Pladevall, Marta, Grossmann, Mark, Garrido, Nicolás, Pons, Maria, Blanco, Joan
Published in Epigenetics (01.10.2012)

Get full text

Journal Article

Methylation screening of reciprocal genome-wide UPDs identifies novel human-specific imprinted genes

Methylation screening of reciprocal genome-wide UPDs identifies novel human-specific imprinted genes

by Nakabayashi, Kazuhiko, Trujillo, Alex Martin, Tayama, Chiharu, Camprubi, Cristina, Yoshida, Wataru, Lapunzina, Pablo, Sanchez, Aurora, Soejima, Hidenobu, Aburatani, Hiroyuki, Nagae, Genta, Ogata, Tsutomu, Hata, Kenichiro, Monk, David
Published in Human molecular genetics (15.08.2011)

Get full text

Journal Article

Screening individuals with intellectual disability, autism and Tourette's syndrome for KCNK9 mutations and aberrant DNA methylation within the 8q24 imprinted cluster

Screening individuals with intellectual disability, autism and Tourette's syndrome for KCNK9 mutations and aberrant DNA methylation within the 8q24 imprinted cluster

by Delgado, Marta Sánchez, Camprubí, Cristina, Tümer, Zeynep, Martínez, Francisco, Milà, Montserrat, Monk, David
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01.09.2014)

Get full text

Journal Article

Lack of association of MTHFR rs1801133 polymorphism and CTCFL mutations with sperm methylation errors in infertile patients

Lack of association of MTHFR rs1801133 polymorphism and CTCFL mutations with sperm methylation errors in infertile patients

by Camprubí, Cristina, Pladevall, Marta, Grossmann, Mark, Garrido, Nicolás, Pons, Maria C., Blanco, Joan
Published in Journal of assisted reproduction and genetics (01.09.2013)

Get full text

Journal Article

Imprinting at the PLAGL1 domain is contained within a 70-kb CTCF/cohesin-mediated non-allelic chromatin loop

Imprinting at the PLAGL1 domain is contained within a 70-kb CTCF/cohesin-mediated non-allelic chromatin loop

by Iglesias-Platas, Isabel, Court, Franck, Camprubi, Cristina, Sparago, Angela, Guillaumet-Adkins, Amy, Martin-Trujillo, Alex, Riccio, Andrea, Moore, Gudrun E, Monk, David
Published in Nucleic acids research (01.02.2013)

Get full text

Journal Article

Does genomic imprinting play a role in autoimmunity?

Does genomic imprinting play a role in autoimmunity?

by Camprubí, Cristina, Monk, David
Published in Advances in experimental medicine and biology (2011)

Get more information

Journal Article

Prader-Willi and Angelman syndromes: genetic counseling

Prader-Willi and Angelman syndromes: genetic counseling

by Camprubí, Cristina, Coll, Maria Dolors, Gabau, Elisabeth, Guitart, Míriam
Published in European journal of human genetics : EJHG (01.02.2010)

Get full text

Journal Article

Epigenetic Transgenerational Inheritance

Epigenetic Transgenerational Inheritance

by Blanco Rodríguez, Joan, Camprubí Sánchez, Cristina
Published in Advances in experimental medicine and biology (01.01.2019)

Get more information

Journal Article

The PEG13-DMR and brain-specific enhancers dictate imprinted expression within the 8q24 intellectual disability risk locus

The PEG13-DMR and brain-specific enhancers dictate imprinted expression within the 8q24 intellectual disability risk locus

by Court, Franck, Camprubi, Cristina, Garcia, Cristina Vicente, Guillaumet-Adkins, Amy, Sparago, Angela, Seruggia, Davide, Sandoval, Juan, Esteller, Manel, Martin-Trujillo, Alex, Riccio, Andrea, Montoliu, Lluis, Monk, David
Published in Epigenetics & chromatin (25.03.2014)

Get full text

Journal Article

Novel UBE3A mutations causing Angelman syndrome: Different parental origin for single nucleotide changes and multiple nucleotide deletions or insertions

Novel UBE3A mutations causing Angelman syndrome: Different parental origin for single nucleotide changes and multiple nucleotide deletions or insertions

by Camprubí, Cristina, Guitart, Miriam, Gabau, Elisabeth, Coll, Maria Dolors, Villatoro, Sergi, Oltra, Silvestre, Roselló, Monica, Ferrer, Irene, Monfort, Sandra, Orellana, Carmen, Martínez, Francisco
Published in American journal of medical genetics. Part A (01.03.2009)

Get full text

Journal Article

Imprinting center analysis in Prader–Willi and Angelman syndrome patients with typical and atypical phenotypes

Imprinting center analysis in Prader–Willi and Angelman syndrome patients with typical and atypical phenotypes

by Camprubí, Cristina, Coll, Maria Dolors, Villatoro, Sergi, Gabau, Elisabeth, Kamli, Amine, Martínez, Maria Jesus, Poyatos, David, Guitart, Miriam
Published in European journal of medical genetics (01.01.2007)

Get full text

Journal Article

Prader Willi syndrome patients: study of 77 patients

Prader Willi syndrome patients: study of 77 patients

by Poyatos, David, Camprubí, Cristina, Gabau, Elisabeth, Nosas, Ramón, Villatoro, Sergi, Coll, María Dolores, Guitart, Miriam
Published in Medicina clínica (07.11.2009)

Get more information

Journal Article

Characterization of novel paternal ncRNAs at the Plagl1 locus, including Hymai, predicted to interact with regulators of active chromatin

Characterization of novel paternal ncRNAs at the Plagl1 locus, including Hymai, predicted to interact with regulators of active chromatin

by Iglesias-Platas, Isabel, Martin-Trujillo, Alex, Cirillo, Davide, Court, Franck, Guillaumet-Adkins, Amy, Camprubi, Cristina, Bourc'his, Deborah, Hata, Kenichiro, Feil, Robert, Tartaglia, Gian, Arnaud, Philippe, Monk, David
Published in PloS one (19.06.2012)

Get full text

Journal Article

Stability of Genomic Imprinting and Gestational-Age Dynamic Methylation in Complicated Pregnancies Conceived Following Assisted Reproductive Technologies1

Stability of Genomic Imprinting and Gestational-Age Dynamic Methylation in Complicated Pregnancies Conceived Following Assisted Reproductive Technologies1

by Camprubí, Cristina, Iglesias-Platas, Isabel, Martin-Trujillo, Alex, Salvador-Alarcon, Cristina, Rodriguez, Maria Angeles, Barredo, Dalia Rodriguez, Court, Franck, Monk, David
Published in Biology of reproduction (01.09.2013)

Get full text

Journal Article

Human imprinted retrogenes exhibit non-canonical imprint chromatin signatures and reside in non-imprinted host genes

Human imprinted retrogenes exhibit non-canonical imprint chromatin signatures and reside in non-imprinted host genes

by Monk, David, Arnaud, Philippe, Frost, Jennifer M., Wood, Andrew J., Cowley, Michael, Martin-Trujillo, Alejandro, Guillaumet-Adkins, Amy, Iglesias Platas, Isabel, Camprubi, Cristina, Bourc'his, Deborah, Feil, Robert, Moore, Gudrun E., Oakey, Rebecca J.
Published in Nucleic acids research (01.06.2011)

Get full text

Journal Article

Methylation screening of reciprocal genome-wide UPDs identifies novel human-specific imprinted genes super()

Methylation screening of reciprocal genome-wide UPDs identifies novel human-specific imprinted genes super()

by Nakabayashi, Kazuhiko, Trujillo, Alex Martin, Tayama, Chiharu, Camprubi, Cristina, Yoshida, Wataru, Lapunzina, Pablo, Sanchez, Aurora, Soejima, Hidenobu, Aburatani, Hiroyuki, Nagae, Genta, Ogata, Tsutomu, Hata, Kenichiro, Monk, David
Published in Human molecular genetics (15.08.2011)

Get full text

Journal Article

Novel UBE3A mutations causing Angelman syndrome: Different parental origin for single nucleotide changes and multiple nucleotide deletions or insertions

Novel UBE3A mutations causing Angelman syndrome: Different parental origin for single nucleotide changes and multiple nucleotide deletions or insertions

by Camprubí, Cristina, Guitart, Miriam, Gabau, Elisabeth, Coll, Maria Dolors, Villatoro, Sergi, Oltra, Silvestre, Roselló, Monica, Ferrer, Irene, Monfort, Sandra, Orellana, Carmen, Martínez, Francisco
Published in American journal of medical genetics. Part A (01.03.2009)

Get full text

Journal Article