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Showing results (91-100 of 100) with videos related to

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Journal of Medical Genetics|July 29, 1999
Analysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlationW W Lam, I Hatada, S Ohishi, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 20, 2004
Placental-specific insulin-like growth factor 2 (Igf2) regulates the diffusional exchange characteristics of the mouse placentaC P Sibley, P M Coan, A C Ferguson-Smith, et al.
Placenta|September 29, 2004
Fetal growth restriction: a workshop reportI Cetin, J-M Foidart, M Miozzo, et al.
Human Molecular Genetics|March 15, 2006
Imprinting of IGF2 P0 transcript and novel alternatively spliced INS-IGF2 isoforms show differences between mouse and humanD Monk, R Sanches, P Arnaud, et al.
Journal of Medical Genetics|November 25, 2003
Silencing of CDKN1C (p57KIP2) is associated with hypomethylation at KvDMR1 in Beckwith-Wiedemann syndromeN Diaz-Meyer, C D Day, K Khatod, et al.
Journal of Medical Genetics|January 15, 2003
Beckwith-Wiedemann syndrome and assisted reproduction technology (ART)E R Maher, L A Brueton, S C Bowdin, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|March 16, 2002
Early malnutrition and programming of adult degenerative diseases: experimental, epidemiological and preventive studiesC Remacle, B Reusens, L Kalbe, et al.
Human Molecular Genetics|June 9, 1998
Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith-Wiedemann syndrome region in chromosome 11p15.5M Paulsen, K R Davies, L M Bowden, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 8, 1999
A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndromeN J Smilinich, C D Day, G V Fitzpatrick, et al.
Nature Biotechnology|September 7, 2021
Integration of spatial and single-cell transcriptomic data elucidates mouse organogenesisT Lohoff, S Ghazanfar, A Missarova, et al.
Pageof 10

Showing results (91-100 of 100) with videos related to

Sort By:
Pageof 10
You have reached the last page of results.This site can display upto 100 results.
Journal of Medical Genetics|July 29, 1999
Analysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlationW W Lam, I Hatada, S Ohishi, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 20, 2004
Placental-specific insulin-like growth factor 2 (Igf2) regulates the diffusional exchange characteristics of the mouse placentaC P Sibley, P M Coan, A C Ferguson-Smith, et al.
Placenta|September 29, 2004
Fetal growth restriction: a workshop reportI Cetin, J-M Foidart, M Miozzo, et al.
Human Molecular Genetics|March 15, 2006
Imprinting of IGF2 P0 transcript and novel alternatively spliced INS-IGF2 isoforms show differences between mouse and humanD Monk, R Sanches, P Arnaud, et al.
Journal of Medical Genetics|November 25, 2003
Silencing of CDKN1C (p57KIP2) is associated with hypomethylation at KvDMR1 in Beckwith-Wiedemann syndromeN Diaz-Meyer, C D Day, K Khatod, et al.
Journal of Medical Genetics|January 15, 2003
Beckwith-Wiedemann syndrome and assisted reproduction technology (ART)E R Maher, L A Brueton, S C Bowdin, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|March 16, 2002
Early malnutrition and programming of adult degenerative diseases: experimental, epidemiological and preventive studiesC Remacle, B Reusens, L Kalbe, et al.
Human Molecular Genetics|June 9, 1998
Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith-Wiedemann syndrome region in chromosome 11p15.5M Paulsen, K R Davies, L M Bowden, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 8, 1999
A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndromeN J Smilinich, C D Day, G V Fitzpatrick, et al.
Nature Biotechnology|September 7, 2021
Integration of spatial and single-cell transcriptomic data elucidates mouse organogenesisT Lohoff, S Ghazanfar, A Missarova, et al.
Pageof 10