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F Saunders

Showing results (281-290 of 365) with videos related to

Pageof 37
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Blood|June 1, 1988
A myeloid-related sequence that localizes to human chromosome 8q21.1-22W M Mars, P van Tuinen, H A Drabkin, et al.
Bone Marrow Transplantation|March 29, 2000
Matched unrelated bone marrow transplantation for combined immunodeficiencyI Dalal, B Reid, J Doyle, et al.
Genomics|September 6, 2002
Functional and structural characterization of the human gene BHLHB5, encoding a basic helix-loop-helix transcription factorZheng-Ping Xu, Amalia Dutra, Christine M Stellrecht, et al.
American Journal of Human Genetics|January 1, 1995
WT1 exon 1 deletion/insertion mutations in Wilms tumor patients, associated with di- and trinucleotide repeats and deletion hotspot consensus sequencesV Huff, N Jaffe, G F Saunders, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1973
125 I-labeled DNA-RNA hybrids in cytological preparationsL C Altenburg, M J Getz, W R Crain, et al.
Nature|October 6, 1997
Haem-ligand switching during catalysis in crystals of a nitrogen-cycle enzymeP A Williams, V Fülöp, E F Garman, et al.
Endocrine Reviews|November 1, 1991
The human placental lactogen genes: structure, function, evolution and transcriptional regulationW H Walker, S L Fitzpatrick, H A Barrera-Saldaña, et al.
The Journal of Urology|October 1, 1990
Familial renal cell carcinoma: hereditary or coincidental?A K Levinson, D E Johnson, L C Strong, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 2, 2002
Iris hypoplasia in mice that lack the alternatively spliced Pax6(5a) isoformSanjaya Singh, Rajnikant Mishra, Nelson A Arango, et al.
Ophthalmic Paediatrics and Genetics|December 1, 1991
DNA diagnosis in a family with autosomal dominant aniridiaF D Verbraak, M A Mannens, E J Redeker, et al.
Pageof 37

Showing results (281-290 of 365) with videos related to

Sort By:
Pageof 37
Blood|June 1, 1988
A myeloid-related sequence that localizes to human chromosome 8q21.1-22W M Mars, P van Tuinen, H A Drabkin, et al.
Bone Marrow Transplantation|March 29, 2000
Matched unrelated bone marrow transplantation for combined immunodeficiencyI Dalal, B Reid, J Doyle, et al.
Genomics|September 6, 2002
Functional and structural characterization of the human gene BHLHB5, encoding a basic helix-loop-helix transcription factorZheng-Ping Xu, Amalia Dutra, Christine M Stellrecht, et al.
American Journal of Human Genetics|January 1, 1995
WT1 exon 1 deletion/insertion mutations in Wilms tumor patients, associated with di- and trinucleotide repeats and deletion hotspot consensus sequencesV Huff, N Jaffe, G F Saunders, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1973
125 I-labeled DNA-RNA hybrids in cytological preparationsL C Altenburg, M J Getz, W R Crain, et al.
Nature|October 6, 1997
Haem-ligand switching during catalysis in crystals of a nitrogen-cycle enzymeP A Williams, V Fülöp, E F Garman, et al.
Endocrine Reviews|November 1, 1991
The human placental lactogen genes: structure, function, evolution and transcriptional regulationW H Walker, S L Fitzpatrick, H A Barrera-Saldaña, et al.
The Journal of Urology|October 1, 1990
Familial renal cell carcinoma: hereditary or coincidental?A K Levinson, D E Johnson, L C Strong, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 2, 2002
Iris hypoplasia in mice that lack the alternatively spliced Pax6(5a) isoformSanjaya Singh, Rajnikant Mishra, Nelson A Arango, et al.
Ophthalmic Paediatrics and Genetics|December 1, 1991
DNA diagnosis in a family with autosomal dominant aniridiaF D Verbraak, M A Mannens, E J Redeker, et al.
Pageof 37