J M Opitz|P Mullen - JoVE Visualize

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Protein Science : a Publication of the Protein Society|June 1, 1997

Secondary and tertiary structural changes in gamma delta resolvase: comparison of the wild-type enzyme, the I110R mutant, and the C-terminal DNA binding domain in solutionB Pan, Z Deng, D Liu, et al.

Plos One|January 10, 2013

Investigation of prolific sheep from UK and Ireland for evidence on origin of the mutations in BMP15 (FecX(G), FecX(B)) and GDF9 (FecG(H)) in Belclare and Cambridge sheepMichael P Mullen, James P Hanrahan, Dawn J Howard, et al.

Pediatric Cardiology|January 24, 2019

Pulmonary Artery Banding in Post-tricuspid Congenital Cardiac Shunting Defects with High Pulmonary Vascular ResistanceThomas J Kulik, Julia E McSweeney, Joseph Tella, et al.

Journal of Chemical Ecology|January 22, 2008

Identification and characterization of cuticular hydrocarbons from a rapid species radiation of Hawaiian swordtailed crickets (Gryllidae: Trigonidiinae: Laupala)Sean P Mullen, Jocelyn G Millar, Coby Schal, et al.

Anesthesiology|May 30, 2006

Characterization of ryanodine receptor-mediated calcium release in human B cells: relevance to diagnostic testing for malignant hyperthermiaLeslie C McKinney, Thomas Butler, Shawn P Mullen, et al.

American Journal of Medical Genetics|April 14, 1997

Another "new" form, the palagonia type of acrofacial dysostosis in a Sicilian familyG Sorge, L Pavone, A Polizzi, et al.

European Journal of Pediatrics|January 2, 1976

Studies of malformation syndromes of man XIB: the cerebro-hepato-renal syndrome of Zellweger: comparative pathologyK W Gilchrist, E F Gilbert, S Goldfarb, et al.

American Journal of Medical Genetics|November 1, 1994

Microcephaly, lymphedema, and chorioretinal dysplasia: report of two additional casesB Angle, S Holgado, B K Burton, et al.

European Journal of Pediatrics|August 1, 1980

A fetus with upper limb amelia, "caudal regression" and Dandy-Walker defect with an insulin-dependent diabetic motherH J Bruyere, C Viseskul, J M Opitz, et al.

Proceedings of the National Academy of Sciences of the United States of America|January 1, 1972

Cytological mapping of human X-linked genes by use of somatic cell hybrids involving an X-autosome translocation (mouse-hamster-human X-linked markers)K H Grzeschik, P W Allderdice, A Grzeschik, et al.

Pageof 59

Showing results (181-190 of 585) with videos related to

Sort By:

Pageof 59

Protein Science : a Publication of the Protein Society|June 1, 1997

Secondary and tertiary structural changes in gamma delta resolvase: comparison of the wild-type enzyme, the I110R mutant, and the C-terminal DNA binding domain in solutionB Pan, Z Deng, D Liu, et al.

Plos One|January 10, 2013

Investigation of prolific sheep from UK and Ireland for evidence on origin of the mutations in BMP15 (FecX(G), FecX(B)) and GDF9 (FecG(H)) in Belclare and Cambridge sheepMichael P Mullen, James P Hanrahan, Dawn J Howard, et al.

Pediatric Cardiology|January 24, 2019

Pulmonary Artery Banding in Post-tricuspid Congenital Cardiac Shunting Defects with High Pulmonary Vascular ResistanceThomas J Kulik, Julia E McSweeney, Joseph Tella, et al.

Journal of Chemical Ecology|January 22, 2008

Identification and characterization of cuticular hydrocarbons from a rapid species radiation of Hawaiian swordtailed crickets (Gryllidae: Trigonidiinae: Laupala)Sean P Mullen, Jocelyn G Millar, Coby Schal, et al.

Anesthesiology|May 30, 2006

Characterization of ryanodine receptor-mediated calcium release in human B cells: relevance to diagnostic testing for malignant hyperthermiaLeslie C McKinney, Thomas Butler, Shawn P Mullen, et al.

American Journal of Medical Genetics|April 14, 1997

Another "new" form, the palagonia type of acrofacial dysostosis in a Sicilian familyG Sorge, L Pavone, A Polizzi, et al.

European Journal of Pediatrics|January 2, 1976

Studies of malformation syndromes of man XIB: the cerebro-hepato-renal syndrome of Zellweger: comparative pathologyK W Gilchrist, E F Gilbert, S Goldfarb, et al.

American Journal of Medical Genetics|November 1, 1994

Microcephaly, lymphedema, and chorioretinal dysplasia: report of two additional casesB Angle, S Holgado, B K Burton, et al.

European Journal of Pediatrics|August 1, 1980

A fetus with upper limb amelia, "caudal regression" and Dandy-Walker defect with an insulin-dependent diabetic motherH J Bruyere, C Viseskul, J M Opitz, et al.

Proceedings of the National Academy of Sciences of the United States of America|January 1, 1972

Cytological mapping of human X-linked genes by use of somatic cell hybrids involving an X-autosome translocation (mouse-hamster-human X-linked markers)K H Grzeschik, P W Allderdice, A Grzeschik, et al.

Pageof 59