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M Winter

Showing results (671-680 of 1,528) with videos related to

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Zeitschrift Fur Orthopadie Und Ihre Grenzgebiete|September 1, 1983
[Experimental results of stepped titanium shafts for hip endoprostheses]D Stock, J Gottstein, P Griss, et al.
International Journal of Biological Sciences|March 2, 2016
The Landscape of Pancreatic Cancer Therapeutic Resistance MechanismsSaswati Chand, Kevin O'Hayer, Fernando F Blanco, et al.
Frontiers in Endocrinology|April 4, 2022
Corrigendum: When to Start and Stop Bone-Protecting Medication for Preventing Glucocorticoid-Induced OsteoporosisKaleen N Hayes, Ulrike Baschant, Barbara Hauser, et al.
Marine Drugs|June 27, 2023
Expanding the Utility of Bioinformatic Data for the Full Stereostructural Assignments of Marinolides A and B, 24- and 26-Membered Macrolactones Produced by a Chemically Exceptional Marine-Derived BacteriumMin Cheol Kim, Jaclyn M Winter, Reiko Cullum, et al.
American Journal of Medical Genetics. Part A|February 28, 2003
Complex chromosomal rearrangement and associated counseling issues in a family with Pelizaeus-Merzbacher diseaseKaren Woodward, Maria Cundall, Rodger Palmer, et al.
Clinical Dysmorphology|April 18, 1998
Mutation of the MITF gene in albinism-deafness syndrome (Tietz syndrome)J Amiel, P M Watkin, M Tassabehji, et al.
Journal of Medical Genetics|June 1, 1992
Confirmation of an association between RFLPs at the transforming growth factor-alpha locus and non-syndromic cleft lip and palateS E Holder, G M Vintiner, B Farren, et al.
Clinical Dysmorphology|October 18, 2003
The appearance of the feet in Pfeiffer syndrome caused by FGFR1 P252R mutationMassimiliano Rossi, Rachel L Jones, Gail Norbury, et al.
Clinical Dysmorphology|April 20, 2001
Diagnostic dilemmas in four infants with nephrotic syndrome, microcephaly and severe developmental delayB B de Vries, W G van'tHoff, R A Surtees, et al.
Advances in Experimental Medicine and Biology|December 19, 2007
Possible roles of the weakly inward rectifying k+ channel Kir4.1 (KCNJ10) in the pre-Bötzinger complexNestoras Papadopoulos, Stefan M Winter, Kai Härtel, et al.
Pageof 153

Showing results (671-680 of 1,528) with videos related to

Sort By:
Pageof 153
Zeitschrift Fur Orthopadie Und Ihre Grenzgebiete|September 1, 1983
[Experimental results of stepped titanium shafts for hip endoprostheses]D Stock, J Gottstein, P Griss, et al.
International Journal of Biological Sciences|March 2, 2016
The Landscape of Pancreatic Cancer Therapeutic Resistance MechanismsSaswati Chand, Kevin O'Hayer, Fernando F Blanco, et al.
Frontiers in Endocrinology|April 4, 2022
Corrigendum: When to Start and Stop Bone-Protecting Medication for Preventing Glucocorticoid-Induced OsteoporosisKaleen N Hayes, Ulrike Baschant, Barbara Hauser, et al.
Marine Drugs|June 27, 2023
Expanding the Utility of Bioinformatic Data for the Full Stereostructural Assignments of Marinolides A and B, 24- and 26-Membered Macrolactones Produced by a Chemically Exceptional Marine-Derived BacteriumMin Cheol Kim, Jaclyn M Winter, Reiko Cullum, et al.
American Journal of Medical Genetics. Part A|February 28, 2003
Complex chromosomal rearrangement and associated counseling issues in a family with Pelizaeus-Merzbacher diseaseKaren Woodward, Maria Cundall, Rodger Palmer, et al.
Clinical Dysmorphology|April 18, 1998
Mutation of the MITF gene in albinism-deafness syndrome (Tietz syndrome)J Amiel, P M Watkin, M Tassabehji, et al.
Journal of Medical Genetics|June 1, 1992
Confirmation of an association between RFLPs at the transforming growth factor-alpha locus and non-syndromic cleft lip and palateS E Holder, G M Vintiner, B Farren, et al.
Clinical Dysmorphology|October 18, 2003
The appearance of the feet in Pfeiffer syndrome caused by FGFR1 P252R mutationMassimiliano Rossi, Rachel L Jones, Gail Norbury, et al.
Clinical Dysmorphology|April 20, 2001
Diagnostic dilemmas in four infants with nephrotic syndrome, microcephaly and severe developmental delayB B de Vries, W G van'tHoff, R A Surtees, et al.
Advances in Experimental Medicine and Biology|December 19, 2007
Possible roles of the weakly inward rectifying k+ channel Kir4.1 (KCNJ10) in the pre-Bötzinger complexNestoras Papadopoulos, Stefan M Winter, Kai Härtel, et al.
Pageof 153