B Steinmann|M Raghunath - JoVE Visualize

Showing results (141-150 of 230) with videos related to

Pageof 23

Sort By:

Genomics|September 15, 1996

A point mutation creating an extra N-glycosylation site in fibrillin-1 results in neonatal Marfan syndromeL Lönnqvist, L Karttunen, T Rantamäki, et al.

Neuroscience|April 9, 2014

Increased macromolecular damage due to oxidative stress in the neocortex and hippocampus of WNIN/Ob, a novel rat model of premature agingJ K Sinha, S Ghosh, U Swain, et al.

Journal of Autoimmunity|December 1, 1989

Detection of human autoantibody against intercalated cells of kidney-collecting tubuleM Raghunath, P Gilbert, I Miedaner-Maier, et al.

Prenatal Diagnosis|December 1, 1995

Prenatal diagnosis of Marfan syndrome: identification of a fibrillin-1 mutation in chorionic villus sampleT Rantamäki, M Raghunath, L Karttunen, et al.

Annals of Nutrition & Metabolism|July 16, 2005

Addition of milk does not alter the antioxidant activity of black teaVijayakumar C Reddy, G V Vidya Sagar, D Sreeramulu, et al.

Nature Genetics|November 1, 1992

A homozygous stop codon in the lysyl hydroxylase gene in two siblings with Ehlers-Danlos syndrome type VIJ Hyland, L Ala-Kokko, P Royce, et al.

Journal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|April 1, 1982

A new high performance liquid chromatography (HPLC) method for the quantitation of strychnine in urine and tissue extractsT Egloff, A Niederwieser, K Pfister, et al.

American Journal of Human Genetics|January 1, 1990

Missense mutations associated with RFLP haplotypes 1 and 4 of the human phenylalanine hydroxylase geneY Okano, T Wang, R C Eisensmith, et al.

Journal of Reproductive Immunology|January 13, 2006

Local immunity in Indian women with bacterial vaginosisP Yasodhara, M Raghunath, D Sreeramulu, et al.

American Journal of Medical Genetics|September 1, 1989

Ehlers-Danlos syndrome type IV: a subset of patients distinguished by low serum levels of the amino-terminal propeptide of type III procollagenB Steinmann, A Superti-Furga, H I Joller-Jemelka, et al.

Pageof 23

Showing results (141-150 of 230) with videos related to

Sort By:

Pageof 23

Genomics|September 15, 1996

A point mutation creating an extra N-glycosylation site in fibrillin-1 results in neonatal Marfan syndromeL Lönnqvist, L Karttunen, T Rantamäki, et al.

Neuroscience|April 9, 2014

Increased macromolecular damage due to oxidative stress in the neocortex and hippocampus of WNIN/Ob, a novel rat model of premature agingJ K Sinha, S Ghosh, U Swain, et al.

Journal of Autoimmunity|December 1, 1989

Detection of human autoantibody against intercalated cells of kidney-collecting tubuleM Raghunath, P Gilbert, I Miedaner-Maier, et al.

Prenatal Diagnosis|December 1, 1995

Prenatal diagnosis of Marfan syndrome: identification of a fibrillin-1 mutation in chorionic villus sampleT Rantamäki, M Raghunath, L Karttunen, et al.

Annals of Nutrition & Metabolism|July 16, 2005

Addition of milk does not alter the antioxidant activity of black teaVijayakumar C Reddy, G V Vidya Sagar, D Sreeramulu, et al.

Nature Genetics|November 1, 1992

A homozygous stop codon in the lysyl hydroxylase gene in two siblings with Ehlers-Danlos syndrome type VIJ Hyland, L Ala-Kokko, P Royce, et al.

Journal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|April 1, 1982

A new high performance liquid chromatography (HPLC) method for the quantitation of strychnine in urine and tissue extractsT Egloff, A Niederwieser, K Pfister, et al.

American Journal of Human Genetics|January 1, 1990

Missense mutations associated with RFLP haplotypes 1 and 4 of the human phenylalanine hydroxylase geneY Okano, T Wang, R C Eisensmith, et al.

Journal of Reproductive Immunology|January 13, 2006

Local immunity in Indian women with bacterial vaginosisP Yasodhara, M Raghunath, D Sreeramulu, et al.

American Journal of Medical Genetics|September 1, 1989

Ehlers-Danlos syndrome type IV: a subset of patients distinguished by low serum levels of the amino-terminal propeptide of type III procollagenB Steinmann, A Superti-Furga, H I Joller-Jemelka, et al.

Pageof 23