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Showing results (91-100 of 106) with videos related to

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Cancer Research|June 5, 2001
Extensive somatic microsatellite mutations in normal human tissueS Vilkki, J L Tsao, A Loukola, et al.
The Journal of Clinical Endocrinology and Metabolism|November 4, 2000
Expression of transcription factor GATA-4 during human testicular development and diseaseI Ketola, V Pentikäinen, T Vaskivuo, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 15, 2001
Inherited susceptibility to uterine leiomyomas and renal cell cancerV Launonen, O Vierimaa, M Kiuru, et al.
American Journal of Human Genetics|July 31, 1998
Assignment of the disease locus for lethal congenital contracture syndrome to a restricted region of chromosome 9q34, by genome scan using five affected individualsP Mäkelä-Bengs, N Järvinen, K Vuopala, et al.
Pediatrics|March 4, 2000
Childhood encephalopathies and myopathies: a prospective study in a defined population to assess the frequency of mitochondrial disordersJ Uusimaa, A M Remes, H Rantala, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|March 1, 1997
Collagenase-3 (MMP-13) is expressed by hypertrophic chondrocytes, periosteal cells, and osteoblasts during human fetal bone developmentN Johansson, U Saarialho-Kere, K Airola, et al.
Anesthesiology|December 1, 1991
Behavioral and histopathologic effects following intrathecal administration of butorphanol, sufentanil, and nalbuphine in sheepN Rawal, L Nuutinen, P P Raj, et al.
The Journal of Clinical Endocrinology and Metabolism|July 10, 2001
Survival of human ovarian follicles from fetal to adult life: apoptosis, apoptosis-related proteins, and transcription factor GATA-4T E Vaskivuo, M Anttonen, R Herva, et al.
American Journal of Human Genetics|May 1, 1985
Mapping DNA sequences in a human X-chromosome deletion which extends across the region of the Duchenne muscular dystrophy mutationC Ingle, R Williamson, A de la Chapelle, et al.
The American Journal of Pathology|September 11, 2001
Familial cutaneous leiomyomatosis is a two-hit condition associated with renal cell cancer of characteristic histopathologyM Kiuru, V Launonen, M Hietala, et al.
Pageof 11

Showing results (91-100 of 106) with videos related to

Sort By:
Pageof 11
Cancer Research|June 5, 2001
Extensive somatic microsatellite mutations in normal human tissueS Vilkki, J L Tsao, A Loukola, et al.
The Journal of Clinical Endocrinology and Metabolism|November 4, 2000
Expression of transcription factor GATA-4 during human testicular development and diseaseI Ketola, V Pentikäinen, T Vaskivuo, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 15, 2001
Inherited susceptibility to uterine leiomyomas and renal cell cancerV Launonen, O Vierimaa, M Kiuru, et al.
American Journal of Human Genetics|July 31, 1998
Assignment of the disease locus for lethal congenital contracture syndrome to a restricted region of chromosome 9q34, by genome scan using five affected individualsP Mäkelä-Bengs, N Järvinen, K Vuopala, et al.
Pediatrics|March 4, 2000
Childhood encephalopathies and myopathies: a prospective study in a defined population to assess the frequency of mitochondrial disordersJ Uusimaa, A M Remes, H Rantala, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists|March 1, 1997
Collagenase-3 (MMP-13) is expressed by hypertrophic chondrocytes, periosteal cells, and osteoblasts during human fetal bone developmentN Johansson, U Saarialho-Kere, K Airola, et al.
Anesthesiology|December 1, 1991
Behavioral and histopathologic effects following intrathecal administration of butorphanol, sufentanil, and nalbuphine in sheepN Rawal, L Nuutinen, P P Raj, et al.
The Journal of Clinical Endocrinology and Metabolism|July 10, 2001
Survival of human ovarian follicles from fetal to adult life: apoptosis, apoptosis-related proteins, and transcription factor GATA-4T E Vaskivuo, M Anttonen, R Herva, et al.
American Journal of Human Genetics|May 1, 1985
Mapping DNA sequences in a human X-chromosome deletion which extends across the region of the Duchenne muscular dystrophy mutationC Ingle, R Williamson, A de la Chapelle, et al.
The American Journal of Pathology|September 11, 2001
Familial cutaneous leiomyomatosis is a two-hit condition associated with renal cell cancer of characteristic histopathologyM Kiuru, V Launonen, M Hietala, et al.
Pageof 11