Results
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241.
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A five-base pair deletion in the sedlin gene causes spondyloepiphyseal dysplasia tarda in a six-generation Arkansas kindred. [electronic resource] by
- Mumm, S
- Christie, P T
- Finnegan, P
- Jones, J
- Dixon, P H
- Pannett, A A
- Harding, B
- Gottesman, G S
- Thakker, R V
- Whyte, M P
Producer: 20001016
In:
The Journal of clinical endocrinology and metabolism vol. 85
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242.
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243.
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Mutation analysis of coding sequences for type I procollagen in individuals with low bone density. [electronic resource] by
- Spotila, L D
- Colige, A
- Sereda, L
- Constantinou-Deltas, C D
- Whyte, M P
- Riggs, B L
- Shaker, J L
- Spector, T D
- Hume, E
- Olsen, N
Producer: 19941006
In:
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research vol. 9
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244.
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Mutations in TNFRSF11A, affecting the signal peptide of RANK, cause familial expansile osteolysis. [electronic resource] by
- Hughes, A E
- Ralston, S H
- Marken, J
- Bell, C
- MacPherson, H
- Wallace, R G
- van Hul, W
- Whyte, M P
- Nakatsuka, K
- Hovy, L
- Anderson, D M
Producer: 20000210
In:
Nature genetics vol. 24
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245.
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Calcium-sensing receptor mutations in familial benign hypercalcemia and neonatal hyperparathyroidism. [electronic resource] by
- Pearce, S H
- Trump, D
- Wooding, C
- Besser, G M
- Chew, S L
- Grant, D B
- Heath, D A
- Hughes, I A
- Paterson, C R
- Whyte, M P
Producer: 19960813
In:
The Journal of clinical investigation vol. 96
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246.
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Albers-Schönberg disease (autosomal dominant osteopetrosis, type II) results from mutations in the ClCN7 chloride channel gene. [electronic resource] by
- Cleiren, E
- Bénichou, O
- Van Hul, E
- Gram, J
- Bollerslev, J
- Singer, F R
- Beaverson, K
- Aledo, A
- Whyte, M P
- Yoneyama, T
- deVernejoul, M C
- Van Hul, W
Producer: 20020207
In:
Human molecular genetics vol. 10
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247.
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Alkaline phosphatase knock-out mice recapitulate the metabolic and skeletal defects of infantile hypophosphatasia. [electronic resource] by
- Fedde, K N
- Blair, L
- Silverstein, J
- Coburn, S P
- Ryan, L M
- Weinstein, R S
- Waymire, K
- Narisawa, S
- Millán, J L
- MacGregor, G R
- Whyte, M P
Producer: 20000127
In:
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research vol. 14
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248.
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Periodontal Defects in the A116T Knock-in Murine Model of Odontohypophosphatasia. [electronic resource] by
- Foster, B L
- Sheen, C R
- Hatch, N E
- Liu, J
- Cory, E
- Narisawa, S
- Kiffer-Moreira, T
- Sah, R L
- Whyte, M P
- Somerman, M J
- Millán, J L
Producer: 20150630
In:
Journal of dental research vol. 94
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249.
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Insulin-like growth factor system abnormalities in hepatitis C-associated osteosclerosis. Potential insights into increasing bone mass in adults. [electronic resource] by
- Khosla, S
- Hassoun, A A
- Baker, B K
- Liu, F
- Zein, N N
- Whyte, M P
- Reasner, C A
- Nippoldt, T B
- Tiegs, R D
- Hintz, R L
- Conover, C A
Producer: 19980619
In:
The Journal of clinical investigation vol. 101
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250.
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Increased risk of fibrosing alveolitis associated with interleukin-1 receptor antagonist and tumor necrosis factor-alpha gene polymorphisms. [electronic resource] by
- Whyte, M
- Hubbard, R
- Meliconi, R
- Whidborne, M
- Eaton, V
- Bingle, C
- Timms, J
- Duff, G
- Facchini, A
- Pacilli, A
- Fabbri, M
- Hall, I
- Britton, J
- Johnston, I
- Di Giovine, F
Producer: 20000915
In:
American journal of respiratory and critical care medicine vol. 162
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251.
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Polymorphisms in the endothelin-1 (EDN1) are associated with asthma in two populations. [electronic resource] by
- Zhu, G
- Carlsen, K
- Carlsen, K-H
- Lenney, W
- Silverman, M
- Whyte, M K
- Hosking, L
- Helms, P
- Roses, A D
- Hay, D W
- Barnes, M R
- Anderson, W H
- Pillai, S G
Producer: 20080327
In:
Genes and immunity vol. 9
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252.
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First-stage autosomal genome screen in extended pedigrees suggests genes predisposing to low bone mineral density on chromosomes 1p, 2p and 4q. [electronic resource] by
- Devoto, M
- Shimoya, K
- Caminis, J
- Ott, J
- Tenenhouse, A
- Whyte, M P
- Sereda, L
- Hall, S
- Considine, E
- Williams, C J
- Tromp, G
- Kuivaniemi, H
- Ala-Kokko, L
- Prockop, D J
- Spotila, L D
Producer: 19981027
In:
European journal of human genetics : EJHG vol. 6
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253.
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Paget bone disease involving young adults in 3 generations of a Korean family. [electronic resource] by
- Kim, G S
- Kim, S H
- Cho, J K
- Park, J Y
- Shin, M J
- Shong, Y K
- Lee, K U
- Han, H
- Kim, T G
- Teitelbaum, S L
- Reinus, W R
- Whyte, M P
Producer: 19970717
In:
Medicine vol. 76
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254.
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Mutational analysis of PHEX gene in X-linked hypophosphatemia. [electronic resource] by
- Dixon, P H
- Christie, P T
- Wooding, C
- Trump, D
- Grieff, M
- Holm, I
- Gertner, J M
- Schmidtke, J
- Shah, B
- Shaw, N
- Smith, C
- Tau, C
- Schlessinger, D
- Whyte, M P
- Thakker, R V
Producer: 19981105
In:
The Journal of clinical endocrinology and metabolism vol. 83
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255.
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Exercise training reduces fatty acid availability and improves the insulin sensitivity of glucose metabolism. [electronic resource] by
- Shojaee-Moradie, F
- Baynes, K C R
- Pentecost, C
- Bell, J D
- Thomas, E L
- Jackson, N C
- Stolinski, M
- Whyte, M
- Lovell, D
- Bowes, S B
- Gibney, J
- Jones, R H
- Umpleby, A M
Producer: 20070926
In:
Diabetologia vol. 50
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256.
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Traditional risk factors and ischemic stroke in young adults: the Baltimore-Washington Cooperative Young Stroke Study. [electronic resource] by
- Rohr, J
- Kittner, S
- Feeser, B
- Hebel, J R
- Whyte, M G
- Weinstein, A
- Kanarak, N
- Buchholz, D
- Earley, C
- Johnson, C
- Macko, R
- Price, T
- Sloan, M
- Stern, B
- Wityk, R
- Wozniak, M
- Sherwin, R
Producer: 19961126
In:
Archives of neurology vol. 53
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257.
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Interstitial lung disease guideline: the British Thoracic Society in collaboration with the Thoracic Society of Australia and New Zealand and the Irish Thoracic Society. [electronic resource] by
- Bradley, B
- Branley, H M
- Egan, J J
- Greaves, M S
- Hansell, D M
- Harrison, N K
- Hirani, N
- Hubbard, R
- Lake, F
- Millar, A B
- Wallace, W A H
- Wells, A U
- Whyte, M K
- Wilsher, M L
Producer: 20080915
In:
Thorax vol. 63 Suppl 5
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258.
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Factor analysis in the Genetics of Asthma International Network family study identifies five major quantitative asthma phenotypes. [electronic resource] by
- Pillai, S G
- Tang, Y
- van den Oord, E
- Klotsman, M
- Barnes, K
- Carlsen, K
- Gerritsen, J
- Lenney, W
- Silverman, M
- Sly, P
- Sundy, J
- Tsanakas, J
- von Berg, A
- Whyte, M
- Ortega, H G
- Anderson, W H
- Helms, P J
Producer: 20080407
In:
Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology vol. 38
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259.
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Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementia. [electronic resource] by
- Kovach, M J
- Waggoner, B
- Leal, S M
- Gelber, D
- Khardori, R
- Levenstien, M A
- Shanks, C A
- Gregg, G
- Al-Lozi, M T
- Miller, T
- Rakowicz, W
- Lopate, G
- Florence, J
- Glosser, G
- Simmons, Z
- Morris, J C
- Whyte, M P
- Pestronk, A
- Kimonis, V E
Producer: 20020313
In:
Molecular genetics and metabolism vol. 74
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260.
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Alendronate for the treatment of pediatric osteogenesis imperfecta: a randomized placebo-controlled study. [electronic resource] by
- Ward, L M
- Rauch, F
- Whyte, M P
- D'Astous, J
- Gates, P E
- Grogan, D
- Lester, E L
- McCall, R E
- Pressly, T A
- Sanders, J O
- Smith, P A
- Steiner, R D
- Sullivan, E
- Tyerman, G
- Smith-Wright, D L
- Verbruggen, N
- Heyden, N
- Lombardi, A
- Glorieux, F H
Producer: 20110321
In:
The Journal of clinical endocrinology and metabolism vol. 96
Availability: No items available.
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