Graeme Scobie - Concepedia

Concepedia

Author

Graeme Scobie

University of Wales

Also Known As

G A Scobie, G Scobie, G. A. Scobie, G. SCOBIE, G. Scobie, G.A. Scobie, GRAEME SCOBIE, Graeme A Scobie, Graeme A. Scobie, Graeme SCOBIE

25

Publications

1.1K

Citations

14

H-Index

61

Concepts

All Affiliations

University of Wales MRC Centre for Reproductive Health Queen's Medical Centre Oxford Brookes University Medical Research Council

GS

About

Graeme Scobie is an author at University of Wales specializing in medicine, molecular genetics, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	10	414
2	Natural Sciences	3	3	62
3	Allergy	2	2	26
4	Public Health	1	1	15
5	Allergy Medicine	1	1	11

Graeme Scobie

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15

Publications

1.1K

Citations

13

H-Index

	Year	Citations
A novel mammalian receptor for the evolutionarily conserved type II GnRH Robert P. Millar, Steven Lowe, Darrell Conklin, Proceedings of the National Academy of Sciences	2001	310
Differential Expression of Estrogen Receptor-α and -β and Androgen Receptor in the Ovaries of Marmosets and Humans Philippa T. K. Saunders, Michael Millar, Karin Williams, Biology of Reproduction	2000	176
Angiogenesis During Follicular Development in the Primate and its Inhibition by Treatment with Truncated Flt-1-Fc (Vascular Endothelial Growth Factor TrapA40)* Christine Wulff, Stanley J. Wiegand, Philippa T. K. Saunders, Endocrinology	2001	134
ERβ1 and the ERβ2 Splice Variant (ERβcx/β2) Are Expressed in Distinct Cell Populations in the Adult Human Testis Philippa T. K. Saunders, Michael Millar, Sheila Macpherson, The Journal of Clinical Endocrinology & Metabolism SpermatogenesisGeneticsEstrogen ActionMolecular GeneticsReproductive Biology	2002	133
Human oestrogen receptors: differential expression of ERalpha and beta and the identification of ERbeta variants Graeme Scobie, Sheila Macpherson, Michael Millar, Steroids Endocrine MechanismDifferential ExpressionHormonal ReceptorDiabetesPhysiology	2002	84
Mutation in an α1-antitrypsin enhancer results in an interleukin-6 deficient acute-phase response due to loss of cooperativity between transcription factors Kevin Morgan, Graeme Scobie, P. Marsters, Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease InflammationCytokineTranscriptional RegulationImmunogeneticsImmunology	1997	43
Acute intermittent porphyria caused by a C?T mutation that produces a stop codon in the porphobilinogen deaminase gene Graeme Scobie, David H. Llewellyn, Andy Urquhart, Human Genetics BiologyT MutationGeneticsPathogenesisStop Codon	1990	38
Acute intermittent porphyria caused by defective splicing of porphobilinogen deaminase RNA: a synonymous codon mutation at -22 bp from the 5' splice site causes skipping of exon 3. David H. Llewellyn, Graeme Scobie, Andy Urquhart, Journal of Medical Genetics Synonymous Codon MutationGeneticsRna SplicingPathologyMolecular Genetics	1996	29
Point mutation in a 3′ flanking sequence of the alpha-1-antitrypsin gene associated with chronic respiratory disease occurs in a regulatory sequence Kevin Morgan, Graeme Scobie, Noor Kalsheker Human Molecular Genetics	1993	28
Identification of a Novel Missense Mutation That Is as Damaging to DAX-1 Repressor Function as a Nonsense Mutation Pamela Brown, Graeme Scobie, Julie Townsend, The Journal of Clinical Endocrinology & Metabolism GeneticsHuman Chorionic GonadotropinMolecular BiologyMolecular GeneticsReproductive Biology	2003	24

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