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The publication data currently available has been vetted by Vanderbilt faculty, staff, administrators and trainees. The data itself is retrieved directly from NCBI's PubMed and is automatically updated on a weekly basis to ensure accuracy and completeness.

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Results: 1 to 10 of 10

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C. elegans dopaminergic D2-like receptors delimit recurrent cholinergic-mediated motor programs during a goal-oriented behavior.
Correa P, LeBoeuf B, GarcĂ­a LR
(2012) PLoS Genet 8: e1003015
MeSH Terms: Animals, Caenorhabditis elegans, Caenorhabditis elegans Proteins, Cholinergic Antagonists, Cholinergic Neurons, Copulation, Disorders of Sex Development, Dopamine, Female, Male, Muscle Contraction, Receptors, Cholinergic, Receptors, Dopamine D2, Sexual Behavior, Animal, Signal Transduction, Vulva
Added September 3, 2013
0 Communities
1 Members
0 Resources
16 MeSH Terms
Clinical, genetic, and enzymatic characterization of P450 oxidoreductase deficiency in four patients.
Sahakitrungruang T, Huang N, Tee MK, Agrawal V, Russell WE, Crock P, Murphy N, Migeon CJ, Miller WL
(2009) J Clin Endocrinol Metab 94: 4992-5000
MeSH Terms: Adolescent, Adult, Bone and Bones, Catalysis, Cytochromes c, DNA, Disorders of Sex Development, Escherichia coli, Female, Genetic Vectors, Genitalia, Hormones, Humans, Infant, Newborn, Infertility, Male, Mutation, NADP, NADPH-Ferrihemoprotein Reductase, Pregnancy, Steroid 17-alpha-Hydroxylase, Syndrome
Added May 5, 2016
0 Communities
1 Members
0 Resources
22 MeSH Terms
Activation of the Hedgehog pathway in the mouse fetal ovary leads to ectopic appearance of fetal Leydig cells and female pseudohermaphroditism.
Barsoum IB, Bingham NC, Parker KL, Jorgensen JS, Yao HH
(2009) Dev Biol 329: 96-103
MeSH Terms: Animals, Cell Differentiation, Disorders of Sex Development, Embryo, Mammalian, Female, Fetus, Hedgehog Proteins, Immunohistochemistry, In Situ Hybridization, Leydig Cells, Male, Mice, Mice, Transgenic, Ovary, Sex Differentiation, Signal Transduction
Added October 13, 2015
0 Communities
1 Members
0 Resources
16 MeSH Terms
Major sperm protein signaling promotes oocyte microtubule reorganization prior to fertilization in Caenorhabditis elegans.
Harris JE, Govindan JA, Yamamoto I, Schwartz J, Kaverina I, Greenstein D
(2006) Dev Biol 299: 105-21
MeSH Terms: Animals, Caenorhabditis elegans, Caenorhabditis elegans Proteins, Cell Cycle Proteins, Cell Polarity, Disorders of Sex Development, Enzyme Activation, Fertilization, Fluorescence Recovery After Photobleaching, GTP-Binding Protein alpha Subunits, Gi-Go, GTP-Binding Protein alpha Subunits, Gs, Gap Junctions, Helminth Proteins, Microtubules, Mitogen-Activated Protein Kinases, Oocytes, Receptor Protein-Tyrosine Kinases, Signal Transduction, Sperm-Ovum Interactions
Added December 10, 2013
0 Communities
1 Members
0 Resources
19 MeSH Terms
A microdeletion in the ligand binding domain of human steroidogenic factor 1 causes XY sex reversal without adrenal insufficiency.
Correa RV, Domenice S, Bingham NC, Billerbeck AE, Rainey WE, Parker KL, Mendonca BB
(2004) J Clin Endocrinol Metab 89: 1767-72
MeSH Terms: Adrenal Glands, Adult, Base Sequence, DNA-Binding Proteins, Disorders of Sex Development, Female, Fushi Tarazu Transcription Factors, Gene Deletion, Genes, Dominant, Genitalia, Female, Homeodomain Proteins, Humans, Ligands, Mutation, Receptors, Cytoplasmic and Nuclear, Steroidogenic Factor 1, Transcription Factors, Transcription, Genetic
Added October 13, 2015
0 Communities
1 Members
0 Resources
18 MeSH Terms
A sperm cytoskeletal protein that signals oocyte meiotic maturation and ovulation.
Miller MA, Nguyen VQ, Lee MH, Kosinski M, Schedl T, Caprioli RM, Greenstein D
(2001) Science 291: 2144-7
MeSH Terms: Amino Acid Sequence, Animals, Caenorhabditis elegans, Carrier Proteins, Cytoskeleton, Disorders of Sex Development, Enzyme Activation, Evolution, Molecular, Female, Gonads, Helminth Proteins, MAP Kinase Signaling System, Male, Meiosis, Membrane Proteins, Microinjections, Mitogen-Activated Protein Kinases, Molecular Sequence Data, Oocytes, Ovulation, Phylogeny, Protein Folding, Protein Structure, Tertiary, Pseudopodia, Recombinant Proteins, Signal Transduction, Sperm Motility, Spermatozoa
Added March 5, 2014
0 Communities
1 Members
0 Resources
28 MeSH Terms
No mutation in cytochrome P450 side chain cleavage in a patient with congenital lipoid adrenal hyperplasia.
Sakai Y, Yanase T, Okabe Y, Hara T, Waterman MR, Takayanagi R, Haji M, Nawata H
(1994) J Clin Endocrinol Metab 79: 1198-201
MeSH Terms: Adolescent, Adrenal Hyperplasia, Congenital, Adrenodoxin, Base Sequence, Cholesterol Side-Chain Cleavage Enzyme, Disorders of Sex Development, Female, Ferredoxin-NADP Reductase, Hormones, Humans, Male, Middle Aged, Mitochondria, Molecular Probes, Molecular Sequence Data, Mutation, Testis
Added February 12, 2015
0 Communities
1 Members
0 Resources
17 MeSH Terms
Pseudohermaphroditism, glomerulopathy, and Wilms tumor (Drash syndrome): frequency in end-stage renal failure.
Eddy AA, Mauer SM
(1985) J Pediatr 106: 584-7
MeSH Terms: Disorders of Sex Development, Female, Glomerulosclerosis, Focal Segmental, Humans, Infant, Kidney, Kidney Failure, Chronic, Nephrectomy, Risk, Syndrome, Ultrasonography, Wilms Tumor
Added February 3, 2012
0 Communities
1 Members
0 Resources
12 MeSH Terms
Compound heterozygous mutations (Arg 239----stop, Pro 342----Thr) in the CYP17 (P45017 alpha) gene lead to ambiguous external genitalia in a male patient with partial combined 17 alpha-hydroxylase/17,20-lyase deficiency.
Ahlgren R, Yanase T, Simpson ER, Winter JS, Waterman MR
(1992) J Clin Endocrinol Metab 74: 667-72
MeSH Terms: Adrenal Hyperplasia, Congenital, Aldehyde-Lyases, Alleles, Amino Acid Sequence, Animals, Arginine, Base Sequence, Blotting, Southern, Cell Line, Child, Cytochrome P-450 Enzyme System, DNA, Disorders of Sex Development, Heterozygote, Humans, Leukocytes, Male, Molecular Sequence Data, Mutation, Oligodeoxyribonucleotides, Polymerase Chain Reaction, Proline, Restriction Mapping, Steroid 17-alpha-Hydroxylase, Threonine, Transfection
Added February 12, 2015
0 Communities
1 Members
0 Resources
26 MeSH Terms
Molecular basis of apparent isolated 17,20-lyase deficiency: compound heterozygous mutations in the C-terminal region (Arg(496)----Cys, Gln(461)----Stop) actually cause combined 17 alpha-hydroxylase/17,20-lyase deficiency.
Yanase T, Waterman MR, Zachmann M, Winter JS, Simpson ER, Kagimoto M
(1992) Biochim Biophys Acta 1139: 275-9
MeSH Terms: Adolescent, Adrenal Hyperplasia, Congenital, Aldehyde-Lyases, Amino Acid Sequence, Base Sequence, Cell Line, Cytochrome P-450 Enzyme System, Disorders of Sex Development, Heterozygote, Humans, Male, Molecular Sequence Data, Mutation, Transfection
Added February 12, 2015
0 Communities
1 Members
0 Resources
14 MeSH Terms