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Research Output 1985 2019

2019

Disruption of PHF21A causes syndromic intellectual disability with craniofacial anomalies, epilepsy, hypotonia, and neurobehavioral problems including autism

Kim, H. G., Rosenfeld, J. A., Scott, D. A., Bénédicte, G., Labonne, J. D., Brown, J., McGuire, M., Mahida, S., Naidu, S., Gutierrez, J., Lesca, G., Des Portes, V., Bruel, A. L., Sorlin, A., Xia, F., Capri, Y., Muller, E., McKnight, D., Torti, E., Rüschendorf, F. & 8 others, Hummel, O., Islam, Z., Kolatkar, P. R., Layman, L. C., Ryu, D., Kong, I. K., Madan-Khetarpal, S. & Kim, C. H., Oct 22 2019, In : Molecular Autism. 10, 1, 35.

Research output: Contribution to journalArticle

Open Access
Muscle Hypotonia
Autistic Disorder
Intellectual Disability
Epilepsy
Haploinsufficiency

The Use of Whole Exome Sequencing in a Cohort of Transgender Individuals to Identify Rare Genetic Variants

Theisen, J. G., Sundaram, V., Filchak, M. S., Chorich, L. P., Sullivan, M. E., Knight, J., Kim, H. G. & Layman, L. C., Dec 1 2019, In : Scientific Reports. 9, 1, 20099.

Research output: Contribution to journalArticle

Open Access
Transgender Persons
Exome
Genes
Brain
Social Distance
2018
2 Citations (Scopus)

Copy number variation and regions of homozygosity analysis in patients with MÜLLERIAN aplasia

Demir Eksi, D., Shen, Y., Erman, M., Chorich, L. P., Sullivan, M. E., Bilekdemir, M., Yllmaz, E., Luleci, G., Kim, H. G., Alper, O. M. & Layman, L. C., Feb 3 2018, In : Molecular Cytogenetics. 11, 1, 13.

Research output: Contribution to journalArticle

Genes
Microarrays
Chromosomes
Animals
Western World
2 Citations (Scopus)

JAK/STAT signaling pathway gene expression is reduced following Nelf knockdown in GnRH neurons

Ko, E. K., Chorich, L. P., Sullivan, M. E., Cameron, R. S. & Layman, L. C., Jul 15 2018, In : Molecular and Cellular Endocrinology. 470, p. 151-159 9 p.

Research output: Contribution to journalArticle

Janus Kinases
Transcription
Transducers
Gene expression
Gonadotropin-Releasing Hormone
4 Citations (Scopus)

WDR11-mediated Hedgehog signalling defects underlie a new ciliopathy related to Kallmann syndrome

Kim, Y. J., Osborn, D. P. S., Lee, J. Y., Araki, M., Araki, K., Mohun, T., Känsäkoski, J., Brandstack, N., Kim, H. T., Miralles, F., Kim, C. H., Brown, N. A., Kim, H. G., Martinez-Barbera, J. P., Ataliotis, P., Raivio, T., Layman, L. C. & Kim, S. H., Feb 1 2018, In : EMBO Reports. 19, 2, p. 269-289 21 p.

Research output: Contribution to journalArticle

Kallmann Syndrome
Hedgehogs
Hypogonadism
Defects
Gene expression
2017
8 Citations (Scopus)

Genetic analysis of Mayer-Rokitansky-Kuster-Hauser syndrome in a large cohort of families

Williams, L. S., Demir Eksi, D., Shen, Y., Lossie, A. C., Chorich, L. P., Sullivan, M. E., Phillips, J. A., Erman, M., Kim, H. G., Alper, O. M. & Layman, L. C., Jul 2017, In : Fertility and sterility. 108, 1, p. 145-151.e2

Research output: Contribution to journalArticle

Point Mutation
Mullerian aplasia
Genetic Association Studies
Pedigree
Microarray Analysis
2 Citations (Scopus)

Genetic basis of eugonadal and hypogonadal female reproductive disorders

Trofimova, T., Lizneva, D., Suturina, L., Walker, W., Chen, Y-H., Azziz, R. & Layman, L. C., Oct 1 2017, In : Best Practice and Research: Clinical Obstetrics and Gynaecology. 44, p. 3-14 12 p.

Research output: Contribution to journalReview article

Hypogonadism
Kallmann Syndrome
Ovarian Hyperstimulation Syndrome
Primary Ovarian Insufficiency
Turner Syndrome
2016
4 Citations (Scopus)

A balanced chromosomal translocation involving chromosomes 3 and 16 in a patient with Mayer-Rokitansky-Kuster-Hauser syndrome reveals new candidate genes at 3p22.3 and 16p13.3

Williams, L. S., Kim, H. G., Kalscheuer, V. M., Tuck, J. M., Chorich, L. P., Sullivan, M. E., Falkenstrom, A., Reindollar, R. H. & Layman, L. C., Jul 30 2016, In : Molecular Cytogenetics. 9, 1, 57.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 16
Genetic Translocation
Chromosomes, Human, Pair 3
Chromosomes
Genes
9 Citations (Scopus)

A microdeletion at Xq22.2 implicates a glycine receptor GLRA4 involved in intellectual disability, behavioral problems and craniofacial anomalies

Labonne, J. D. J., Graves, T. D., Shen, Y., Jones, J. R., Kong, I. K., Layman, L. C. & Kim, H. G., Aug 9 2016, In : BMC Neurology. 16, 1, 132.

Research output: Contribution to journalArticle

Glycine Receptors
Intellectual Disability
Genes
Pelizaeus-Merzbacher Disease
X-Linked Genes
15 Citations (Scopus)

An atypical 12q24.31 microdeletion implicates six genes including a histone demethylase KDM2B and a histone methyltransferase SETD1B in syndromic intellectual disability

Labonne, J. D. J., Lee, K. H., Iwase, S., Kong, I. K., Diamond, M. P., Layman, L. C., Kim, C. H. & Kim, H. G., Jul 1 2016, In : Human Genetics. 135, 7, p. 757-771 15 p.

Research output: Contribution to journalArticle

Histone Demethylases
Intellectual Disability
Genes
Untranslated RNA
Zebrafish
2 Citations (Scopus)

Berberine Inhibits Uterine Leiomyoma Cell Proliferation via Downregulation of Cyclooxygenase 2 and Pituitary Tumor-Transforming Gene 1

Chuang, T. Y., Min, J., Wu, H. L., McCrary, C., Layman, L. C., Diamond, M. P., Azziz, R., Al-Hendy, A. & Chen, Y. H., Oct 30 2016, In : Reproductive Sciences. 24, 7, p. 1005-1013 9 p.

Research output: Contribution to journalArticle

Berberine
Leiomyoma
Pituitary Neoplasms
Cyclooxygenase 2
Oncogenes
4 Citations (Scopus)
Megalencephaly
Intellectual Disability
Genes
Microarrays
Chromosomes
4 Citations (Scopus)

Concomitant partial exon skipping by a unique missense mutation of RPS6KA3 causes Coffin-Lowry syndrome

Labonne, J. D. J., Chung, M. J., Jones, J. R., Anand, P., Wenzel, W., Iacoboni, D., Layman, L. C. & Kim, H. G., Jan 1 2016, In : Gene. 575, 1, p. 42-47 6 p.

Research output: Contribution to journalArticle

Coffin-Lowry Syndrome
Missense Mutation
Exons
Peptides
Mutation
1 Citation (Scopus)

Steric clash in the SET domain of histone methyltransferase NSD1 as a cause of sotos syndrome and its genetic heterogeneity in a Brazilian cohort

Ha, K., Anand, P., Lee, J. A., Jones, J. R., Kim, C. A., Bertola, D. R., Labonne, J. D. J., Layman, L. C., Wenzel, W. & Kim, H. G., Nov 2016, In : Genes. 7, 11, 96.

Research output: Contribution to journalArticle

Sotos Syndrome
Genetic Heterogeneity
Mutation
Missense Mutation
Intellectual Disability
18 Citations (Scopus)

Targeted next generation sequencing approach identifies eighteen new candidate genes in normosmic hypogonadotropic hypogonadism and Kallmann syndrome

Quaynor, S. D., Bosley, M. E., Duckworth, C. G., Porter, K. R., Kim, S. H., Kim, H. G., Chorich, L. P., Sullivan, M. E., Choi, J. H., Cameron, R. S. & Layman, L. C., Dec 5 2016, In : Molecular and Cellular Endocrinology. 437, p. 86-96 11 p.

Research output: Contribution to journalArticle

Kallmann Syndrome
Hypogonadism
Genes
Olfactory Pathways
Mutation
2015
8 Citations (Scopus)

A microdeletion encompassing PHF21A in an individual with global developmental delay and craniofacial anomalies

Labonne, J. D. J., Vogt, J., Reali, L., Kong, I. K., Layman, L. C. & Kim, H. G., Dec 1 2015, In : American Journal of Medical Genetics, Part A. 167, 12, p. 3011-3018 8 p.

Research output: Contribution to journalArticle

Genes
Phenotype
Multiple Hereditary Exostoses
Genetic Association Studies
Extremities
10 Citations (Scopus)

Expanding the spectrum of founder mutations causing isolated gonadotropin-releasing hormone deficiency

Choi, J. H., Balasubramanian, R., Lee, P. H., Shaw, N. D., Hall, J. E., Plummer, L., Buck, C. L., Kottler, M. L., Jarzabek, K., Wołczynski, S., Quinton, R., Latronico, A. C., Dode, C., Ogata, T., Kim, H. G., Layman, L. C., Gusella, J. F. & Crowley, W. F., Oct 1 2015, In : Journal of Clinical Endocrinology and Metabolism. 100, 10, p. E1378-E1385

Research output: Contribution to journalArticle

Gonadotropin-Releasing Hormone
Genes
Mutation
Alleles
Heterozygote
4 Citations (Scopus)

Long-term follow-up of females with unbalanced X;Y translocations - Reproductive and nonreproductive consequences

Dobek, W. A., Kim, H. G., Walls, C. A., Chorich, L. P., Tho, S. P., Wang, Z. X., McDonough, P. G. & Layman, L. C., Dec 12 2015, In : Molecular Cytogenetics. 8, 1, 13.

Research output: Contribution to journalArticle

Genes
Gonadoblastoma
Kallmann Syndrome
Eye Abnormalities
Defects
33 Citations (Scopus)

MicroRNA-223 expression is upregulated in insulin resistant human adipose tissue

Chuang, T. Y., Wu, H. L., Chen, C. C., Gamboa, G. M., Layman, L. C., Diamond, M. P., Azziz, R. & Chen, Y-H., Jan 1 2015, In : Journal of Diabetes Research. 2015, 943659.

Research output: Contribution to journalArticle

MicroRNAs
Insulin Resistance
Adipose Tissue
Insulin
Facilitative Glucose Transport Proteins
11 Citations (Scopus)

NELF knockout is associated with impaired pubertal development and subfertility

Quaynor, S. D., Ko, E. K., Chorich, L. P., Sullivan, M. E., Demir, D., Waller, J. L., Kim, H. G., Cameron, R. S. & Layman, L. C., May 5 2015, In : Molecular and Cellular Endocrinology. 407, p. 26-36 11 p.

Research output: Contribution to journalArticle

Luteinizing Hormone
Nose
Infertility
Gonadotropin-Releasing Hormone
Neurons
41 Citations (Scopus)

Novel MED12 gene somatic mutations in women from the Southern United States with symptomatic uterine fibroids

Halder, S. K., Laknaur, A., Miller, J., Layman, L. C., Diamond, M. & Al-Hendy, A., Mar 17 2015, In : Molecular Genetics and Genomics. 290, 2, p. 505-511 7 p.

Research output: Contribution to journalArticle

Mediator Complex
Leiomyoma
Mutation
Genes
Exons
2014
3 Citations (Scopus)

Differential expression of nasal embryonic LHRH factor (NELF) variants in immortalized GnRH neuronal cell lines

Quaynor, S. D., Goldberg, L. Y., Ko, E. K., Stanley, R. K., Demir, D., Kim, H. G., Chorich, L. P., Cameron, R. S. & Layman, L. C., Mar 5 2014, In : Molecular and Cellular Endocrinology. 383, 1, p. 32-37 6 p.

Research output: Contribution to journalArticle

Nose
Gonadotropin-Releasing Hormone
Cells
Cell Line
Nuclear Localization Signals
12 Citations (Scopus)

Familial 46,XY sex reversal without campomelic dysplasia caused by a deletion upstream of the SOX9 gene

Bhagavath, B., Layman, L. C., Ullmann, R., Shen, Y., Ha, K., Rehman, K., Looney, S., McDonough, P. G., Kim, H. G. & Carr, B. R., Aug 5 2014, In : Molecular and Cellular Endocrinology. 393, 1-2, p. 1-7 7 p.

Research output: Contribution to journalArticle

Campomelic Dysplasia
Siblings
Genes
Polymerase chain reaction
DNA
1 Citation (Scopus)

Interstitial microduplication at 2p11.2 in a patient with syndromic intellectual disability: 30-year follow-up

Jun, K. R., Ullmann, R., Khan, S., Layman, L. C. & Kim, H. G., Aug 19 2014, In : Molecular Cytogenetics. 7, 1, 52.

Research output: Contribution to journalArticle

RNA-Directed DNA Polymerase
Chromosomes
Intellectual Disability
Genes
Reverse Transcriptase Polymerase Chain Reaction
2 Citations (Scopus)

Spectrum of genes involved in a unique case of potocki schaffer syndrome with a large chromosome 11 deletion

Romeike, B. F. M., Shen, Y., Nishimoto, H. K., Morton, C. C., Layman, L. C. & Kim, H. G., 2014, In : Clinical Neuropathology. 33, 3, p. 238-244 7 p.

Research output: Contribution to journalLetter

Multiple Hereditary Exostoses
Chromosome Disorders
Chromosome Deletion
Chromosomes, Human, Pair 11
Transcriptome
15 Citations (Scopus)

The expression of the miR-25/93/106b family of micro-RNAs in the adipose tissue of women with polycystic ovary syndrome

Wu, H. L., Heneidi, S., Chuang, T. Y., Diamond, M. P., Layman, L. C., Azziz, R. & Chen, Y. H., Dec 1 2014, In : Journal of Clinical Endocrinology and Metabolism. 99, 12, p. E2754-E2761

Research output: Contribution to journalArticle

Polycystic Ovary Syndrome
MicroRNAs
Insulin Resistance
Adipose Tissue
Insulin
3 Citations (Scopus)

The genetics of Mullerian aplasia

Layman, L. C., Jan 1 2014, In : Expert Review of Endocrinology and Metabolism. 9, 4, p. 411-419 9 p.

Research output: Contribution to journalReview article

Exome
Inborn Genetic Diseases
Gene Dosage
Microarray Analysis
Methylation
14 Citations (Scopus)

The historical Coffin-Lowry syndrome family revisited: Identification of two novel mutations of RPS6KA3 in three male patients

Nishimoto, H. K., Ha, K., Jones, J. R., Dwivedi, A., Cho, H. M., Layman, L. C. & Kim, H. G., Sep 2014, In : American Journal of Medical Genetics, Part A. 164, 9, p. 2172-2179 8 p.

Research output: Contribution to journalArticle

Coffin-Lowry Syndrome
Mutation
Phosphotransferases
Craniofacial Abnormalities
Muscle Hypotonia
2013
20 Citations (Scopus)

Clinical genetic testing for Kallmann syndrome

Layman, L. C., May 1 2013, In : Journal of Clinical Endocrinology and Metabolism. 98, 5, p. 1860-1862 3 p.

Research output: Contribution to journalReview article

Nerve Tissue Proteins
Fibroblast Growth Factor 8
Kallmann Syndrome
Receptor, Fibroblast Growth Factor, Type 1
DNA Helicases
57 Citations (Scopus)

Contribution of copy number variants involving nonsense-mediated mRNA decay pathway genes to neuro-developmental disorders

Nguyen, L. S., Kim, H. G., Rosenfeld, J. A., Shen, Y., Gusella, J. F., Lacassie, Y., Layman, L. C., Shaffer, L. G. & Gécz, J., May 1 2013, In : Human Molecular Genetics. 22, 9, p. 1816-1825 10 p., ddt035.

Research output: Contribution to journalArticle

Nonsense Mediated mRNA Decay
Intellectual Disability
Genes
Mutation
Nonsense Codon
74 Citations (Scopus)

Delayed puberty and estrogen resistance in a woman with estrogen receptor α variant

Quaynor, S. D., Stradtman, E. W., Kim, H. G., Shen, Y., Chorich, L. P., Schreihofer, D. A. & Layman, L. C., Jan 1 2013, In : New England Journal of Medicine. 369, 2, p. 164-171 8 p.

Research output: Contribution to journalArticle

Delayed Puberty
Estrogen Receptors
Estrogens
Mutation
Androgen Receptors

Effects of an estrogen receptor α variant.

Quaynor, S. D., Schreihofer, D. A. & Layman, L. C., Oct 24 2013, In : The New England journal of medicine. 369, 17, 1 p.

Research output: Contribution to journalComment/debate

Delayed Puberty
Estrogen Receptor alpha
Missense Mutation
Estradiol
Estrogens

Genetics of Female Infertility in Humans

Bhagavath, B. & Layman, L. C., Aug 29 2013, Emery and Rimoin's Principles and Practice of Medical Genetics. Elsevier Ltd., p. 1-24 24 p.

Research output: Chapter in Book/Report/Conference proceedingChapter

Female Infertility
15 Citations (Scopus)

Identification of HESX1 mutations in Kallmann syndrome

Newbern, K., Natrajan, N., Kim, H. G., Chorich, L. P., Halvorson, L. M., Cameron, R. S. & Layman, L. C., Jun 1 2013, In : Fertility and sterility. 99, 7, p. 1831-1837 7 p.

Research output: Contribution to journalArticle

Kallmann Syndrome
Mutation
Missense Mutation
Phenotype
DNA
98 Citations (Scopus)

Liquid chromatography-tandem mass spectrometry analysis of human adrenal vein 19-carbon steroids before and after ACTH stimulation

Rege, J., Nakamura, Y., Satoh, F., Morimoto, R., Kennedy, M. R., Layman, L. C., Honma, S., Sasano, H. & Rainey, W. E., Mar 1 2013, In : Journal of Clinical Endocrinology and Metabolism. 98, 3, p. 1182-1188 7 p.

Research output: Contribution to journalArticle

Liquid chromatography
Tandem Mass Spectrometry
Liquid Chromatography
Adrenocorticotropic Hormone
Androgens
111 Citations (Scopus)

Mirna-93 inhibits glut4 and is overexpressed in adipose tissue of polycystic ovary syndrome patients and women with insulin resistance

Chen, Y. H., Heneidi, S., Lee, J. M., Layman, L. C., Stepp, D. W., Gamboa, G. M., Chen, B. S., Chazenbalk, G. & Azziz, R., Jul 2013, In : Diabetes. 62, 7, p. 2278-2286 9 p.

Research output: Contribution to journalArticle

Polycystic Ovary Syndrome
MicroRNAs
Insulin Resistance
Adipose Tissue
Insulin

The authors reply

Quaynor, S. D., Schreihofer, D. A. & Layman, L. C., Oct 29 2013, In : New England Journal of Medicine. 369, 17, 1 p.

Research output: Contribution to journalLetter

27 Citations (Scopus)

The genetic basis of female reproductive disorders: Etiology and clinical testing

Layman, L. C., May 6 2013, In : Molecular and Cellular Endocrinology. 370, 1-2, p. 138-148 11 p.

Research output: Contribution to journalReview article

Hypogonadism
Genes
Mutation
Ovarian Hyperstimulation Syndrome
Testing
40 Citations (Scopus)

The molecular basis of impaired follicle-stimulating hormone action: Evidence from human mutations and mouse models

Siegel, E. T., Kim, H. G., Nishimoto, H. K. & Layman, L. C., Mar 1 2013, In : Reproductive Sciences. 20, 3, p. 211-233 23 p.

Research output: Contribution to journalReview article

Follicle Stimulating Hormone
Mutation
Spermatogenesis
Ligands
Ovarian Hyperstimulation Syndrome
2012

Disorders of the hypothalamic-pituitary-gonadal axis

Layman, L. C., Dec 1 2012, Handbook of Neuroendocrinology. Elsevier Inc., p. 659-683 25 p.

Research output: Chapter in Book/Report/Conference proceedingChapter

Pituitary Diseases
Hypogonadism
Puberty
Gonadal Disorders
Delayed Puberty
60 Citations (Scopus)

Genetic considerations in the patient with Turner syndrome - 45,X with or without mosaicism

Zhong, Q. & Layman, L. C., Jan 1 2012, In : Fertility and sterility. 98, 4, p. 775-779 5 p.

Research output: Contribution to journalReview article

Turner Syndrome
Mosaicism
Cell Line
X Chromosome
Karyotype
41 Citations (Scopus)

Role of ART in imprinting disorders

Eroglu, A. & Layman, L. C., May 2 2012, In : Seminars in Reproductive Medicine. 30, 2, p. 92-104 13 p.

Research output: Contribution to journalArticle

Assisted Reproductive Techniques
Beckwith-Wiedemann Syndrome
Angelman Syndrome
Retinoblastoma
Infertility
29 Citations (Scopus)

Translocations disrupting PHF21A in the Potocki-Shaffer-syndrome region are associated with intellectual disability and craniofacial anomalies

Kim, H. G., Kim, H. T., Leach, N. T., Lan, F., Ullmann, R., Silahtaroglu, A., Kurth, I., Nowka, A., Seong, I. S., Shen, Y., Talkowski, M. E., Ruderfer, D., Lee, J. H., Glotzbach, C., Ha, K., Kjaergaard, S., Levin, A. V., Romeike, B. F., Kleefstra, T., Bartsch, O. & 15 others, Elsea, S. H., Jabs, E. W., MacDonald, M. E., Harris, D. J., Quade, B. J., Ropers, H. H., Shaffer, L. G., Kutsche, K., Layman, L. C., Tommerup, N., Kalscheuer, V. M., Shi, Y., Morton, C. C., Kim, C. H. & Gusella, J. F., Jul 13 2012, In : American journal of human genetics. 91, 1, p. 56-72 17 p.

Research output: Contribution to journalArticle

Intellectual Disability
Genes
Multiple Hereditary Exostoses
Haploinsufficiency
Lysine
2011
41 Citations (Scopus)

Nasal embryonic LHRH factor (NELF) mutations in patients with normosmic hypogonadotropic hypogonadism and Kallmann syndrome

Xu, N., Kim, H. G., Bhagavath, B., Cho, S. G., Lee, J. H., Ha, K., Meliciani, I., Wenzel, W., Podolsky, R. H., Chorich, L. P., Stackhouse, K. A., Grove, A. M. H., Odom, L. N., Ozata, M., Bick, D. P., Sherins, R. J., Kim, S. H., Cameron, R. S. & Layman, L. C., Apr 2011, In : Fertility and sterility. 95, 5, p. 1613-1620.e7

Research output: Contribution to journalArticle

Kallmann Syndrome
Hypogonadism
Nose
Gonadotropin-Releasing Hormone
Mutation
53 Citations (Scopus)

The prevalence of digenic mutations in patients with normosmic hypogonadotropic hypogonadism and Kallmann syndrome

Quaynor, S. D., Kim, H. G., Cappello, E. M., Williams, T., Chorich, L. P., Bick, D. P., Sherins, R. J. & Layman, L. C., Jan 1 2011, In : Fertility and sterility. 96, 6

Research output: Contribution to journalArticle

Kallmann Syndrome
Hypogonadism
Mutation
Genes
Idiopathic Hypogonadotropic Hypogonadism
28 Citations (Scopus)
Kallmann Syndrome
CHARGE Syndrome
DNA-Binding Proteins
Genes
Mutation
2010
3 Citations (Scopus)

Genetic Diagnosis of Hypogonadotropic Hypogonadism and Kallmann Syndrome

Layman, L. C., Dec 1 2010, Genetic Diagnosis of Endocrine Disorders. Elsevier Inc., p. 217-225 9 p.

Research output: Chapter in Book/Report/Conference proceedingChapter

Kallmann Syndrome
Hypogonadism
Delayed Puberty
Genes
Mutation
18 Citations (Scopus)

Genotype and phenotype of patients with gonadotropin-releasing hormone receptor mutations

Kim, H. G., Pedersen-White, J., Bhagavath, B. & Layman, L. C., Apr 8 2010, In : Frontiers of Hormone Research. 39, p. 94-110 17 p.

Research output: Contribution to journalArticle

LHRH Receptors
Genes
Genotype
Phenotype
Mutation
4 Citations (Scopus)
Hematocolpos
Vagina
Mucous Membrane
Catheters
Pressure
15 Citations (Scopus)

NELF is a nuclear protein involved in hypothalamic GnRH neuronal migration

Xu, N., Bhagavath, B., Kim, H. G., Halvorson, L., Podolsky, R. S., Chorich, L. P., Prasad, P. D., Xiong, W., Cameron, R. S. & Layman, L. C., May 5 2010, In : Molecular and Cellular Endocrinology. 319, 1-2, p. 47-55 9 p.

Research output: Contribution to journalArticle

Nuclear Proteins
Nose
Gonadotropin-Releasing Hormone
Neurons
Nuclear Localization Signals