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Regulatory variant in FZD6 gene contributes to nonsyndromic cleft lip and palate in an African-American family.

Molecular genetics & genomic medicine

Cvjetkovic N, Maili L, Weymouth KS, Hashmi SS, Mulliken JB, Topczewski J, Letra A, Yuan Q, Blanton SH, Swindell EC, Hecht JT.
PMID: 26436110
Mol Genet Genomic Med. 2015 Sep;3(5):440-51. doi: 10.1002/mgg3.155. Epub 2015 May 07.

Nonsyndromic cleft lip with or without cleft palate (NSCLP) is a common birth defect affecting 135,000 newborns worldwide each year. While a multifactorial etiology has been suggested as the cause, despite decades of research, the genetic underpinnings of NSCLP...

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Cvjetkovic N, Maili L, Weymouth KS, et al. Regulatory variant in FZD6 gene contributes to nonsyndromic cleft lip and palate in an African-American family. Mol Genet Genomic Med. 2015;3(5):440-51doi: 10.1002/mgg3.155.
Cvjetkovic, N., Maili, L., Weymouth, K. S., Hashmi, S. S., Mulliken, J. B., Topczewski, J., Letra, A., Yuan, Q., Blanton, S. H., Swindell, E. C., & Hecht, J. T. (2015). Regulatory variant in FZD6 gene contributes to nonsyndromic cleft lip and palate in an African-American family. Molecular genetics & genomic medicine, 3(5), 440-51. https://doi.org/10.1002/mgg3.155
Cvjetkovic, Nevena, et al. "Regulatory variant in FZD6 gene contributes to nonsyndromic cleft lip and palate in an African-American family." Molecular genetics & genomic medicine vol. 3,5 (2015): 440-51. doi: https://doi.org/10.1002/mgg3.155
Cvjetkovic N, Maili L, Weymouth KS, Hashmi SS, Mulliken JB, Topczewski J, Letra A, Yuan Q, Blanton SH, Swindell EC, Hecht JT. Regulatory variant in FZD6 gene contributes to nonsyndromic cleft lip and palate in an African-American family. Mol Genet Genomic Med. 2015 Sep;3(5):440-51. doi: 10.1002/mgg3.155. Epub 2015 May 07. PMID: 26436110; PMCID: PMC4585452.
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The evolution of comparative genomics.

Molecular genetics & genomic medicine

Mullikin JC.
PMID: 25333060
Mol Genet Genomic Med. 2014 Sep;2(5):363-8. doi: 10.1002/mgg3.112.

No abstract available.

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Mullikin JC. The evolution of comparative genomics. Mol Genet Genomic Med. 2014;2(5):363-8doi: 10.1002/mgg3.112.
Mullikin, J. C. (2014). The evolution of comparative genomics. Molecular genetics & genomic medicine, 2(5), 363-8. https://doi.org/10.1002/mgg3.112
Mullikin, James C. "The evolution of comparative genomics." Molecular genetics & genomic medicine vol. 2,5 (2014): 363-8. doi: https://doi.org/10.1002/mgg3.112
Mullikin JC. The evolution of comparative genomics. Mol Genet Genomic Med. 2014 Sep;2(5):363-8. doi: 10.1002/mgg3.112. PMID: 25333060; PMCID: PMC4190870.
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Implicit learning modulates attention capture: evidence from an item-specific proportion congruency manipulation.

Frontiers in psychology

Thomson DR, Willoughby K, Milliken B.
PMID: 24926280
Front Psychol. 2014 Jun 04;5:551. doi: 10.3389/fpsyg.2014.00551. eCollection 2014.

A host of research has now shown that our explicit goals and intentions can, in large part, overcome the capture of visual attention by objects that differ from their surroundings in terms of size, shape, or color. Surprisingly however,...

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Thomson DR, Willoughby K, Milliken B. Implicit learning modulates attention capture: evidence from an item-specific proportion congruency manipulation. Front Psychol. 2014;5:551doi: 10.3389/fpsyg.2014.00551.
Thomson, D. R., Willoughby, K., & Milliken, B. (2014). Implicit learning modulates attention capture: evidence from an item-specific proportion congruency manipulation. Frontiers in psychology, 5551. https://doi.org/10.3389/fpsyg.2014.00551
Thomson, David R, et al. "Implicit learning modulates attention capture: evidence from an item-specific proportion congruency manipulation." Frontiers in psychology vol. 5 (2014): 551. doi: https://doi.org/10.3389/fpsyg.2014.00551
Thomson DR, Willoughby K, Milliken B. Implicit learning modulates attention capture: evidence from an item-specific proportion congruency manipulation. Front Psychol. 2014 Jun 04;5:551. doi: 10.3389/fpsyg.2014.00551. eCollection 2014. PMID: 24926280; PMCID: PMC4044972.
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Molecular basis of vascular anomalies.

Trends in cardiovascular medicine

Vikkula M, Boon LM, Mulliken JB, Olsen BR.
PMID: 14987552
Trends Cardiovasc Med. 1998 Oct;8(7):281-92. doi: 10.1016/s1050-1738(98)00024-3.

Vascular anomalies comprise a heterogeneous group of disorders that are divided into tumors (hemangiomas) and malformations. Recent advances in biomedical research provide insights into the molecular basis of these disorders and a deeper understanding of vascular morphogenesis. In the...

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Vikkula M, Boon LM, Mulliken JB, et al. Molecular basis of vascular anomalies. Trends Cardiovasc Med. 1998;8(7):281-92doi: 10.1016/s1050-1738(98)00024-3.
Vikkula, M., Boon, L. M., Mulliken, J. B., & Olsen, B. R. (1998). Molecular basis of vascular anomalies. Trends in cardiovascular medicine, 8(7), 281-92. https://doi.org/10.1016/s1050-1738(98)00024-3
Vikkula, M, et al. "Molecular basis of vascular anomalies." Trends in cardiovascular medicine vol. 8,7 (1998): 281-92. doi: https://doi.org/10.1016/s1050-1738(98)00024-3
Vikkula M, Boon LM, Mulliken JB, Olsen BR. Molecular basis of vascular anomalies. Trends Cardiovasc Med. 1998 Oct;8(7):281-92. doi: 10.1016/s1050-1738(98)00024-3. PMID: 14987552.
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THE PEACE RESOLUTION OF SCIENTIFIC WORKERS.

Science (New York, N.Y.)

Mulliken RS.
PMID: 17777622
Science. 1940 May 31;91(2370):525-6. doi: 10.1126/science.91.2370.525-b.

No abstract available.

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Mulliken RS. THE PEACE RESOLUTION OF SCIENTIFIC WORKERS. Science. 1940;91(2370):525-6doi: 10.1126/science.91.2370.525-b.
Mulliken, R. S. (1940). THE PEACE RESOLUTION OF SCIENTIFIC WORKERS. Science (New York, N.Y.), 91(2370), 525-6. https://doi.org/10.1126/science.91.2370.525-b
Mulliken, R S. "THE PEACE RESOLUTION OF SCIENTIFIC WORKERS." Science (New York, N.Y.) vol. 91,2370 (1940): 525-6. doi: https://doi.org/10.1126/science.91.2370.525-b
Mulliken RS. THE PEACE RESOLUTION OF SCIENTIFIC WORKERS. Science. 1940 May 31;91(2370):525-6. doi: 10.1126/science.91.2370.525-b. PMID: 17777622.
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Systematic Relations between Electronic Structure and Band-Spectrum Structure in Diatomic Molecules: I.

Proceedings of the National Academy of Sciences of the United States of America

Mulliken RS.
PMID: 16576966
Proc Natl Acad Sci U S A. 1926 Mar;12(3):144-51. doi: 10.1073/pnas.12.3.144.

No abstract available.

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Mulliken RS. Systematic Relations between Electronic Structure and Band-Spectrum Structure in Diatomic Molecules: I. Proc Natl Acad Sci U S A. 1926;12(3):144-51doi: 10.1073/pnas.12.3.144.
Mulliken, R. S. (1926). Systematic Relations between Electronic Structure and Band-Spectrum Structure in Diatomic Molecules: I. Proceedings of the National Academy of Sciences of the United States of America, 12(3), 144-51. https://doi.org/10.1073/pnas.12.3.144
Mulliken, R S. "Systematic Relations between Electronic Structure and Band-Spectrum Structure in Diatomic Molecules: I." Proceedings of the National Academy of Sciences of the United States of America vol. 12,3 (1926): 144-51. doi: https://doi.org/10.1073/pnas.12.3.144
Mulliken RS. Systematic Relations between Electronic Structure and Band-Spectrum Structure in Diatomic Molecules: I. Proc Natl Acad Sci U S A. 1926 Mar;12(3):144-51. doi: 10.1073/pnas.12.3.144. PMID: 16576966; PMCID: PMC1084475.
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Mutations in the VEGFR3 signaling pathway explain 36% of familial lymphedema.

Molecular syndromology

Mendola A, Schlögel MJ, Ghalamkarpour A, Irrthum A, Nguyen HL, Fastré E, Bygum A, van der Vleuten C, Fagerberg C, Baselga E, Quere I, Mulliken JB, Boon LM, Brouillard P, Vikkula M.
PMID: 24167460
Mol Syndromol. 2013 Sep;4(6):257-66. doi: 10.1159/000354097. Epub 2013 Aug 21.

Lymphedema is caused by dysfunction of lymphatic vessels, leading to disabling swelling that occurs mostly on the extremities. Lymphedema can be either primary (congenital) or secondary (acquired). Familial primary lymphedema commonly segregates in an autosomal dominant or recessive manner....

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Mendola A, Schlögel MJ, Ghalamkarpour A, et al. Mutations in the VEGFR3 signaling pathway explain 36% of familial lymphedema. Mol Syndromol. 2013;4(6):257-66doi: 10.1159/000354097.
Mendola, A., Schlögel, M. J., Ghalamkarpour, A., Irrthum, A., Nguyen, H. L., Fastré, E., Bygum, A., van der Vleuten, C., Fagerberg, C., Baselga, E., Quere, I., Mulliken, J. B., Boon, L. M., Brouillard, P., Vikkula, M. (2013). Mutations in the VEGFR3 signaling pathway explain 36% of familial lymphedema. Molecular syndromology, 4(6), 257-66. https://doi.org/10.1159/000354097
Mendola, A, et al. "Mutations in the VEGFR3 signaling pathway explain 36% of familial lymphedema." Molecular syndromology vol. 4,6 (2013): 257-66. doi: https://doi.org/10.1159/000354097
Mendola A, Schlögel MJ, Ghalamkarpour A, Irrthum A, Nguyen HL, Fastré E, Bygum A, van der Vleuten C, Fagerberg C, Baselga E, Quere I, Mulliken JB, Boon LM, Brouillard P, Vikkula M. Mutations in the VEGFR3 signaling pathway explain 36% of familial lymphedema. Mol Syndromol. 2013 Sep;4(6):257-66. doi: 10.1159/000354097. Epub 2013 Aug 21. PMID: 24167460; PMCID: PMC3776465.
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Genomic insights into Wnt signaling in an early diverging metazoan, the ctenophore Mnemiopsis leidyi.

EvoDevo

Pang K, Ryan JF, Mullikin JC, Baxevanis AD, Martindale MQ.
PMID: 20920349
Evodevo. 2010 Oct 04;1(1):10. doi: 10.1186/2041-9139-1-10.

BACKGROUND: Intercellular signaling pathways are a fundamental component of the integrating cellular behavior required for the evolution of multicellularity. The genomes of three of the four early branching animal phyla (Cnidaria, Placozoa and Porifera) have been surveyed for key...

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Pang K, Ryan JF, et al. Genomic insights into Wnt signaling in an early diverging metazoan, the ctenophore Mnemiopsis leidyi. Evodevo. 2010;1(1):10doi: 10.1186/2041-9139-1-10.
Pang, K., Ryan, J. F., Mullikin, J. C., Baxevanis, A. D., & Martindale, M. Q. (2010). Genomic insights into Wnt signaling in an early diverging metazoan, the ctenophore Mnemiopsis leidyi. EvoDevo, 1(1), 10. https://doi.org/10.1186/2041-9139-1-10
Pang, Kevin, et al. "Genomic insights into Wnt signaling in an early diverging metazoan, the ctenophore Mnemiopsis leidyi." EvoDevo vol. 1,1 (2010): 10. doi: https://doi.org/10.1186/2041-9139-1-10
Pang K, Ryan JF, Mullikin JC, Baxevanis AD, Martindale MQ. Genomic insights into Wnt signaling in an early diverging metazoan, the ctenophore Mnemiopsis leidyi. Evodevo. 2010 Oct 04;1(1):10. doi: 10.1186/2041-9139-1-10. PMID: 20920349; PMCID: PMC2959043.
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Gene-Specific Substitution Profiles Describe the Types and Frequencies of Amino Acid Changes during Antibody Somatic Hypermutation.

Frontiers in immunology

Sheng Z, Schramm CA, Kong R, Mullikin JC, Mascola JR, Kwong PD, Shapiro L.
PMID: 28539926
Front Immunol. 2017 May 10;8:537. doi: 10.3389/fimmu.2017.00537. eCollection 2017.

Somatic hypermutation (SHM) plays a critical role in the maturation of antibodies, optimizing recognition initiated by recombination of V(D)J genes. Previous studies have shown that the propensity to mutate is modulated by the context of surrounding nucleotides and that...

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Sheng Z, Schramm CA, Kong R. Gene-Specific Substitution Profiles Describe the Types and Frequencies of Amino Acid Changes during Antibody Somatic Hypermutation. Front Immunol. 2017;8:537doi: 10.3389/fimmu.2017.00537.
Sheng, Z., Schramm, C. A., Kong, R., Mullikin, J. C., Mascola, J. R., Kwong, P. D., & Shapiro, L. (2017). Gene-Specific Substitution Profiles Describe the Types and Frequencies of Amino Acid Changes during Antibody Somatic Hypermutation. Frontiers in immunology, 8537. https://doi.org/10.3389/fimmu.2017.00537
Sheng, Zizhang, et al. "Gene-Specific Substitution Profiles Describe the Types and Frequencies of Amino Acid Changes during Antibody Somatic Hypermutation." Frontiers in immunology vol. 8 (2017): 537. doi: https://doi.org/10.3389/fimmu.2017.00537
Sheng Z, Schramm CA, Kong R, Mullikin JC, Mascola JR, Kwong PD, Shapiro L. Gene-Specific Substitution Profiles Describe the Types and Frequencies of Amino Acid Changes during Antibody Somatic Hypermutation. Front Immunol. 2017 May 10;8:537. doi: 10.3389/fimmu.2017.00537. eCollection 2017. PMID: 28539926; PMCID: PMC5424261.
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Exome sequencing of family trios from the National Birth Defects Prevention Study: Tapping into a rich resource of genetic and environmental data.

Birth defects research

Jenkins MM, Almli LM, Pangilinan F, Chong JX, Blue EE, Shapira SK, White J, McGoldrick D, Smith JD, Mullikin JC, Bean CJ, Nembhard WN, Lou XY, Shaw GM, Romitti PA, Keppler-Noreuil K, Yazdy MM, Kay DM, Carter TC, Olshan AF, Moore KJ, Nascone-Yoder N, Finnell RH, Lupo PJ, Feldkamp ML, Nickerson DA, Bamshad MJ, Brody LC, Reefhuis J.
PMID: 31328417
Birth Defects Res. 2019 Dec 01;111(20):1618-1632. doi: 10.1002/bdr2.1554. Epub 2019 Jul 21.

BACKGROUND: The National Birth Defects Prevention Study (NBDPS) is a multisite, population-based, case-control study of genetic and nongenetic risk factors for major structural birth defects. Eligible women had a pregnancy affected by a birth defect or a liveborn child...

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Jenkins MM, Almli LM, Pangilinan F, et al. Exome sequencing of family trios from the National Birth Defects Prevention Study: Tapping into a rich resource of genetic and environmental data. Birth Defects Res. 2019;111(20):1618-1632doi: 10.1002/bdr2.1554.
Jenkins, M. M., Almli, L. M., Pangilinan, F., Chong, J. X., Blue, E. E., Shapira, S. K., White, J., McGoldrick, D., Smith, J. D., Mullikin, J. C., Bean, C. J., Nembhard, W. N., Lou, X. Y., Shaw, G. M., Romitti, P. A., Keppler-Noreuil, K., Yazdy, M. M., Kay, D. M., Carter, T. C., Olshan, A. F., Moore, K. J., Nascone-Yoder, N., Finnell, R. H., Lupo, P. J., Feldkamp, M. L., Nickerson, D. A., Bamshad, M. J., Brody, L. C., Reefhuis, J. (2019). Exome sequencing of family trios from the National Birth Defects Prevention Study: Tapping into a rich resource of genetic and environmental data. Birth defects research, 111(20), 1618-1632. https://doi.org/10.1002/bdr2.1554
Jenkins, Mary M, et al. "Exome sequencing of family trios from the National Birth Defects Prevention Study: Tapping into a rich resource of genetic and environmental data." Birth defects research vol. 111,20 (2019): 1618-1632. doi: https://doi.org/10.1002/bdr2.1554
Jenkins MM, Almli LM, Pangilinan F, Chong JX, Blue EE, Shapira SK, White J, McGoldrick D, Smith JD, Mullikin JC, Bean CJ, Nembhard WN, Lou XY, Shaw GM, Romitti PA, Keppler-Noreuil K, Yazdy MM, Kay DM, Carter TC, Olshan AF, Moore KJ, Nascone-Yoder N, Finnell RH, Lupo PJ, Feldkamp ML, Nickerson DA, Bamshad MJ, Brody LC, Reefhuis J. Exome sequencing of family trios from the National Birth Defects Prevention Study: Tapping into a rich resource of genetic and environmental data. Birth Defects Res. 2019 Dec 01;111(20):1618-1632. doi: 10.1002/bdr2.1554. Epub 2019 Jul 21. PMID: 31328417; PMCID: PMC6889076.
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Verrucous Venous Malformation-Subcutaneous Variant.

The American Journal of dermatopathology

Schmidt BAR, El Zein S, Cuoto J, Al-Ibraheemi A, Liang MG, Paltiel HJ, Anderson ME, Labow BI, Upton J, Fishman SJ, Mulliken JB, Greene AK, Warman ML, Kozakewich H.
PMID: 33899768
Am J Dermatopathol. 2021 Dec 01;43(12):e181-e184. doi: 10.1097/DAD.0000000000001963.

BACKGROUND: Verrucous venous malformation (VVM), previously called "verrucous hemangioma," typically involves the dermis and the subcutaneous fat. We have encountered patients with VVM confined to the hypodermis.MATERIALS AND METHODS: During a nearly 20-year period, 13 patients, aged 2-17 years,...

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Schmidt BAR, El Zein S, Cuoto J, et al. Verrucous Venous Malformation-Subcutaneous Variant. Am J Dermatopathol. 2021;43(12):e181-e184doi: 10.1097/DAD.0000000000001963.
Schmidt, B. A. R., El Zein, S., Cuoto, J., Al-Ibraheemi, A., Liang, M. G., Paltiel, H. J., Anderson, M. E., Labow, B. I., Upton, J., Fishman, S. J., Mulliken, J. B., Greene, A. K., Warman, M. L., & Kozakewich, H. (2021). Verrucous Venous Malformation-Subcutaneous Variant. The American Journal of dermatopathology, 43(12), e181-e184. https://doi.org/10.1097/DAD.0000000000001963
Schmidt, Birgitta A R, et al. "Verrucous Venous Malformation-Subcutaneous Variant." The American Journal of dermatopathology vol. 43,12 (2021): e181-e184. doi: https://doi.org/10.1097/DAD.0000000000001963
Schmidt BAR, El Zein S, Cuoto J, Al-Ibraheemi A, Liang MG, Paltiel HJ, Anderson ME, Labow BI, Upton J, Fishman SJ, Mulliken JB, Greene AK, Warman ML, Kozakewich H. Verrucous Venous Malformation-Subcutaneous Variant. Am J Dermatopathol. 2021 Dec 01;43(12):e181-e184. doi: 10.1097/DAD.0000000000001963. PMID: 33899768.
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Congenital Disseminated Pyogenic Granuloma: Characterization of an Aggressive Multisystemic Disorder.

The Journal of pediatrics

Alomari MH, Kozakewich HPW, Kerr CL, Uller W, Davis SL, Chaudry G, Liang MG, Orbach DB, Mulliken JB, Greene AK, Afshar S, Fishman SJ, Taghinia AH, Al-Ibraheemi A, Alomari AI.
PMID: 32622671
J Pediatr. 2020 Nov;226:157-166. doi: 10.1016/j.jpeds.2020.06.079. Epub 2020 Jul 02.

OBJECTIVE: To describe the clinical, radiologic, and histopathologic features of "congenital disseminated pyogenic granuloma" involving various organs with high morbidity related to cerebral hemorrhagic involvement.STUDY DESIGN: We searched the database of the Vascular Anomalies Center at Boston Children's Hospital...

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Alomari MH, Kozakewich HPW, Kerr CL, et al. Congenital Disseminated Pyogenic Granuloma: Characterization of an Aggressive Multisystemic Disorder. J Pediatr. 2020;226:157-166doi: 10.1016/j.jpeds.2020.06.079.
Alomari, M. H., Kozakewich, H. P. W., Kerr, C. L., Uller, W., Davis, S. L., Chaudry, G., Liang, M. G., Orbach, D. B., Mulliken, J. B., Greene, A. K., Afshar, S., Fishman, S. J., Taghinia, A. H., Al-Ibraheemi, A., & Alomari, A. I. (2020). Congenital Disseminated Pyogenic Granuloma: Characterization of an Aggressive Multisystemic Disorder. The Journal of pediatrics, 226157-166. https://doi.org/10.1016/j.jpeds.2020.06.079
Alomari, Mohammed H, et al. "Congenital Disseminated Pyogenic Granuloma: Characterization of an Aggressive Multisystemic Disorder." The Journal of pediatrics vol. 226 (2020): 157-166. doi: https://doi.org/10.1016/j.jpeds.2020.06.079
Alomari MH, Kozakewich HPW, Kerr CL, Uller W, Davis SL, Chaudry G, Liang MG, Orbach DB, Mulliken JB, Greene AK, Afshar S, Fishman SJ, Taghinia AH, Al-Ibraheemi A, Alomari AI. Congenital Disseminated Pyogenic Granuloma: Characterization of an Aggressive Multisystemic Disorder. J Pediatr. 2020 Nov;226:157-166. doi: 10.1016/j.jpeds.2020.06.079. Epub 2020 Jul 02. PMID: 32622671.
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