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[Shaping of the length, width and cranial index in human fetuses].

Folia morphologica

Malinowski A.
PMID: 5313172
Folia Morphol (Warsz). 1970;29(4):495-501.

No abstract available.

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Malinowski A. Kształtowanie sie długości, szerokości oraz wskaźnika głowy u płodów ludzkich. [Shaping of the length, width and cranial index in human fetuses]. Folia Morphol (Warsz). 1970;29(4):495-501
Malinowski, A. (1970). Kształtowanie sie długości, szerokości oraz wskaźnika głowy u płodów ludzkich. [Shaping of the length, width and cranial index in human fetuses]. Folia morphologica, 29(4), 495-501.
Malinowski, A. "Kształtowanie sie długości, szerokości oraz wskaźnika głowy u płodów ludzkich." [Shaping of the length, width and cranial index in human fetuses]. Folia morphologica vol. 29,4 (1970): 495-501.
Malinowski A. Kształtowanie sie długości, szerokości oraz wskaźnika głowy u płodów ludzkich. [Shaping of the length, width and cranial index in human fetuses]. Folia Morphol (Warsz). 1970;29(4):495-501. Polish. PMID: 5313172.
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Immunohistochemical assays incorporating SP142 and 22C3 monoclonal antibodies for detection of PD-L1 expression in NSCLC patients with known status of .

Oncotarget

Krawczyk P, Jarosz B, Kucharczyk T, Grenda A, Reszka K, Pankowski J, Wojas-Krawczyk K, Nicoś M, Szumiło J, Trojanowski T, Milanowski J.
PMID: 28969070
Oncotarget. 2017 Jul 31;8(38):64283-64293. doi: 10.18632/oncotarget.19724. eCollection 2017 Sep 08.

Different immunohistochemical (IHC) assays were approved for PD-L1 expression examination on tumor cells in qualification to immune-checkpoint inhibitors therapy in NSCLC patients. These assays have some similarities, but also very serious differences. We assessed 2 IHC tests for PD-L1...

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Krawczyk P, Jarosz B, Kucharczyk T, et al. Immunohistochemical assays incorporating SP142 and 22C3 monoclonal antibodies for detection of PD-L1 expression in NSCLC patients with known status of . Oncotarget. 2017;8(38):64283-64293doi: 10.18632/oncotarget.19724.
Krawczyk, P., Jarosz, B., Kucharczyk, T., Grenda, A., Reszka, K., Pankowski, J., Wojas-Krawczyk, K., Nicoś, M., Szumiło, J., Trojanowski, T., & Milanowski, J. (2017). Immunohistochemical assays incorporating SP142 and 22C3 monoclonal antibodies for detection of PD-L1 expression in NSCLC patients with known status of . Oncotarget, 8(38), 64283-64293. https://doi.org/10.18632/oncotarget.19724
Krawczyk, Paweł, et al. "Immunohistochemical assays incorporating SP142 and 22C3 monoclonal antibodies for detection of PD-L1 expression in NSCLC patients with known status of ." Oncotarget vol. 8,38 (2017): 64283-64293. doi: https://doi.org/10.18632/oncotarget.19724
Krawczyk P, Jarosz B, Kucharczyk T, Grenda A, Reszka K, Pankowski J, Wojas-Krawczyk K, Nicoś M, Szumiło J, Trojanowski T, Milanowski J. Immunohistochemical assays incorporating SP142 and 22C3 monoclonal antibodies for detection of PD-L1 expression in NSCLC patients with known status of . Oncotarget. 2017 Jul 31;8(38):64283-64293. doi: 10.18632/oncotarget.19724. eCollection 2017 Sep 08. PMID: 28969070; PMCID: PMC5610002.
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PHYLOGENY AND SYSTEMATICS OF EUGLENA (EUGLENACEAE) SPECIES WITH AXIAL, STELLATE CHLOROPLASTS BASED ON MORPHOLOGICAL AND MOLECULAR DATA-NEW TAXA, EMENDED DIAGNOSES, AND EPITYPIFICATIONS(1).

Journal of phycology

Kosmala S, Karnkowska-Ishikawa A, Milanowski R, Kwiatowski J, Zakryś B.
PMID: 27033825
J Phycol. 2009 Apr;45(2):464-81. doi: 10.1111/j.1529-8817.2009.00653.x.

Morphological and molecular studies, as well as original literature reexamination, necessitate establishment of five Euglena species with a single axial, stellate chloroplast [Euglena viridis (O. F. Müller) Ehrenberg 1830, Euglena pseudoviridis Chadefaud 1937, Euglena stellata Mainx 1926, Euglena pseudostellata...

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Kosmala S, Karnkowska-Ishikawa A, Milanowski R, et al. PHYLOGENY AND SYSTEMATICS OF EUGLENA (EUGLENACEAE) SPECIES WITH AXIAL, STELLATE CHLOROPLASTS BASED ON MORPHOLOGICAL AND MOLECULAR DATA-NEW TAXA, EMENDED DIAGNOSES, AND EPITYPIFICATIONS(1). J Phycol. 2009;45(2):464-81doi: 10.1111/j.1529-8817.2009.00653.x.
Kosmala, S., Karnkowska-Ishikawa, A., Milanowski, R., Kwiatowski, J., & Zakryś, B. (2009). PHYLOGENY AND SYSTEMATICS OF EUGLENA (EUGLENACEAE) SPECIES WITH AXIAL, STELLATE CHLOROPLASTS BASED ON MORPHOLOGICAL AND MOLECULAR DATA-NEW TAXA, EMENDED DIAGNOSES, AND EPITYPIFICATIONS(1). Journal of phycology, 45(2), 464-81. https://doi.org/10.1111/j.1529-8817.2009.00653.x
Kosmala, Sylwia, et al. "PHYLOGENY AND SYSTEMATICS OF EUGLENA (EUGLENACEAE) SPECIES WITH AXIAL, STELLATE CHLOROPLASTS BASED ON MORPHOLOGICAL AND MOLECULAR DATA-NEW TAXA, EMENDED DIAGNOSES, AND EPITYPIFICATIONS(1)." Journal of phycology vol. 45,2 (2009): 464-81. doi: https://doi.org/10.1111/j.1529-8817.2009.00653.x
Kosmala S, Karnkowska-Ishikawa A, Milanowski R, Kwiatowski J, Zakryś B. PHYLOGENY AND SYSTEMATICS OF EUGLENA (EUGLENACEAE) SPECIES WITH AXIAL, STELLATE CHLOROPLASTS BASED ON MORPHOLOGICAL AND MOLECULAR DATA-NEW TAXA, EMENDED DIAGNOSES, AND EPITYPIFICATIONS(1). J Phycol. 2009 Apr;45(2):464-81. doi: 10.1111/j.1529-8817.2009.00653.x. PMID: 27033825.
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Ring lithiation of 1,8-bis(dimethylamino)naphthalene: another side of the 'proton sponge coin'.

Dalton transactions (Cambridge, England : 2003)

Antonov AS, Pozharskii AF, Ozeryanskii VA, Filarowski A, Suponitsky KY, Tolstoy PM, Vovk MA.
PMID: 26399216
Dalton Trans. 2015 Oct 28;44(40):17756-66. doi: 10.1039/c5dt02482j. Epub 2015 Sep 23.

It has been found that 1,8-bis(dimethylamino)naphthalene (DMAN), unlike N,N-dimethylaniline, undergoes ring metallation in the n-BuLi-TMEDA-Et2O system with a low selectivity and in poor total yields. The situation is significantly improved in the t-BuLi-TMEDA-n-hexane system when 3- and 4-lithium derivatives...

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Antonov AS, Pozharskii AF, Ozeryanskii VA, et al. Ring lithiation of 1,8-bis(dimethylamino)naphthalene: another side of the 'proton sponge coin'. Dalton Trans. 2015;44(40):17756-66doi: 10.1039/c5dt02482j.
Antonov, A. S., Pozharskii, A. F., Ozeryanskii, V. A., Filarowski, A., Suponitsky, K. Y., Tolstoy, P. M., & Vovk, M. A. (2015). Ring lithiation of 1,8-bis(dimethylamino)naphthalene: another side of the 'proton sponge coin'. Dalton transactions (Cambridge, England : 2003), 44(40), 17756-66. https://doi.org/10.1039/c5dt02482j
Antonov, Alexander S, et al. "Ring lithiation of 1,8-bis(dimethylamino)naphthalene: another side of the 'proton sponge coin'." Dalton transactions (Cambridge, England : 2003) vol. 44,40 (2015): 17756-66. doi: https://doi.org/10.1039/c5dt02482j
Antonov AS, Pozharskii AF, Ozeryanskii VA, Filarowski A, Suponitsky KY, Tolstoy PM, Vovk MA. Ring lithiation of 1,8-bis(dimethylamino)naphthalene: another side of the 'proton sponge coin'. Dalton Trans. 2015 Oct 28;44(40):17756-66. doi: 10.1039/c5dt02482j. Epub 2015 Sep 23. PMID: 26399216.
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Conformational state of β-hydroxynaphthylamides: Barriers for the rotation of the amide group around CN bond and dynamics of the morpholine ring.

Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy

Kozlecki T, Tolstoy PM, Kwocz A, Vovk MA, Kochel A, Polowczyk I, Tretyakov PY, Filarowski A.
PMID: 25965172
Spectrochim Acta A Mol Biomol Spectrosc. 2015 Oct 05;149:254-62. doi: 10.1016/j.saa.2015.04.052. Epub 2015 Apr 28.

Three β-hydroxynaphthylamides (morpholine, pyrrolidine and dimethylamine derivatives) have been synthesized and their conformational state was analyzed by NMR, X-ray and DFT calculations. In aprotic solution the molecules contain intramolecular OHO hydrogen bonds, which change into intermolecular ones in solid...

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Kozlecki T, Tolstoy PM, Kwocz A, et al. Conformational state of β-hydroxynaphthylamides: Barriers for the rotation of the amide group around CN bond and dynamics of the morpholine ring. Spectrochim Acta A Mol Biomol Spectrosc. 2015;149:254-62doi: 10.1016/j.saa.2015.04.052.
Kozlecki, T., Tolstoy, P. M., Kwocz, A., Vovk, M. A., Kochel, A., Polowczyk, I., Tretyakov, P. Y., & Filarowski, A. (2015). Conformational state of β-hydroxynaphthylamides: Barriers for the rotation of the amide group around CN bond and dynamics of the morpholine ring. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 149254-62. https://doi.org/10.1016/j.saa.2015.04.052
Kozlecki, Tomasz, et al. "Conformational state of β-hydroxynaphthylamides: Barriers for the rotation of the amide group around CN bond and dynamics of the morpholine ring." Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy vol. 149 (2015): 254-62. doi: https://doi.org/10.1016/j.saa.2015.04.052
Kozlecki T, Tolstoy PM, Kwocz A, Vovk MA, Kochel A, Polowczyk I, Tretyakov PY, Filarowski A. Conformational state of β-hydroxynaphthylamides: Barriers for the rotation of the amide group around CN bond and dynamics of the morpholine ring. Spectrochim Acta A Mol Biomol Spectrosc. 2015 Oct 05;149:254-62. doi: 10.1016/j.saa.2015.04.052. Epub 2015 Apr 28. PMID: 25965172.
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Solvatochromism of BODIPY-Schiff dye.

The journal of physical chemistry. B

Filarowski A, Lopatkova M, Lipkowski P, Van der Auweraer M, Leen V, Dehaen W.
PMID: 25470764
J Phys Chem B. 2015 Feb 12;119(6):2576-84. doi: 10.1021/jp508718d. Epub 2014 Dec 18.

A boron-dipyrrin chromophore connected with an o-hydroxyaryl aldimine by a diazo bridge (BODIPY-Schiff dye) has been developed. The photophysical properties of the BODIPY-Schiff dye have been investigated with UV, steady-state, and time-resolved fluorimetry. The spectral features have been characterized...

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Filarowski A, Lopatkova M, Lipkowski P, et al. Solvatochromism of BODIPY-Schiff dye. J Phys Chem B. 2014;119(6):2576-84doi: 10.1021/jp508718d.
Filarowski, A., Lopatkova, M., Lipkowski, P., Van der Auweraer, M., Leen, V., & Dehaen, W. (2015). Solvatochromism of BODIPY-Schiff dye. The journal of physical chemistry. B, 119(6), 2576-84. https://doi.org/10.1021/jp508718d
Filarowski, Aleksander, et al. "Solvatochromism of BODIPY-Schiff dye." The journal of physical chemistry. B vol. 119,6 (2015): 2576-84. doi: https://doi.org/10.1021/jp508718d
Filarowski A, Lopatkova M, Lipkowski P, Van der Auweraer M, Leen V, Dehaen W. Solvatochromism of BODIPY-Schiff dye. J Phys Chem B. 2015 Feb 12;119(6):2576-84. doi: 10.1021/jp508718d. Epub 2014 Dec 18. PMID: 25470764.
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Design and synthesis of 4-heteroaryl 1,2,3,4-tetrahydroisoquinolines as triple reuptake inhibitors.

ACS medicinal chemistry letters

Liu S, Zha C, Nacro K, Hu M, Cui W, Yang YL, Bhatt U, Sambandam A, Isherwood M, Yet L, Herr MT, Ebeltoft S, Hassler C, Fleming L, Pechulis AD, Payen-Fornicola A, Holman N, Milanowski D, Cotterill I, Mozhaev V, Khmelnitsky Y, Guzzo PR, Sargent BJ, Molino BF, Olson R, King D, Lelas S, Li YW, Johnson K, Molski T, Orie A, Ng A, Haskell R, Clarke W, Bertekap R, O'Connell J, Lodge N, Sinz M, Adams S, Zaczek R, Macor JE.
PMID: 25050161
ACS Med Chem Lett. 2014 May 13;5(7):760-5. doi: 10.1021/ml500053b. eCollection 2014 Jul 10.

A series of 4-bicyclic heteroaryl 1,2,3,4-tetrahydroisoquinoline inhibitors of the serotonin transporter (SERT), norepinephrine transporter (NET), and dopamine transporter (DAT) was discovered. The synthesis and structure-activity relationship (SAR) of these triple reuptake inhibitors (TRIs) will be discussed. Compound 10i (AMR-2),...

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Liu S, Zha C, Nacro K, et al. Design and synthesis of 4-heteroaryl 1,2,3,4-tetrahydroisoquinolines as triple reuptake inhibitors. ACS Med Chem Lett. 2014;5(7):760-5doi: 10.1021/ml500053b.
Liu, S., Zha, C., Nacro, K., Hu, M., Cui, W., Yang, Y. L., Bhatt, U., Sambandam, A., Isherwood, M., Yet, L., Herr, M. T., Ebeltoft, S., Hassler, C., Fleming, L., Pechulis, A. D., Payen-Fornicola, A., Holman, N., Milanowski, D., Cotterill, I., Mozhaev, V., Khmelnitsky, Y., Guzzo, P. R., Sargent, B. J., Molino, B. F., Olson, R., King, D., Lelas, S., Li, Y. W., Johnson, K., Molski, T., Orie, A., Ng, A., Haskell, R., Clarke, W., Bertekap, R., O'Connell, J., Lodge, N., Sinz, M., Adams, S., Zaczek, R., & Macor, J. E. (2014). Design and synthesis of 4-heteroaryl 1,2,3,4-tetrahydroisoquinolines as triple reuptake inhibitors. ACS medicinal chemistry letters, 5(7), 760-5. https://doi.org/10.1021/ml500053b
Liu, Shuang, et al. "Design and synthesis of 4-heteroaryl 1,2,3,4-tetrahydroisoquinolines as triple reuptake inhibitors." ACS medicinal chemistry letters vol. 5,7 (2014): 760-5. doi: https://doi.org/10.1021/ml500053b
Liu S, Zha C, Nacro K, Hu M, Cui W, Yang YL, Bhatt U, Sambandam A, Isherwood M, Yet L, Herr MT, Ebeltoft S, Hassler C, Fleming L, Pechulis AD, Payen-Fornicola A, Holman N, Milanowski D, Cotterill I, Mozhaev V, Khmelnitsky Y, Guzzo PR, Sargent BJ, Molino BF, Olson R, King D, Lelas S, Li YW, Johnson K, Molski T, Orie A, Ng A, Haskell R, Clarke W, Bertekap R, O'Connell J, Lodge N, Sinz M, Adams S, Zaczek R, Macor JE. Design and synthesis of 4-heteroaryl 1,2,3,4-tetrahydroisoquinolines as triple reuptake inhibitors. ACS Med Chem Lett. 2014 May 13;5(7):760-5. doi: 10.1021/ml500053b. eCollection 2014 Jul 10. PMID: 25050161; PMCID: PMC4094255.
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Heat Stress Affects Pi-related Genes Expression and Inorganic Phosphate Deposition/Accumulation in Barley.

Frontiers in plant science

Pacak A, Barciszewska-Pacak M, Swida-Barteczka A, Kruszka K, Sega P, Milanowska K, Jakobsen I, Jarmolowski A, Szweykowska-Kulinska Z.
PMID: 27446155
Front Plant Sci. 2016 Jun 24;7:926. doi: 10.3389/fpls.2016.00926. eCollection 2016.

Phosphorus (P) in plants is taken from soil as an inorganic phosphate (Pi) and is one of the most important macroelements in growth and development. Plants actively react to Pi starvation by the induced expression of Pi transporters, MIR399,...

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Pacak A, Barciszewska-Pacak M, Swida-Barteczka A, et al. Heat Stress Affects Pi-related Genes Expression and Inorganic Phosphate Deposition/Accumulation in Barley. Front Plant Sci. 2016;7:926doi: 10.3389/fpls.2016.00926.
Pacak, A., Barciszewska-Pacak, M., Swida-Barteczka, A., Kruszka, K., Sega, P., Milanowska, K., Jakobsen, I., Jarmolowski, A., & Szweykowska-Kulinska, Z. (2016). Heat Stress Affects Pi-related Genes Expression and Inorganic Phosphate Deposition/Accumulation in Barley. Frontiers in plant science, 7926. https://doi.org/10.3389/fpls.2016.00926
Pacak, Andrzej, et al. "Heat Stress Affects Pi-related Genes Expression and Inorganic Phosphate Deposition/Accumulation in Barley." Frontiers in plant science vol. 7 (2016): 926. doi: https://doi.org/10.3389/fpls.2016.00926
Pacak A, Barciszewska-Pacak M, Swida-Barteczka A, Kruszka K, Sega P, Milanowska K, Jakobsen I, Jarmolowski A, Szweykowska-Kulinska Z. Heat Stress Affects Pi-related Genes Expression and Inorganic Phosphate Deposition/Accumulation in Barley. Front Plant Sci. 2016 Jun 24;7:926. doi: 10.3389/fpls.2016.00926. eCollection 2016. PMID: 27446155; PMCID: PMC4919326.
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Factor analysis of deuterium isotope effects on 13C NMR chemical shifts in Schiff bases.

Chemistry (Weinheim an der Bergstrasse, Germany)

Dominiak PM, Filarowski A, Hansen PE, Woźniak K.
PMID: 15924288
Chemistry. 2005 Aug 05;11(16):4758-66. doi: 10.1002/chem.200401350.

We have analyzed deuterium isotope effects on (13)C chemical shifts in a series of o-hydroxy Schiff bases by applying factor analysis. Two orthogonal factors were obtained that explain about 80 and 10 % of the variance of the data....

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Dominiak PM, Filarowski A, Hansen PE, et al. Factor analysis of deuterium isotope effects on 13C NMR chemical shifts in Schiff bases. Chemistry. 2005;11(16):4758-66doi: 10.1002/chem.200401350.
Dominiak, P. M., Filarowski, A., Hansen, P. E., & Woźniak, K. (2005). Factor analysis of deuterium isotope effects on 13C NMR chemical shifts in Schiff bases. Chemistry (Weinheim an der Bergstrasse, Germany), 11(16), 4758-66. https://doi.org/10.1002/chem.200401350
Dominiak, Paulina M, et al. "Factor analysis of deuterium isotope effects on 13C NMR chemical shifts in Schiff bases." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 11,16 (2005): 4758-66. doi: https://doi.org/10.1002/chem.200401350
Dominiak PM, Filarowski A, Hansen PE, Woźniak K. Factor analysis of deuterium isotope effects on 13C NMR chemical shifts in Schiff bases. Chemistry. 2005 Aug 05;11(16):4758-66. doi: 10.1002/chem.200401350. PMID: 15924288.
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2-alpha-hydroxyalkyl- and 2,7-di(alpha-hydroxyalkyl)-1,8-bis(dimethylamino)naphthalenes: stabilization of nonconventional in/out conformers of "proton sponges" via N...H-O intramolecular hydrogen bonding. A remarkable kind of tandem nitrogen inversion.

The Journal of organic chemistry

Pozharskii AF, Degtyarev AV, Ryabtsova OV, Ozeryanskii VA, Kletskii ME, Starikova ZA, Sobczyk L, Filarowski A.
PMID: 17378612
J Org Chem. 2007 Apr 13;72(8):3006-19. doi: 10.1021/jo062667v. Epub 2007 Mar 23.

A regular set of 2-(alpha-hydroxymethyl)- and 2,7-di(alpha-hydroxymethyl)-1,8-bis(dimethylamino)naphthalenes has been prepared. Their X-ray, NMR, and IR studies have demonstrated that in tertiary mono-alcohols the orientation of free nitrogen electron pairs in crystals and solution corresponds to nonconventional in/out conformers stabilized...

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Pozharskii AF, Degtyarev AV, Ryabtsova OV, et al. 2-alpha-hydroxyalkyl- and 2,7-di(alpha-hydroxyalkyl)-1,8-bis(dimethylamino)naphthalenes: stabilization of nonconventional in/out conformers of "proton sponges" via N...H-O intramolecular hydrogen bonding. A remarkable kind of tandem nitrogen inversion. J Org Chem. 2007;72(8):3006-19doi: 10.1021/jo062667v.
Pozharskii, A. F., Degtyarev, A. V., Ryabtsova, O. V., Ozeryanskii, V. A., Kletskii, M. E., Starikova, Z. A., Sobczyk, L., & Filarowski, A. (2007). 2-alpha-hydroxyalkyl- and 2,7-di(alpha-hydroxyalkyl)-1,8-bis(dimethylamino)naphthalenes: stabilization of nonconventional in/out conformers of "proton sponges" via N...H-O intramolecular hydrogen bonding. A remarkable kind of tandem nitrogen inversion. The Journal of organic chemistry, 72(8), 3006-19. https://doi.org/10.1021/jo062667v
Pozharskii, Alexander F, et al. "2-alpha-hydroxyalkyl- and 2,7-di(alpha-hydroxyalkyl)-1,8-bis(dimethylamino)naphthalenes: stabilization of nonconventional in/out conformers of "proton sponges" via N...H-O intramolecular hydrogen bonding. A remarkable kind of tandem nitrogen inversion." The Journal of organic chemistry vol. 72,8 (2007): 3006-19. doi: https://doi.org/10.1021/jo062667v
Pozharskii AF, Degtyarev AV, Ryabtsova OV, Ozeryanskii VA, Kletskii ME, Starikova ZA, Sobczyk L, Filarowski A. 2-alpha-hydroxyalkyl- and 2,7-di(alpha-hydroxyalkyl)-1,8-bis(dimethylamino)naphthalenes: stabilization of nonconventional in/out conformers of "proton sponges" via N...H-O intramolecular hydrogen bonding. A remarkable kind of tandem nitrogen inversion. J Org Chem. 2007 Apr 13;72(8):3006-19. doi: 10.1021/jo062667v. Epub 2007 Mar 23. PMID: 17378612.
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Unproved methods and theories in allergy.

Allergy and asthma proceedings

Miranowski AC, Greenberger PA.
PMID: 15515386
Allergy Asthma Proc. 2004 Jul-Aug;25(4):S61-3.

No abstract available.

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Miranowski AC, Greenberger PA. Unproved methods and theories in allergy. Allergy Asthma Proc. 2004;25(4):S61-3
Miranowski, A. C., & Greenberger, P. A. (2004). Unproved methods and theories in allergy. Allergy and asthma proceedings, 25(4), S61-3.
Miranowski, Anne C, and Greenberger, Paul A. "Unproved methods and theories in allergy." Allergy and asthma proceedings vol. 25,4 (2004): S61-3.
Miranowski AC, Greenberger PA. Unproved methods and theories in allergy. Allergy Asthma Proc. 2004 Jul-Aug;25(4):S61-3. PMID: 15515386.
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The epidermis of grhl3-null mice displays altered lipid processing and cellular hyperproliferation.

Organogenesis

Ting SB, Caddy J, Wilanowski T, Auden A, Cunningham JM, Elias PM, Holleran WM, Jane SM.
PMID: 19521564
Organogenesis. 2005 Apr;2(2):33-5. doi: 10.4161/org.2.2.2167.

The presence of an impermeable surface barrier is an essential homeostatic mechanism in almost all living organisms. We have recently described a novel gene that is critical for the developmental instruction and repair of the integument in mammals. This...

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Ting SB, Caddy J, Wilanowski T, et al. The epidermis of grhl3-null mice displays altered lipid processing and cellular hyperproliferation. Organogenesis. 2005;2(2):33-5doi: 10.4161/org.2.2.2167.
Ting, S. B., Caddy, J., Wilanowski, T., Auden, A., Cunningham, J. M., Elias, P. M., Holleran, W. M., & Jane, S. M. (2005). The epidermis of grhl3-null mice displays altered lipid processing and cellular hyperproliferation. Organogenesis, 2(2), 33-5. https://doi.org/10.4161/org.2.2.2167
Ting, Stephen B, et al. "The epidermis of grhl3-null mice displays altered lipid processing and cellular hyperproliferation." Organogenesis vol. 2,2 (2005): 33-5. doi: https://doi.org/10.4161/org.2.2.2167
Ting SB, Caddy J, Wilanowski T, Auden A, Cunningham JM, Elias PM, Holleran WM, Jane SM. The epidermis of grhl3-null mice displays altered lipid processing and cellular hyperproliferation. Organogenesis. 2005 Apr;2(2):33-5. doi: 10.4161/org.2.2.2167. PMID: 19521564; PMCID: PMC2634083.
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