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Biology and Biochemistry

D-Index
102
Citations
40431
World Ranking
1358
National Ranking
786

Overview

William B. Guggino is affiliated with Johns Hopkins University in the United States, focusing primarily on research within medicine and biochemistry, genetics, and molecular biology. Their research spans multiple subfields, including pulmonary and respiratory medicine, genetics, molecular biology, epidemiology, and nephrology.

The scientist has contributed to topics centered on cystic fibrosis research advances, virus-based gene therapy research, respiratory viral infections research, energy harvesting in wireless networks, neonatal respiratory health research, genetic and kidney cyst diseases, and chronic kidney disease and diabetes.

Recent publications by William B. Guggino include:

  • Gene Therapy for Cystic Fibrosis Paved the Way for the Use of Adeno-Associated Virus in Gene Therapy, 2020, Human Gene Therapy
  • Transduction of Surface and Basal Cells in Rhesus Macaque Lung Following Repeat Dosing with AAV1CFTR, 2020, Human Gene Therapy

Other notable papers related to their frequent collaborators or fields of study include:

  • Megalin-mediated albumin endocytosis in renal proximal tubules is involved in the antiproteinuric effect of angiotensin II type 1 receptor blocker in a subclinical acute kidney injury animal model, 2021, Biochimica et Biophysica Acta (BBA) - General Subjects
  • The Mitochondrial Ca2+ import complex is altered in ADPKD, 2021, Cell Calcium
  • Transduction of Ferret Surface and Basal Cells of Airways, Lung, Liver, and Pancreas via Intratracheal or Intravenous Delivery of Adeno-Associated Virus 1 or 6, 2023, Human Gene Therapy

William B. Guggino frequently collaborates with several researchers, including Liudmila Cebotaru, Murali K. Yanda, Cristian Ciobanu, Vartika Tomar, and Cristina V. Cebotaru.

Their publications have appeared predominantly in the following venues:

  • Human Gene Therapy
  • UNC Libraries
  • Journal of Cystic Fibrosis
  • Biochimica et Biophysica Acta (BBA) - General Subjects
  • Cell Calcium

Best Publications

  • Appearance of water channels in Xenopus oocytes expressing red cell CHIP28 protein.

    Gregory M. Preston;Tiziana Piazza Carroll;William B. Guggino;Peter Agre

  • In vivo transfer of the human cystic fibrosis transmembrane conductance regulator gene to the airway epithelium

    Melissa A. Rosenfeld;Kunihiko Yoshimura;Bruce C. Trapnell;Koichi Yoneyama

  • Aquaporin CHIP: the archetypal molecular water channel

    P. Agre;G. M. Preston;B. L. Smith;Jin Sup Jung

  • Molecular characterization of an aquaporin cDNA from brain: candidate osmoreceptor and regulator of water balance

    Jin Sup Jung;Ratan V. Bhat;Gregory M. Preston;William B. Guggino

  • Co-assembly of polycystin-1 and -2 produces unique cation-permeable currents

    Kazushige Hanaoka;Feng Qian;Alessandra Boletta;Anil K. Bhunia

  • Molecular structure of the water channel through aquaporin CHIP. The hourglass model.

    Jin Sup Jung;G. M. Preston;B. L. Smith;W. B. Guggino

  • CFTR regulates outwardly rectifying chloride channels through an autocrine mechanism involving ATP.

    Erik M. Schwiebert;Marie E. Egan;Tae Ho Hwang;Stephanie B. Fulmer

  • Identification of a urate transporter, ABCG2, with a common functional polymorphism causing gout

    Owen M. Woodward;Anna Köttgen;Josef Coresh;Eric Boerwinkle

  • Stable in vivo expression of the cystic fibrosis transmembrane conductance regulator with an adeno-associated virus vector.

    Terence R. Flotte;Sandra A. Afione;Carol Conrad;Sharon A. McGrath

  • The mercury-sensitive residue at cysteine 189 in the CHIP28 water channel.

    G. M. Preston;Jin Sup Jung;W. B. Guggino;P. Agre

  • CHIP28 water channels are localized in constitutively water-permeable segments of the nephron.

    S Nielsen;B L Smith;E I Christensen;M A Knepper

  • Cloning of the gamma-aminobutyric acid (GABA) rho 1 cDNA: a GABA receptor subunit highly expressed in the retina.

    G R Cutting;L Lu;B F O'Hara;L M Kasch

  • Molecular Characterization of a Broad Selectivity Neutral Solute Channel

    Hiroyasu Tsukaguchi;Chairat Shayakul;Urs V. Berger;Bryan Mackenzie

  • CFTR Is a Conductance Regulator as well as a Chloride Channel

    Erik M. Schwiebert;Dale J. Benos;Marie E. Egan;Monroe Jack Stutts

  • From CFTR biology toward combinatorial pharmacotherapy: expanded classification of cystic fibrosis mutations.

    Gudio Veit;Radu G. Avramescu;Annette N. Chiang;Scott A. Houck

  • New insights into cystic fibrosis: molecular switches that regulate CFTR.

    William B. Guggino;Bruce A. Stanton

  • MOLECULAR CLONING AND CHARACTERIZATION OF AN AQUAPORIN CDNA FROM SALIVARY,LACRIMAL, AND RESPIRATORY TISSUES

    Surabhi Raina;Gregory M. Preston;William B. Guggino;Peter Agre

  • Defective regulation of outwardly rectifying Cl− channels by protein kinase A corrected by insertion of CFTR

    Marie Egan;Terence Flotte;Terence Flotte;Sandra Afione;Rikki Solow

  • Immunocytochemical localization of the cystic fibrosis gene product CFTR.

    Isabelle Crawford;Peter C. Maloney;Pamela L. Zeitlin;William B. Guggino

  • Structure of nucleotide-binding domain 1 of the cystic fibrosis transmembrane conductance regulator

    Hal A Lewis;Sean G Buchanan;Stephen K Burley;Kris Conners

Frequent Co-Authors

Erik M. Schwiebert
Erik M. Schwiebert University of Alabama at Birmingham
Garry R. Cutting
Garry R. Cutting Johns Hopkins University School of Medicine
Terence R. Flotte
Terence R. Flotte University of Massachusetts Chan Medical School
Pamela L. Zeitlin
Pamela L. Zeitlin National Jewish Health
Olivier Devuyst
Olivier Devuyst University of Zurich
Peter Agre
Peter Agre Johns Hopkins University
Harvey B. Pollard
Harvey B. Pollard Uniformed Services University of the Health Sciences
Barrie J. Carter
Barrie J. Carter National Institutes of Health
Pierre J. Courtoy
Pierre J. Courtoy Université Catholique de Louvain
Min Li
Min Li Chinese Academy of Sciences

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