@article{ludwig_hallowell_womble_o'neil_2023, title={Bilateral patellar aplasia in a foal}, ISSN={["2053-1095"]}, DOI={10.1002/vms3.1083}, abstractNote={Abstract}, journal={VETERINARY MEDICINE AND SCIENCE}, author={Ludwig, Elsa K. and Hallowell, Kim and Womble, Mandy and O'Neil, Erin}, year={2023}, month={Feb} }
 @article{multani_cohen_haas_borst_womble_musulin_2023, title={Pancreatic Torsion Resulting in Acute Pancreatic Necrosis in a Young Dog}, volume={59}, ISSN={["1547-3317"]}, DOI={10.5326/JAAHA-MS-7382}, abstractNote={ABSTRACT}, number={6}, journal={JOURNAL OF THE AMERICAN ANIMAL HOSPITAL ASSOCIATION}, author={Multani, Rajdeep and Cohen, Eli B. and Haas, Jason and Borst, Luke and Womble, Mandy and Musulin, Sarah}, year={2023}, pages={297–301} }
 @article{kang_womble_cullen_harrison_premanandan_schreeg_2023, title={Severe bronchiectasis resulting from chronic bacterial bronchitis and bronchopneumonia in a jungle cat}, volume={11}, ISSN={["1943-4936"]}, DOI={10.1177/10406387231216181}, abstractNote={ Bronchiectasis is irreversible bronchial dilation that can be congenital or acquired secondary to chronic airway obstruction. Feline bronchiectasis is rare and, to our knowledge, has not been reported previously in a non-domestic felid. An ~10-y-old female jungle cat ( Felis chaus) was presented for evaluation of an abdominal mass and suspected pulmonary metastasis. The animal died during exploratory laparotomy and was submitted for postmortem examination. Gross examination revealed consolidation of the left caudal lung lobe and hila of the cranial lung lobes. Elsewhere in the lungs were several pale-yellow pleural foci of endogenous lipid pneumonia. On cut section, there was severe distension of bronchi with abundant white mucoid fluid. The remaining lung lobes were multifocally expanded by marginal emphysema. Histologically, ectatic bronchi, bronchioles, and fewer alveoli contained degenerate neutrophils, fibrin, and mucin (suppurative bronchopneumonia) with rare gram-negative bacteria. Aerobic culture yielded low growth of Proteus mirabilis and Escherichia coli. There was chronic bronchitis, marked by moderate bronchial gland hyperplasia, lymphoplasmacytic inflammation, and lymphoid hyperplasia. The palpated abdominal mass was a uterine endometrial polyp, which was considered an incidental, but novel, finding. Chronic bronchitis and bronchopneumonia should be considered as a cause of bronchiectasis and a differential diagnosis for respiratory disease in non-domestic felids. }, journal={JOURNAL OF VETERINARY DIAGNOSTIC INVESTIGATION}, author={Kang, Danyue and Womble, Mandy and Cullen, John M. and Harrison, Tara M. and Premanandan, Christopher and Schreeg, Megan E.}, year={2023}, month={Nov} }
 @article{hastain_buchy_dombrowski_womble_armwood_gruber_2023, title={What is your diagnosis? Ulcerative shell lesions from a diamond-backed terrapin (Malaclemys terrapin)}, volume={7}, ISSN={["1939-165X"]}, url={https://doi.org/10.1111/vcp.13291}, DOI={10.1111/vcp.13291}, abstractNote={An adult female intact diamond-backed terrapin (Malaclemys terrapin) at the North Carolina Museum of Natural Sciences presented for an episode of scute sloughing and cystic ulcerative pitting lesions on the carapace and plastron. The patient was wild-caught as a hatchling or juvenile by another institution in 2004 and obtained by the museum in 2007. Since acquisition, this turtle has had a chronic history of pitting shell lesions, keratin scute flaking, and excessive keratin scute buildup. This turtle had two notable episodes with deep shell lesions and scute sloughing, the first of which completely resolved with topical antibiotics. During the second episode, the multifocal deep ulcerative lesions cultured positive for multiple aerobic bacteria that were initially susceptible to topical and injectable antibiotics. Healing was prolonged due to the development of antibiotic resistance, and antibiotic therapy was altered according to sensitivity results. Complete gross resolution occurred after 4 months of treatment. On presentation, multiple ulcerated and hemorrhagic lesions were present on the carapace after acute sloughing of the scutes, most notably between the right first and second costal scutes. The deep ulcers were associated with tan to yellow dry caseous granuloma-like exudative lesions that penetrated into the bone. Swabs from these lesions were submitted for cytology (Figure 1). The patient was otherwise active and eating well. Fungal hyphae with mild heterophilic inflammation The sample is of low cellularity consisting mostly of keratinized squamous epithelial cells. Focal areas of the slides contain low numbers of poorly preserved heterophils (not pictured). Numerous variably staining fungal hyphae are associated with many of the keratin aggregates. The hyphae are found individually and in mats. Hyphae are approximately 2–4 μm in diameter and septate, with thin nonstaining walls that are mostly parallel but occasionally nonparallel. They display internal complexity, often containing variably sized clear, distinct vacuoles. Rare acute and right-angled lateral branching is observed. Gross examination of the dermal fragments and multiple fragments of surrounding tissue reveals multifocal to coalescing pale tan plaques, nodules, and pitting lesions (Figure 2). On histopathologic examination, the superficial dermis is expanded by epithelial inclusion cysts. Cyst structures are lined by well-differentiated stratified squamous epithelium with central keratinization and the accumulation of lamellated layers of keratin debris (Figure 3A). Embedded within the central layers of keratin are numerous fungal hyphae highlighted by Grocott's methenamine silver stain (Figure 3B). Hyphae are approximately 4 μm in diameter with nonparallel cell walls and display acute and right-angle branching and septation. The dermal fragments display marked orthokeratotic to parakeratotic hyperkeratosis, with conglomerates of keratin debris, degenerative leukocytes, and eosinophilic fluid also containing the fungal hyphae (not pictured). A pooled swab prepared from the oral cavity, cloaca, and shell submitted to the University of Illinois College of Veterinary Medicine Zoological Pathology Program Molecular Diagnostic Laboratory tested positive for Emydomyces testavorans by quantitative PCR. Ulcerative shell disease is a common cause of morbidity and mortality in captive and free-ranging populations of turtles,1, 2 and clinical signs include shell erosions, lethargy, and emaciation.3 Reported causes of ulcerative shell disease include trauma, malnutrition (eg, calcium and vitamin D3 deficiencies), and various bacterial and fungal etiologies, though the cause is often unknown.1, 4 In captive individuals, poor husbandry practices such as inappropriate temperature, humidity, lighting, and/or nutrition are considered predisposing factors.4 Infectious causes are most often identified as gram-negative commensals within the Enterobacteriae order, including Escherichia, Klebsiella, and Enterobacter spp.4 Bacterial ulcerative shell disease has the potential to progress to septicemic cutaneous ulcerative disease (SCUD), in which bacterial dermatitis and osteomyelitis may be identified.1 Fungal causes of ulcerative shell disease are rarely reported, and the majority of published reports are from nonaquatic turtle species.2 Emydomyces testavorans is a keratinophilic fungal organism in the Onygenales order.5 Onygenalean fungi have been identified as primary pathogens for ulcerative dermatitis in captive and free-ranging reptilian species, including crocodilians, lizards, and snakes.1 E. testavorans has only been recently described and has been isolated from ulcerative shell lesions in aquatic turtles, causing keratin discoloration, flaking and textural change, erosion, ulceration, and osteonecrosis.2, 5 The most consistent and striking histopathologic lesion with E. testavorans infection is the presence of epithelial inclusion cysts, identified in more than 90% of cases.2 Epithelial inclusion cysts are cystic spaces lined by stratified squamous epithelium with central keratinization. E. testavorans hyphae are typically embedded in keratin debris.5 Although the underlying mechanism of epithelial inclusion cyst formation with E. testavorans infection is unclear, it is presumed that the excessive keratinization occurs secondary to the fungal infection rather than fungal infection with tropism for previously established epithelial inclusion cysts. Since epithelial inclusion cysts in other species are not often associated with fungal infections, it is possible that immunosuppression is contributing to the pathogenesis in aquatic turtles. Definitive diagnosis of E. testavorans typically requires PCR with or without DNA sequencing. Although culture can be performed, it may be complicated by sample contamination with other common environmental bacterial and fungal organisms and by the requirement for reptile keratin-enriched media. Preferred samples are lesion swabs and biopsy material that should be refrigerated for culture and frozen for molecular diagnostics.5 In summary, this case described the cytologic features of the onygenalean fungus E. testavorans, a newly described cause of ulcerative shell lesions in aquatic turtles. The frequent association of fungal hyphae with keratin and concurrent inflammation is consistent with histologic findings of epithelial inclusion cysts associated with E. testavorans.2 The heterophilic inflammation, in this case, could be in response to the fungus, keratin, and/or concurrent bacterial infection. Although bacteria were not identified cytologically, bacterial culture was not performed to exclude this possibility. A thorough examination of keratin aggregates for fungal hyphae elements is warranted in samples from ulcerative shell lesions in aquatic turtles. The authors have no affiliations or financial involvement with any organization or entity with a financial interest in, or in financial compensation with, the subject matter or materials discussed in this article.}, journal={VETERINARY CLINICAL PATHOLOGY}, author={Hastain, Sydney A. A. and Buchy, Jessica M. M. and Dombrowski, Daniel S. S. and Womble, Mandy A. A. and Armwood, Abigail R. R. and Gruber, Erika J. J.}, year={2023}, month={Jul} }
 @article{anderson_murillo_womble_gibbs_harrell_watanabe_2022, title={Case Report: Novel Disseminated Paecilomyces formosus Infection in a Dog}, volume={9}, ISSN={["2297-1769"]}, DOI={10.3389/fvets.2022.878327}, abstractNote={A 2.5-year-old, 25.5 kg, spayed female Australian Shepherd dog had a 2-month history of shifting leg lameness in all limbs, tetraparesis, progressive lethargy, and severe pain. On the physical examination, fever (40.61°C), tachycardia, tachypnea, mild diffuse pelvic limb muscular atrophy, left prescapular and right popliteal lymphadenomegaly were observed. Due to the poor prognosis and difficult pain management, humane euthanasia was elected. Macroscopic and histological findings revealed multifocal to coalescing granulomas with central areas of lytic necrosis within the right femur, left humerus, left scapula, left biceps brachii, right semimembranosus muscle, liver, spleen, and lymph nodes. The necrotic areas contained myriad intralesional, intracellular, and extracellular negatively stained, non-pigmented, septate acute angle branching hyphae with parallel walls measuring 3–6 μm in width with polar bulbous projections measuring 7–13 μm in width. Fresh samples of the liver were submitted for fungal culture. Panfungal PCR targeting the major conserved genes-ITS, TUB, CAL-confirmed Paecilomyces formosus. Paecilomyces spp. are members of anamorphic fungi classified under the phylum Ascomycota. Paecilomycosis is an uncommon fungal infection caused by Paecilomyces spp with a disease reported in humans and animals ranging from superficial to systemic clinical forms affecting both immunocompromised and immunocompetent individuals. In dogs, disseminated paecilomycosis has been reported, but the species of fungi are not always determined. To our knowledge, this is the first case of disseminated paecilomycosis caused by P. formosus infection in a dog.}, journal={FRONTIERS IN VETERINARY SCIENCE}, author={Anderson, Stephanie and Murillo, Daniel Felipe Barrantes and Womble, Mandy and Gibbs, Nicole and Harrell, Karyn and Watanabe, Tatiane Terumi Negrao}, year={2022}, month={May} }
 @article{womble_cabot_harrison_watanabe_2022, title={Outbreak in African lions of Yersinia pseudotuberculosis infection, with aberrant bacterial morphology}, volume={1}, ISSN={["1943-4936"]}, DOI={10.1177/10406387211072822}, abstractNote={ A concurrent outbreak of infection with Yersinia pseudotuberculosis occurred in adult captive African lions ( Panthera leo). Two 17-y-old male lions and one 14-y-old female lion developed respiratory distress, lethargy, ataxia, and hyporexia. Within 3–5 d of the onset of clinical signs, one male and the female lion died and were submitted for postmortem examination. Macroscopically, the liver and spleen had multifocal-to-coalescing, semi-firm, pale-tan nodules throughout the parenchyma. The lungs were non-collapsed and marked by petechiae. Histologic examination identified lytic, necrosuppurative foci in the liver, spleen, lungs, and kidney, with abundant intralesional gram-negative coccobacilli in the male lion. Similar findings were seen in the female lion in the liver, spleen, kidney, and mesenteric lymph node; however, the intralesional bacterial colonies were more pleomorphic, comprising rod and filamentous morphologies. Aerobic bacterial culture of the liver, spleen, and lung revealed Y. pseudotuberculosis growth. The source of infection is unknown, and an epidemiologic study was performed. Sources to be considered are from the predation of rodent and/or bird reservoirs, or contaminated soil or water. Mortality associated with Y. pseudotuberculosis has been described in an African lion cub, however, to our knowledge, Y. pseudotuberculosis has not been reported in adult African lions, and this is only the second report of Y. pseudotuberculosis with aberrant bacterial morphology observed histologically. }, journal={JOURNAL OF VETERINARY DIAGNOSTIC INVESTIGATION}, author={Womble, Mandy and Cabot, Megan L. and Harrison, Tara and Watanabe, Tatiane Terumi Negrao}, year={2022}, month={Jan} }
 @article{cabot_watanabe_womble_harrison_2022, title={YERSINIA PSEUDOTUBERCULOSIS INFECTION IN LIONS (PANTHERA LEO) AT A ZOOLOGICAL PARK}, volume={53}, ISSN={["1937-2825"]}, DOI={10.1638/2021-0106}, abstractNote={Abstract: Two co-housed 17-yr-old male lions (Panthera leo) and one 15-yr-old female lion in an adjacent enclosure developed acute lethargy, depression, anorexia, and ataxia at a zoological park in central North Carolina, United States. One of the male lions and the female lion were found dead 5 and 4 d after the onset of clinical signs, respectively. The other male lion recovered without any clinical treatment. A third male lion housed with the female lion never developed clinical signs. Postmortem examination, microscopic evaluation, and bacterial culture of the liver from both deceased lions confirmed systemic Yersinia pseudotuberculosis infection. Susceptibility testing revealed resistance to amoxicillin–clavulanic acid and cefazolin. To investigate the extent of the outbreak, qualitative real-time polymerase chain reaction (PCR) for Y. pseudotuberculosis was performed on feces and substrate from 15 enclosures housing nondomestic felids and canids, resulting in a positive sample from one enclosure housing four asymptomatic lions. This enclosure was adjacent to housing of the deceased female lion. Enrofloxacin was administered to all animals in the vicinity at doses of 5 mg/kg in nondomestic felids and 10 mg/kg in nondomestic canids, orally q24h for 14 d. Repeated fecal PCR performed 1 wk after completing the antibiotic treatment protocol found no positive samples. The source of the infection was not identified despite PCR testing of environmental samples from all enclosures in the vicinity, the remains of a prey item fed out prior to the outbreak, and a single dead rodent found on grounds. No further clinical cases have occurred within the following year.}, number={3}, journal={JOURNAL OF ZOO AND WILDLIFE MEDICINE}, author={Cabot, Megan L. and Watanabe, Tatiane Terumi Negrao and Womble, Mandy and Harrison, Tara M.}, year={2022}, month={Sep}, pages={593–599} }
 @article{womble_schreeg_hoch_meira_foster_premanandan_watanabe_2021, title={Concurrent Clostridial Enteritis and Oviductal Adenocarcinoma with Carcinomatosis in an Adult Alpaca (Vicugna pacos)}, volume={189}, ISSN={["1532-3129"]}, DOI={10.1016/j.jcpa.2021.09.007}, abstractNote={An adult alpaca (Vicugna pacos) with a history of colic and anorexia was euthanized because of failure to respond to treatment. Macroscopically, pale-tan, multifocal to coalescing, firm nodules and plaques markedly expanded the omentum, mesentery and the parietal and visceral peritoneum of multiple abdominal organs, especially the right oviduct and associated mesosalpinx. Abundant dark-red watery digesta were present in the duodenum and jejunum. Histological evaluation of the right oviduct, abdominal visceral nodules and plaques and mesenteric lymph nodes revealed transmural expansion and replacement by an epithelial malignant neoplasm, comprised of tubules and acini of ciliated columnar cells supported by abundant fibrous connective tissue. Both ovaries were histologically normal. On the basis of the ciliated morphology of the neoplastic cells, the focus on the proximal reproductive tract and the unremarkable ovaries, a reproductive tubal adenocarcinoma with carcinomatosis was diagnosed, with both the endometrium and oviduct considered as the tissues of origin. The prominent ciliated morphology of the neoplastic cells and the classification of human fallopian tube (oviduct) neoplasia lead us to propose oviductal adenocarcinoma with widespread carcinomatosis as the definitive diagnosis. The lamina propria of the small intestine was infiltrated segmentally by lymphocytes, plasma cells and neutrophils, and Clostridium perfringens with beta2 toxin production was identified by polymerase chain reaction in the small intestinal contents. To our knowledge, this is the first report of these two distinct diseases in an alpaca.}, journal={JOURNAL OF COMPARATIVE PATHOLOGY}, author={Womble, Mandy and Schreeg, Megan E. and Hoch, Allison and Meira, Enoch B. de Souza, Jr. and Foster, Derek and Premanandan, Christopher and Watanabe, Tatiane T. Negrao}, year={2021}, month={Nov}, pages={52–58} }
 @misc{womble_georoff_helmick_carpenter_joslin_tupa_tetzloff_mcaloose_2021, title={MORTALITY REVIEW FOR THE NORTH AMERICAN SNOW LEOPARD (PANTHERA UNCIA) ZOO POPULATION FROM JANUARY 1999 TO DECEMBER 2019}, volume={52}, ISSN={["1937-2825"]}, DOI={10.1638/2020-0132}, abstractNote={Abstract: The objective of this 20-yr retrospective study was to review and summarize causes of mortality in the North American (NA) snow leopard population to inform and enhance animal health and husbandry practices. Pathology reports were requested from all NA zoological institutions housing snow leopards that died between 01 January 1999 and 31 December 2019. Data were reviewed and cause of death (COD) and concurrent diseases were summarized and compared by age group, organ system, and disease process. The 241 snow leopards in this report include 109 males, 130 females, and two of undetermined sex. Among them were 116 geriatric snow leopards (>15 yr), 72 adults (15–3 yr), 16 juveniles (3 yr to 2 mo), 32 neonates (2 mo to 0 days), and five fetuses (<0 days). Overall, noninfectious diseases were the most common COD across all age groups (73%). In adult and geriatric snow leopards, chronic renal disease (CRD) (38.8%) and malignant neoplasia (19.7%), including oral squamous cell carcinoma (6.4%), were a common COD. In juveniles and neonates, perinatal death and congenital diseases, including ocular coloboma (15.6%), were a common COD. Individuals with CRD were 13.5 and 4.36 times more likely to have veno-occlusive disease and cardiac fibrosis, respectively. Snow leopards with urolithiasis were 5.27 times more likely to have CRD. Infectious (14.1%) and inflammatory diseases (8.7%) for which no specific etiology was identified were less common overall and more common in juveniles and neonates (25% and 21%, respectively). Neoplasms not previously reported in snow leopards or that are generally uncommon in the veterinary literature included transitional cell carcinoma of the urinary bladder (n = 7) and mesothelioma (n = 1).}, number={1}, journal={JOURNAL OF ZOO AND WILDLIFE MEDICINE}, author={Womble, Mandy and Georoff, Timothy A. and Helmick, Kelly and Carpenter, Nancy A. and Joslin, Janis and Tupa, Lynn and Tetzloff, Jay and McAloose, Denise}, year={2021}, month={Mar}, pages={145–156} }
 @article{womble_lewbart_shive_2020, title={Pathologic Lesions of the Budgett Frog (Lepidobatrachus laevis), an Emerging Laboratory Animal Model}, volume={70}, ISSN={["1532-0820"]}, DOI={10.30802/AALAS-CM-19-000071}, abstractNote={Lepidobatrachus laevis, commonly called the Budgett frog, is a member of the horned frog family (Ceratophryidae), which has become increasingly popular among amphibian hobbyists. L. laevis is also used in biologic research on embryonic development, providing a novel model
 species for the study of organogenesis, regeneration, evolution, and biologic scaling. However, little scientific literature details disease processes or histologic lesions in this species. Our objective was to describe spontaneous pathologic lesions in L. laevis to identify disease
 phenotypes. We performed a retrospective analysis of 14 captive L. laevis frogs (wild-caught and captive-bred), necropsied at the NC State University College of Veterinary Medicine between 2008 and 2018. The majority of frogs exhibited renal changes, including varying combinations of
 tubular epithelial binucleation, karyomegaly, and cytoplasmic vacuolation; polycystic kidney disease; and renal carcinoma. Many of the renal changes are reminiscent of a condition described in Japanese (Bufo japonicus) and Chinese (Bufo raddei) toad hybrids that progresses from
 tubular epithelial atypia and tubular dilation to polycystic kidney disease to renal carcinoma. A second common finding was variably sized, randomly distributed bile duct clusters (biliary proliferation). Other noteworthy findings included regional or generalized edema, intestinal adenocarcinoma,
 aspiration pneumonia, and parasitism. This retrospective analysis is the first description of histologic lesions identified in captive L. laevis populations, providing new insight into spontaneous disease processes occurring in this species for use in disease diagnosis and clinical
 management.}, number={3}, journal={COMPARATIVE MEDICINE}, author={Womble, Mandy A. and Lewbart, Gregory A. and Shive, Heather R.}, year={2020}, month={Jun}, pages={239–247} }
 @article{houck_cohen_womble_lewbart_petritz_2019, title={Radiographic anatomy and barium sulfate contrast study of the gastrointestinal tract of eastern box turtles (Terrapene carolina carolina)}, volume={60}, ISSN={["1740-8261"]}, url={https://doi.org/10.1111/vru.12792}, DOI={10.1111/vru.12792}, abstractNote={Abstract}, number={5}, journal={VETERINARY RADIOLOGY & ULTRASOUND}, publisher={Wiley}, author={Houck, Emma L. and Cohen, Eli B. and Womble, Mandy and Lewbart, Gregory A. and Petritz, Olivia A.}, year={2019}, month={Sep}, pages={473–484} }
 @misc{womble_pickett_nascone-yoder_2016, title={Frogs as integrative models for understanding digestive organ development and evolution}, volume={51}, ISSN={["1084-9521"]}, DOI={10.1016/j.semcdb.2016.02.001}, abstractNote={The digestive system comprises numerous cells, tissues and organs that are essential for the proper assimilation of nutrients and energy. Many aspects of digestive organ function are highly conserved among vertebrates, yet the final anatomical configuration of the gut varies widely between species, especially those with different diets. Improved understanding of the complex molecular and cellular events that orchestrate digestive organ development is pertinent to many areas of biology and medicine, including the regeneration or replacement of diseased organs, the etiology of digestive organ birth defects, and the evolution of specialized features of digestive anatomy. In this review, we highlight specific examples of how investigations using Xenopus laevis frog embryos have revealed insight into the molecular and cellular dynamics of digestive organ patterning and morphogenesis that would have been difficult to obtain in other animal models. Additionally, we discuss recent studies of gut development in non-model frog species with unique feeding strategies, such as Lepidobatrachus laevis and Eleutherodactylous coqui, which are beginning to provide glimpses of the evolutionary mechanisms that may generate morphological variation in the digestive tract. The unparalleled experimental versatility of frog embryos make them excellent, integrative models for studying digestive organ development across multiple disciplines.}, journal={SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY}, author={Womble, Mandy and Pickett, Melissa and Nascone-Yoder, Nanette}, year={2016}, month={Mar}, pages={92–105} }
 @article{amin_womble_ledon-rettig_hull_dickinson_nascone-yoder_2015, title={Budgett's frog (Lepidobatrachus laevis): A new amphibian embryo for developmental biology}, volume={405}, ISSN={["1095-564X"]}, DOI={10.1016/j.ydbio.2015.06.007}, abstractNote={The large size and rapid development of amphibian embryos has facilitated ground-breaking discoveries in developmental biology. Here, we describe the embryogenesis of the Budgett's frog (Lepidobatrachus laevis), an unusual species with eggs that are over twice the diameter of laboratory Xenopus, and embryos that can tolerate higher temperatures to develop into a tadpole four times more rapidly. In addition to detailing their early development, we demonstrate that, like Xenopus, these embryos are amenable to explant culture assays and can express exogenous transcripts in a tissue-specific manner. Moreover, the steep developmental trajectory and large scale of Lepidobatrachus make it exceptionally well-suited for morphogenesis research. For example, the developing organs of the Budgett's frog are massive compared to those of most model species, and are composed of larger individual cells, thereby affording increased subcellular resolution of early vertebrate organogenesis. Furthermore, we found that complete limb regeneration, which typically requires months to achieve in most vertebrate models, occurs in a matter of days in the Budgett's tadpole, which substantially accelerates the pace of experimentation. Thus, the unusual combination of the greater size and speed of the Budgett's frog model provides inimitable advantages for developmental studies—and a novel inroad to address the mechanisms of spatiotemporal scaling during evolution.}, number={2}, journal={DEVELOPMENTAL BIOLOGY}, author={Amin, Nirav M. and Womble, Mandy and Ledon-Rettig, Cristina and Hull, Margaret and Dickinson, Amanda and Nascone-Yoder, Nanette}, year={2015}, month={Sep}, pages={291–303} }
 @article{reed_womble_dush_tull_bloom_morckel_devlin_nascone-yoder_2009, title={Morphogenesis of the Primitive Gut Tube Is Generated by Rho/ROCK/Myosin II-Mediated Endoderm Rearrangements}, volume={238}, ISSN={["1097-0177"]}, DOI={10.1002/dvdy.22157}, abstractNote={Abstract}, number={12}, journal={DEVELOPMENTAL DYNAMICS}, author={Reed, Rachel A. and Womble, Mandy A. and Dush, Michel K. and Tull, Rhesa R. and Bloom, Stephanie K. and Morckel, Allison R. and Devlin, Edward W. and Nascone-Yoder, Nanette M.}, year={2009}, month={Dec}, pages={3111–3125} }