WILLIAM E. GOTTLIEB, M.D.

FRISCO, CO

Research Active
Orthopaedic Surgery - Sports Medicine NPI registered 21+ years 15 publications 1976 – 2007 NPI: 1780680660
RNA, MessengerDNAMolecular Sequence DataSpermatozoaIn Vitro TechniquesChromosome BandingPolymorphism, Restriction Fragment LengthAcrosomeBody FluidsChromosome DeletionElectrophoresis, Polyacrylamide GelDNA ProbesChromosomes, Human, Pair 15Angelman SyndromePrader-Willi Syndrome

Practice Location

360 PEAK ONE DRIVE
FRISCO, CO 80443

Phone: (970) 668-3633

What does WILLIAM GOTTLIEB research?

Dr. Gottlieb studies several important medical areas, including the genetic underpinnings of Prader-Willi and Angelman syndromes, which are both linked to abnormalities on chromosome 15. He investigates how these conditions arise and their genetic components, helping to illuminate underlying causes that can inform better diagnosis and treatment options. Additionally, Dr. Gottlieb examines surgical techniques, such as breast augmentation and reduction, focusing on methods that minimize scarring and enhance recovery.

Key findings

  • In a study of Angelman syndrome, 85% of participants had deletions on chromosome 15 linked to the condition, indicating a strong genetic basis for diagnosis.
  • Research found that 60% of patients with Prader-Willi syndrome without clear genetic deletions displayed maternal uniparental disomy, contributing to improved diagnostic accuracy.
  • In evaluating silicone gel breast implants, it was determined that while improvements have been made for natural appearance, issues like capsular contracture can still arise.
  • His studies on the human sperm acrosome reaction indicated that after exposure to follicular fluid, 40% of sperm completed the activation process within 3 minutes, enhancing understanding of fertilization processes.
  • A crucial finding regarding medical instruments highlighted that many hospital-acquired infections stemmed from improper sterilization of equipment, underscoring the need for stringent safety practices.

Frequently asked questions

Does Dr. Gottlieb study Prader-Willi syndrome?
Yes, he conducts research on the genetic causes and implications of Prader-Willi syndrome.
What treatments has Dr. Gottlieb researched?
He has researched silicone gel implants for breast augmentation and various techniques for breast surgery.
Is Dr. Gottlieb's work relevant to patients with Angelman syndrome?
Absolutely, his research focuses on the genetic aspects of Angelman syndrome, aiding in understanding and diagnosis.
What are the complications of vertical mammaplasty?
Dr. Gottlieb's study indicates that while vertical mammaplasty can yield great results, it requires practice to master and can lead to complications.
How does Dr. Gottlieb's work help patients undergoing fertility treatments?
His research on the sperm acrosome reaction provides insights that can improve reproductive techniques and fertility outcomes.

Publications in plain English

Silicone gel implants in breast augmentation and reconstruction.

2007

Annals of plastic surgery

Gampper TJ, Khoury H, Gottlieb W, Morgan RF

Plain English
This research focused on silicone gel implants used for breast augmentation and reconstruction. The study found that while silicone gel implants have been improved over the years to look and feel more natural, issues like capsular contracture can still occur, causing discomfort and distortion. Despite concerns leading to restrictions on their use in the U.S., these implants are still available in clinical trials and are widely used in other countries. Who this helps: This benefits patients seeking breast enhancement or reconstruction options.

PubMed

Chromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints.

1999

American journal of human genetics

Amos-Landgraf JM, Ji Y, Gottlieb W, Depinet T, Wandstrat AE +5 more

Plain English
This study looked at the genetic changes that cause Prader-Willi syndrome (PWS) and Angelman syndrome (AS), two disorders linked to a deletion on chromosome 15. Researchers found that sequences of DNA, called END repeats, near the breakpoints of chromosome 15 are involved in these deletions. Specifically, in the cases they analyzed, 1 in 5 patients had a specific alteration in a gene related to these deletions, suggesting that active DNA sequences in reproductive cells might increase the likelihood of these genetic changes happening. Who this helps: This helps patients with Prader-Willi and Angelman syndromes by providing insights into the underlying causes of their conditions.

PubMed

Vertical mammaplasty: technique and complications.

1998

Surgical technology international

Restifo RJ, Gottlieb W, Ward BA, Lalikos JF

Plain English
This study focuses on a surgical technique called vertical mammaplasty, which aims to reduce scarring when performing breast surgery. The researchers found that while this method can provide very good results, it requires significant practice to master, and some complications can occur during the procedure. Understanding these details is important for improving patient safety and the overall success of the surgery. Who this helps: This helps patients seeking breast surgery with less visible scarring.

PubMed

A common insertion/deletion polymorphism in the Prader-Willi syndrome minimal critical region.

1994

Human molecular genetics

Gabriel J, Gottlieb W, Garcia A, Rogan PK, Saitoh S +1 more

PubMed

Evaluation of potential models for imprinted and nonimprinted components of human chromosome 15q11-q13 syndromes by fine-structure homology mapping in the mouse.

1993

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

Nicholls RD, Gottlieb W, Russell LB, Davda M, Horsthemke B +1 more

Plain English
This study explored genetic regions linked to Prader-Willi and Angelman syndromes, which are disorders impacting behavior and development, by examining a similar region in mice. Researchers identified four key genetic areas on mouse chromosome 7 that are involved in these syndromes, with specific focus on the Gabrb3 gene, which plays a role in the brain's function. They found that this gene is expressed equally from both parental chromosomes and does not have the same genetic imprinting seen in humans, suggesting that animal models can help investigate these conditions in more detail. Who this helps: This research benefits scientists and doctors working on genetic disorders, particularly those related to Prader-Willi and Angelman syndromes.

PubMed

Cytogenetic and molecular analysis in Angelman syndrome.

1993

American journal of medical genetics

Zackowski JL, Nicholls RD, Gray BA, Bent-Williams A, Gottlieb W +5 more

Plain English
This study examined 29 individuals with Angelman syndrome, focusing on their genetic makeup to understand the causes of the condition. The researchers found that 85% of the participants had deletions on a specific part of chromosome 15 that is linked to Angelman syndrome, with the deletions typically inherited from their mothers. The results are important because they provide clear genetic evidence that can help in diagnosing and understanding the condition better. Who this helps: This helps patients and their families, as well as doctors who work with Angelman syndrome.

PubMed

The frequency of uniparental disomy in Prader-Willi syndrome. Implications for molecular diagnosis.

1992

The New England journal of medicine

Mascari MJ, Gottlieb W, Rogan PK, Butler MG, Waller DA +4 more

Plain English
This study looked at the genetic causes of Prader-Willi syndrome, a condition that can be hard to diagnose in young children. Researchers found that 60% of the 30 patients without noticeable genetic deletions had a specific type of inheritance called maternal uniparental disomy, where they inherited two copies of chromosome 15 from their mother. Understanding these genetic causes is important because it helps in diagnosing this syndrome accurately, which can assist in planning better care for patients. Who this helps: This helps patients with Prader-Willi syndrome and their families by providing accurate diagnoses and tailored treatment plans.

PubMed

Paternal uniparental disomy of chromosome 15 in a child with Angelman syndrome.

1992

Annals of neurology

Nicholls RD, Pai GS, Gottlieb W, Cantú ES

Plain English
This study looked at a child with Angelman syndrome to see if they had a rare genetic inheritance pattern where both copies of chromosome 15 were inherited from their father. The researchers found that this child had paternal uniparental disomy for chromosome 15, which is unusual, as it is rarely seen in Angelman syndrome cases. Their findings help clarify the genetics behind Angelman syndrome and how it differs from Prader-Willi syndrome. Who this helps: This helps doctors and researchers understand the genetic causes of Angelman syndrome, improving diagnosis and care for affected patients.

PubMed

The Mr 115 kd fiber cell-specific protein is a component of the lens cytoskeleton.

1989

Current eye research

FitzGerald PG, Gottlieb W

Plain English
This study focused on a specific protein found in lens fiber cells of the eye, known as the Mr 115 kd protein. Researchers used advanced imaging techniques to identify that this protein is part of the lens cell's internal structure, called the cytoskeleton, which helps maintain the shape and function of these cells. Understanding this protein's role is important because it could provide insights into how lens cells work and lead to better treatments for vision problems. Who this helps: This helps patients with vision issues, particularly those related to the lens of the eye.

PubMed

Ultrastructural studies of the early events of the human sperm acrosome reaction as initiated by human follicular fluid.

1988

Gamete research

Yudin AI, Gottlieb W, Meizel S

Plain English
This study looked at how human sperm start the acrosome reaction (AR), which is critical for fertilization, after being exposed to fluid from human ovarian follicles. Researchers found that within just 5 seconds, 2% of sperm began the AR, and after 180 seconds, 40% had completed the process. Understanding these early stages of sperm activation can help improve reproductive techniques and fertility treatments. Who this helps: This research benefits patients undergoing fertility treatments.

PubMed

Partial characterization of a fraction from human follicular fluid that initiates the human sperm acrosome reaction in vitro.

1988

Gamete research

Siiteri JE, Gottlieb W, Meizel S

Plain English
The study examined a specific component from human follicular fluid, which has been found to trigger the sperm acrosome reaction, an essential process for fertilization, in lab conditions. Researchers identified that this component has a molecular weight of approximately 50,000 and that its activity peaks just five minutes after being introduced to sperm. They discovered that this activity might involve both a larger factor and a smaller one that can be released through enzymatic treatment, suggesting it could be linked to particular carbohydrates on proteins. Who this helps: This research benefits fertility specialists and patients undergoing fertility treatments.

PubMed

Biochemical studies of metalloendoprotease activity in the spermatozoa of three mammalian species.

1987

Journal of andrology

Gottlieb W, Meizel S

Plain English
This study looked at the activity of specific enzymes called metalloendoproteases in sperm from pigs, humans, and hamsters. Researchers found that all three types of sperm tested showed this enzyme activity, with hamster sperm having a different reaction than the others. Specifically, the optimal enzyme activity level was found to be at a pH of 6.2 for intact sperm and 7.0 for hamster cytoplasmic droplets. Who this helps: This research helps reproductive scientists and fertility specialists understand the biochemical processes in sperm that may affect fertility treatments.

PubMed

Nocturnal doses of ranitidine and nizatidine do not affect the disposition of diazepam.

1987

Journal of clinical pharmacology

Klotz U, Gottlieb W, Keohane PP, Dammann HG

Plain English
This study looked at how the medications ranitidine and nizatidine affect the way the body processes diazepam, a drug often used to treat anxiety. Researchers found that taking either ranitidine or nizatidine at night did not change how long diazepam stayed in the body or how quickly it was cleared out, with diazepam's half-life remaining around 35 hours on average. This is important because it shows that these common medications can be safely used together without affecting the efficacy of diazepam. Who this helps: This research benefits patients who use diazepam and also take ranitidine or nizatidine for other conditions.

PubMed

Medical instrumentation and nosocomial infection.

1979

Journal of clinical engineering

Ben-Zvi S, Gottlieb W

Plain English
This study looked at how improper cleaning and use of medical equipment can lead to infections acquired in hospitals. It found that many of these infections can occur due to poorly sterilized instruments, highlighting the need for clinical engineers to train hospital staff on proper sterilization and usage techniques. This is important because reducing these infections can improve patient safety and outcomes. Who this helps: This helps patients in hospitals by reducing their risk of infections.

PubMed

The hospital instrumentation department: delivering clinical engineering services to the hospital community.

1976

Journal of clinical engineering

Ben-Zvi S, Gottlieb W

PubMed

Frequent Co-Authors

R D Nicholls P K Rogan S Meizel D J Driscoll S Ben-Zvi Thomas J Gampper Habib Khoury Raymond F Morgan J M Amos-Landgraf Y Ji

Physician data sourced from the NPPES NPI Registry . Publication data from PubMed . Plain-English summaries generated by AI. Not medical advice.